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	<title>Yourlawyer.com (Risperdal News)</title>
	<link>http://www.yourlawyer.com/topics/overview/risperdal</link>
	<description></description>
	<pubDate>Sat, 21 Nov 2009 03:05:48 -0800</pubDate>

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		<title>Atypical Antipsychotics Linked to Worrisome Weight Gains, Other Outcomes, in Children</title>
		<link>http://www.yourlawyer.com/articles/read/17191</link>		
		<pubDate>Wed, 28 Oct 2009 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/17191</guid>
		<description><![CDATA[Yet another study has linked significant weight gains in children to some antipsychotic medication. Forbes reported that an emerging study found that weight gains of 10-to-20 pounds were not unusual in children during their first three months on the medications like Zyprexa, Seroquel, Risperdal and Abilify. Also, cholesterol, triglyceride, and other metabolic &ldquo;parameters&rdquo; were elevated, said Forbes.It has long been known and we have...]]></description>
			<content:encoded><![CDATA[Yet another study has linked significant weight gains in children to some antipsychotic medication. Forbes reported that an emerging study found that weight gains of 10-to-20 pounds were not unusual in children during their first three months on the medications like <a href="http://www.yourlawyer.com/topics/overview/zyprexa">Zyprexa</a>, <a href="http://www.yourlawyer.com/topics/overview/Seroquel-And-Cardiac-Death">Seroquel</a>, <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> and <a href="http://www.yourlawyer.com/topics/overview/abilify">Abilify</a>. Also, cholesterol, triglyceride, and other metabolic &ldquo;parameters&rdquo; were elevated, said Forbes.<br /><br />It has long been known and we have long written about the association between weight gain and antipsychotics; however, this new study points to even deeper increases, said Forbes. Tracking 272 children, aged four to 19 ,who were initially prescribed popular antipsychotic medications between 2001 and 2007, the researchers discovered that while increases in weight were dependent on the drug, the gains appeared in the entire spectrum of atypical antipsychotic medications, reported Forbes. The study was conducted at the Zucker Hillside Hospital in Queens, New York and the findings are being published in the Journal of the American Medical Association, said Forbes.<br /><br />&quot;Weight gain was pervasive even in medications usually considered to be weight neutral in adults,&quot; said study lead Christoph Correll, an Albert Einstein College of Medicine psychiatrist, quoted Forbes. &quot;The worry is that weight gain sustained over long periods of time can cause adverse outcomes like diabetes and heart attacks and strokes,&quot; Correll added.<br /><br />According to the research, children on Eli Lilly&rsquo;s Zyprexa gained 19 pounds in three months; children taking AstraZeneca&rsquo;s Seroquel, Johnson &amp; Johnson&rsquo;s Risperdal, and Bristol-Myers Squibb&rsquo;s Abilify gained 10 to 13 pounds in the same time frame, said Forbes. Meanwhile, Seroquel and Zyprexa were linked to &ldquo;statistically significant&rdquo; cholesterol level increases and Seroquel, Zyprexa, and Risperdal were found to increase triglyceride levels, added Forbes, which explained that triglycerides are fatty particles in the blood. <br /><br />&quot;It is an enormous amount of weight,&quot; said Christopher Varley a child psychiatrist with the University of Washington School of Medicine, quoted Forbes. &quot;It might be a time bomb about to go off, I don't think we know the answer,&quot; Varley added, saying that once children take these medications, &quot;there is just a strong physiologic drive to eat more that is irresistible.&quot; Varley wrote an accompanying editorial to the study.<br /><br />A serious issue with the findings is that children are being prescribed these powerful medications for diagnoses that are not psychotic in nature, such as aggression, sleep problems, and attention deficit disorder (ADD), noted Forbes. Experts feel these children would benefit from milder drugs and counseling. Another issue is a diagnosis that is growing in popularity. Pediatric bipolar disorder can be treated with atypical antipsychotics; however, diagnosis criteria is considered weak, reported Forbes.<br /><br /><br />]]></content:encoded>
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		<title>Risperdal Said to be Responsible for Breast Growth in Boys</title>
		<link>http://www.yourlawyer.com/articles/read/16680</link>		
		<pubDate>Thu, 25 Jun 2009 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/16680</guid>
		<description><![CDATA[Risperdal has been linked to breast growth, and even lactation, in boys&nbsp; under 18 who take the powerful antipsychotic drug. The condition is known as gynecomastia (male breast growth), and is usually permanent.&nbsp; In most cases, boys with Risperdal-associated gynecomastia must undergo breast reduction surgery, and even mastectomy, to correct the condition.Risperdal was originally approved by the Food &amp; Drug Administration (FDA) in...]]></description>
			<content:encoded><![CDATA[<a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> has been linked to breast growth, and even lactation, in boys&nbsp; under 18 who take the powerful antipsychotic drug. The condition is known as gynecomastia (male breast growth), and is usually permanent.&nbsp; In most cases, boys with Risperdal-associated gynecomastia must undergo breast reduction surgery, and even mastectomy, to correct the condition.<br /><br />Risperdal was originally approved by the <a href="http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.Overview&amp;DrugName=RISPERDAL">Food &amp; Drug Administration</a> (FDA) in 1993 to treat schizophrenia in adults.&nbsp; Later, its approved uses were expanded to include bipolar disorder I in adults, as well as irritability associated with autistic disorders in children from 5 to 16 years of age.&nbsp; Then in August 2007, Risperdal was approved for treatment of schizophrenia in adolescents aged from 13 to 17, as well as the&nbsp; short term treatment of manic or mixed episodes of bipolar I disorder in children aged between 10 and 17.&nbsp; It is not approved as a treatment for Attention Deficit Disorder (ADHD) though it is often prescribed off-label to treat children with the condition.<br /><br />Risperdal causes a release of prolactin from the pituitary gland.&nbsp; Prolactin is a hormone that stimulates breast development and lactation.&nbsp; Recently, a report aired on CBS News that discussed the problem of gynecomastia in boys taking Risperdal.&nbsp; The boys highlighted in the CBS News report were often being given Risperdal off-label to treat&nbsp; ADHD.<br /><br />One child cited&nbsp; by CBS, only age four, began developing a breast on one side of his body after he began taking Risperdal.&nbsp; At that young age, his breast had even begun producing milk.&nbsp; The child has undergone mastectomies to correct the problem.<br /><br />Another boy, now 19, who began developing breasts as a result of Risperdal when he was 14, still&nbsp; suffers psychological affects even though he underwent a double mastectomy.<br /><br />It is not clear how often boys taking Risperdal suffer from male breast growth. According to CBS, the drug's maker, Janssen, found that in a clinical trial it conducted involving fewer than 2,000 children, 43 developed the abnormal breasts. &nbsp;<br /><br />In 2008, Duke University psychiatrist P. Murali Doraiswamy told The Wall Street Journal that Risperdal had the strongest link with gynecomastia in children and adolescents of any of the newer antipsychotic drugs&ndash;accounting for 70% of the cases analyzed. He has also found that some girls taking Risperdal begin to lactate before they reach puberty.&nbsp; In 2006, Doraiswamy&nbsp; co-authored of a study on antipsychotics and prolactin with FDA scientist.&nbsp; He told the Journal that the changes in hormones linked to Risperdal could not be considered harmless.<br /><br />The surgery - usually a mastectomy - boys undergo to correct gynecomastia is painful.&nbsp; And the psychological problems suffered by many of these Risperdal victims can be even more difficult.&nbsp; That is why many families of these boys have chosen to file&nbsp; lawsuits against Janssen.&nbsp; According to CBS News, such lawsuits claim Janssen marketed Risperdal for unapproved uses in children, and downplayed serious side effects.&nbsp;&nbsp; These lawsuits point out that&nbsp; breast growth wasn't even mentioned under the &quot;Warnings&quot; section of the Risperdal label, but was only listed under &quot;Precautions.&quot;&nbsp;&nbsp; They also allege that the language regarding gynecomastia in the Risperdal label was worded in &quot;obscure&quot; terms.<br /><br />]]></content:encoded>
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		<title>Risperdal Researcher Promised Drug Maker Positive Results from Clinical Trials</title>
		<link>http://www.yourlawyer.com/articles/read/16270</link>		
		<pubDate>Fri, 20 Mar 2009 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/16270</guid>
		<description><![CDATA[A prominent Harvard psychiatrist promised positive results to Johnson &amp; Johnson before the start of some clinical trials for Risperdal.&nbsp; According to The Wall Street Journal, the revelations regarding Dr. Joseph Biederman came to light in court documents that are part of&nbsp; a lawsuit involving Risperdal and other atypical antipsychotic drugs.&nbsp; While he is not a defendant in the case, Biederman was called as a witness to...]]></description>
			<content:encoded><![CDATA[A prominent Harvard psychiatrist promised positive results to Johnson &amp; Johnson before the start of some clinical trials for <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a>.&nbsp; According to The Wall Street Journal, the revelations regarding Dr. Joseph Biederman came to light in court documents that are part of&nbsp; a lawsuit involving Risperdal and other atypical antipsychotic drugs.&nbsp; While he is not a defendant in the case, Biederman was called as a witness to illustrate the questionable financial ties between drug makers and the research community.<br /><br />Some of the 2,000&nbsp; plaintiffs involved in the multi-state lawsuit are children.&nbsp; Risperdal wasn&rsquo;t approved for use in children until 2007. However, it is known that doctors prescribed the drug off-label for thousands of children years before that.&nbsp; While off-label prescribing is legal, drug companies are legally barred from marketing off-label uses.&nbsp; But according to The Boston Globe, the companies often skirt that prohibition by paying&nbsp; respected &ldquo;opinion leaders&rdquo; - usually top experts in their field - to discuss their off-label prescribing experiences at &ldquo;educational&rdquo; talks or meetings.<br /><br />As we reported last November, Biederman was one of those opinion leaders.&nbsp; Biederman has long advocated the use of atypical antipsychotics, like Risperdal, to treat children diagnosed with bipolar disorder.&nbsp; The lawsuit has raised questions about Biederman&rsquo;s role in convincing Johnson &amp; Johnson&rsquo;s to fund a center on pediatric bipolar disorder at Harvard's Massachusetts General Hospital.<br /><br />According to a Boston Globe article published at the time, emails written between executives at Johnson &amp; Johnson subsidiary Janssen Pharmaceuticals indicate Biederman&nbsp; had repeatedly proposed that the company&nbsp; help fund the center.&nbsp; One of the emails, written in 2002, stated that &ldquo;the rationale of this center is to generate and disseminate data supporting the use of risperidone (Risperdal) in this patient population.&rdquo;&nbsp; Another email mentions at least $700,000 in Johnson &amp; Johnson payments to the center, the Globe said.<br /><br />Biederman&rsquo;s dealings with drug companies have been questioned before.&nbsp; According to The Wall Street Journal,&nbsp; an investigation by<a href="http://grassley.senate.gov"> Sen. Charles Grassley</a> (R-Iowa)&nbsp; found that&nbsp; from 2000 through 2007, Biederman received $1.6 million from Johnson &amp; Johnson.&nbsp; However, only a fraction of that was reported to Harvard. Earlier this year, Biederman agreed to step down from a number of industry-funded clinical trials until Massachusetts General Hospital investigates that lack of disclosure.<br /><br />Now The Wall Street Journal is reporting that a Powerpoint presentation given by Biederman to Johnson &amp; Johnson executives included a slide that said a future clinical trial&nbsp; aimed at evaluating the use of Risperdal in preschool children &ldquo;will support the safety and effectiveness of risperidone (Risperdal) in this age group.&quot;<br /><br />Another slide that addressed a Risperdal trial meant to compare the drug to others in treating pediatric bipolar disorder promised the study would &quot;clarify the competitive advantages of risperidone vs. other neuroleptics,&quot; the Journal said.<br /><br />Meanwhile, the Boston Globe reported today that Biederman is trying to have his own testimony in the antipsychotic lawsuit&nbsp; sealed.&nbsp; According report, Biederman's lawyers have argued that making his testimony public &ldquo;could be immensely damaging to him, both personally and professionally.&quot;<br /><br />]]></content:encoded>
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		<title>Misleading  Risperdal, Duragesic Patch Claims Prompt Fines in West Virginia Lawsuit</title>
		<link>http://www.yourlawyer.com/articles/read/16171</link>		
		<pubDate>Wed, 04 Mar 2009 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/16171</guid>
		<description><![CDATA[Risperdal maker Johnson &amp; Johnson has been ordered by a West Virginia judge to pay a hefty fine over a 2003 letter to doctors that obfuscated the antipsychotic drug's diabetes risk. According to Bloomberg News, the same judge also assessed a smaller fine after finding that doctors were misled about the risks and benefits of the company's Duragesic pain patch.Risperdal is one of class of drugs called atypical antipsychotics.&nbsp; Other...]]></description>
			<content:encoded><![CDATA[<a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> maker Johnson &amp; Johnson has been ordered by a West Virginia judge to pay a hefty fine over a 2003 letter to doctors that obfuscated the antipsychotic drug's diabetes risk. According to Bloomberg News, the same judge also assessed a smaller fine after finding that doctors were misled about the risks and benefits of the company's <a href="http://www.yourlawyer.com/topics/overview/duragesic_patch">Duragesic pain patch</a>.<br /><br />Risperdal is one of class of drugs called atypical antipsychotics.&nbsp; Other atypical antipsychotics include Eli Lilly's Zyprexa, and AstraZeneca's Seroquel.&nbsp; These drugs have long been linked to an increased risk of weight gain and diabetes. According to Bloomberg News, in 2003, the <a href="http://www.fda.gov/">Food &amp; Drug Administration</a> (FDA) required the makers of antipsychotics to warn about this risk.<br /><br />The State of West Virginia had brought suit against Johnson &amp; Johnson and its Janssen unit over claims made in the 2003 letter to doctors, Bloomberg News said.&nbsp;&nbsp; The FDA had already cited the same letter for being misleading. West Virginia Circuit Court Judge Martin Gaughan agreed, writing that the letter was &quot;deliberately constructed to circumvent the FDA's mandated warning for an increased risk of diabetes, and deliberately constructed to mislead health-care professionals.&quot;<br /><br />According to Bloomberg News, the judge fined Johnson &amp; Johnson $1.95 million for the letter and an additional $2 million for Risperdal sales calls made in West Virginia from November 2003 to July 2004.<br /><br />The makers of antipsychotics have faced increasing scrutiny over the way these drugs are marketed.&nbsp; Hundreds of lawsuits have been filed by individuals who claim the drug's diabetes risks were hidden.&nbsp; Meanwhile, federal and state authorities have, like West Virginia,&nbsp; filed lawsuits over the drugs' illegal promotion.<br /><br />Earlier this year, Eli Lilly agreed to pay $1.4 billion in fines to settle federal charges over its promotion of&nbsp; Zyprexa.&nbsp; Documents unsealed in Seroquel litigation indicate that, among other things, AstraZeneca directed sales reps to downplay the drug's diabetes risks.<br /><br />In West Virginia, Judge Gaughan also assessed&nbsp;&nbsp; Johnson &amp; Johnson and Janssen a $525,000 fine for distributing a brochure that contained misleading information about the&nbsp; Duragesic patch.&nbsp; According to a report on WOWKTV.com, the FDA had also warned the companies that the brochure was misleading. &nbsp;<br /><br />In his order, Judge Gaughan wrote that &quot;The defendants were twice put on notice by previous [FDA] warning letters that its promotional materials for Duragesic contained false or misleading statements; however . . . the defendants then willfully sent the false or misleading Duragesic [brochure] to West Virginia health care providers to make its medication Duragesic more appealing for sale.&rdquo;&nbsp; &nbsp;<br /><br />Fentanyl patches, like the Duragesic Patch, have long been linked to accidental overdoses.&nbsp; In December 2007, FDA issued an alert, warning patients and doctors that there was a high danger of accidental overdose associated with the use of fentanyl patches, including the&nbsp; Duragesic Pain Patch. At the time, the FDA attributed the overdoses to patch &ldquo;misuse&rdquo; and ordered all fentanyl patch makers to create special &ldquo;medication guides&rdquo; for patients that spell out the dangers of overdoses and improper use in easy-to-understand language.<br /><br />]]></content:encoded>
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		<title>Atypical Antipsychotic Drugs Double Heart Risks</title>
		<link>http://www.yourlawyer.com/articles/read/15863</link>		
		<pubDate>Thu, 15 Jan 2009 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15863</guid>
		<description><![CDATA[Atypical antipsychotic drugs, including Seroquel, Zyprexa and Risperdal, double the risk of heart failure and death, according to a new study published in The New England Journal of Medicine.&nbsp; According to Reuters.com, the new study raises questions about claims that atypical antipsychotics are safer than older generation antipsychotics.Atypical antipsychotics, among the best-selling in the world, are used to treat schizophrenia and other...]]></description>
			<content:encoded><![CDATA[Atypical antipsychotic drugs, including <a href="http://www.yourlawyer.com/topics/overview/seroquel">Seroquel</a>, Zyprexa and <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a>, double the risk of heart failure and death, according to a new study published in The New England Journal of Medicine.&nbsp; According to Reuters.com, the new study raises questions about claims that atypical antipsychotics are safer than older generation antipsychotics.<br /><br />Atypical antipsychotics, among the best-selling in the world, are used to treat schizophrenia and other mental problems.&nbsp; But according to Reuters, they are also widely used off-label to treat dementia and childhood hyperactivity.&nbsp; Many experts and patient advocates have called for a halt to such practices, and this study will likely add ammunition to their arguments.<br /><br />For this latest&nbsp; study, researchers at the University of Vanderbilt studied nearly 277,000 people in Tennessee. About 46,000 were taking atypical antipsychotic drugs and 44,000 were taking typical antipsychotic drugs. About 187,000 weren't taking any of the drugs. Patients ranged in age from 30 to 74 years; the average age was about 46.<br /><br />The study found that those&nbsp; taking the highest dose of the new antipsychotics had the greatest risk of heart failure and death, Reuters said.&nbsp; The danger faded once they stopped taking the drugs. The risk spanned all age groups, including younger people. &nbsp;<br /><br />The drugs studied in this group included clozapine, made generically, Johnson &amp; Johnson's Risperdal,&nbsp; Zyprexa, and Seroquel, made by AstraZeneca, Reuters said. The &quot;typical&quot; drugs used for comparison were haloperidol and thioridazine, both generics.<br /><br />According to The Wall Street Journal, an editorial accompanying the study said the use of such drugs should be &quot;reduced sharply&quot; among children and elderly patients<br /><br />Last week, we reported that another study conducted by scientists at the Wolfson Centre for Age-Related Diseases at King&rsquo;s College London found that use of antipsychotic drugs to treat Alzheimer's disease patients doubled their chance of dying.&nbsp; While they are not approved for that use, antipsychotics are used in dementia patients, including those with Alzheimer's to control dementia.&nbsp; Researchers conducting the British study concluded that the risks of the drugs in these patients outweighed any potential benefits. &nbsp;<br /><br />According to Reuters, in June the U.S. Food and Drug Administration (FDA) said older, conventional antipsychotic medications should carry a warning on the packaging about the risk of death. The FDA issued a similar warning in 2005 for newer antipsychotics.<br /><br />]]></content:encoded>
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		<title>Alzheimer's Patients on Risperdal, Thorazine, Other Anti-Psychotic Drugs, More Likely to Die</title>
		<link>http://www.yourlawyer.com/articles/read/15819</link>		
		<pubDate>Fri, 09 Jan 2009 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15819</guid>
		<description><![CDATA[Using anti-psychotic drugs, such as Risperdal and Thorazine, to treat Alzheimer's disease patients isn't worth the increased risk of death, a new study concludes.&nbsp; Such drugs are often used to stem aggression sometimes exhibited by Alzheimer's patients, but the new study conducted by British researchers found these medications could also double patients' chance of dying.The research, conducted by scientists at the Wolfson Centre for...]]></description>
			<content:encoded><![CDATA[Using anti-psychotic drugs, such as <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> and Thorazine, to treat Alzheimer's disease patients isn't worth the increased risk of death, a new study concludes.&nbsp; Such drugs are often used to stem aggression sometimes exhibited by Alzheimer's patients, but the new study conducted by British researchers found these medications could also double patients' chance of dying.<br /><br />The research, conducted by scientists at the Wolfson Centre for Age-Related Diseases at King's College London, was published in today's issue of the journal <a href="http://www.thelancet.com/journals/laneur/article/PIIS1474-4422(08)70295-3/fulltext">Lancet</a>.&nbsp; For the study, the researchers followed 165 British patients aged 67 to 100 years with moderate to severe Alzheimer's disease from 2001 to 2004. Half were being treated with anti-psychotic drugs, including&nbsp; Risperdal, Thorazine and Stelazine. The other half got placebos. <br /><br />After a year, 39 patients of the 83 receiving anti-psychotic drugs had died.&nbsp; Of the 82 taking placebos, 27 were dead after a year. Only 46 percent of those taking anti-psychotic were still alive after two years, while 71 percent remained alive in the placebo group.&nbsp; After three years, the numbers of those living in the drug group dropped to 30 percent, while 59 percent of those in the placebo group were still living.&nbsp; <br /><br />This is just the latest study to show a correlation between anti-psychotic drugs and a higher death rate in Alzheimer's patients.&nbsp; According to a report in the Associated Press, no one knows exactly why this association exists, but some surmise that they could be damaging to the brain.&nbsp; Another theory is that their sedative effects make patients less mobile, which can make them more vulnerable to infection, the Associated Press said.<br /><br />According to the Associated Press, anti-psychotic drugs are routinely given to up to 60 percent of dementia patients living in nursing homes.&nbsp; They are used to control aggression, as well as the hallucinations they sometimes experience.&nbsp; But guidelines recommend that such medications be used &quot;cautiously and temporarily&quot;, the Associated Press said. In addition to the increased risk of death, anti-psychotic drugs are linked to other side effects, including respiratory problems, stroke and diabetes.<br /><br />Clive Ballard, lead author of the Lancet article, told the Associated Press that the risks associated with anti-psychotic drugs are not worth the benefits.&nbsp; &quot;Would I want to take a drug that slightly reduced my aggression but doubled my risk of dying? I'm not sure I would,&quot; Ballard said.<br /><br />]]></content:encoded>
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		<title>Doctor Agrees to Cut Drug Firm Ties</title>
		<link>http://www.yourlawyer.com/articles/read/15788</link>		
		<pubDate>Mon, 05 Jan 2009 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15788</guid>
		<description><![CDATA[Dr. Joseph Biederman is the latest doctor whose activities with big pharmaceutical are under review.&nbsp; According to the Boston Globe&rsquo;s Boston.com, Biederman, a well-known child psychiatrist who has advocated the use of antipsychotics to treat bipolar disorder in children, will be suspending his financial relationships with pharmaceutical companies until such time that an agreement with Massachusetts General Hospital...]]></description>
			<content:encoded><![CDATA[<p>Dr. Joseph Biederman is the latest doctor whose activities with big pharmaceutical are under review.&nbsp; According to the Boston Globe&rsquo;s Boston.com, Biederman, a well-known child psychiatrist who has advocated the use of antipsychotics to treat bipolar disorder in children, will be suspending his financial relationships with pharmaceutical companies until such time that an agreement with Massachusetts General Hospital &mdash;Biederman&rsquo;s employer&mdash;can be reached. &nbsp;</p><p>Biederman is well known as being one of this country&rsquo;s strongest proponents of diagnosing pediatric bipolar disorder noted the Boston Globe. As we&rsquo;ve reported previously, Biederman has long advocated the use of atypical antipsychotics, like <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a>, to treat children diagnosed with bipolar disorder. According to a report in the WSJ in November,&nbsp; Biederman and colleagues published many favorable Risperdal studies while he was receiving payments from the drugs maker, Johnson &amp; Johnson.&nbsp; </p><p>Charles E. Grassley&mdash;Republican-Iowa&mdash;accused Beiderman of not disclosing over $1 million received from drug makers and a congressional investigation was initiated by Grassley this summer; Harvard Medical School is investigating the allegations said the Boston Globe.&nbsp; <br /></p><p>Massachussetts General's&nbsp; agreement with Beiderman says, in part, that he will &quot;not participate in any outside activities that are paid for or sponsored by industry, such as consulting activities and speaking engagements,&quot; reported the Boston Globe, which also noted Biederman is to cease any involvement with industry-funded activities within the hospital.&nbsp; These activities include research, the Boston Globe pointed out.<br /><br />The Boston Globe also reported that a hospital spokeswomen said Beiderman has stepped down from a number of industry-funded clinical trials, although the doctor continues to see patients.&nbsp; Spokewoman Peggy Slasman would not provide information on the studies, said the Wall Street Journal (WSJ), but did confirm studies would continue, but without Beiderman leading them.&nbsp; The hospital agreement will remain in place until reviews of Beiderman&rsquo;s relationships&mdash;including if he completely disclosed drug industry funding&mdash;with drug companies are completed said the Boston Globe. <br /><br />Meanwhile, scandals involving undisclosed drug money for research and promotion are a growing trend among medical researchers.&nbsp; Fierce Healthcare noted that Emory University stripped the chairmanship from one of its psychiatric researchers when an investigation revealed he had not reported industry-sourced income.&nbsp; Prominent researcher Charles Nemeroff agreed to step down as chair of Emory&rsquo; Department of Psychiatry and Behavioral Sciences following an internal investigation into his financial ties to drug makers.&nbsp; It seemed, said the WSJ, Nemeroff failed to report to Emory over $800,000 he received from GlaxoSmithKline for over 250 speaking engagements from January 2000 to January 2006.&nbsp; According to the Atlanta Constitution-Journal, Emory&rsquo;s investigation found Nemeroff also received income from other drug makers.<br /><br />Also, David Sinclair, a professor at Harvard Medical School who sat on the scientific advisory board of supplement maker Shaklee Corporation where he helped promote a product that claimed to possess life-extending properties has stepped down.&nbsp; Sinclair left his seat after the WSJ raised questions about his support of Shaklee&rsquo;s Vivix Cellular Anti-Aging Tonic.&nbsp; It seems, said the WSJ, that Sinclair touted Vivix&mdash;with resveratrol&mdash;for six months; that he told Shaklee salespeople at a summer conference, that &ldquo;over a year ago, we set out together to do this, to make a product that you could actually activate these genetic pathways that can slow down aging&rdquo;; and that he appeared on the radio with Shaklee&rsquo;s chief doctor promoting Vivix.&nbsp; Sinclair continues as co-chief adviser to Sirtris Pharmaceuticals, a division Glaxo, which is studying resveratrol for use as a drug. Sinclair received over $8 million when Glaxo acquired Sirtris; the company pays him $297,000 annually as a consultant, said the WSJ.<br /><br /></p>]]></content:encoded>
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		<title>Risperdal Promotion Questioned in Lawsuit</title>
		<link>http://www.yourlawyer.com/articles/read/15570</link>		
		<pubDate>Tue, 25 Nov 2008 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15570</guid>
		<description><![CDATA[A prominent Harvard psychiatrist may have&nbsp; promised that his work at a psychiatric research institute would promote the off-label pediatric use of Risperdal in a bid to convince Johnson &amp; Johnson to fund the facility, The Boston Globe reported today.&nbsp; The revelations come from emails and other documents released in a lawsuit involving Risperdal and other atypical antipsychotics. &nbsp;Risperdal wasn't approved for use in children...]]></description>
			<content:encoded><![CDATA[A prominent Harvard psychiatrist may have&nbsp; promised that his work at a psychiatric research institute would promote the off-label pediatric use of <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> in a bid to convince Johnson &amp; Johnson to fund the facility, The Boston Globe reported today.&nbsp; The revelations come from emails and other documents released in a lawsuit involving Risperdal and other atypical antipsychotics. &nbsp;<br /><br />Risperdal wasn't approved for use in children until 2007. However, it is known that doctors prescribed the drug off-label for thousands of children years before that.&nbsp; While off-label prescribing is legal, drug companies are legally barred from marketing off-label uses.&nbsp; But according to The Boston Globe, the companies often skirt that prohibition by paying&nbsp; respected &quot;opinion leaders&quot; - usually top experts in their field - to discuss their off-label prescribing experiences at &quot;educational&quot; talks or meetings.<br /><br />According to the Boston Globe, Harvard psychiatrist Dr. Joseph Biederman -one of the country's top experts on bipolar disorder in children - is one of those &quot;opinion leaders&quot;.&nbsp;&nbsp; As we've reported previously, Biederman has long advocated the use of atypical antipsychotics, like Risperdal, to treat children diagnosed with bipolar disorder.<br /><br />Biederman's dealings with drug companies have been questioned before.&nbsp; According to The Wall Street Journal,&nbsp; an investigation by <a href="http://grassley.senate.gov/">Sen. Charles Grassley</a> (R-Iowa)&nbsp; found that&nbsp; from 2000 through 2007, Biederman received $1.6 million from Johnson &amp; Johnson.&nbsp; However, only a fraction of that was reported to Harvard. &nbsp;<br /><br />According to the Journal,&nbsp; Biederman and colleagues published many favorable Risperdal studies while he was on the Johnson &amp; Johnson payroll.&nbsp;&nbsp; A 2005 study, for instance, concluded that &quot;risperidone (Risperdal) treatment was associated with a significant short-term improvement of symptoms of pediatric bipolar disorder.&quot;<br /><br />Now, documents released as part of a huge, multi-state lawsuit have raised questions about Biederman's role in convincing Johnson &amp; Johnson's to fund a center on pediatric bipolar disorder at Massachusetts General.&nbsp; According to the Boston Globe, the lawsuit was brought on behalf of more than 2,000 patients, including children, who claim to have been injured by atypical antipsychotics, including Risperdal.&nbsp; Though Biederman is not a defendant in the suit, the Globe reports that plaintiffs lawyers are using his relationship with Johnson &amp; Johnson to illustrate how researchers and drug companies conspired to boost off-label prescriptions&nbsp; of atypical antipsychotics.<br /><br />According to the Globe article, emails written between executives at Johnson &amp; Johnson subsidiary Janssen Pharmaceuticals indicate Biederman&nbsp; had repeatedly proposed that the company&nbsp; help fund the center.&nbsp; One of the emails, written in 2002, stated that &quot;the rationale of this center is to generate and disseminate data supporting the use of risperidone (Risperdal) in this patient population.&quot;&nbsp; Another email mentions at least $700,000 in Johnson &amp; Johnson payments to the center, the Globe said.<br /><br />The Boston Globe also reports that the research institute's 2002 annual report states that one of the center's &quot;essential features&quot; is its ability to conduct research that &quot;will move forward the commercial goals of J&amp;J (Johnson &amp; Johnson)&quot;<br /><br />Hopefully, Biederman himself will be able to shed more light on his dealings with Johnson &amp; Johnson.&nbsp; According to the Globe, lawyers representing plaintiffs in the atypical antipsychotic lawsuit recently won their bid to compel an interview with Biederman. The Globe said he is expected to be interviewed under oath by January.<br /><br />]]></content:encoded>
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		<title>Panel Questions Antipsychotics for Kids</title>
		<link>http://www.yourlawyer.com/articles/read/15551</link>		
		<pubDate>Thu, 20 Nov 2008 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15551</guid>
		<description><![CDATA[Reuters is reporting that a panel of external experts is urging the U.S. Food and Drug Administration (FDA) and &ldquo;other U.S. health agencies&rdquo; to look at &ldquo;the long-term effects&rdquo; of antipsychotic drugs on children.The group met to review the safety of Risperdal&mdash;known generically as risperidone, and manufactured by Johnson &amp; Johnson&mdash;and Zyprexa&mdash;manufactured by Eli Lilly and Company&nbsp; and known...]]></description>
			<content:encoded><![CDATA[Reuters is reporting that a panel of external experts is urging the U.S. Food and Drug Administration (FDA) and &ldquo;other U.S. health agencies&rdquo; to look at &ldquo;the long-term effects&rdquo; of antipsychotic drugs on children.<br /><br />The group met to review the safety of <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a>&mdash;known generically as risperidone, and manufactured by Johnson &amp; Johnson&mdash;and <a href="http://www.yourlawyer.com/topics/overview/zyprexa">Zyprexa</a>&mdash;manufactured by Eli Lilly and Company&nbsp; and known generically as olanzapine, reported Reuters.&nbsp; Reuters said the panel, which met this week, &ldquo;unanimously requested more long-term data on the side effects of using these drugs in children.&rdquo;&nbsp; Both medications are atypical antipsychotics and have made headlines for their increased and unapproved use in children, said Reuters.<br /><br />&quot;These drugs have very high potential for benefit but also have a fairly well recognized set of risks,&quot; Dr. Carl D'Angio, of the University of Rochester in Rochester, New York, and a panel member, quoted Reuters.&nbsp; <br /><br />Risperdal, which is prescribed to treat schizophrenia, has been linked to diabetes, neuroleptic malignant syndrome (NMS), tardive dyskinesia, no less than 37 reports of stroke or stroke-like events, and 16 deaths.&nbsp; Risperdal has also been known to cause irregular heartbeats, muscle weakness and spasms, high fever, constipation, weight gain and headaches.&nbsp; <br /><br />Zyprexa, another popular schizophrenia medication, has been linked to serious side effects including diabetes, hyperglycemia, and other blood sugar disorders.&nbsp; One study that included both drugs found them to cause diabetes 50 percent more often than older antipsychotics.<br /><br />Reuters noted that close to 400,000 Risperdal prescriptions - 25 percent of all those written for the drug -&nbsp; were filled for children and teenagers last year.&nbsp; Of those, 240,000&nbsp; went to children under age of 12.&nbsp; In children&nbsp; under age 17, the drugs were used most often to given to children with&nbsp; autism and ADHD. <br /><br />Reuters also reported that based on &ldquo;documents submitted to the panel,&rdquo; in the years &ldquo;between 1993 and March 2008, some 1,200 children on&rdquo; Risperdal experienced &ldquo;severe side effects,&rdquo; with 31 ending in death.&nbsp; <br /><br />&ldquo;We are concerned about some of the side effects that they have because these drugs affect multiple organ systems,&quot; Dr. Keith Kocis, a panel member from the University of North Carolina at Chapel Hill, told Reuters.&nbsp; <br /><br />According to Reuters, FDA spokeswoman Sandy Walsh said the panel was &ldquo;surprised&rdquo; to learn that such a &ldquo;high percentage&rdquo; of Risperdal's &ldquo;total usage is in children,&rdquo; adding that the committee was concerned with its off-label use in children with ADHD.&nbsp; Reuters quoted Walsh as saying in an email that the agency would be meeting with the National Institutes of Health (NIH) &quot;to discuss long-term study of drugs in this class and will begin looking closely at specifically how these products are actually being used in treating pediatric patients and their effects.&quot;<br /><br />It is widely accepted and understood that doctors can use their best judgment in prescribing practices and can prescribe FDA-approved drugs for approved and nonapproved purposes.&nbsp; However, as Reuters points outs, some doctors are pushing this freedom, especially in the case of antipsychotics and children.<br /><br />]]></content:encoded>
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		<title>American Children Take the Most Psychotropic Drugs</title>
		<link>http://www.yourlawyer.com/articles/read/15224</link>		
		<pubDate>Fri, 26 Sep 2008 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15224</guid>
		<description><![CDATA[A new study reports that American children are about three times likelier to be prescribed psychotropic medications than children in Europe.&nbsp; The study states that the differences may be attributable to regulatory practices and cultural beliefs about the role of medication in emotional and behavioral problems.Julie Zito led the team comprised of researchers from the U.S., Germany, and the Netherlands.&nbsp; The group investigated...]]></description>
			<content:encoded><![CDATA[A new study reports that American children are about three times likelier to be prescribed <a href="http://www.yourlawyer.com/practice_areas/defective_drugs">psychotropic medications</a> than children in Europe.&nbsp; The study states that the differences may be attributable to regulatory practices and cultural beliefs about the role of medication in emotional and behavioral problems.<br /><br />Julie Zito led the team comprised of researchers from the U.S., Germany, and the Netherlands.&nbsp; The group investigated prescription levels in the three countries.&nbsp; Zito reported that, &quot;Antidepressant and stimulant prevalence were three or more times greater in the U.S. than in the Netherlands and Germany, while antipsychotic prevalence was 1.5 to 2.2 times greater.&quot;&nbsp; The use of antidepressants, such as Prozac, and stimulants, such as Ritalin, in children has been the subject of much controversy; this study is believed to quantify the differences in practice between the US and Western Europe.<br /><br />Study authors believe the differences may be partly due to different diagnostic classification systems.&nbsp; For instance, &quot;The US trend of increasing bipolar diagnosis in children and adolescents does not reflect European practice.&quot;&nbsp; The team also discussed government cost restrictions in Europe, the increased amount of child psychiatrists per capita in the U.S., as well as the U.S. practice of using two or more different psychotropic drugs in a single year as possible explanations.&nbsp; &quot;Direct to consumer drug advertising, which is common in the U.S., is also likely to account for some of the differences.&nbsp; The increased use of medication in the US also reflects the individualist and activist therapeutic mentality of US medical culture,&quot; Zito added.<br /><br />Earlier this month we reported about one million children and teenagers are treated for schizophrenia and prescription rates for atypicals&mdash;the anti-psychotic drugs most prescribed for these disorders&mdash;have increased more than five-fold for children over the past 15 years and are also being used to control outbursts and aggression in children with a wide variety of diagnoses representing about 80 percent of the prescriptions written for maladies such as autism, ADHD, bipolar disorder, depression, and anxiety, despite the drugs&rsquo; serious side effects.&nbsp; Some uses are off-label, or not approved by the Food and Drug Administration (FDA).&nbsp; Approximately three million Americans suffer from schizophrenia and about 20 percent begin to show symptoms as children or teens.<br /><br />Meanwhile, state officials are finding atypical antipsychotics have become the largest drug class in Medicaid and many question if this is due to marketing or need; several states are suing drug makers for off-label promotion and commissioning &quot;ghost-written&quot; articles to increase use. But, drug makers continue to obtain new approvals from the FDA to treat more conditions.&nbsp; In the last two years, Risperdal received approval to treat schizophrenia in adolescents and the irritability of autism in children ages five to 16.&nbsp; Nicola Huff, whose son, John Aaron, took Risperdal for seven years to resolve behavioral problems said at age 14, he developed female-sized breasts that had to be surgically removed.&nbsp; Tammy Wandling, whose son Austin has autism, said a psychiatrist put him on Risperdal at age four.&nbsp; In less than nine months, Austin developed a baseball-size growth in his right breast.&nbsp; Research suggests Risperdal can cause an increase in the hormone prolactin, which causes breasts to enlarge and produce milk.<br /><br />]]></content:encoded>
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		<title>All Antipsychotic Drugs Pose Stroke Risk</title>
		<link>http://www.yourlawyer.com/articles/read/15050</link>		
		<pubDate>Fri, 29 Aug 2008 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/15050</guid>
		<description><![CDATA[United Kingdom researchers report that more people than was at first believed could be at a higher risk of suffering a stroke due to antipsychotic drugs.&nbsp; Earlier research only pointed to some types of the drug as increasing the risk, especially for those diagnosed with dementia.&nbsp; Now, a study published in the British Medical Journal says all forms of antipsychotic drugs increase stroke risk and this increase occurs in all...]]></description>
			<content:encoded><![CDATA[United Kingdom researchers report that more people than was at first believed could be at a higher risk of suffering a stroke due to <a href="http://www.yourlawyer.com/practice_areas/defective_drugs">antipsychotic drugs</a>.&nbsp; Earlier research only pointed to some types of the drug as increasing the risk, especially for those diagnosed with dementia.&nbsp; Now, a study published in the British Medical Journal says all forms of antipsychotic drugs increase stroke risk and this increase occurs in all patients.<br /><br />Typically, antipsychotics are prescribed to control psychotic symptoms in patients with schizophrenia and some severe forms of depression.&nbsp; Atypically, antipsychotic drugs are believed to be widely used to control some dementia symptoms, such as aggression; many experts disagree on this use.&nbsp; Anitpsychotics are characterized into two categories:&nbsp; The newer &quot;atypical&quot; - including Zyprexa, Seroquel and Risperdal -&nbsp; and the older &quot;typical&quot; antipsychotics.&nbsp; In 2002, when concerns were raised over antipsychotic use, the focus was on &quot;atypicals,&rdquo; which led to a recommendation from drug safety advocates in the United Kingdom that such drugs should not be prescribed to dementia patients.&nbsp; The UK government has been urged to strengthen this suggestion when completing its pending dementia strategy.<br /><br />The first anti-psychotics, like Thorazine, helped many but came with severe side effects, such as tardive dyskinesia and involuntary and debilitating movements.&nbsp; The second generation, dubbed atypicals, emerged in the 1990s and cause fewer involuntary movements, but weight gain and diabetes can result, said Tom Clark, clinical affairs director for the American Society of Consultant Pharmacists Foundation.<br /><br />These newest findings&mdash;released from researchers at the London School of Hygiene and Tropical Medicine---confirm fears long associated with the treatment of dementia patients, but also raise broader issues.&nbsp; For instance, the researchers identified 6,700 patients with an average age of 80 and found a greater than three-fold risk for dementia patients suffering stroke while taking any sort of anti-psychotic drug.&nbsp; Patients without dementia taking any sort of antipsychotic realized a 40% increase in risk.<br /><br />The researchers repeated the recommendation that patients with dementia should not be prescribed these drugs. &quot;The over-prescription of antipsychotics is a serious breach of human rights, these drugs should only be a last resort,&rdquo; said Neil Hunt, from the Alzheimer's Society and that doctors must now pay attention to these warnings.&nbsp; &quot;The forthcoming National Dementia Strategy is a crucial opportunity to stop this dangerous over-prescribing and we look forward to its launch in the autumn.&quot;&nbsp; Meanwhile, Marjorie Wallace, the chief executive of the mental health charity Sane, said that while the drugs were capable of transforming lives, different patients reacted differently to their side-effects, &quot;This study should remind us all that antipsychotics are powerful drugs which can both be essential for some people, while carrying other risks.&nbsp; This is another warning that all antipsychotics should be prescribed with great thought and care and be subject to rigorous follow-up.&quot;<br /><br />In the United States, over 26 percent of the nation's nursing home residents were on antipsychotics in early 2007, compared with 19.4 percent in 1999, federal surveys show.&nbsp; Those drugs do little to help dementia patients, said Lon S. Schneider, a California psychiatrist and lead investigator of the CATIE-AD study of outpatients with Alzheimer's.&nbsp; He and his colleagues found that patients on anti-psychotics for 12 weeks had a slightly greater risk of dying sooner than those on placebo.<br /><br />]]></content:encoded>
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		<title>Antipsychotics Do More Harm than Good In Dementia Patients</title>
		<link>http://www.yourlawyer.com/articles/read/14641</link>		
		<pubDate>Tue, 24 Jun 2008 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/14641</guid>
		<description><![CDATA[Antipsychotic drugs use to reduce symptoms of agitation, aggression, and violence in dementia patients is on the rise, as can be seen in soaring sales of antipsychotics like Risperdal, Seroquel, and Zyprexa.&nbsp; These drugs experienced a $4 billion dollar increase in sales since 2000 for a total of $13.1 billion in 2007, due, in part, to an increase in such prescriptions in nursing homes.&nbsp; As a matter-of fact, researchers estimate that...]]></description>
			<content:encoded><![CDATA[Antipsychotic drugs use to reduce symptoms of agitation, aggression, and violence in dementia patients is on the rise, as can be seen in soaring sales of antipsychotics like <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a>,<a href="http://www.yourlawyer.com/topics/overview/seroquel"> Seroquel</a>, and <a href="http://www.yourlawyer.com/topics/overview/zyprexa">Zyprexa</a>.&nbsp; These drugs experienced a $4 billion dollar increase in sales since 2000 for a total of $13.1 billion in 2007, due, in part, to an increase in such prescriptions in nursing homes.&nbsp; As a matter-of fact, researchers estimate that nearly 30 percent of all nursing home patients have received antipsychotic drugs at one time or another.<br /><br />But, a 2006 study of Alzheimer&rsquo;s patients revealed that in most, antipsychotics provided no significant improvement over placebos in treating aggression and delusions.&nbsp; A year earlier, the <a href="http://www.fda.gov/cder/drug/InfoSheets/HCP/antipsychotics_conventional.htm">Food and Drug Administration</a> (FDA) ordered newer antipsychotics be labeled with a &ldquo;black box&rdquo; label warning of an increased risk of death.&nbsp; Last week, the FDA required a similar warning on older antipsychotics, as well.&nbsp; First generation antipsychotics, like Haldol, carry a significant risk of repetitive movement disorders and sedation.&nbsp; Second-generation antipsychotics, called atypicals, are commonly prescribed because the risk of movement disorders is lower; however, they can cause sedation and can contribute to weight gain and diabetes; some experts cite a lack of research for these drugs used in behavioral problems.&nbsp; If patients begin showing behavioral symptoms of dementia, doctors said, they should have complete medical and psychiatric workups first, especially if symptoms develop suddenly.<br /><br />The FDA has not approved marketing of antispychotics for older dementia patients; however, the drugs are routinely prescribed &ldquo;off label.&rdquo;&nbsp; Off-label prescribing is perfectly legal and left to the discretion of the prescribing physician; marketing of drugs for off-label, unapproved purposes is illegal and several states are suing big name antipsychotic drug makers on charges of false and misleading marketing.<br /><br />Other, recent research revealed community-dwelling adults receiving a prescription for a newer antipsychotic medication were 3.2 times more likely than individuals who received no antipsychotic therapy to be hospitalized or to die during 30 days of follow-up.&nbsp; Those who received older antipsychotic therapy were 3.8 times more likely to have such an event compared to those who received no antipsychotic therapy.&nbsp; In nursing home groups, those taking older antipsychotics were 2.4 times more likely to be hospitalized or die, while those taking newer drugs were 1.9 times more likely to die or be hospitalized during the 30 day follow-up.&nbsp; Meanwhile, a recent British study concluded that the continuing use of antipsychotic drugs provides neither cognitive nor neuropsychiatric benefits when taken by Alzheimer&rsquo;s patients.<br /><br />Some nursing homes are trying a different approach, so-called environmental intervention, tactics that include reducing boredom, providing intellectual and physical stimulation, exercise, calming music, pet therapy, and improving how staff approaches and talks to dementia patients.&nbsp; Such approaches are time consuming, do not help all patients, can be prohibitively expensive, and are more difficult to provide as Alzheimer&rsquo;s continues to increase.&nbsp; Also, nursing homes are understaffed and insurers do not typically reimburse for the type of one-on-one psychosocial therapy that advocates recommend.&nbsp; Despite dangerous side effects, sedatives and antipsychotics, are often prescribed because they offer a quick fix.<br /><br />]]></content:encoded>
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		<title>Antipsychotics Harmful for Dementia Patients</title>
		<link>http://www.yourlawyer.com/articles/read/14463</link>		
		<pubDate>Tue, 27 May 2008 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/14463</guid>
		<description><![CDATA[Antipsychotics, even when taken for a very short time period, are likelier to land elderly people with dementia in the hospital.&nbsp; In some cases, patients died.&nbsp; Researchers stress the underlying problems, which require the need for these medications&mdash;behavioral problems such as aggression and agitation&mdash;pose real issues.&nbsp; Alternatives are limited, the researchers added.&nbsp; &quot;A misreading of the findings would be...]]></description>
			<content:encoded><![CDATA[<a href="http://www.yourlawyer.com/practice_areas/defective_drugs">Antipsychotics</a>, even when taken for a very short time period, are likelier to land elderly people with dementia in the hospital.&nbsp; In some cases, patients died.&nbsp; Researchers stress the underlying problems, which require the need for these medications&mdash;behavioral problems such as aggression and agitation&mdash;pose real issues.&nbsp; Alternatives are limited, the researchers added.&nbsp; &quot;A misreading of the findings would be we don't need to do something for these nursing home residents,&quot; said study author Dr. Gary J. Kennedy, head of geriatric psychiatry for Montefiore Medical Center in New York City.&nbsp; The findings were published in the May 26 issue of the Archives of Internal Medicine.<br /><br />Many experts feel behavioral interventions should be tried first and antipsychotics used as a last resort, &quot;when the behavior or the psychiatric symptoms are really out of control and causing complete distress not only for the person suffering from Alzheimer's, but for caregivers all around them,&quot; said Maria Carrillo, director of medical and scientific affairs at the Alzheimer's Association in Chicago. &quot;It's important to work these things out with the physician and, of course, do follow-up very closely together, so you can make sure these antipsychotics are having the effect you want and, if not, discontinue them immediately.&quot;<br /><br />Antipsychotics are generally prescribed to treat some behavioral complications of dementia, including delirium.&nbsp; Some newer antipsychotic medications such as Zyprexa (olanzapine) and Risperdal (risperidone) have been on the market for about a decade and have nearly replaced their older counterparts.<br /><br />Researchers from the Institute for Clinical Evaluative Sciences in Ontario, Canada, compared 20,682 older adults with dementia living in the community with 20,559 older adults with dementia living in a nursing home between April 1, 1997, and March 31, 2004.&nbsp; Each group was divided into three subgroups:&nbsp; Those not receiving any antipsychotics, those taking newer antipsychotics, and those taking older antipsychotics such as Haldol (haloperidol).<br /><br />The research revealed community-dwelling adults who recently received a prescription for a newer antipsychotic medication were 3.2 times more likely than individuals who received no antipsychotic therapy to be hospitalized or to die during 30 days of follow-up.&nbsp; Those who received older antipsychotic therapy were 3.8 times more likely to have such an event compared to those who received no antipsychotic therapy.&nbsp; In nursing home groups, those taking older antipsychotics were 2.4 times more likely to be hospitalized or die, while those taking newer drugs were 1.9 times more likely to die or be hospitalized during the 30 day follow-up.<br /><br />&quot;It's a carefully done study,&quot; Kennedy said. &quot;One flaw is that the [participants] weren't randomly administered antipsychotics.&nbsp; There was some reason they were given an antipsychotic, such as aggression or agitation.&rdquo;&nbsp; The authors confirmed about 17 percent of patients entering nursing homes begin an antipsychotic within 100 days.&quot;<br /><br />Meanwhile, a recent British study concluded that the continuing use of antipsychotic drugs provides neither cognitive nor neuropsychiatric benefits when taken by Alzheimer&rsquo;s patients. Research was conducted by King's College Hospital in London where 165 patients who were already being treated with antipsychotic drugs were studied.&nbsp; The patients were divided into two groups:&nbsp; One continued treatment with the drugs; the other group stopped treatment.<br /><br />]]></content:encoded>
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		<title>Atypical Antipsychotic Drugs Used Inappropriately, Prescribed too Often, Critics Charge</title>
		<link>http://www.yourlawyer.com/articles/read/13896</link>		
		<pubDate>Mon, 18 Feb 2008 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/13896</guid>
		<description><![CDATA[Zyprexa, Seroquel, Abilify and other atypical antipsychotic drugs, meant to be used sparingly for severe mental illness like schizophrenia and bi-polar disorder, are being prescribed in increasing numbers to young children and the elderly.&nbsp; Doctors have helped to turn atypical antipsychotics like Zyprexa into blockbusters by prescribing them for more common conditions such as dementia and aggression.&nbsp; Some have accused drug makers of...]]></description>
			<content:encoded><![CDATA[Zyprexa, Seroquel, Abilify and other <a href="http://www.yourlawyer.com/practice_areas/defective_drugs">atypical antipsychotic drugs</a>, meant to be used sparingly for severe mental illness like schizophrenia and bi-polar disorder, are being prescribed in increasing numbers to young children and the elderly.&nbsp; Doctors have helped to turn atypical antipsychotics like Zyprexa into blockbusters by prescribing them for more common conditions such as dementia and aggression.&nbsp; Some have accused drug makers of illegally promoting off-label uses as the reason behind this surge in atypical antipsychotic drug prescriptions.&nbsp; Yet even as the use of atypical antipsychotic medications has grown, so have the number studies questioning some of the drugs' benefits, especially in light of their link to serious side effects such as sedation, obesity, and diabetes.<br /><br />Drugs receive US <a href="http://www.fda.gov/">Food and Drug Administration</a> (FDA) approval for specific purposes; however, medications are often prescribed as off-label&mdash;purposes other than that for which they were approved&mdash;on some difficult-to-treat conditions.&nbsp; Off-label prescribing is legal at physician discretion; however, off-label marketing by drug companies is in violation of federal law.<br /><br />The first antipsychotics, like Thorazine, helped many but came with severe side effects, such as tardive dyskinesia, involuntary and debilitating movements.&nbsp; The second generation, dubbed atypicals, emerged in the 1990s and cause fewer involuntary movements, but weight gain and diabetes can result from their use, said Tom Clark, clinical affairs director for the American Society of Consultant Pharmacists Foundation.&nbsp; Atypicals include Risperdal, made by Janssen Pharmaceutica, part of Johnson &amp; Johnson; Zyprexa from Eli Lilly &amp; Co.; Seroquel by AstraZeneca P.L.C.; Geodon by Pfizer Inc.; and Abilify by Bristol-Myers Squibb Co.<br /><br />State officials are finding atypicals have become the largest drug class in Medicaid and many question if this is due to illegal off-label marketing or true patient need.&nbsp; Several states are suing drug makers for off-label promotion and commissioning &quot;ghost-written&quot; articles to increase use of their products.&nbsp; Meanwhile, drug makers are obtaining new approvals from the FDA to treat more conditions.&nbsp; For instance, in the last two years, Risperdal received approval to treat schizophrenia in adolescents and the irritability of autism in children ages five to 16.<br /><br />However, increased use of these new antipsychotics can have unforeseen results.&nbsp; Nicola Huff, whose son, John Aaron, took Risperdal for seven years to resolve behavioral problems said at age 14, he developed female-sized breasts that had to be surgically removed.&nbsp; Tammy Wandling, whose son Austin has autism, said a psychiatrist put him on Risperdal at age four.&nbsp; In less than nine months, Austin developed a baseball-size growth in his right breast.&nbsp; Research suggests Risperdal can cause an increase in the hormone prolactin, which causes breasts to enlarge and make milk.<br /><br />More than 26 percent of the nation's nursing home residents were on antipsychotics in early 2007, compared with 19.4 percent in 1999, federal surveys show.&nbsp; Those drugs do little to help dementia patients, said Lon S. Schneider, a California psychiatrist and lead investigator of the CATIE-AD study of outpatients with Alzheimer's.&nbsp; He and his colleagues found that patients on anti-psychotics for 12 weeks had a slightly greater risk of dying sooner than those on placebo.<br /><br />Zyprexa-maker Lilly set aside $1.2 billion to settle 31,000 claims and still faces 1,200 cases and a federal probe.&nbsp; Bristol-Myers Squibb, maker of Abilify, agreed to pay $515 million last year, in part to settle off-label marketing allegations; the firms also face thousands of additional claims.&nbsp; AstraZeneca has 8,000 suits pending for Seroquel.<br /><br />]]></content:encoded>
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		<title>Risperdal, Haldol and other Antipsychotic Drugs Little Help in Managing Aggression</title>
		<link>http://www.yourlawyer.com/articles/read/13616</link>		
		<pubDate>Fri, 04 Jan 2008 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/13616</guid>
		<description><![CDATA[Antipsychotic drugs used to manage aggressive outbursts in intellectually disabled people are no more effective than placebos for most patients and may be less so, researchers report, challenging established worldwide medical practice.&nbsp; Researchers focused on Janssen&rsquo;s Risperdal and Haldol but said findings applied to similar medications such as Zyprexa.&nbsp; These drugs account for over $10 billion in annual sales and at least half...]]></description>
			<content:encoded><![CDATA[Antipsychotic drugs used to manage aggressive outbursts in intellectually disabled people are no more effective than placebos for most patients and may be less so, researchers report, challenging established worldwide medical practice.&nbsp; Researchers focused on Janssen&rsquo;s <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> and Haldol but said findings applied to similar medications such as Zyprexa.&nbsp; These drugs account for over $10 billion in annual sales and at least half of all prescriptions are for unapproved off label uses to treat aggression or irritation.&nbsp; While it is illegal for drug companies to market approved medications for off label uses, how a drug is used remains at the prescribing physician&rsquo;s discretion; many use antipsychotics&mdash;developed for schizophrenia&mdash;as tranquilizers for children with attention-deficit problems, college students with depression, Alzheimer&rsquo;s patients, and intellectually handicapped people.<br /><br />The study tracked 86 adults&mdash;aged 18 to 65&mdash;with low IQs living in community housing in England, Wales, and Australia for more than a month and found a 79 percent reduction in aggressive behavior among those on placebos as compared to a 65 percent or less reduction in those on antipsychotics.&nbsp; Dr. Peter J. Tyrer, professor of psychiatry at Imperial College London, led the team.&nbsp; Patients were given Risperdal, Haldol, or a placebo and behavior was tracked&mdash;many with very low IQs tend to lash out at others and themselves quickly.&nbsp; Patients in all three groups improved; those on the placebo improved significantly compared to those on medication.<br /><br />Researchers said the results would likely spur requests for government review of British treatment standards.&nbsp; Others feel these findings will add to the continuing debate over the widening use of antipsychotic drugs and patient advocates and some psychiatrists feel the medications are overused.&nbsp; While studies have been mixed, the drugs do have serious side effects and doctors have little to guide them.&nbsp; Johnny L. Matson, a professor of psychology at Louisiana State University in Baton Rouge, co-author of an editorial with the study in the journal Lancet said, &ldquo;The message to doctors should be, think twice about prescribing or just don&rsquo;t do it.&nbsp; We know that behavioral treatments can work very well with many patients.&rdquo;&nbsp; Others disagreed, saying the study did not reflect previous research or their experience.&nbsp; Janssen, a Johnson &amp; Johnson subsidiary, said Risperdal only promotes approved uses, which in Great Britain, includes treating autism-related irritability.&nbsp; Tyrer said there was no reason to believe other antipsychotics used for aggression, like Zyprexa from Eli Lilly or Seroquel from AstraZeneca, would be more effective.&nbsp; &ldquo;These people tend to get so little company normally, they&rsquo;re neglected, they tend to be pushed into the background and this extra attention has a much bigger effect on them that it would on a person of more normal intelligence level,&rdquo; said Tyler.<br /><br />Study authors included researchers from the University of Wales and the University of Birmingham in Britain and the University of Queensland in Brisbane, Australia.&nbsp; Authors claim results &ldquo;should not be interpreted as an indication that antipsychotic drugs have no place in the treatment of some aspects of behavior disturbance,&rdquo; but the routine prescription of drugs for aggression &ldquo;should no longer be regarded as a satisfactory form of care.&rdquo;<br /><br />]]></content:encoded>
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		<title>Abuse of Risperdal, Seroquel, Other Antipsychotic Drugs in Nursing Homes Widespread</title>
		<link>http://www.yourlawyer.com/articles/read/13548</link>		
		<pubDate>Thu, 20 Dec 2007 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/13548</guid>
		<description><![CDATA[Use of antipsychotic drugs like Risperdal and Seroquel to control dementia patients has risen in recent years, despite the Food and Drug Administration's (FDA) &quot;black box&quot; warning labels that these drugs can increase the risk of death for elderly dementia sufferers.&nbsp; About 30% of nursing home residents are on antipsychotic drugs, according to the Centers for Medicare &amp; Medicaid Services (CMS), most of them on newer, atypical...]]></description>
			<content:encoded><![CDATA[Use of antipsychotic drugs like <a href="http://www.yourlawyer.com/topics/overview/risperdal">Risperdal</a> and <a href="http://www.yourlawyer.com/topics/overview/seroquel">Seroquel</a> to control dementia patients has risen in recent years, despite the <a href="http://www.fda.gov/">Food and Drug Administration'</a>s (FDA) &quot;black box&quot; warning labels that these drugs can increase the risk of death for elderly dementia sufferers.&nbsp; About 30% of nursing home residents are on antipsychotic drugs, according to the Centers for Medicare &amp; Medicaid Services (CMS), most of them on newer, atypical antipsychotics.&nbsp; Federal law strongly discourages nursing homes from physically restraining unruly patients, but federal health-care programs such as Medicaid pay for drugs that may help calm aggressive behavior and agitation associated with Alzheimer's.<br /><br />In 2005, Medicaid spent $5.4 billion on atypical antipsychotic medicines&mdash;more than it spent on any other drug class, including antibiotics, AIDS drugs, or high blood pressure.&nbsp; Atypical antipsychotics are approved for schizophrenia and bipolar disorder, but in what is known as &quot;off label&quot; use&mdash;use not approved by the FDA for FDA-approved medications&mdash;doctors often prescribe the drugs to dementia patients.&nbsp; The widespread use of antipsychotics among the elderly has begun to draw criticism from regulators, researchers, lawmakers, and the nursing-home industry.&nbsp; Senator Charles Grassley, the ranking Republican on the Senate Finance Committee, asked several drug manufacturers for records on how they may have marketed these drugs for use in geriatric patients and also has asked the Inspector General of the Department of Health and Human Services to investigate use of the drugs in nursing homes.<br /><br />The $122 billion nursing-home industry has moved toward large, often understaffed, institutions where use of psychotropic drugs is rising.&nbsp; According to CMS, nearly 21% of nursing-home patients who don't have a psychosis diagnosis are on antipsychotics.&nbsp; A 2005 study found antipsychotics were prescribed not only for psychosis, but for depression, confusion, memory loss, and feelings of isolation.&nbsp; Last year, CMS instituted new guidelines to limit the use of antipsychotics; however, it's still easier for nursing homes to get reimbursed for giving patients extra pills than it is for hiring extra staff.<br /><br />An Alzheimer's patient often cannot refuse antipsychotic drugs, says Cynthia Rudder, of the Long-Term Care Community Coalition. &quot;You are basically quieting them against their will and it is absolutely horrendous,&quot; she says.&nbsp; Family members can object to the use of such drugs, but risk having their relative discharged for unruly behavior.<br /><br />At CMS, officials stress the need to shift to smaller, less-rigid facilities as a way to reduce antipsychotic usage.&nbsp; Some nursing-home-industry officials agree change is needed, yet replacing drugs with approaches that require a more human touch is easier said than done.<br /><br />There are some Alzheimer's patients for whom nonpharmacological approaches simply don't work, says William Thies, a vice president at the Alzheimer's Association in Chicago, and in these cases antipsychotics may be warranted.&nbsp; But the drugs need to be used very carefully, at the lowest dose and after ruling out a medical problem, says Thies, who has a doctorate in pharmacology.<br /><br />A spokesman for AstraZeneca Pharmaceuticals LP, maker of Seroquel, says &quot;decisions about medical treatment are made by physicians&quot; and the company doesn't recommend the drug &quot;for uses other than its approved indications in schizophrenia and bipolar disorder.&quot;<br /><br />But according to the Wall Street Journal, some pharmaceutical companies have attracted scrutiny for marketing drugs for unapproved uses.&nbsp;&nbsp; It is illegal for drug makers to promote off-label uses, but doctors may prescribe medications as they see fit.&nbsp;&nbsp; Last month, the Arkansas attorney general filed suit against Johnson &amp; Johnson and two of its units, claiming, among other things, that they &quot;engaged in a false and misleading campaign&quot; to promote its antipsychotic drug Risperdal to geriatric patients.<br /><br />]]></content:encoded>
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		<title>Study: Seniors Face Risks with All Antipsychotic Drugs</title>
		<link>http://www.yourlawyer.com/articles/read/12612</link>		
		<pubDate>Tue, 27 Feb 2007 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/12612</guid>
		<description><![CDATA[For the last couple of years, there have been a lot of questions raised about the cost, effectiveness, and safety of second-generation (or atypical) antipsychotic drugs such as Zyprexa, Seroquel, and Risperdal. However, a new Canadian study has found that older, conventional antipsychotic medications pose a similar risk of death to elderly patients perhaps an even greater risk than the atypical class.  A new report published in the current issue...]]></description>
			<content:encoded><![CDATA[For the last couple of years, there have been a lot of questions raised about the cost, effectiveness, and safety of second-generation (or atypical) antipsychotic drugs such as Zyprexa, Seroquel, and Risperdal. However, a new Canadian study has found that older, conventional antipsychotic medications pose a similar risk of death to elderly patients perhaps an even greater risk than the atypical class.<br /> <br /> A new report published in the current issue of the Canadian Medical Association Journal (CMAJ) claims that, among elderly patients, &ldquo;the risk of death associated with conventional antipsychotic medications is comparable to and possibly greater than the risk of death associated with atypical antipsychotic medications. Until further evidence is available, physicians should consider all antipsychotic medications to be equally risky in elderly patients.&rdquo;<br /> <br /> Researchers studied more than 37,000 seniors and discovered that, within the first 180 days of treatment, 14.1 percent of the conventional-drug group died, compared to 9.6 percent of the atypical-drug group. Patients taking high dosages of conventional drugs faced a 67 percent increase in mortality. In addition, the study found that patients who had taken a conventional medication had a 32 percent greater (dose-dependent) risk of death within 180 days than those who were given an atypical agent.<br /> <br /> In 2005, Health Canada, the government&rsquo;s public-health watchdog, reported that atypical antipsychotic medications increased the risk of death by 60 percent in trials involving elderly patients with dementia. However, researchers were concerned that warnings about the new atypical antipsychotic drugs were causing physicians to prescribe conventional antipsychotic treatments more frequently--even though their overall safety has not been proven either. <br /> <br /> The authors of the study believe that regulatory product warnings should be expanded to account for these new findings. &ldquo;The results from our study strongly suggest that Health Canada and the FDA should include conventional antipsychotic medications in their public health advisories, which currently warn only of the increased risk of death associated with the use of atypical antipsychotic medications in elderly patients with dementia.&rdquo;<br /> <br /> They also note, &ldquo;Antipsychotic medications are disproportionately used in elderly populations and have been prescribed to over a quarter of U.S. Medicare beneficiaries in nursing homes&rdquo; and that &ldquo;much use is outside approved indications.&rdquo;]]></content:encoded>
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		<title>Antipsychotic drugs linked to higher risk of death among seniors</title>
		<link>http://www.yourlawyer.com/articles/read/12609</link>		
		<pubDate>Mon, 26 Feb 2007 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/12609</guid>
		<description><![CDATA[Doctors should consider all antipsychotic medications to be equally risky for seniors, say researchers, who suggested additional warnings for the drugs are warranted.  In 2005, both Health Canada and the U.S. Food and Drug Administration warned that newer antipsychotic drugs increased the risk of death among elderly patients with dementia.  The newer antipsychotics such as Zyprexa (olanzapine), Seroquel (quetiapine) and Risperdal (risperidone)...]]></description>
			<content:encoded><![CDATA[Doctors should consider all antipsychotic medications to be equally risky for seniors, say researchers, who suggested additional warnings for the drugs are warranted.<br /> <br /> In 2005, both Health Canada and the U.S. Food and Drug Administration warned that newer antipsychotic drugs increased the risk of death among elderly patients with dementia.<br /> <br /> The newer antipsychotics such as Zyprexa (olanzapine), Seroquel (quetiapine) and Risperdal (risperidone) were developed for schizophrenia, but doctors may prescribe them for dementia. There is no strong evidence that the drugs are effective for Alzheimer's.<br /> <br /> The warnings left the impression that older, conventional antipsychotics were safer.<br /> <br /> To test the idea, Dr. Sebastian Schneeweiss of Harvard Medical School in Boston and his colleagues reviewed death rates among more than 37,000 people aged 65 and older in British Columbia who took antipsychotic drugs between January 1996 and December 2004.<br /> <br /> Some people in the study took older antipsychotic such as haloperidol and chlorpromazine while others took the newer, atypical variety.<br /> <br /> Patients prescribed the conventional antipsychotics showed a 32 per cent greater risk of death within 180 days compared with those given an atypical antipsychotic, the team reports in Tuesday's issue of the Canadian Medical Association Journal.<br /> Expand warning<br /> <br /> The increased risk of death was larger than that from all other health conditions measured in the study except congestive heart failure and HIV infection, the researchers said.<br /> <br /> &quot;Together with earlier findings, the results from our study strongly suggest that Health Canada and the FDA should include conventional antipsychotic medications in their public health advisories, which currently warn only of the increased risk of death associated with the use of atypical antipsychotic medications in elderly patients with dementia,&quot; the study's authors concluded.<br /> <br /> It is possible that doctors prescribed the older antipsychotic haloperidol more often than newer medications in patients who were more likely to die, or that patients using the antipsychotic drugs were more impaired physically and cognitively, the researchers acknowledged.<br /> <br /> Scientists do not know why conventional antipsychotic medications seem to increase short-term mortality.<br /> 4 additional deaths<br /> <br /> Using patient data from British Columbia, the authors compared 12,882 people over age 65 taking the older drugs to 24,359 seniors taking the atypical drugs.<br /> <br /> Within the first six months of treatment, 14.1 per cent of the people on the conventional drugs died, compared to 9.6 per cent in the atypical antipsychotics group.<br /> <br /> &quot;In these analyses, the adjusted risk difference &hellip; meant that, for every 100 patients prescribed a conventional antipsychotic drug instead of an atypical drug, there were about four additional deaths,&quot; they wrote.<br /> <br /> Reasons for the increased risk of death aren't clear, they note, though some evidence points to increased risk of heart-related conditions, impact on blood pressure and swallowing problems as potential explanations.]]></content:encoded>
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		<title>Link Found Between Antipsychotic Drugs and Weight Gain</title>
		<link>http://www.yourlawyer.com/articles/read/12531</link>		
		<pubDate>Tue, 13 Feb 2007 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/12531</guid>
		<description><![CDATA[In what may be a major breakthrough for the research and development of antipsychotic drugs, brain scientists at Johns Hopkins University believe they have discovered a major cause of the weight gain suffered by many patients taking antipsychotic medication. Scientists now claim that powerful drugs such as Zyprexa (olanzapine), Clozaril (clozapine), and Risperdal (risperidone) may affect production of an enzyme known as AMPK, which influences...]]></description>
			<content:encoded><![CDATA[In what may be a major breakthrough for the research and development of antipsychotic drugs, brain scientists at Johns Hopkins University believe they have discovered a major cause of the weight gain suffered by many patients taking antipsychotic medication. Scientists now claim that powerful drugs such as Zyprexa (olanzapine), Clozaril (clozapine), and Risperdal (risperidone) may affect production of an enzyme known as AMPK, which influences appetite.<br /> <br /> &ldquo;We&rsquo;ve now connected a whole class of antipsychotics to natural brain chemicals that trigger appetite,&rdquo; said Dr. Solomon H. Snyder, professor of neuroscience at the Johns Hopkins School of Medicine. &ldquo;Our identification of the molecular players that link such drugs to increased food intake means there&rsquo;s now hope for finding a newer generation of drugs without the weight-gain side effects.&rdquo;<br /> <br /> The researchers tested their theory by injecting mice with clozapine, and they found that those mice &ldquo;showed quadrupled AMPK activity.&rdquo; A spike in AMPK production and activity leads to an increased appetite in mice, and researchers believe that AMPK has the same appetite-control function in humans. The authors of the study think that the increased AMPK activity caused by these drugs is a result of the effects the drugs have on the protein histamine and its receptor. The drugs may work to block the histamine receptor, which spurs AMPK activity.<br /> <br /> &ldquo;Histamine also has a long history as a suspect in weight control, but no one ever could put a finger on the exact link,&rdquo; Dr. Snyder said. &ldquo;The connection we&rsquo;ve made between its receptor and appetite control is incredibly intriguing and opens new avenues for research on weight control, possibly including drugs that suppress appetite safely.&rdquo;<br /> <br /> The findings are significant because of the increase in diabetes and heart disease associated with the weight gain caused by these types of drugs. The research, which was funded by the U.S. Public Health Service, Canadian Institute of Health Research, National Institutes of Health, and National Multiple Sclerosis Society, will be published in the Proceedings of the National Academy of Sciences later this month. <br /> <br /> In related news, an FDA scientist, Dr. David Graham, testified today before Congress, claiming that the agency&rsquo;s scrutiny and oversight of Zyprexa and similar antipsychotic drugs was lax and that the FDA is acutely aware of and concerned by the connection these medications have to weight gain, diabetes, and heart disease.]]></content:encoded>
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		<title>Antipsychotic Drug May Be Linked to Pituitary Tumors</title>
		<link>http://www.yourlawyer.com/articles/read/11980</link>		
		<pubDate>Thu, 13 Jul 2006 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11980</guid>
		<description><![CDATA[A link may exist between the development of pituitary tumors and the use of some drugs commonly used to treat schizophrenia, according to research from Duke University Medical Center and the U.S. Food and Drug Administration (FDA). Although a connection has been suspected for more than 20 years, this is the first systematic study to document an association between specific antipsychotic medications and adverse reports of pituitary tumors in...]]></description>
			<content:encoded><![CDATA[A link may exist between the development of pituitary tumors and the use of some drugs commonly used to treat schizophrenia, according to research from Duke University Medical Center and the U.S. Food and Drug Administration (FDA). Although a connection has been suspected for more than 20 years, this is the first systematic study to document an association between specific antipsychotic medications and adverse reports of pituitary tumors in humans.<br /> <br /> Of seven antipsychotic medications, risperidone (trade name Risperdal), was linked to 70 percent of pituitary tumors reported to the FDA's Adverse Events Reporting System database. Risperidone is the most widely used medication within the class of drugs called atypical antipsychotics, which are used to treat schizophrenia, paranoia and manic-depressive disorders, according to the study authors.<br /> <br /> The findings appear in the June 2, 2006 issue of Pharmacotherapy. The study was funded by the author's respective research departments. Coauthors include lead author Ana Szarfman, Joseph Tonning and Jonathan Levine, all of the FDA.<br /> <br /> The researchers cautioned that the study, although suggestive, does not prove that the medications actually cause pituitary tumors.<br /> <br /> &quot;Our findings do not prove a causal relationship between antipsychotic medications and pituitary tumors, but health professionals and patients should be aware of such potentially adverse effects,&quot; said P. Murali Doraiswamy, M.D., a psychiatrist at Duke and co-author of the study.<br /> <br /> &quot;Atypical antipsychotics are lifesaving medications for a lot of people. By no means are we advocating that people stop using them, especially risperidone,&quot; he said. &quot;But we do need to learn more about possible differences in their long-term side-effects, and I believe this should be a high priority for investigation.&quot;<br /> <br /> Doraiswamy cautions that the study merely suggests an association between the drugs, pituitary tumors and several other side-effects &ndash; not a true causal relationship. Further studies are needed to offer such conclusive evidence. If future studies confirm the findings, stronger warning labels should be considered for these drugs, he said.<br /> <br /> &quot;The actual numbers of people known to have developed pituitary tumors as a possible side-effect due to any of these medications remains unclear because many adverse drug reactions are not reported to the FDA,&quot; Doraiswamy cautioned. &quot;We also don't have exact numbers of how many people currently take these drugs. Another caveat is that pituitary tumors can occur incidentally among the population in general.&quot;<br /> <br /> The team chose six atypical antipsychotics and one typical antipsychotic to examine in a &quot;data mining&quot; analysis using a sophisticated software algorithm. The algorithm, called the Multi-item Gamma Poisson Shrinker (MGPS), was used to &quot;mine&quot; data contained in the FDA's Adverse Event Reporting System (AERS) database. Using the algorithm software, the researchers looked for disproportionate reporting patterns of pituitary tumors linked to use of risperidone, aripiprazole, clozapine, olanzapine, quetiapine, ziprasidone and haloperidol, the typical antipsychotic.<br /> <br /> They found 77 reports of pituitary tumors associated with the seven antipsychotics. Risperidone was associated with 54 (70 percent) of those reports and had the highest adjusted reporting ratio for pituitary tumors, followed by haloperidol and ziprasidone. Complications included nine reports of visual problems, two reports of convulsions, four reports of headaches, three reports of cerebrovascular events and seven reports of patients who needed surgical intervention.<br /> <br /> The antipsychotic drugs in question are all dopamine D2 receptor antagonists that work by blocking dopamine, a neurotransmitter. A key function of dopamine is to suppress the release of prolactin, a hormone, from the pituitary gland.<br /> <br /> Elevation of blood prolactin levels is a well known side-effect of potent dopamine D2 blocking antipsychotics and, because antipsychotic medications vary in their potency, some medications appear to increase prolactin levels more intensely than other medications in their class, Doraiswamy said.<br /> <br /> Increased cellular production of prolactin can cause enlargement of the pituitary gland and disrupt production of other hormones, creating hormonal imbalances in the body. It can also lead to the development of pituitary tumors. Most pituitary tumors are benign, and pituitary cancer is extremely rare.<br /> <br /> Enlargement of the pituitary can cause other problems as well. The gland is located close to the optic nerve, so its enlargement can compress the nerve and cause visual problems, including partial blindness. Any swelling or abnormal growth within the pituitary can press on the brain and lead to headaches, bleeding, and, in some cases, convulsions, Doraiswamy added.<br /> <br /> Indeed, reported side-effects to the FDA database included 796 reports of increased blood levels of the hormone prolactin (hyperprolactinemia); 503 reports of the cessation of menses in women (amenorrhea); 630 reports of production of breast milk in adults and children of both sexes (galactorrhea); and male breast development. Ninety of the reports of hyperprolactinemia and 96 of the reports of galactorrhea occurred in children and adolescents. According to Doraiswamy, these symptoms can be indicative of a pituitary disturbance but not necessarily of a pituitary tumor.<br /> <br /> All reported side-effects were most strongly associated with risperidone, which also accounted for 82 percent of all reported occurrences of side-effects in children and adolescents, Doraiswamy said.<br /> <br /> The researchers are concerned that development of pituitary tumors following chronic use of potent antipsychotics may pose a problem in mentally ill patients, particularly children.<br /> <br /> &quot;In this population, we worry that symptoms may not be evaluated quickly enough, which, if due to a tumor, could lead to complications such as visual problems or localized bleeding near the pituitary gland,&quot; Doraiswamy said. &quot;Although such serious side-effects are quite rare, prescribing physicians, patients and their family members should watch for them because they can be controlled.&quot;<br /> <br /> Doraiswamy noted that the patterns of reported side-effects contained in a database as large as the FDA's may never have been fully appreciated without the use of the MGPS algorithm method, which was developed in part by Szarfman, the study's lead author.<br /> <br /> More than 1,000 adverse drug events are added to the FDA's drug safety database every day, and the system now holds more than 2.5 million entries. The large numbers suggest millions of possible combinations between medications and side-effects that no human could ever compute, monitor or contextualize on their own, Doraiswamy said.<br /> <br /> Doraiswamy has previously received funding and consulting fees from all companies that manufacture the antipsychotic medications examined in this study. They are Janssen Pharmaceutica, the manufacturer of risperidone (Risperdal); Bristol-Myers Squibb Company/Otsuka America Pharmaceuticals, manufacturers of aripiprazole (Abilify); Novartis Pharmaceuticals, manufacturer of clozapine (Clozaril); Eli Lilly and Company, manufacturer of olanzapine (Zyprexa); AstraZeneca Pharmaceuticals LP, manufacturer of quetiapine (Seroquel); and McNeill Laboratories/Janssen Pharmaceutica, manufacturer and developer of the typical antipsychotic haloperidol (Haldol).<br /> ]]></content:encoded>
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		<title>Antipsychotic drugs linked to pituitary tumors</title>
		<link>http://www.yourlawyer.com/articles/read/11816</link>		
		<pubDate>Sat, 03 Jun 2006 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11816</guid>
		<description><![CDATA[Treatment with potent D2-receptor antagonists such as risperidone (Risperdal, Janssen-Ortho) may be associated with pituitary tumors, researchers say. In the June 2006 issue of Pharmacotherapy, the team notes that while they haven't uncovered a causal relationship between the drugs and tumors, this important adverse effect is something clinicians and patients should be aware of.  &quot;Atypical antipsychotics are lifesaving medications for a lot...]]></description>
			<content:encoded><![CDATA[Treatment with potent D2-receptor antagonists such as risperidone (Risperdal, Janssen-Ortho) may be associated with pituitary tumors, researchers say. In the June 2006 issue of Pharmacotherapy, the team notes that while they haven't uncovered a causal relationship between the drugs and tumors, this important adverse effect is something clinicians and patients should be aware of.<br /> <br /> &quot;Atypical antipsychotics are lifesaving medications for a lot of people. By no means are we advocating that people stop using them especially risperidone,&quot; senior author Murali Doraiswamy, MD, a psychiatrist at Duke University, Durham, North Carolina, told reporters. &quot;But we do need to learn more about possible differences in their long-term side effects, and I believe this should be a high priority for investigation.&quot;<br /> <br /> Doraiswamy says that if additional studies confirm the current findings, stronger warning labels should be considered for these drugs.<br /> <br /> His group studied six atypical antipsychotics and one typical. They used data from the US Food and Drug Administration's (FDA's) adverse-event reporting system database. With algorithm software, they searched for disproportionate reporting patterns of pituitary tumors.<br /> <br /> Risperidone was linked to 54 (70%) out of 77 cases of pituitary tumors reported in the FDA's database and was followed by haloperidol and ziprasidone. Risperidone is the most widely prescribed of the atypical antipsychotics and is generally used to treat schizophrenia and related psychotic disorders. <br /> <br /> D2-receptor antagonists inhibit dopamine production. A key function of dopamine is to suppress the release of prolactin, a hormone from the pituitary gland. Increased cellular production of prolactin can cause enlargement of the pituitary gland and disrupt production of other hormones. It can also lead to the development of pituitary tumors. <br /> <br /> &quot;The actual numbers of people known to have developed pituitary tumors as a possible side effect due to any of these medications remains unclear, because many adverse drug reactions are not reported to the FDA,&quot; Doraiswamy added in a news release. &quot;We also don't have exact numbers of how many people currently take these drugs. Another caveat is that pituitary tumors can occur incidentally among the population in general.&quot;<br /> <br /> The researchers are also concerned about children developing pituitary tumors following the chronic use of antipsychotics. &quot;In this population, we worry that symptoms may not be evaluated quickly enough, which, if due to a tumor, could lead to complications such as visual problems or localized bleeding near the pituitary gland,&quot; Doraiswamy said. &quot;Although such serious side effects are quite rare, prescribing physicians, patients, and their family members should watch for them because they can be controlled.&quot;<br /> <br /> Doraiswamy points out that because antipsychotic medications vary in their potency, some medications appear to increase prolactin levels more intensely than others.<br /> <br /> While a connection between these drugs and tumors has been suspected for over 20 years, this is the first systematic study to document an association between specific antipsychotic medications and adverse reports of pituitary tumors in humans.<br />]]></content:encoded>
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		<title>Adult anti-psychotics can worsen troubles</title>
		<link>http://www.yourlawyer.com/articles/read/11627</link>		
		<pubDate>Tue, 02 May 2006 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11627</guid>
		<description><![CDATA[Evan Kitchens, a cheerful fourth-grader who loves basketball and idolizes his 16-year-old brother, had been hospitalized for mental illness by the time he was 8.  The boy from Bandera, Texas, was aggressive and hyperactive and had been diagnosed with a variety of other ailments, including obsessive-compulsive disorder and an autism spectrum disorder.  A couple of years ago, Evan was taking five psychiatric drugs, says his mother, Mary Kitchens....]]></description>
			<content:encoded><![CDATA[<p>Evan Kitchens, a cheerful fourth-grader who loves basketball and idolizes his 16-year-old brother, had been hospitalized for mental illness by the time he was 8.<br /> <br /> The boy from Bandera, Texas, was aggressive and hyperactive and had been diagnosed with a variety of other ailments, including obsessive-compulsive disorder and an autism spectrum disorder.<br /> <br /> A couple of years ago, Evan was taking five psychiatric drugs, says his mother, Mary Kitchens. Two were so-called atypical anti-psychotics, a group of relatively new drugs approved by the Food and Drug Administration for treating adults with schizophrenia or bipolar disorder.<br /> <br /> &quot;Evan was a walking zombie on all those drugs,&quot; Kitchens says. At the harrowing nadir two years ago, she wondered whether her son would survive, let alone live a normal life.<br /> <br /> Evan shook with severe body tremors and hardly talked. He had crossed eyes, a dangerously low white blood cell count and a thyroid disorder, all symptoms that emerged after he started the atypical anti-psychotic drugs, Kitchens says. Now, he has been weaned from the drugs and takes medicine only for attention-deficit disorder, she says. And he is mentally healthier than he has ever been.<br /> <br /> These six new anti-psychotic drugs: Clozaril, Risperdal, Zyprexa, Seroquel, Abilify and Geodon are not approved for children, but doctors can prescribe them to kids &quot;off label.&quot; And prescribing atypical anti-psychotics for aggressive children such as Evan is leading the field in a growing pediatric business, according to a new analysis of a federal survey by Vanderbilt Medical School researchers.<br /> <br /> Outpatient prescriptions for children ages 2 to 18 jumped about fivefold from just under half a million to about 2.5 million from 1995 to 2002, the survey shows.<br /> <br /> At the same time, reports of deaths and dangerous side effects potentially linked to the drugs are increasing. A USA TODAY analysis of Food and Drug Administration data shows at least 45 deaths of children from 2000 to 2004 where an atypical was considered the &quot;primary suspect.&quot; More than 1,300 cases reported bad side effects, including some that can be life threatening, such as convulsions and a low white blood cell count.<br /> <br /> <strong>Non-drug treatments</strong><br /> <br /> Treating children's disruptive behavior with pills is a complicated issue and the subject of debate among experts.<br /> <br /> FOSTER CHILDREN: Oversight of prescriptions is scarce<br /> <br /> &quot;In my experience, and that of many psychiatrists, anti-psychotics are often overused for aggression in young patients,&quot; says Ronald Pies, a clinical professor at Tufts University and author of Handbook of Essential Psychopharmacology.<br /> <br /> That doesn't mean it's necessarily wrong to give the pills, he adds.<br /> <br /> Nobody disputes that the lives of schizophrenic or severely manic children might be saved by anti-psychotics. But many non-drug treatments can help to keep aggressive, disruptive children off the atypicals, says John March, chief of child and adolescent psychiatry at Duke University School of Medicine.<br /> <br /> So much hinges on whether safer treatments can work for a child.<br /> <br /> Kids who show up on anti-psychotics for aggression often can be weaned off if there are family changes, says behavioral pediatrician Lawrence Diller of Walnut Creek, Calif. For instance, adolescents may lash out angrily if their parents are fighting or discipline is inconsistent, Diller says. In a divorce, the child sometimes ends up with the less effective parent.<br /> <br /> Last year, Diller saw an 8-year-old boy on four psychiatric drugs, including an atypical. He lived with his mother, &quot;a highly anxious, incompetent parent.&quot; When he went to live with his father, his symptoms virtually disappeared, and he didn't need any drugs, Diller says.<br /> <br /> Child psychiatrist George Stewart says he has seen dozens of aggressive children weaned off the atypical anti-psychotic drugs in his consulting work and as medical director of a residential treatment facility in Concord, Calif. Too often, he says, doctors give the drugs without considering family conditions or life experiences that cause aggressive behavior, which can be changed with intensive counseling. Three examples he offers:<br /> </p> <ul>   <li>A boy younger than 3 was treated with two anti-psychotics at a therapeutic preschool for kids with severe behavior problems. Stewart got a full family history, discovering his teen mother had a series of abusive boyfriends. &quot;He was acting out due to that, but nobody took the time to find out what was going on at home,&quot; says Stewart, who worked with the mom to improve conditions. &quot;She settled down.&quot; The child was taken off atypicals and is doing fine.</li>   <li>A 12-year-old boy with out-of-control rage &quot;we're talking smearing poop all over the 'quiet room' &quot; was treated at Stewart's center. Intensive therapy identified the sources of his rage and taught the boy how to cope. He returned home, off all meds.</li>   <li>A teen girl seemed to be intractably violent. &quot;She was trying to stab pencils in people's eyes,&quot; Stewart says. It turned out she had been raped and experienced other severe trauma. She was weaned off anti-psychotics and counseled. Now in her late teens, she's living independently and doing well with no psychiatric drugs.</li> </ul> <p>One of the most disturbing, potentially dangerous trends linked to atypicals is called &quot;polypharmacy&quot;: routinely giving kids several psychiatric drugs, says child psychiatrist Joseph Penn of Bradley Hospital and Brown University School of Medicine in Providence. &quot;We know very little about the interaction of these drugs, the effects they could be having on kids,&quot; he says.<br /> <br /> The benefits of prescribing multiple drugs may outweigh risks in some cases, but Penn says he is appalled at how many times he has seen the mega-powerful atypicals prescribed to children suffering from insomnia when they're taking other medicines.<br /> <br /> &quot;I've seen hundreds of cases,&quot; he says, &quot;and often parents don't seem to have been told about the many less risky prescription and non-prescription options out there.&quot;<br /> <br /> Sometimes medical conditions or drugs for attention-deficit hyperactivity disorder cause the insomnia. Rather than attacking causes, doctors add an atypical to the mix, he says.<br /> <strong><br /> More research needed</strong><br /> <br /> There has been little carefully controlled, long-term research on children taking most psychiatric drugs, including the atypical anti-psychotics. The FDA is trying to get more pediatric research on the atypicals, says Thomas Laughren, the agency's director of the psychiatry products division.<br /> <br /> The FDA has asked five pharmaceutical companies that make the drugs to test them in children with schizophrenia and bipolar disorder, the uses they're approved for in adults. Under law, they can get a six-month extension on their patents for doing these studies.<br /> <br /> Also, the drug companies are doing their own pediatric studies on children with disorders as diverse as ADHD, autism, conduct disorder and Tourette's syndrome.<br /> <br /> Janssen LP has applied to the FDA for approval to use its atypical anti-psychotic, Risperdal, in the treatment of symptoms of autism, says Ramy Mahmoud, vice president of medical affairs for Janssen.<br /> <br /> The National Institute of Mental Health also is conducting pediatric studies, but the research is primarily funded and supervised by pharmaceutical companies.<br /> <br /> Even if the companies win approval, it won't guarantee safety or effectiveness of the drugs in children, says David Graham of the FDA Office of Drug Safety, who emphasizes he doesn't speak for the agency. &quot;You basically know the drug isn't cyanide. You don't know much else,&quot; says Graham, who was the whistle-blower in the 2004 Vioxx heart disease scandal. Industry-funded trials are four to five times more likely than independent studies to show effectiveness for a drug, he says.<br /> <br /> According to a research review published in February, 90% of drug-company-funded studies come up with findings that support the company's drug.<br /> <br /> In head-to-head research testing more than one atypical anti-psychotic drug, the outcomes are contradictory, coming down on the side of whichever company is paying for the research. (The research included studies of Risperdal, Zyprexa, Clozaril and Geodon, but none on Seroquel or Abilify.)<br /> <br /> &quot;It appears that whichever company sponsors the trial produces the better anti-psychotic drug,&quot; writes lead author Stephan Heres of the Technical University of Munich in the American Journal of Psychiatry.<br /> <br /> And the short-term, smaller studies required of companies rarely detect any but the most glaring problems, Graham says.<br /> <br /> &quot;The American public is operating under the illusion that a drug is safe just because it's approved by the FDA,&quot; says Jeffrey Lieberman, chairman of psychiatry at the Columbia College of Physicians and Surgeons in New York. Studies lasting a few weeks to a few months, with a couple of thousand patients total, won't reveal all that's wrong with a drug, he says.<br /> <br /> Laughren agrees that &quot;it's very difficult to answer every question we'd like to answer with these studies, because obviously they're not huge. Sometimes bad things that happen are going to be discovered only when a drug is used more widely.&quot;<br /> <br /> He says he, too, shares concern about the anti-psychotics prescribed for children without proof of safety or effectiveness. Much more pediatric information on the atypicals will be available within five years, he says.<br /> <br /> <strong>Recommended changes</strong><br /> <br /> Others favor fundamental changes to get the needed facts about drug safety. Lieberman thinks one solution would be for the FDA to be given a new legal authority: the right to require drug companies seeking to gain approval of a drug to contribute to a collective pool at the National Institutes of Health. The NIH could supervise larger safety and effectiveness studies of medicines after they're on the market.<br /> <br /> A national electronic medical records database that would capture all bad side effects of drugs, and require ages and diagnoses, could do a lot to protect children from careless prescribing and reveal the effects of anti-psychotics, Duke's March says.<br /> <br /> &quot;We know so little about what's happening to all the kids who are getting these powerful anti-psychotics,&quot; he says.<br /> <br /> March also thinks more private insurers ought to insist that aggressive children with short fuses try non-drug therapies proven to help before doctors jump in with anti-psychotics. These pills can seem like an appealing &quot;quick fix,&quot; he says, so they're popular.<br /> <br /> For foster children with mental health problems, medication is a mainstay, says Ira Burnim, legal director at the Bazelon Center for Mental Health Law, an advocacy group for those with mental disabilities. There's proof that the most effective care is &quot;wraparound,&quot; he says, meaning that caseworkers touch base regularly with a child's school, doctor, foster and perhaps birth families, in addition to ensuring therapy or medication as needed.<br /> <br /> &quot;Now they're medicating many kids instead of giving them the services they need. But there's very little time spent with psychiatrists and not much attention paid to side effects from these heavy drugs,&quot; Burnim says.<br /> <br /> States vary in how much wraparound care they provide for foster kids, &quot;but a typical pattern is patches here and there,&quot; Burnim says. &quot;They rely heavily on medications like the anti-psychotics. This costs more than wraparound in the long run, and it's less safe for the kids.&quot;<br /> <br /> March considers the widespread use of anti-psychotics on children without proof of safety or effectiveness &quot;a very large experiment.&quot; Many kids are getting the short end of the stick, he says. &quot;We're not even gathering good data on the outcome of the experiment. It's the worst of all possible worlds.&quot; <br /> </p> ]]></content:encoded>
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		<title>Drug therapy caused some scary side effects</title>
		<link>http://www.yourlawyer.com/articles/read/11628</link>		
		<pubDate>Tue, 02 May 2006 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
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		<description><![CDATA[Erin Evans is one parent who wishes she had never heard of anti-psychotics.  As a military couple, she and her husband, Joe, moved around frequently. Their son, Rex, 13, was babied a lot. His mother now feels that he was not ready for school when he reached kindergarten age.  He had trouble focusing in the classroom and was diagnosed with attention-deficit disorder at age 6. He started on an ADHD medicine and began hallucinating about worms and...]]></description>
			<content:encoded><![CDATA[Erin Evans is one parent who wishes she had never heard of anti-psychotics.<br /> <br /> As a military couple, she and her husband, Joe, moved around frequently. Their son, Rex, 13, was babied a lot. His mother now feels that he was not ready for school when he reached kindergarten age.<br /> <br /> He had trouble focusing in the classroom and was diagnosed with attention-deficit disorder at age 6. He started on an ADHD medicine and began hallucinating about worms and bugs in his food.<br /> <br /> Soon he was also on Prozac for anxiety, but the nervousness and paranoia persisted.<br /> <br /> At age 8, Rex was given Risperdal by a Tennessee child psychiatrist in private practice who consulted for the military. He said the boy probably had obsessive-compulsive disorder, too, Evans says.<br /> <br /> &quot;(He) didn't tell us it had never been approved for children or warn us about any side effects,&quot; she says.<br /> <br /> For the first few weeks, Risperdal helped a little; Rex became less anxious and hyper. &quot;But then it wore right off, so the doctor kept increasing the dose,&quot; she says.<br /> <br /> After one month on Risperdal, Rex started having tremors; within a few months, his hands shook so severely that he could barely write at school, &quot;and I'd have to guide the cup of milk to his mouth in the morning,&quot; Evans says.<br /> <br /> But the psychiatrist said the tremors weren't so bad, Evans says, and urged the family to continue the drug.<br /> <br /> The psychiatrist didn't pressure them, she says, &quot;but I'm from the generation where, when a doctor says something, you believe it.&quot;<br /> <br /> Then, about a year after Rex started Risperdal, the Evanses found out that he might have schizoaffective disorder, a psychotic illness that children rarely get. A doctor's report said Rex probably would need to be institutionalized.<br /> <br /> That year, when Rex was 9, the family moved to Colorado Springs. The parents started to learn more about Risperdal and, for the first time, they realized that Rex's symptoms could be side effects, so they started to wean him off the drug. In a few weeks they noticed his jaw was scrunching up and his facial expressions were becoming distorted. By then, Evans says, she had read up on tardive dyskinesia (TD), a neurological disorder that can be caused by anti-psychotics.<br /> <br /> Rex became less anxious, but the TD worsened. &quot;He had a horrible, ugly look on his face all the time,&quot; Evans says. Friends no longer came to play. Rex went from winning an award for best reader in the third grade to claiming he couldn't remember how to spell his own name in fourth grade.<br /> <br /> Then in fifth grade, Rex slowly began to improve. A medical exam showed spasms in his thorax, perhaps linked to the upper body spasms, restricting the flow of oxygen to his brain.<br /> <br /> He began oxygen therapy, and he quickly became more responsive to others and did better at school, Evans says. He also had behavioral therapies. At the end of elementary school, Rex had episodes only a few times a week.<br /> <br /> But junior high has brought more stress and bullying, and the episodes have become more frequent. &quot;His movement-disorder specialist said he expected Rex to have this for the rest of his life,&quot; Evans says.<br /> <br /> Now she is bitter. &quot;I trusted the doctors, I trusted the FDA ... and I feel betrayed by both,&quot; she says.<br /> <br /> The Food and Drug Administration &quot;does not regulate the practice of medicine,&quot; says Thomas Laughren, head of the division of psychiatry products. He adds that he's concerned about the use of such drugs in kids without systematic safety data.<br /> <br /> Nobody knows how many children on atypicals get TD, says Ramy Mahmoud of Janssen LP, maker of Risperdal, but it's rare in adults. &quot;Our drug isn't indicated for children,&quot; he says. &quot;It's a strong drug. It has risks and benefits. Doctors and patients together have to weigh the benefits, at the start and on a continuing basis, along with the harm and suffering.&quot;]]></content:encoded>
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		<title>New antipsychotic drugs carry risks for children</title>
		<link>http://www.yourlawyer.com/articles/read/11629</link>		
		<pubDate>Tue, 02 May 2006 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
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		<description><![CDATA[Nancy Thomas remembers the bad old days when she had to wear long-sleeve clothes to church to cover bite marks all over her arms from her daughter Alexa's rages.  At age 8, Alexa was diagnosed with bipolar disorder. She was a violent child with sharp mood swings and meltdowns that drove her to tear up the house. Antidepressants and drugs for attention-deficit disorder had only made Alexa more aggressive, Thomas says.  A mix of medicines...]]></description>
			<content:encoded><![CDATA[<p>Nancy Thomas remembers the bad old days when she had to wear long-sleeve clothes to church to cover bite marks all over her arms from her daughter Alexa's rages.<br /> <br /> At age 8, Alexa was diagnosed with bipolar disorder. She was a violent child with sharp mood swings and meltdowns that drove her to tear up the house. Antidepressants and drugs for attention-deficit disorder had only made Alexa more aggressive, Thomas says.<br /> <br /> A mix of medicines including so-called atypical antipsychotics drugs approved only for adults finally stabilized Alexa's moods. Now at 15, she is able to live a more normal life as long as she takes the medication.<br /> <br /> Even so, the Russellville, Mo., teen is paying a price: On one of the atypical antipsychotics, Alexa gained about 100 pounds in a year, putting her at risk for a host of health problems, including diabetes. It has taken her three years to lose a third of that extra weight; she is still struggling with the rest.<br /> <br /> Atypicals are a new generation of antipsychotic drugs approved by the Food and Drug Administration for adult schizophrenia and bipolar disorder (manic depression). None of the six drugs: Clozaril, Risperdal, Zyprexa, Seroquel, Abilify and Geodon are approved for kids, but doctors can prescribe them as &quot;off-label&quot; medications.<br /> <br /> Psychiatrists say the drugs can be helpful for children with serious mental illnesses and have been known to save young lives. But diagnosis often is difficult, making appropriate prescribing tricky. And many experts, including behavioral pediatrician Lawrence Diller, author of Should I Medicate My Child?, say there is growing overuse of these powerful antipsychotics.<br /> <br /> Schizophrenia is rare in children under 18: It strikes about 1 in 40,000, as opposed to 1 in 100 adults, according to the National Institute of Mental Health. Nobody knows exactly how many kids have bipolar disorder; psychiatrists don't even agree on criteria to diagnose the disease in childhood.<br /> <br /> Research on how the drugs affect children is sparse, and experts increasingly are concerned that the drugs are being prescribed too often for children with behavior problems, such as attention-deficit disorder and aggression.<br /> <br /> John March, chief of child and adolescent psychiatry at Duke University School of Medicine, prescribes the drugs to kids in some cases of serious illness when he thinks the benefits outweigh the risks. But he says prescribing them for behavior problems alone may be a mistake. &quot;We have no evidence about the safety of these agents or their effectiveness in controlling aggression,&quot; he says. &quot;Why are we doing this?&quot;<br /> <br /> At the same time, reports of deaths and dangerous side effects linked to the drugs are mounting. A USA TODAY study of FDA data collected from 2000 to 2004 shows at least 45 deaths of children in which an atypical antipsychotic was listed in the FDA database as the &quot;primary suspect.&quot; There also were 1,328 reports of bad side effects, some of them life-threatening.<br /> <br /> Drug companies are required to file any reports they have to the FDA, but consumers and doctors report such events on a voluntary basis. Studies suggest the FDA's Adverse Events Reporting System database captures only 1% to 10% of drug-induced side effects and deaths, &quot;maybe even less than 1%,&quot; says clinical pharmacologist Alastair J.J. Wood, an associate dean at Vanderbilt Medical School in Nashville. So the real number of cases is almost certainly much higher.<br /> <br /> &quot;We're conducting a very large experiment on our children,&quot; March says.<br /> <br /> Side effects that linger<br /> <br /> Some parents tell stories of serious effects that linger long after their kids stop taking the drugs.<br /> <br /> Rex Evans' parents are bitter about what happened to their son. They believe the 13-year-old Colorado Springs boy was harmed permanently by an atypical antipsychotic he took several years ago. Rex now has a serious case of tardive dyskinesia (TD), suffering daily episodes of involuntary jerking movements and facial grimacing, says Erin Evans, his mother.<br /> <br /> Antipsychotics are known to cause TD, but it's thought to be a rare effect for the newer atypicals.<br /> <br /> Despite such reports, outpatient prescriptions for kids ages 2 to 18 leaped fivefold from just under half a million to about 2.5 million&nbsp; from 1995 to 2002, according to a new analysis of a federal survey by Vanderbilt Medical School researchers. This doesn't include prescriptions at psychiatric hospitals or residential treatment centers.<br /> <br /> And even though the drugs are approved only for adults, the rate of children treated with atypicals &quot;is growing dramatically faster than the rate for adults,&quot; says Robert Epstein, chief medical officer for Medco Health Solutions, pharmacy benefit managers.<br /> <br /> Medco did an analysis of outpatient prescriptions for USA TODAY and found that, in a sampling of about 2.5 million of Medco's 55 million members, the rate of children 19 and under with at least one atypical prescription jumped 80% from 2001 to 2005 from 3.6 per 1,000 to 6.5 per 1,000. And that only represents kids who are privately insured, not those in foster care or others on Medicaid.<br /> <br /> &quot;We know these are very strong medicines,&quot; Epstein says. &quot;You'd want to be absolutely sure the child needs it.&quot;<br /> <br /> The more serious risks<br /> <br /> Because of the nature of the FDA data, they don't prove that these drugs caused the deaths or the side effects. Many side effects for which an atypical is listed as the &quot;primary suspect&quot; occurred in the normal course of using the drug, but the database also includes cases involving drug abuse, overdoses, suicides and homicides. Entries are sometimes cryptic, and the FDA enters verbatim misspellings and all what's reported on the form.<br /> <br /> Still, the data &quot;can be a useful signaling device&quot; suggesting problems with a drug that warrant conclusive studies, says Jerome Avorn, a pharmacology specialist at Harvard Medical School and author of the book Powerful Medicines.<br /> <br /> One-fourth of the cases in the database studied by USA TODAY did not list the patient's age. But in cases that listed an age under 18:<br /></p> <ul>   <li> A condition called dystonia was most often cited as an &quot;adverse event&quot; suffered by someone taking one of the drugs, with 103 reports. Dystonia produces involuntary, often painful muscle contractions.</li>   <li>Tremors, weight gain and sedation often were cited, along with neurological effects such as TD. Symptoms of TD can vary from slight twitching to full-blown jerking of the body.</li>   <li> A condition called neuroleptic malignant syndrome, with 41 pediatric cases over the five years, was the most troubling effect listed, says child psychiatrist Joseph Penn of Bradley Hospital and Brown University School of Medicine. It is life-threatening and can kill within 24 hours of diagnosis. It's been linked to drugs that act on the brain's dopamine receptors, which would include the atypicals, Penn says.</li> </ul> <p> The FDA office of drug safety checks the database, &quot;and we haven't been alerted to any particular or unusual concern,&quot; says Thomas Laughren, director of the agency's division of psychiatry products. &quot;The effects (in kids) are similar to what we're seeing in adults. We have not systematically looked at the data for children&quot; because the drugs aren't approved for them, he says.<br /> <br /> The 45 deaths<br /> <br /> Among the 45 pediatric deaths in which atypicals were the primary suspect, at least six were related to diabetes, atypicals carry warnings that the drugs may increase the risk of high blood sugar and diabetes. Other causes of death ranged from heart and pulmonary problems to suicide, choking and liver failure.<br /> <br /> An 8-year-old boy had cardiac arrest. A 15-year-old boy died of an overdose. A 13-year-old girl experienced diabetic ketoacidosis, a deficiency of insulin.<br /> <br /> More than half of the kids who died were on at least one other psychiatric drug besides the atypical antipsychotic, and many were taking drugs for other ailments.<br /> <br /> The youngest, a 4-year-old boy whose symptoms suggested diabetes complications, was taking 10 other drugs.<br /> <br /> The reports don't tell the child's general state of health or other factors that could predispose him to trouble. Also, neither Clozaril, which is rarely used, nor Abilify, the newest atypical, was listed as a primary suspect in any deaths.<br /> <br /> All the drugmakers emphasize that their products are not approved for children, and they say the drugs are safe and effective for adults with schizophrenia or bipolar disorder who are monitored for side effects. Still, &quot;there are worrisome questions here,&quot; says Avorn. Large, longer-term database studies could provide answers, he says.<br /> <br /> There's some evidence that the drugs can help young schizophrenics and may be helpful in treating bipolar disorder in children, says Robert Findling, a child psychiatrist at University Hospitals of Cleveland.<br /> <br /> But the data from controlled studies &quot;are too few to guide treatment decisions&quot; on bipolar disorder, concluded Findling's research team in a summary of pediatric studies published in the Journal of Clinical Psychiatry.<br /> <br /> These antipsychotics are the most widely used class of drugs to treat disruptive kids who attack others and defy adults, Findling says. Again, there's a paucity of proof that the drugs help.<br /> <br /> There are only a handful of carefully controlled, sizable studies testing the drugs for any pediatric disorder, and they're mostly short-term, says Benedetto Vitiello, chief of child and adolescent psychiatry at the national mental health institute. The most serious, widespread problem found to be caused by the medicines is weight gain, he says. The effect varies by drug, but kids typically put on twice the pounds they should in their first six months on atypicals.<br /> <br /> In the first three months on the drugs, children add about 2 to 3 inches to their waistlines, says research psychiatrist Christoph Correll of Zucker Hillside Hospital in Glen Oaks, N.Y. A lot of this is abdominal fat, which increases the risk of diabetes and heart disease. Obese children are twice as likely as normal-weight children to have diabetes, according to a new University of Michigan study.<br /> <br /> &quot;Some patients gain weight on Zyprexa and others do not,&quot; says Calvin Sumner, a medical adviser to Eli Lilly Research Laboratories. Lilly makes the drug, which has been associated with weight gains in adult studies. Sumner stresses that Zyprexa isn't approved for kids.<br /> <br /> There's no proof atypicals cause diabetes, says Ramy Mahmoud of Janssen LP, maker of Risperdal. He says the FDA added a label warning of increased diabetes risk &quot;to make people aware of the possibility.&quot;<br /> <br /> One key question about atypicals is whether they will have long-term, unknown effects on the brains of children.<br /> <br /> The brain system that the drugs work on develops through childhood and adolescence, says Cynthia Kuhn, a Duke University pharmacologist. &quot;We really don't know the impact of chronically perturbing that system in childhood.&quot;<br /> <br /> Why atypicals get prescribed<br /> <br /> Given all the potential problems, why would doctors prescribe these drugs to children to begin with?<br /> <br /> Nobody disputes that the lives of schizophrenic or severely manic children may be saved by antipsychotics. &quot;I use them myself for patients,&quot; says March, the Duke psychiatrist. &quot;I have a 9-year-old who threatened to jump out of a second-story window if her mom didn't give her the car keys to drive down to the 7-Eleven to get a Coke. If I took her off antipsychotics, she'd disintegrate.&quot;<br /> <br /> But several factors can lead to misprescribing of antipsychotics.<br /> <br /> It can be difficult to tell one behavioral disorder or illness from another in kids. For example, the aggression and irritability of bipolar disorder can mimic attention-deficit hyperactivity disorder or depression, the mental health institute says. Also, the environment can be a key cause of symptoms that may be mistakenly diagnosed as mental disorders, says Diller, the behavioral pediatrician. Some events in a child's life can trigger acting-out or other symptoms. Adults can explain what happened to them; children, especially the youngest, may be more reticent.<br /> <br /> Doctors often face time pressures that prevent them from finding out what's going on in kids' lives, knowledge that might suggest alternative treatments, Penn says. For example, abuse of drugs such as methamphetamine, OxyContin and cocaine is fairly common among teens, he says. Kids begin acting strangely, hearing voices, becoming paranoid. The symptoms can mimic psychosis or behavioral disorders, and doctors can end up giving these children unneeded antipsychotic drugs, he says.<br /> <br /> Insurance coverage rules may encourage the soaring use of antipsychotics for children, as well. &quot;With some companies, the only thing they reimburse for is prescribing. There's little or no therapy,&quot; says Ronald Brown, editor of the Journal of Pediatric Psychology and a dean at Temple University.<br /> <br /> Also, kids with serious mental health problems often have at least one hospitalization, but policies cover only a week or two.<br /> <br /> It can take a couple of weeks just to get medical records and family histories, Penn says, but insurers often extend time if there's a new medicine started, which encourages drug dabbling for children who are not ready to go home.<br /> <br /> In the end, some parents say their children have such severe behavior disorders or mental illness that the benefits outweigh risks.<br /> <br /> Parents of children such as Alexa Thomas, who have bipolar disorder, say the atypicals often help. &quot;We were very fortunate,&quot; says Alexa's mother, special-education director for the Russellville, Mo., school district. &quot;The medication worked for my daughter. It doesn't work for everybody.&quot;<br /> <br /> Misdiagnosis common<br /> <br /> The Vanderbilt study of antipsychotic prescribing finds at least 13% of pediatric prescriptions are for bipolar disorder. But there is some concern about over-diagnosis and &quot;jumping to this (bipolar) label too quickly,&quot; says psychiatrist Peter Jensen, head of the Center for the Advancement of Children's Mental Health at Columbia University.<br /> <br /> Sandra Spencer's son, Stephen, was diagnosed as bipolar at age 6 and put on atypicals. He developed liver abnormalities and obesity, his mother says. &quot;He's been on a smorgasbord of meds,&quot; she says. None worked well for very long.<br /> <br /> By the time he was in sixth grade, doctors said they weren't sure Stephen was bipolar after all. Now 15, he is on low doses of an antidepressant and mood stabilizer. He's being weaned off both, says Spencer, executive director of the Federation of Families for Children's Mental Health, a support group.<br /> <br /> She worries about how the drugs have affected Stephen, who is black: As little psychiatric drug research as there is on children, there's least of all on minority kids. Some drugs are known to affect black adults differently from whites. &quot;He probably had ADHD all along,&quot; Spencer says. &quot;Psychiatry is so not an exact science.&quot;<br /> <br /> Child psychiatrist Barbara Geller, a bipolar expert at Washington University in St. Louis, agrees: &quot;The science is nowhere near where it is in other branches of medicine.&quot;<br /> <br /> So parents struggle to make the right decisions for very troubled kids. &quot;There's a lot of fear among parents,&quot; Spencer says. &quot;You don't know what the effects of these drugs are going to be. You're at the mercy of your doctor.<br /> <br /> &quot;I have had to make a lot of decisions, and they were fear-driven. You don't have enough information to make an intelligent decision.&quot; <br /></p> ]]></content:encoded>
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		<title>A rush to overprescribe?</title>
		<link>http://www.yourlawyer.com/articles/read/11637</link>		
		<pubDate>Tue, 02 May 2006 00:00:00 -0700</pubDate>
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		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11637</guid>
		<description><![CDATA[Rising numbers of U.S. children are taking a new generation of anti-psychotic drugs called atypicals. Although the six drugs: Clozaril, Risperdal, Zyprexa, Seroquel, Abilify and Geodon can be helpful in treating children with mental illness, critics say that the drugs are overprescribed and that many kids suffer serious side effects from drugs they never needed.   USA TODAY's Marilyn Elias talks to one mother who believes that's what happened to...]]></description>
			<content:encoded><![CDATA[Rising numbers of U.S. children are taking a new generation of anti-psychotic drugs called atypicals. Although the six drugs: Clozaril, Risperdal, Zyprexa, Seroquel, Abilify and Geodon can be helpful in treating children with mental illness, critics say that the drugs are overprescribed and that many kids suffer serious side effects from drugs they never needed. <br /> <br /> USA TODAY's Marilyn Elias talks to one mother who believes that's what happened to her son.<br /> <br /> Evan Kitchens had problems from birth. He suffered from lack of oxygen during a difficult delivery. As a baby, he wouldn't nurse properly, didn't want to be held and screamed for hours.<br /> <br /> &quot;He hardly slept at all,&quot; says his mother, Mary Kitchens, a florist in Bandera, Texas.<br /> <br /> At 18 months old, Evan was diagnosed with an autism spectrum disorder and prescribed Adderall, a drug to treat attention-deficit hyperactivity disorder.<br /> <br /> But Evan just got more aggressive and hyperactive. When he was 2, he knocked out the front teeth of his younger brother with a flashlight. The family began a constant round of appointments with child psychiatrists and other doctors.<br /> <br /> At 2&frac12;, Evan was diagnosed with obsessive-compulsive disorder. When he was 3, doctors put him on Risperdal, his first anti-psychotic. But in a &quot;special needs&quot; preschool, his aggressive behavior continued. He was out of control, racing out of the classroom, hitting other kids.<br /> <br /> At 5 Evan was hospitalized for the first time. He was still on Risperdal and two other drugs, supposedly to stabilize his moods and curb hyperactivity. But nothing had worked well for long.<br /> <br /> Kitchens says she tried doctor after doctor. She had insurance only on and off; her husband disappeared when twins were born 16 months after Evan, she says, so she became the family's sole support.<br /> <br /> &quot;Every drug created new symptoms, and then you had to treat those symptoms,&quot; she says. &quot;We were constantly changing meds. I see now what we were really managing was symptoms of the drugs, not his underlying problem.&quot;<br /> <br /> In April 2004, at age 8, Evan set fire to the bedroom carpet with a candle. Fortunately, 14-year-old Ethan, Evan's older brother, saw the fire before anyone was hurt.<br /> <br /> Evan was hospitalized in San Antonio. The family drove three hours every day, Kitchens says, to bring Evan dinner and spend time with him. Now doctors said he might have bipolar disorder.<br /> <br /> Evan had been on Risperdal and the mood stabilizer Lithium. Doctors added Seroquel to the mix. Within a month, he showed tremors, Kitchens says. &quot;They got so bad, he was shaking all the time.&quot; Evan's eyes started to cross. Still, doctors thought it was important to keep him on the drugs. They added two more mood stabilizers. Soon Evan had a thyroid disorder and an abnormally low white blood cell count, Kitchens says.<br /> <br /> In August, Evan was transferred to another center and weaned off everything but Seroquel and a drug for attention-deficit disorder. His alertness returned, but other symptoms lingered for months.<br /> <br /> In January 2005, Evan came home. Kitchens gradually took him off Seroquel and says he's doing better than ever just taking medicine for ADD. He has had intensive behavior-management therapy; so has the whole family. His alarming symptoms are gone, but his eyes still cross occasionally if he's tired.<br /> <br /> Many child psychiatrists are frustrated by the lack of drugs to treat kids with mental disorders, says Wayne Macfadden, U.S. medical director for Seroquel, which is made by AstraZeneca. But Seroquel isn't approved for children, he says. &quot;Obviously, prescribers have to weigh the risks and benefits.&quot;<br /> <br /> Evan made the honor roll in regular school his first semester home, Kitchens says. He sang in the school's Christmas choir, played basketball and is making friends.<br /> <br /> His mother wishes she had gone the non-drug route earlier. &quot;I didn't even know what was available. I totally relied on the doctors.&quot;<br /> <br /> Evan says his time of live-in care &quot;is like a blur. I remember my stomach would hurt, and my head would hurt. I slept a whole lot. And then I started to see two of things. I was very scared.&quot; He says he's happy to be home: &quot;Nothing hurts anymore.&quot;<br /> <br /> If doctors recommend the drugs he took for other kids, Evan has some advice for their parents: &quot;Sometimes it's good for them, sometimes it's bad for them. I would warn them about the bad things that can happen.&quot;<br /> ]]></content:encoded>
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		<title>For foster kids, oversight of prescriptions is scarce</title>
		<link>http://www.yourlawyer.com/articles/read/11638</link>		
		<pubDate>Tue, 02 May 2006 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11638</guid>
		<description><![CDATA[Foster children are of special concern to some experts who fear atypical anti-psychotics may be prescribed without the careful oversight usually provided by birth parents.  The vigilant medical monitoring that is needed by foster children on anti-psychotics &quot;is still unusual, unfortunately&quot; in the USA, says Moira Szilagyi, a Rochester, N.Y., pediatric endocrinologist who specializes in foster children.  There are no numbers collected...]]></description>
			<content:encoded><![CDATA[<div class=&#8243;&Prime;inside-copy&Prime;&#8243;>Foster children are of special concern to some experts who fear atypical anti-psychotics may be prescribed without the careful oversight usually provided by birth parents.</div>  <p class=&#8243;&Prime;inside-copy&Prime;&#8243;>The vigilant medical monitoring that is needed by foster children on anti-psychotics &quot;is still unusual, unfortunately&quot; in the USA, says Moira Szilagyi, a Rochester, N.Y., pediatric endocrinologist who specializes in foster children.</p>  <p class=&#8243;&Prime;inside-copy&Prime;&#8243;>There are no numbers collected nationally, but Paul Vincent of the Child Welfare Policy and Practice Group believes there has been an upswing in the use of atypicals by foster kids in the past few years. His Montgomery, Ala., firm consults for state child welfare agencies, reviewing many of their health services.</p>  <p class=&#8243;&Prime;inside-copy&Prime;&#8243;>Some state data obtained by USA TODAY through Freedom of  Information Act requests appear to support his observations.</p> <ul>   <li>In California, Med-Cal prescription claims for atypicals for kids in foster care increased 77% between 2001 and 2005, to 70,879. The actual number is probably higher because the state does not get complete data from managed-care providers, which cover the majority of foster children.</li>   <li>In Illinois, the number of children covered under the state's public health care program not just foster children who had an atypical prescription went up 39% between fiscal years 2003 and 2005, to 17,746.</li> </ul>               <p class=&#8243;&Prime;inside-copy&Prime;&#8243;>Kids as young as 4 are getting prescriptions for anti-psychotics, Vincent says, sometimes from unqualified counselors. &quot;They aren't psychiatrists or even psychologists. I have considerable worry about the accuracy of these diagnoses.&quot;<br /> <br /> The safety of these drugs is of most concern to Andrea Moore, a Coral Springs, Fla., attorney. Judges appointed her to represent foster kids a few years ago. Several children she represented started lactating after taking anti-psychotics, a recognized side effect of the drugs. A 12-year-old girl with a history of heart problems became short of breath on Geodon, an atypical that can cause arrhythmias. &quot;The doctor prescribing it did not even have her medical history,&quot; Moore says.<br /> <br /> Geodon has a proven &quot;modest&quot; effect on heart rhythms in adults, says Ilise Lombardo, medical director for the U.S. Geodon team at Pfizer Inc., maker of the drug. The clinical impact of this rhythm change is unknown but is being studied in adults, she says; safety and effectiveness studies in kids are underway, too. The drug's label says patients with certain heart problems shouldn't take it.<br /> <br /> In February, Florida's health care agency ordered an independent investigation into why the number of Medicaid children taking anti-psychotics nearly doubled in the past five years. The numbers jumped from 9,500 to 17,900.<br /> <br /> A new Florida law adds some protections for foster children, but it has loopholes, Moore says. &quot;I'm still hearing about problems with overprescribing and under-monitoring.&quot;</p>]]></content:encoded>
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		<title>More kids get drugs that treat psychosis</title>
		<link>http://www.yourlawyer.com/articles/read/11503</link>		
		<pubDate>Fri, 17 Mar 2006 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11503</guid>
		<description><![CDATA[        Soaring numbers of U.S. children are being prescribed anti-psychotic drugs in many cases, for attention deficit disorder or other behavioral problems for which these medications have not been proven to work, a study found.  The annual number of children prescribed anti-psychotic drugs jumped fivefold from 1995 to 2002, to an estimated 2.5 million, the study said. That is an increase from 8.6 out of every 1,000 children in the mid-1990s...]]></description>
			<content:encoded><![CDATA[        <p class=&#8243;&Prime;&Prime;&Prime;&Prime;MsoNormal&Prime;&Prime;&Prime;&Prime;&#8243;>Soaring numbers of U.S. children are being prescribed anti-psychotic drugs in many cases, for attention deficit disorder or other behavioral problems for which these medications have not been proven to work, a study found.<br /> <br /> The annual number of children prescribed anti-psychotic drugs jumped fivefold from 1995 to 2002, to an estimated 2.5 million, the study said. That is an increase from 8.6 out of every 1,000 children in the mid-1990s to nearly 40 out of 1,000.<br /> <br /> But more than half of the prescriptions were for attention deficit and other non-psychotic conditions, the researchers said.</p>         <p class=&#8243;&Prime;&Prime;&Prime;&Prime;MsoNormal&Prime;&Prime;&Prime;&Prime;&#8243;>The findings are worrisome &quot;because it looks like these medications are being used for large numbers of children in a setting where we don't know if they work,&quot; said lead author Dr. William Cooper, a pediatrician at Vanderbilt Children's Hospital.<br /> <br /> The increasing use of anti-psychotics since the mid-1990s corresponds with the introduction of costly and heavily marketed medications such as Zyprexa, made by Eli Lilly and Co. and used to treat schizophrenia, and Risperdal. The packaging information for both says their safety and effectiveness in children have not been established.</p>      <p class=&#8243;&Prime;&Prime;&Prime;&Prime;MsoNormal&Prime;&Prime;&Prime;&Prime;&#8243;>Anti-psychotics are intended for use against schizophrenia and other psychotic illnesses.</p>   <p class=&#8243;&Prime;&Prime;&Prime;&Prime;MsoNormal&Prime;&Prime;&Prime;&Prime;&#8243;>However, attention deficit disorder is sometimes accompanied by temper outbursts and other disruptive behavior. As a result, some doctors prescribe anti-psychotics to these children to calm them down a strategy some doctors and parents say works.<br /> <br /> The drugs, which typically cost several dollars per pill, are considered safer than older anti-psychotics at least in adults but they still can have serious side effects, including weight gain, elevated cholesterol and diabetes.</p><p class=&#8243;&Prime;&Prime;&Prime;&Prime;MsoNormal&Prime;&Prime;&Prime;&Prime;&#8243;>The researcher&rsquo;s analyzed data on youngsters age 13 on average who were involved in annual national health surveys. The surveys involved prescriptions given during 119,752 doctor visits. The researchers used that data to come up with national estimates.</p>   <p class=&#8243;&Prime;&Prime;&Prime;&Prime;MsoNormal&Prime;&Prime;&Prime;&Prime;&#8243;>Cooper said some of the increases might reflect repeat prescriptions given to the same child, but he said that is unlikely and noted that his findings echo results from smaller studies.</p>]]></content:encoded>
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		<title>America&amp;#039;s Top-Selling Prescription Drugs &amp;#150; a Who&amp;#039;s Who of Blockbusters</title>
		<link>http://www.yourlawyer.com/articles/read/11442</link>		
		<pubDate>Sat, 04 Mar 2006 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11442</guid>
		<description><![CDATA[According to a recent article in Forbes.com (2/27/06) that was based on figures obtained from IMS Health, a healthcare information company, the top 20 prescription drugs in the U.S. in 2005, with combined sales of $64.6 billion, were as follow:1.&nbsp;&nbsp;&nbsp; LIPITOR &ndash; Pfizer &ndash; Treats high cholesterol: $8.4 billion2.&nbsp;&nbsp;&nbsp; ZOCOR &ndash; Merck &ndash;Treats high cholesterol: $4.4 billion3.&nbsp;&nbsp;&nbsp; NEXIUM...]]></description>
			<content:encoded><![CDATA[According to a recent article in Forbes.com (2/27/06) that was based on figures obtained from IMS Health, a healthcare information company, the top 20 prescription drugs in the U.S. in 2005, with combined sales of $64.6 billion, were as follow:<br /><br />1.&nbsp;&nbsp;&nbsp; LIPITOR &ndash; Pfizer &ndash; Treats high cholesterol: $8.4 billion<br /><br />2.&nbsp;&nbsp;&nbsp; ZOCOR &ndash; Merck &ndash;Treats high cholesterol: $4.4 billion<br /><br />3.&nbsp;&nbsp;&nbsp; NEXIUM &ndash; AstraZeneca &ndash; Treats heartburn: $4.4 billion <br /><br />4.&nbsp;&nbsp;&nbsp; PREVACID &ndash; Abbott &amp; Takeda &ndash; Treats heartburn: $3.8 billion <br /><br />5.&nbsp;&nbsp;&nbsp; ADVAIR DISKUS &ndash; GlaxoSmithKline &ndash; Treats asthma: $3.6 billion <br /><br />6.&nbsp;&nbsp;&nbsp; PLAVIX &ndash; Bristol-Meyers Squibb &amp; Sanofi-Aventis &ndash; Treats heart disease $3.5 billion <br /><br />7.&nbsp;&nbsp;&nbsp; ZOLOFT &ndash; Pfizer &ndash; Treats depression: $3.1 billion <br /><br />8.&nbsp;&nbsp;&nbsp; EPOGEN &ndash; Amgen &ndash; Treats anemia: $3.0 billion <br /><br />9.&nbsp;&nbsp;&nbsp; PROCRIT &ndash; Johnson &amp; Johnson &ndash; Treats anemia: $3.0 billion <br /><br />10.&nbsp;&nbsp;&nbsp; ARANESP &ndash; Amgen &ndash; Treats anemia: $2.8 billion <br /><br />11.&nbsp;&nbsp;&nbsp; ENBREL &ndash; Amgen &amp; Wyeth &ndash; Treats rheumatoid arthritis: $2.7 billion<br /><br />12.&nbsp;&nbsp;&nbsp; NORVASC &ndash; Pfizer &ndash; Treats high blood pressure: $2.6 billion <br /><br />13.&nbsp;&nbsp;&nbsp; SEROQUEL &ndash; AstraZeneca &ndash; Treats schizophrenia: $2.6 billion <br /><br />14.&nbsp;&nbsp;&nbsp; EFFEXOR XR &ndash; Wyeth &ndash; Treats depression: $2.6 billion <br /><br />15.&nbsp;&nbsp;&nbsp; ZYPREXA &ndash; Eli Lilly &ndash; Treats: schizophrenia: $2.5 billion <br /><br />16.&nbsp;&nbsp;&nbsp; SINGULAIR &ndash; Merck &ndash; Treats asthma and allergies: $2.5 billion <br /><br />17.&nbsp;&nbsp;&nbsp; PROTONIX &ndash; Wyeth &ndash; Treats heartburn: $2.4 billion <br /><br />18.&nbsp;&nbsp;&nbsp; RISPERDAL &ndash; Johnson &amp; Johnson &ndash; Treats schizophrenia: $2.3 billion<br /><br />19.&nbsp;&nbsp;&nbsp; NEULASTA &ndash; Amgen &ndash; Treats chemotherapy side effects: $2.2 billion<br /><br />20.&nbsp;&nbsp;&nbsp; REMICADE &ndash; Johnson &amp; Johnson &ndash; Treats rheumatoid arthritis: $2.2 billion]]></content:encoded>
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		<title>Study Finds Hyperglycemia Linked to Antipsychotic Medications &amp;#150; Validates Prior Research and Zyprexa Litigation Claims</title>
		<link>http://www.yourlawyer.com/articles/read/11122</link>		
		<pubDate>Thu, 01 Dec 2005 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/11122</guid>
		<description><![CDATA[A new study at the VA Connecticut Healthcare System, New Haven, Connecticut found that those taking atypical antipsychotic drugs may be at risk for developing high blood sugar (hyperglycemia).The research, which was conducted by a team led by Dr. Michael J. Sernyak, monitored the frequency of undiagnosed high blood sugar in 647 patients taking various atypical antipsychotics, including: Clozaril (clozapine), Risperdal (risperidone), Zyprexa...]]></description>
			<content:encoded><![CDATA[A new study at the VA Connecticut Healthcare System, New Haven, Connecticut found that those taking atypical antipsychotic drugs may be at risk for developing high blood sugar (hyperglycemia).<br /><br />The research, which was conducted by a team led by Dr. Michael J. Sernyak, monitored the frequency of undiagnosed high blood sugar in 647 patients taking various atypical antipsychotics, including: Clozaril (clozapine), Risperdal (risperidone), Zyprexa (olanzapine), Seroquel (quetiapine), or Geodon (ziprasadone). Over the course of two years, 153 of the participants had a fasting blood sugar result.<br /><br />The study&rsquo;s findings, published in the Journal of Clinical Psychiatry for December 2005, show that blood sugar levels were normal for 70% of the subjects, raised in 25% and extremely elevated in just over 5% of the participants. <br /><br />Race, ethnicity, age, body mass index (BMI), or psychiatric diagnosis did not appear to have an impact on the development of high blood sugar.<br /><br />Of all the antipsychotic medications, Clozaril was found to raise blood sugar in significantly more individuals than any of the other medications. The researchers did not find substantial differences for any of the other drugs.<br /><br />According to the study, almost one in three patients taking atypical antipsychotics who thought their blood sugar levels were normal actually had abnormalities. The authors believe this finding should prompt the implementation of periodic screening even in large outpatient populations.<br /><br />On June 10, newsinfern.com reported that Eli Lilly had agreed to pay $690 million to settle some 8,000 claims regarding its failure to adequately warn patients that Zyprexa posed an increased risk of diabetes and hyperglycemia.<br /><br />Specifically, the claims were based on allegations that prior to September 2003, Lilly failed to adequately warn those taking Zyprexa of an increased risk of developing diabetes, hyperglycemia, and related illnesses.<br /><br />While the pharmaceutical giant did not admit its best-selling drug caused the injuries in question, its potential exposure in the litigation far exceeded the settlement figure. Thus, as a business decision, resolving about 75% of the claims six months before trial made sense. <br /><br />At the time, Jerrold S. Parker, senior partner in the prominent New York personal injury law firm of Parker &amp; Waichman, told reporters that: &ldquo;It&rsquo;s really remarkable to arrive at a settlement of this magnitude so far in advance of trial.&rdquo; <br /><br />Mr. Parker said that the plaintiffs&rsquo; litigation team, made up of some of the foremost products liability attorneys, &ldquo;was able to convince Lilly that plaintiffs&rsquo; case was a strong one, with a good likelihood of success, if it proceeded to trial.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;<br />&nbsp;<br />The fund will be administered by a panel named by the plaintiffs&rsquo; attorneys which will allocate compensation to the plaintiffs based mostly on the extent of their injuries which range from weight gain to death.<br /><br />Zyprexa, like two other powerful antipsychotic drugs, Risperdal (Jannsen Pharmaceuticals) and Seroquel (AstraZeneca), has been found to cause serious side effects in patients, especially those who have already been diagnosed with diabetes and related illnesses. <br /><br />Knowledge of the dangers of Zyprexa was discovered as a result of a series of findings beginning in 2001 when the FDA was alerted to 19 case reports of diabetes associated with the drug. <br /><br />One of these cases resulted in death due to necrotizing pancreatitis, a condition in which cells in the pancreas die. In May 2003, forty additional reports of hyperglycemia (elevated blood sugar), diabetes mellitus, or exacerbation of diabetes were received in the UK including one which proved to be fatal.<br /><br />An emergency report issued by the Japanese Health and Welfare Ministry in April of 2002 concerning the side effects of Zyprexa noted that there had been two deaths of patients who had diabetes prior to taking the anti-psychotic medication. It also reported that there had been seven other patients who lost consciousness or slipped into comas after taking the drug. <br /><br />In April of 2003, the Wall Street Journal ran a front page article on Zyprexa and other anti-psychotics and their link to the development of diabetes. The article estimated that somewhere around 11 million people have taken Zyprexa. <br /><br />An eight-year study found that nearly 300 patients developed diabetes, 75 became seriously ill, and 23 died. Although the FDA was aware of these cases, it did not require Lilly (and the manufactures of similar antipsychotic drugs) to add a significant warning regarding these risks until September 2003.<br /><br />Zyprexa has been prescribed to more than 17 million people worldwide since it was first marketed in 1996.&nbsp; It became Lilly&rsquo;s best selling medication, after Prozac lost U.S. patent protection in 2001, with annual sales of $4.4 billion or almost 33% of Lilly&rsquo;s total sales of $13.86 billion.<br /><br />The results of the newest study serve to confirm the findings reached in previous research as well as the validity of the claims that prompted Lilly&rsquo;s settlement in June.]]></content:encoded>
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		<title>Antipsychotic Drugs Not Advised for Alzheimer's</title>
		<link>http://www.yourlawyer.com/articles/read/10857</link>		
		<pubDate>Tue, 25 Oct 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/10857</guid>
		<description><![CDATA[Frail, elderly patients with Alzheimer's disease who are given widely used antipsychotic drugs such as Zyprexa and Risperdal have a higher risk of dying than patients who are given sugar pills, and doctors should be cautious in prescribing the drugs, according to a new analysis of earlier studies.The report is likely to complicate the limited choices that families face while caring for elderly patients with Alzheimer's. And it lends support to a...]]></description>
			<content:encoded><![CDATA[Frail, elderly patients with Alzheimer's disease who are given widely used antipsychotic drugs such as Zyprexa and Risperdal have a higher risk of dying than patients who are given sugar pills, and doctors should be cautious in prescribing the drugs, according to a new analysis of earlier studies.<br /><br />The report is likely to complicate the limited choices that families face while caring for elderly patients with Alzheimer's. And it lends support to a decision by the Food and Drug Administration earlier this year to require warning labels on the drugs.<br /><br />&quot;These medications are only modestly effective and have significant side effects associated with them,&quot; said Peter Rabins, a professor of psychiatry at Johns Hopkins University School of Medicine who reviewed the new analysis.<br /><br />&quot;The drugs should not be used for trivial problems like difficulty sleeping at night and anxiety,&quot; he added. &quot;Clinicians first need to really weigh the potential risks and benefits in deciding whether the potential harm from the symptoms is worth the risk.&quot;<br /><br />An editorial by Rabins was published last Tuesday, along with the new study, in the Journal of the American Medical Association.<br /><br />About a third of the 4 million to 5 million Americans with the degenerative brain disorder are given antipsychotic drugs, estimated Samuel Gandy, chairman of the medical and scientific advisory council of the Alzheimer's Association, a nonprofit research and advocacy group.<br /><br />The drugs are approved for the treatment of psychoses in adults but have not been specifically approved for use among elderly patients with dementia, so physicians prescribing them for this group are relying on their clinical judgment. Experts said the new study should help doctors better weigh the risks and benefits.<br /><br />&quot;It should make physicians cautious when putting patients with dementia or any frail patient on medicines of this sort that are basically major tranquilizers,&quot; Gandy said. At the same time, he and others noted, the choices are limited when patients fall into the acute grip of agitation and delusions.<br /><br />The lead investigator, Lon Schneider of the University of Southern California, said his meta-analysis of 15 trials involving about 5,000 patients had found that the risk of death rose from 2 percent to 3 percent for patients taking the drugs in studies that lasted around 12 weeks. Most of the deaths came from cardiac problems or respiratory disorders.<br /><br />Schneider said the drugs might increase the risk because they sedate patients and confine them to bed for longer periods, making them more likely to pick up infections.<br /><br />Although Schneider, Gandy and Rabins all agreed the difference in risk was small and the patients were extremely vulnerable to begin with, Gandy said that &quot;because these drugs are so widely used, it could translate into a substantial number of individuals&quot; at risk.<br /><br />Schneider, a professor of psychiatry, neurology and gerontology at USC, said the study should alert clinicians to monitor patients closely, but he added, &quot;I don't know for a fact that elderly patients with dementia are being excessively medicated with antipsychotics.<br /><br />&quot;Maybe the medications are not monitored as carefully or given for too long a time,&quot; he said. &quot;There is a tendency among us to put patients on medications and keep them on for a long period of time.&quot;]]></content:encoded>
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		<title>Alzheimer Drugs May Increase Death Risks</title>
		<link>http://www.yourlawyer.com/articles/read/10838</link>		
		<pubDate>Wed, 19 Oct 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/10838</guid>
		<description><![CDATA[Popular antipsychotic drugs may increase the risk of death when given to people with dementia, according to an analysis done by researchers at the University of California.The research team analyzed 15 trials involving about 5,000 patients to determine if there was a correlation between the use of the antipsychotic drugs and an increased risk for death.&nbsp; During the trails 3,353 patients took the antipsychotics and 1,757 were given...]]></description>
			<content:encoded><![CDATA[Popular antipsychotic drugs may increase the risk of death when given to people with dementia, according to an analysis done by researchers at the University of California.<br /><br />The research team analyzed 15 trials involving about 5,000 patients to determine if there was a correlation between the use of the antipsychotic drugs and an increased risk for death.&nbsp; During the trails 3,353 patients took the antipsychotics and 1,757 were given placebos.&nbsp; The researchers found that the risk of death rose from 2 percent to 3 percent for patients taking the antipsychotic drugs.<br /><br />The research team, led by Lon Schneider, professor of psychiatry, neurology, and gerontology in the Keck School at USC, studied the correlation between aripiprazole (Abilify), olanzapine (Zyprexa), quetiapine (Seroquel), and risperidone (Risperdal) and an increased risk for death.&nbsp; There were 188 deaths associated with the antipsychotic drugs compared to 40 deaths associated with the placebos.<br /><br />When the specific drugs were examined individually, there was no significant difference between the risks conferred by one drug over another.&nbsp; The researchers noted that the differences &ldquo;could not have been recognized by examining any individual trial.&nbsp; The events were too sparse and the trials too small to be able to meaningfully assess for a dose response that might make attribution more compelling.&rdquo;<br /><br />According to the Washington Post, about a third of the 4 million to 5 million Americans with degenerative brain disorder are given antipsychotic drugs.&nbsp; The drugs are approved for the treatment of psychosis in adults, but have not been specifically approved for use among elderly patients with dementia.<br /><br />Mr. Schneider and his team found that most of the deaths came from cardiac problems or respiratory disorders.&nbsp; He said that the drugs might increase the risk because they sedate patients and confine them to bed for longer periods, making them more likely to develop infections.<br /><br />The analysis appears in the October 19 issue of the Journal of the American Medical Association.<br type="_moz"/>]]></content:encoded>
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		<title>Dementia Drugs Can Increase Death Risks</title>
		<link>http://www.yourlawyer.com/articles/read/10835</link>		
		<pubDate>Tue, 18 Oct 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/10835</guid>
		<description><![CDATA[Drugs often used to treat elderly patients with dementia-related aggression and delusions can raise their risk of death, according to a study that reinforces new warning labels required on the medications.The researchers pooled results of 15 previous studies on drugs known as atypical anti-psychotics and sold under the brand names Zyprexa, Risperdal, Seroquel and Abilify.Among more than 5,000 elderly dementia patients, those taking any of the...]]></description>
			<content:encoded><![CDATA[Drugs often used to treat elderly patients with dementia-related aggression and delusions can raise their risk of death, according to a study that reinforces new warning labels required on the medications.<br /><br />The researchers pooled results of 15 previous studies on drugs known as atypical anti-psychotics and sold under the brand names Zyprexa, Risperdal, Seroquel and Abilify.<br /><br />Among more than 5,000 elderly dementia patients, those taking any of the drugs faced a 54 percent increased risk of dying within 12 weeks of starting the medication, compared with patients taking dummy pills.<br /><br />There were 118 deaths among the 3,353 drug users versus 40 in the 1,757-patient placebo group, or 3.5 percent compared with 2.3 percent. The risks were similar for each of the drugs.<br /><br />The drugs are approved for treating schizophrenia and bipolar disease, not elderly dementia. But because schizophrenia-like symptoms are common in elderly patients with Alzheimer's disease or other dementia, doctors frequently prescribe the drugs to these patients, too. Such &quot;off-label&quot; uses are legal.<br /><br />The study gave no information on the causes of death, but the Food and Drug Administration warned in April that the drugs have been linked to deaths from heart failure and pneumonia in elderly dementia patients. At the FDA's request, manufacturers recently revised their drug labels to include strong warnings of the increased risk of death.<br /><br />Dr. Lon Schneider, a University of Southern California psychiatrist and the study's lead author, said the results should instill caution &quot;but not a great sense of fear.&quot;<br /><br />&quot;These drugs are clinically needed and there are actually few alternatives&quot; for elderly dementia patients, Schneider said.<br /><br />Withholding the drugs from patients who need them could also prove dangerous, by increasing the chances they might harm themselves and others, he said.<br /><br />The study appears in Wednesday's Journal of the American Medical Association.<br /><br />Dr. Ronald Landbloom of Zyprexa maker Eli Lilly &amp; Co. said the drugs &quot;can be very helpful with aggressive psychotic patients who are beating up caregivers and nursing home staff, and hurting themselves,&quot; but doctors need to be aware of the risks.<br /><br />William Thies, scientific director of the Alzheimer's Association, said up to about half of all Alzheimer's patients develop problems the drugs can treat.<br /><br />&quot;The trade-off is clearly going to be this small risk,&quot; and for some patients, the risk is worth taking, Thies said.]]></content:encoded>
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		<title>STUDY SUGGESTS THE ANTIPSYCHOTIC DRUG RISPERIDONE (RISPERDAL) MAY BE EFFECTIVE (AND SAFE) FOR TREATMENT OF AUTISM-RELATED AGGRESSION IN CHILDREN</title>
		<link>http://www.yourlawyer.com/articles/read/10160</link>		
		<pubDate>Mon, 04 Jul 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/10160</guid>
		<description><![CDATA[A study in the July edition of the American Journal of Psychiatry, which was sponsored by the National Institute of Mental Health (NIMH), has found that children with autism characterized by tantrums, aggression, and/or self-injury respond favorably to the antipsychotic medication, risperidone (Risperdal).The study involving 101 subjects (82 boys and 19 girls &ndash; ages 5 to 17) claims that these positive results were obtained with limited...]]></description>
			<content:encoded><![CDATA[A study in the July edition of the American Journal of Psychiatry, which was sponsored by the National Institute of Mental Health (NIMH), has found that children with autism characterized by tantrums, aggression, and/or self-injury respond favorably to the antipsychotic medication, risperidone (Risperdal).<br /><br />The study involving 101 subjects (82 boys and 19 girls &ndash; ages 5 to 17) claims that these positive results were obtained with limited side effects. Those side effects were stated to be well-tolerated with some complaints of weight gain.<br /><br />Treatment was for an intermediate term of up to six months for those subjects who improved substantially after the first eight weeks on the drug. The study did find, however, that discontinuation of the medication after six months prompted a rapid return of disruptive and aggressive behavior in most cases.<br />While autism is unquestionably a debilitating chronic condition that impairs social interaction, delays language development, and causes restricted patterns of behavior, this off-label use of a powerful atypical antipsychotic drug should be given more study for a number of reasons.<br /><br />The prescribing of drugs beyond the scope of their approval by the FDA is referred to as &ldquo;off-label&rdquo; use of the drug. The FDA regularly discourages and even warns against such uses of drugs. This has been especially true in the case of powerful antipsychotic medications.<br /><br />The strange thing about off-label use, however, is that doctors may prescribe drugs to treat conditions for which the FDA has denied approval. Thus, while a manufacturer cannot market a drug for an unapproved off-label use, a doctor may prescribe the drug for that use.&nbsp;&nbsp;&nbsp;&nbsp; <br /><br />In the case of risperidone (Risperdal), while it might very well be that favorable results were obtained, it would seem to be somewhat premature to use a limited 6-month study involving only 101 subjects to conclude the drug is &ldquo;safe&rdquo; for children. <br /><br />Risperdal is manufactured by Jannsen Pharmaceuticals, a division of Johnson &amp; Johnson and is prescribed for the treatment of schizophrenia (not autism).<br /><br />The package label submitted by the company and approved by the FDA clearly states under the heading &ldquo;Pediatric Use,&rdquo; that: &ldquo;Safety and effectiveness in children have not been established.&rdquo;<br /><br />Risperdal also comes with some very serious warnings and side effects which should not be so easily discounted simply because a very limited study group using the drug for a short period of time showed limited adverse reactions.<br /><br />Some of the drugs more common side effects may include: Abdominal pain, abnormal walk, agitation, aggression, anxiety, chest pain, constipation, coughing, decreased activity, diarrhea, difficulty with orgasm, diminished sexual desire, dizziness, dry skin, erection and ejaculation problems, excessive menstrual bleeding, fever, headache, inability to sleep, increased dreaming, increased duration of sleep, indigestion, involuntary movements, joint pain, lack of coordination, nasal inflammation, nausea, overactivity, rapid heartbeat, rash, reduced salivation, respiratory infection, sleepiness, sore throat, tremor, underactive reflexes, urination problems, vomiting, weight gain<br /><br />Less common (but recognized) side effects may include: Abnormal vision, back pain, dandruff, difficult or labored breathing, increased saliva, sinus inflammation, toothache.<br /><br />Risperdal should be used with caution by patients with kidney, liver, or heart disease, seizures, breast cancer, thyroid disorders, or any other diseases that affect the metabolism (conversion of food into energy and tissue) as well as by those who have had a stroke or mini-strokes, suffer from fluid loss or dehydration, or expect to be exposed to extremes of temperature. <br /><br />Risperdal may mask signs and symptoms of drug overdose and of conditions such as intestinal obstruction, brain tumor, and Reye's syndrome (a dangerous neurological condition that may follow viral infections, usually occurring in children). Risperdal can also cause difficulty when swallowing, which in turn can cause a type of pneumonia. <br /><br />Risperdal may cause Neuroleptic Malignant Syndrome (NMS), a condition marked by muscle stiffness or rigidity, fast heartbeat or irregular pulse, increased sweating, high fever, and high or low blood pressure. Unchecked, this condition can prove fatal. <br /><br />Patients at high risk for suicide attempts will be prescribed the lowest dose possible to reduce the risk of intentional overdose. <br /><br />Risperdal may impair your ability to drive a car or operate dangerous machinery and patients should not participate in any activities that require being fully alert. <br /><br />Risperdal can cause orthostatic hypotension (low blood pressure when rising to a standing position), with dizziness, rapid heartbeat, and fainting, especially when you first start to take it.<br />Risperdal has been linked to diabetes. This prompted the FDA to request Johnson and Johnson issue a warning to patients and prospective patients. In one recent study, Risperdal increased a patient's chances of developing diabetes by about 50% as compared with older antipsychotics. <br /><br />Risperdal has also been linked to stroke and there have been 37 reports of stroke or stroke-like events, including 16 deaths linked to Risperdal. In April 2003, Johnson &amp; Johnson sent warning letters to U.S. Physicians citing the drug&rsquo;s elevated risk of stroke in elderly patients. <br /><br />Risperdal has also been linked to tardive dyskinesia (TD), a disorder of the central nervous system, which results in involuntary movement of the limbs and twitching of the face and tongue. <br /><br />Risperdal has been known to cause irregular heartbeats, muscle weakness and spasms, high fever, constipation, weight gain and headaches. <br /><br />On April 11, 2005, the FDA announced that older patients with dementia who are given antipsychotic medicines are far more likely to die prematurely than those given placebos. The drug now carries a black-box warning (the FDA&rsquo;s most severe) on the labels.<br /><br />The FDA&rsquo;s own warnings can be found at: http://www.fda.gov/cder/drug/InfoSheets/patient/risperidonePIS.htm. <br /><br />Thus, it would seem to be a bit presumptuous to conclude that this powerful and quite dangerous drug is &ldquo;safe&rdquo; for children based upon this one limited study. While no weapon in the war on autism should be discounted, a very careful risk versus benefit analysis should be done before such a risky medication is routinely prescribed to children with autism.]]></content:encoded>
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		<title>FDA Launches Site to Warn Patients, Doctors of Drug Risks</title>
		<link>http://www.yourlawyer.com/articles/read/9749</link>		
		<pubDate>Fri, 20 May 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/9749</guid>
		<description><![CDATA[The U.S. Food and Drug Administration has begun issuing alerts to patients and doctors on its Web site about emerging drug-safety concerns, including dangers posed by drugs prescribed for unapproved purposes.The new site, called Drug Watch, marks a significant change in how the agency communicates risks to the public. In the past, the FDA has spent months or years privately weighing and debating risk information with drug companies until a final...]]></description>
			<content:encoded><![CDATA[The U.S. Food and Drug Administration has begun issuing alerts to patients and doctors on its Web site about emerging drug-safety concerns, including dangers posed by drugs prescribed for unapproved purposes.<br /><br />The new site, called Drug Watch, marks a significant change in how the agency communicates risks to the public. In the past, the FDA has spent months or years privately weighing and debating risk information with drug companies until a final determination was made on the scientific significance of the danger.<br /><br />After being bashed by Congress and consumers for its slow response to emerging information about heart risks posed by blockbuster pain medications such as Vioxx, the FDA now is beginning to make risk information available to the public much sooner.<br /><br />"This is really a fundamental change," said Dr. Steven Galson, the acting director of the FDA's Center for Drug Evaluation and Research. "We do intend to give companies a heads up before posting something new about their drugs, but we're not going to discuss it with them. They're not going to review it."<br /><br />The safety alerts posted so far on the site http://www.fda.gov/cder/drugSafety.htm are notable also because they emphasize risks posed by doctors prescribing drugs for purposes never approved by the FDA. It's a practice called "off-label prescribing" because it involves using drugs in ways and to treat conditions not covered by the safety and effectiveness determinations on their FDA-approved labels.<br /><br />"That's a very important aspect of this," Galson said. "As you know, we don't regulate the practice of medicine. We have no way of preventing physicians from using drugs off label."<br /><br />But Galson said the agency does have a responsibility to let people know about known risks of off-label uses. "This is very controversial, of course," he said.<br /><br />Some off-label drug uses are beneficial and based on good science, others have little proof of effectiveness and still others have been proved worthless in studies.<br /><br />Officials at the American Medical Association, which represents doctors, and the Pharmaceutical Research and Manufacturers of America, which represents drugmakers, declined to comment, saying they are evaluating the Drug Watch site and will submit formal comments to the FDA.<br /><br />Ed Sagebiel, a spokesman for Indianapolis-based drugmaker Eli Lilly, said the company generally supports the FDA's new effort. The site includes alerts for Eli Lilly drugs Prozac, warning of suicide risks related to it and other antidepressants, and Zyprexa, warning of an increased risk of death when it and other atypical antipsychotics are prescribed off-label to treat dementia in elderly patients.<br /><br />"We just want, from our standpoint, to properly balance warning people and patients of safety concerns without frightening them or inadvertently making them stop taking their medicines," Sagebiel said.<br /><br />Galson said others in the drug industry have expressed similar concerns. "They're worried we may be over-warning and dissuading patients from using products that may do good," he said. "We expected we would get that sort of push-back."<br /><br />Advocates for patients called the site an incremental move in the right direction, even though it requires patients to seek out the information on the Internet, rather than it being given to them when they pick up their medicines. The emphasis on early and off-label risk information is a departure for the FDA, they said.<br /><br />"I don't think they had the political courage even a few years ago to take these kinds of steps," said Larry Sasich, a pharmacist with Public Citizen's Health Research Group, a consumer watchdog that publishes a searchable database of drug risks at www.worstpills.org.<br /><br />Sasich said he thinks the FDA is realizing that the only way to change risky prescribing is for consumers to know more about the drugs they take. Changing the official labeling on drugs and sending letters to doctors about new risks hasn't worked, he said.<br /><br />Sasich expressed concern that elderly patients  who are the biggest consumers of prescription drugs won't have enough access to Drug Watch information that's available only on the Web.<br /><br />Cynthia Pearson, the executive director of the National Women's Health Network in Washington, praised the direct communication of risks listed atop several drugs on the site.<br /><br />"Our position always has been: Get people access to good information and they can make good decisions," Pearson said.<br /><br />The Drug Watch site, still being developed, lists information on about 200 drugs. Most of them include routine prescribing information. Among those tagged with an "FDA Alert:"<br /><br />Accutane, a drug for severe acne. "The FDA continues to assess reports of suicide or suicide attempts" associated with this drug. All patients "should be observed closely for symptoms of depression or suicidal thoughts," the alert warns.<br /><br />Cytotec, also called misoprostol, a drug approved to prevent ulcers. The alert warns of risks in its off-label use in labor and delivery. "These uses are not approved by the FDA. No company has sent the FDA scientific proof that (Cytotec) is safe and effective for these uses. There can be serious side effects, including a torn uterus..." the alert warns.<br /><br />Zyprexa, Risperdal and several other psychiatric drugs called atypical antipsychotics. The FDA warns that when prescribed off label as a treatment for dementia, older patients "had a higher chance for death than patients who did not take the medicine."<br /><br />Amiodarone, marketed also as Cordarone and Pacerone, a popular heart drug approved only to treat a specific life-threatening rhythm disorder. It is widely prescribed off label for non-life-threatening atrial fibrillation. The alert warns of potentially fatal side effects including lung toxicity, liver injury and worsened heart rhythm problems.<br /><br />Gabitril, a drug approved to treat seizures. The alert warns that it risks causing seizures when used off label. Gabitril's "safety and effectiveness have not been established for any other use," the alert notes, adding that the drug's maker, Cephalon, will be educating doctors "to discourage off-label use."<br /><br />Sheryl Williams, a Cephalon spokeswoman, said through Drug Watch, the FDA appears to be trying to do a better job of communicating and addressing the increasing prevalence of off-label prescribing.<br /><br />A Knight Ridder investigation published in 2003 found that patients are being injured and killed when doctors routinely prescribe medications in ways that the FDA has never approved as safe and effective. Off-label prescriptions for top-selling drugs accounted for nearly a quarter of their retail sales.<br /><br />Williams said most of the prescriptions that doctors write for Gabitril are to treat psychiatric conditions - not epileptic seizures. Bipolar disorder is a particularly popular use, she said.<br /><br />"The problem is there is no guidance for them to do so. We haven't done double-blind studies. We haven't even done single-blind studies," Williams said. "Our scientific team doesn't believe there is sufficient evidence that a drug like Gabitril would be effective in bipolar disorder."<br /><br />While Gabitril is effective in reducing the frequency of seizures in people with epilepsy, she said, when used off label the drug has been associated with seizures in people without epilepsy.]]></content:encoded>
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		<title>FDA Issues Warning on Drug Use by Elderly</title>
		<link>http://www.yourlawyer.com/articles/read/9593</link>		
		<pubDate>Mon, 11 Apr 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/9593</guid>
		<description><![CDATA[Elderly patients with dementia were significantly more likely to die prematurely if taking certain anti-psychotic drugs, the government said Monday in an advisory to health care workers and patients.The Food and Drug Administration is asking manufacturers of atypical anti-psychotic drugs to add to their labeling a boxed warning noting the risks and that the drugs were not approved to treat symptoms of dementia in the elderly.Elderly patients...]]></description>
			<content:encoded><![CDATA[Elderly patients with dementia were significantly more likely to die prematurely if taking certain anti-psychotic drugs, the government said Monday in an advisory to health care workers and patients.<br /><br />The Food and Drug Administration is asking manufacturers of atypical anti-psychotic drugs to add to their labeling a boxed warning noting the risks and that the drugs were not approved to treat symptoms of dementia in the elderly.<br /><br />Elderly patients taking the drugs for dementia-related symptoms should consult with their doctors, the FDA said.<br /><br />The drugs were approved for treating schizophrenia and mania, and include such brands as Abilify, Zyprexa, Seroquel, Risperdal, Clozaril and Geodon. Symbyax, which is approved for the treatment of depression associated with bipolar disorder, is also included in the advisory.<br /><br />An analysis of 17 studies covering four drugs showed the rate of death for the elderly patients taking them was about 1.6 to 1.7 times the rate of death for placebo users. The causes of death varied, but most seemed to be either heart-related or from infection.<br /><br />The FDA doesn't have data to indicate how many elderly patients take this class of drugs, but agency officials believe that such prescriptions are common.<br /><br />Carole Copeland, spokesman for Eli Lilly and Co., the maker of Zyprexa, said the company contacted doctors last year to alert them to the higher risk of mortality cited Monday by the FDA. She said the company also changed the drug's label last year to reiterate those higher risks. The company will review the FDA's advisory to determine if further changes were needed, she said.<br /><br />Bristol-Myers Squibb and Otsuka America Pharmaceutical, Inc., which market Abilify, said the companies take the FDA's request seriously and would respond within 30 days. The companies also said a warning was added in February to the package insert accompanying Abilify, which noted a risk of stroke and similar events associated with its use by elderly patients with dementia.]]></content:encoded>
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		<title>Deaths with Antipsychotics in Elderly Patients with Behavioral Disturbances</title>
		<link>http://www.yourlawyer.com/articles/read/9599</link>		
		<pubDate>Mon, 11 Apr 2005 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/9599</guid>
		<description><![CDATA[The Food and Drug Administration has determined that the treatment of behavioral disorders in elderly patients with dementia with atypical (second generation) antipsychotic medications is associated with increased mortality. Of a total of seventeen placebo controlled trials performed with olanzapine (Zyprexa), aripiprazole (Abilify), risperidone (Risperdal), or  quetiapine (Seroquel) in elderly demented patients with behavioral disorders,...]]></description>
			<content:encoded><![CDATA[The Food and Drug Administration has determined that the treatment of behavioral disorders in elderly patients with dementia with atypical (second generation) antipsychotic medications is associated with increased mortality. Of a total of seventeen placebo controlled trials performed with olanzapine (Zyprexa), aripiprazole (Abilify), risperidone (Risperdal), or  quetiapine (Seroquel) in elderly demented patients with behavioral disorders, fifteen showed numerical increases in mortality in the drug-treated group compared to the placebo-treated patients. <br /><br />These studies enrolled a total of 5106 patients, and several analyses have demonstrated an approximately 1.6-1.7 fold increase in mortality in these studies. Examination of the specific causes of these deaths revealed that most were either due to heart related events (e.g., heart failure, sudden death) or infections (mostly pneumonia).<br /><br />The atypical antipsychotics fall into three drug classes based on their chemical structure. Because the increase in mortality was seen with atypical antipsychotic medications in all three chemical classes, the Agency has concluded that the effect is probably related to the common pharmacologic effects of all atypical antipsychotic medications, including those that have not been systematically studied in the dementia population. In addition to the drugs that were studied, the atypical antipsychotic medications include clozapine (Clozaril) and ziprasidone (Geodon). <br /><br />All of tvhe atypical antipsychotics are approved for the treatment of schizophrenia. None, however, is approved for the treatment of behavioral disorders in patients with dementia. Because of these findings, the Agency will ask the manufacturers of these drugs to include a Boxed Warning in their labeling describing this risk and noting that these drugs are not approved for this indication. Symbyax, a combination product containing olanzapine and fluoxetine, approved for the treatment of depressive episodes associated with bipolar disorder, will also be included in the request.<br /><br />The Agency is also considering adding a similar warning to the labeling for older antipsychotic medications because the limited data available suggest a similar increase in mortality for these drugs.]]></content:encoded>
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		<title>FDA Miffed Over Letter On Schizophrenia Drug</title>
		<link>http://www.yourlawyer.com/articles/read/7972</link>		
		<pubDate>Wed, 28 Apr 2004 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/7972</guid>
		<description><![CDATA[Federal regulators yesterday chided Janssen Pharmaceutica, part of the Johnson & Johnson health-care empire, for including misleading information in a letter to physicians about the health risks associated with its schizophrenia medicine, Risperdal. Janssen minimized the diabetic risks associated with the drug, and without supporting data, claimed Risperdal is safer than similar medicines, regulators said in a warning to the company. The letter...]]></description>
			<content:encoded><![CDATA[Federal regulators yesterday chided Janssen Pharmaceutica, part of the Johnson & Johnson health-care empire, for including misleading information in a letter to physicians about the health risks associated with its schizophrenia medicine, Risperdal. <br /><br />Janssen minimized the diabetic risks associated with the drug, and without supporting data, claimed Risperdal is safer than similar medicines, regulators said in a warning to the company. The letter went to 600,000 health-care providers. <br /><br />"The letter misleadingly omits material information about Risperdal, minimizes the potentially fatal risks associated with the drug and claims superior safety without adequate substantiation," the FDA said in its warning. <br /><br />The agency's rebuke puts the spotlight on one of Johnson & Johnson's top-selling medicines, which continues to vie against rivals in the intensely competitive market for anti-psychotic drugs. The market is expected to double in sales, reaching as much as $11.2 billion, by 2006. <br /><br />Johnson & Johnson, which is based in New Brunswick, earlier this month credited sales of Risperdal with helping to lift its prescription drug sales to $2.49 billion for the first quarter of 2004. <br /><br />"We take the FDA's letter seriously, and we are working with the agency to address their concerns as quickly as possible," company spokeswoman Carol Goodrich said. <br /><br />Janssen was ordered to immediately stop distributing promotional material containing the claims and to detail a plan to issue accurate information. The company has until Monday to respond to the FDA's request. <br /><br />"It's not often that a company dances around an issue like this," said Arthur Levin, director of the Center for Medical Consumers, a patient advocacy group in New York City. <br /><br />"It's dangerous," he said, "The question is why aren't they being fined? This is entirely inappropriate." <br /><br />Last year, the Food and Drug Administration instructed Janssen and five other companies that sell similar anti-psychotic medicines to change their product labeling to include warnings about the risk of diabetic-related adverse events, including the possibility of coma and death. <br /><br />The FDA based its decision on a review of clinical study data, post-marketing reports and published case studies, among other things. <br /><br />Janssen complied with the requirement, and the FDA subsequently approved the language proposed by Janssen for its labeling. Then, as a way of alerting physicians to the labeling changes, regulators asked Janssen and the other companies to issue letters to health-care providers. <br /><br />The letter, the FDA said, contradicts the warning in the revised product labeling. <br /><br />Linda Gochfeld, a Princeton psychiatrist, said most doctors were aware of the side effects even without the letter. <br /><br />"With every drug, you're weighing the beneficial effects against the side effects," she said. ]]></content:encoded>
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		<title>Parker &amp; Waichman Files Claims Against Eli Lilly and Company on Behalf of Three Individuals Claiming Injuries Caused by Zyprexa; Plaintiffs Diagnosed with Serious Cases of Diabetes and Pancreatitis</title>
		<link>http://www.yourlawyer.com/articles/read/7798</link>		
		<pubDate>Fri, 19 Mar 2004 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/7798</guid>
		<description><![CDATA[Parker &amp; Waichman LLP (www.yourlawyer.com) filed claims against Eli Lilly and Company (NYSE: LLY - News) on behalf of three individuals who claim to have sustained severe side-effects from Zyprexa. The claims were filed in Federal District Court in the Eastern District of New York. Two plaintiffs have been diagnosed with serious cases of diabetes, and another plaintiff has required lengthy intensive care hospitalization due to a diagnosis of...]]></description>
			<content:encoded><![CDATA[Parker &amp; Waichman LLP (www.yourlawyer.com) filed claims against Eli Lilly and Company (NYSE: LLY - News) on behalf of three individuals who claim to have sustained severe side-effects from Zyprexa. The claims were filed in Federal District Court in the Eastern District of New York. Two plaintiffs have been diagnosed with serious cases of diabetes, and another plaintiff has required lengthy intensive care hospitalization due to a diagnosis of acute pancreatitis. Zyprexa is currently the most popular atypical antipsychotic medication, and is Eli Lilly and Company's best-selling pharmaceutical. Zyprexa users can visit www.zyprexa-side-effects.com for more information on these claims.<br /><br />The British Medical Control Agency and the Japanese Health and Welfare Ministry have both warned about the risk of diabetes in patients who are prescribed Zyprexa. In 2002, a study at Duke University showed a connection between Zyprexa and diabetes. This study documented nearly 300 cases of diabetes in people using Zyprexa. Only recently has Eli Lilly and Company added some language to their labeling in the United States concerning the risk of diabetes from Zyprexa.<br /><br />&quot;We are confident that we will bring justice to our clients whose lives have been permanently affected by the side-effects of a drug that provides little efficacious benefit, but causes life-threatening injuries,&quot; commented Jerrold S. Parker, Co-Founder of Parker &amp; Waichman.<br /><br />&quot;With the alarming studies that have been conducted and the warnings from national health agencies about Zyprexa's link to blood sugar disorders, it is appalling that Eli Lilly has not issued adequate warnings and that they continue to market this drug heavily directly to consumers.&quot;<br /><br />Zyprexa was approved for the treatment of schizophrenia in 1996 and for the treatment of bipolar mania in 2000. It is part of a new generation of antipsychotics known as atypicals, which include Seroquel, Risperdal, Abilify, Clozaril, and Geodon. Ironically, the primary advantage of the newer atypical antipsychotic medications was supposed to be a lower incidence of side effects than the conventional antipsychotics introduced in the 1950s (Haldol, Thorazine, Prolixin, Navane, Stelazine, Trilafon, and Mellaril).<br /><br />More information on Zyprexa side-effects is available at Parker &amp; Waichman's Zyprexa website www.zyprexa-side-effects.com. Current and former Zyprexa users can visit this to request a free legal evaluation.<br /><br />For more information on Parker &amp; Waichman, LLP please visit http://www.yourlawyer.com or call 1-800-LAW-INFO. Current and former shareholders are also encouraged to visit http://www.injurytalk.com. <br /><br />     Contact:<br /><br />     David Krangle, Esq.<br />     Parker &amp; Waichman, LLP<br />     1-800-LAW-INFO (1-800-529-4636)<br />     http://www.yourlawyer.com<br />     dkrangle@yourlawyer.com]]></content:encoded>
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		<title>UK Slow To Clamp Down On Drug That Causes Stroke In Elderly</title>
		<link>http://www.yourlawyer.com/articles/read/7793</link>		
		<pubDate>Sat, 13 Mar 2004 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/7793</guid>
		<description><![CDATA[It took the government's Committee on Safety of Medicines seven months to act on comprehensive evidence that a schizophrenia drug widely given to control the behaviour of elderly people in care homes could cause them to have a stroke. Last week the advisory body recommended doctors should not prescribe risperidone or olanzapine for such patients. But the manufacturer of risperidone brand name Risperdal gave the CSM full data about the risks last...]]></description>
			<content:encoded><![CDATA[It took the government's Committee on Safety of Medicines seven months to act on comprehensive evidence that a schizophrenia drug widely given to control the behaviour of elderly people in care homes could cause them to have a stroke. <br /><br />Last week the advisory body recommended doctors should not prescribe risperidone or olanzapine for such patients. But the manufacturer of risperidone brand name Risperdal gave the CSM full data about the risks last July. <br /><br />Canadian and US drug regulators acted swiftly on early evidence from the manufacturers that Risperdal might cause death in the elderly. <br /><br />In October 2002 Janssen-Ortho wrote to all health professionals, at the request of the Canadian authorities. In April 2003 the US regulators took similar action. <br /><br />The vice-president of medical affairs of Janssen Pharmaceutica in New Jersey wrote: "[Strokes,] including fatalities, were reported in patients (mean age 85 years; range 73-97) in trials of risperidone in elderly patients with dementia-related psychosis. <br /><br />"In placebo-controlled trials, there was a significantly higher incidence of cerebrovascular adverse events in patients treated with risperidone compared to patients treated with placebo. Risperdal has not been shown to be safe or effective in the treatment of patients with dementia-related psychosis." <br /><br />But evidence came to light because the company carried out clinical trials in the hope of applying for a licence to market Risperdal for behavioural problems in the elderly. <br /><br />Doctors were already using Risperdal on such patients. <br /><br />Robert Donnelly, medical director of Janssen in the UK, said that when the first data came in there was "an imbalance" which they reported to the authorities worldwide. <br /><br />That led to the letters in Canada and the US. By last summer they had the full trial data. This went to the UK's Medicines and Healthcare Products Regulatory Authority (MHRA). A Department of Health spokesman said the MHRA had acted at the same time as the Canadians and the Americans by adding a warning to doctors' product information that there might be an increased risk of stroke. <br /><br />In April last year, he said, the company wrote to psycho-geriatricians in the UK. <br /><br />But Robin Keen, who has investigated the worldwide advice since his mother, Urene, suffered a severe stroke while on Risperdal nine months ago, said the warnings would not necessarily have been noticed by doctors, and certainly did not go out to patients. <br /><br />He added: "Practitioners may argue that many drugs have inherent risks, though when knowledge of that risk is clearly available, supported by the presence of clinical trial results, and even more so when that risk is of a life-threatening magnitude, then surely the patient, or that patient's relatives, have the right to that information in order to make an informed decision." <br /><br />The health department said the MHRA had commissioned its own analysis of all the drug data in December after getting reports that those on the drugs were suffering strokes. It received the conclusions in January, and put out its advice to doctors last week. ]]></content:encoded>
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		<title>Caution Urged In Use of Anti-Psychotic Drugs</title>
		<link>http://www.yourlawyer.com/articles/read/7681</link>		
		<pubDate>Thu, 26 Feb 2004 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/7681</guid>
		<description><![CDATA[Reople taking certain drugs for schizophrenia, manic depression, autism, dementia or several other psychiatric disorders should be watched carefully for signs they are developing diabetes, obesity or high cholesterol, four medical societies say.The recommendation follows recent studies that link those potential side effects to certain anti-psychotic drugs.The statement deals with six drugs now available in the United States: Abilify, Clozaril,...]]></description>
			<content:encoded><![CDATA[Reople taking certain drugs for schizophrenia, manic depression, autism, dementia or several other psychiatric disorders should be watched carefully for signs they are developing diabetes, obesity or high cholesterol, four medical societies say.<br /><br />The recommendation follows recent studies that link those potential side effects to certain anti-psychotic drugs.<br /><br />The statement deals with six drugs now available in the United States: Abilify, Clozaril, Geodon, Risperdal, Seroquel and Zyprexa.<br /><br />The recommendation comes from the American Diabetes Association, the American Psychiatric Association, the North American Association for the Study of Obesity, and the American Association of Clinical Endocrinologists. It appears in the February issue of the journal Diabetes Care.<br /><br />The medications differ in their risks of promoting the various side effects, the statement says. So a patient who develops a problem with one drug can be gradually switched to another drug with less potential for that problem. For example, a switchover should be considered if a patient has a weight gain of 5 percent or more, the statement says.<br /><br />Obesity and diabetes, like high cholesterol, raise a person's risk of heart disease.<br /><br />The recommendation says doctors should screen patients before starting them on such a drug or as soon as possible afterward, noting things such as a history of obesity and diabetes in the patient and the family, and the patient's weight, blood pressure and cholesterol levels. Doctors also should monitor the patient once therapy has begun.<br /><br />Patients and family members should be informed of the potential for the side effects, and be told of signs of diabetes and especially those of a life-threatening complication called diabetic ketoacidosis, the statement says. That complication is marked by such symptoms as weight loss, nausea, vomiting, rapid breathing and dehydration.<br /><br />That complication has appeared in some people using anti-psychotics, and it was an early tip-off that the drugs might be linked to diabetes.]]></content:encoded>
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		<title>Anti-Psychotics Caution Advised</title>
		<link>http://www.yourlawyer.com/articles/read/7500</link>		
		<pubDate>Sun, 01 Feb 2004 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/7500</guid>
		<description><![CDATA[People taking certain drugs for schizophrenia, manic-depression, autism, dementia or several other psychiatric disorders should be carefully watched for signs they are developing diabetes, obesity or high cholesterol, four medical societies say. The recommendation follows recent studies that link those potential side effects to certain anti-psychotic drugs. The statement deals with six now available in the United States: Abilify, Clozaril,...]]></description>
			<content:encoded><![CDATA[People taking certain drugs for schizophrenia, manic-depression, autism, dementia or several other psychiatric disorders should be carefully watched for signs they are developing diabetes, obesity or high cholesterol, four medical societies say. <br /><br />The recommendation follows recent studies that link those potential side effects to certain anti-psychotic drugs. <br /><br />The statement deals with six now available in the United States: Abilify, Clozaril, Geodon, Risperdal, Seroquel and Zyprexa. <br /><br />The recommendation, released last week, comes from the American Diabetes Association, the American Psychiatric Association, the North American Association for the Study of Obesity and the American Association of Clinical Endocrinologists. It appears in the February issue of the journal Diabetes Care. <br /><br />The medications differ in their risks of promoting the various side effects, the statement says. So a patient who develops a problem with one drug could be gradually switched over to another drug with less potential for that problem. For example, a switchover should be considered if a patient has a weight gain of 5 percent or more, the statement says. <br /><br />Obesity and diabetes, like high cholesterol, raise a person's risk of heart disease. <br /><br />The recommendation says doctors should screen patients before starting them on such a drug or as soon as possible afterward, noting such things as a history of obesity and diabetes in the patient and the family, and the patient's weight, blood pressure and cholesterol levels. Doctors should also monitor the patient once therapy has begun. <br /><br />Patients and family members should be informed of the potential for the side effects, and be told of signs of diabetes and especially those of a life-threatening complication called diabetic ketoacidosis, the statement says. That complication is marked by such symptoms as weight loss, nausea, vomiting, rapid breathing and dehydration. <br /><br />That complication has appeared in some people using anti-psychotics, and it was an early tip-off that the drugs might be linked to diabetes. ]]></content:encoded>
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		<title>Caution Urged on Anti-Psychotic Drugs</title>
		<link>http://www.yourlawyer.com/articles/read/7484</link>		
		<pubDate>Tue, 27 Jan 2004 00:00:00 -0800</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/7484</guid>
		<description><![CDATA[People taking certain drugs for schizophrenia, manic-depression, autism, dementia or several other psychiatric disorders should be carefully watched for signs they are developing diabetes, obesity or high cholesterol, four medical societies say. The recommendation follows recent studies that link those potential side effects to certain anti-psychotic drugs. The statement deals with six now available in the United States: Abilify, Clozaril,...]]></description>
			<content:encoded><![CDATA[People taking certain drugs for schizophrenia, manic-depression, autism, dementia or several other psychiatric disorders should be carefully watched for signs they are developing diabetes, obesity or high cholesterol, four medical societies say. <br /><br />The recommendation follows recent studies that link those potential side effects to certain anti-psychotic drugs. <br /><br />The statement deals with six now available in the United States: Abilify, Clozaril, Geodon, Risperdal, Seroquel and Zyprexa. <br /><br />The recommendation, released Tuesday, comes from the American Diabetes Association, the American Psychiatric Association, the North American Association for the Study of Obesity, and the American Association of Clinical Endocrinologists. It appears in the February issue of the journal Diabetes Care. <br /><br />The medications differ in their risks of promoting the various side effects, the statement says. So a patient who develops a problem with one drug can be gradually switched over to another drug with less potential for that problem. For example, a switchover should be considered if a patient has a weight gain of 5 percent or more, the statement says. <br /><br />Obesity and diabetes, like high cholesterol, raise a person's risk of heart disease. <br /><br />The recommendation says doctors should screen patients before starting them on such a drug or as soon as possible afterward, noting such things as a history of obesity and diabetes in the patient and the family, and the patient's weight, blood pressure and cholesterol levels. Doctors should also monitor the patient once therapy has begun. <br /><br />Patients and family members should be informed of the potential for the side effects, and be told of signs of diabetes and especially those of a life-threatening complication called diabetic ketoacidosis, the statement says. That complication is marked by such symptoms as weight loss, nausea, vomiting, rapid breathing and dehydration. <br /><br />That complication has appeared in some people using anti-psychotics, and it was an early tip-off that the drugs might be linked to diabetes. ]]></content:encoded>
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		<title>FDA: Antipsychotic Drugs, Diabetes Linked</title>
		<link>http://www.yourlawyer.com/articles/read/6670</link>		
		<pubDate>Thu, 18 Sep 2003 00:00:00 -0700</pubDate>
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		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/6670</guid>
		<description><![CDATA[Federal regulators have asked the makers of a widely used class of six antipsychotic drugs to include labeling language about a possible link with diabetes, Eli Lilly & Co. said Wednesday. Lilly's antipsychotic Zyprexa is the company's top selling drug, accounting for about one-third of the firm's sales. It is also the category's top seller. The Food and Drug Administration's request, made in a letter received this week by the drugs' producers,...]]></description>
			<content:encoded><![CDATA[Federal regulators have asked the makers of a widely used class of six antipsychotic drugs to include labeling language about a possible link with diabetes, Eli Lilly & Co. said Wednesday. <br /><br />Lilly's antipsychotic Zyprexa is the company's top selling drug, accounting for about one-third of the firm's sales. It is also the category's top seller. <br /><br />The Food and Drug Administration's request, made in a letter received this week by the drugs' producers, follows several recent studies exploring a possible diabetes link. Label warnings already have been required for some of the drugs overseas. <br /><br />FDA spokeswoman Susan Cruzan said the agency frequently makes requests for additional drug labeling. Cruzan added she was unaware of any enforcement steps the FDA might take in case a company does not comply, which she said rarely occurs. <br /><br />"It is in their interest to put the information in the labeling," Cruzan said. <br /><br />The other drugs that fall under the FDA's labeling request are: Bristol-Myers Squibb's Abilify, Pfizer's Geodon, Novartis' Clozaril, Janssen's Risperdal and AstraZeneca's Seroquel. <br /><br />The FDA letter recommends patients using the so-called atypical antipsychotics be monitored for blood-sugar abnormalities, particularly if they have risk factors including obesity and a family history of diabetes. <br /><br />The letter said there is no clear link between the drugs and diabetes, but further study is needed. More label changes could be required depending on future findings. <br /><br />Studies have shown a higher incidence of low blood-sugar and diabetes among schizophrenics  regardless of whether they use antipsychotics when compared with the general population. The key question is whether the drugs aggravate the risk. Many of them carry the possible side effect of weight gain, and obesity is a risk factor in diabetes. <br /><br />Lilly spokeswoman Marni Lemons said the company was in discussions with the FDA regarding the new labeling. <br /><br />Bristol-Myers Squibb was "working quickly to respond to the FDA" regarding Abilify, company spokeswoman Tracy Furey said. <br /><br />The FDA's labeling request "levels the playing field among all atypical antipsychotics" in the debate about a possible diabetes link, said analyst Robert Hazlett of SunTrust Robinson Humphrey. <br /><br />He predicted any impact on the drugs' sales would be minor. <br /><br />U.S. sales of the six leading antipsychotics totaled $5.4 billion in the 12-month period ended Aug. 31, with 22.7 million prescriptions written, according to NDCHealth, a health care research company. Zyprexa was the top seller, with nearly $2.4 billion in U.S. sales. <br /><br />Zyprexa has come under pressure because of the emergence of newer rivals Geodon and Abilify. <br /><br />Zyprexa has been singled out by some in the diabetes controversy because of its well-documented link to weight gain in some patients. <br /><br />This year, Lilly also became the target of product-liability lawsuits that attempt to link Zyprexa with life-threatening and fatal cases of diabetes. ]]></content:encoded>
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		<title>Lilly Announces FDA Notification of Class Labeling for Atypical Antipsychotics Regarding Hyperglycemia and Diabetes</title>
		<link>http://www.yourlawyer.com/articles/read/6659</link>		
		<pubDate>Wed, 17 Sep 2003 00:00:00 -0700</pubDate>
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		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/6659</guid>
		<description><![CDATA[Eli Lilly and Company (NYSE:LLY) has received a letter from the U.S. Food and Drug Administration (FDA) requesting updated product labeling for all atypical antipsychotics, to include a warning about additional information on hyperglycemia and diabetes. In addition to Zyprexa(R) (olanzapine), the atypical antipsychotic class includes Clozaril(R) (clozapine, Novartis), Risperdal(R) (risperidone, Janssen), Seroquel(R) (quetiapine, AstraZeneca),...]]></description>
			<content:encoded><![CDATA[Eli Lilly and Company (NYSE:LLY) has received a letter from the U.S. Food and Drug Administration (FDA) requesting updated product labeling for all atypical antipsychotics, to include a warning about additional information on hyperglycemia and diabetes. In addition to Zyprexa(R) (olanzapine), the atypical antipsychotic class includes Clozaril(R) (clozapine, Novartis), Risperdal(R) (risperidone, Janssen), Seroquel(R) (quetiapine, AstraZeneca), Geodon(R) (ziprasidone, Pfizer), and Abilify(R) (aripiprazole, Bristol Myers Squibb). <br /><br />"Increased attention to the signs and symptoms of diabetes mellitus may lead to earlier detection and appropriate treatment, and thus may reduce the risk for the most serious outcomes," the FDA stated in its letter to Eli Lilly and Company received September 15, 2003. <br /><br />"Risk for diabetes should be considered among patients with severe mental illness regardless of medication choice," said Mauricio Tohen, MD, Dr. PH. Lilly Research Fellow and Leader of the Zyprexa Product Team. <br /><br />The Agency recognizes that the relationship between atypical antipsychotic use and hyperglycemia-related adverse events is not completely understood, but epidemiological studies have suggested some increased risk. The requested labeling states, "Assessment of the relationship between atypical antipsychotic use and glucose abnormalities is complicated by the possibility of an increased background risk of diabetes mellitus in patients with schizophrenia and the increasing incidence of diabetes mellitus in the general population." <br /><br />The labeling further states that patients with diabetes who begin taking atypical antipsychotics should be monitored for a worsening of glucose control, and those with risk factors for diabetes (e.g., obesity, family history of diabetes) should undergo fasting glucose testing at baseline, and periodically throughout treatment. Any patient developing suggestive symptoms during treatment with an atypical antipsychotic should be tested for diabetes. <br /><br />"Lilly is committed to continuing to provide resources for complete wellness for patients," Dr. Tohen said. "It is clear that this important area requires more research and Lilly is determined to remain in the forefront of this scientific inquiry," he added. <br /><br />Zyprexa Background <br /><br />Zyprexa is indicated in the United States for the short- and long-term treatment of schizophrenia and for acute bipolar mania. Since Zyprexa was introduced in 1996, it has been prescribed to more than 12 million people worldwide. <br /><br />The most common treatment-emergent adverse event associated with ZYPREXA in placebo-controlled, short-term schizophrenia and bipolar mania trials was somnolence. Other common events were dizziness, weight gain, personality disorder (COSTART term for nonaggressive objectionable behavior), constipation, akathisia, postural hypotension, dry mouth, asthenia, dyspepsia, increased appetite, and tremor. <br /><br />A small number of patients in premarketing trials experienced asymptomatic elevations of hepatic transaminase; none of these patients developed jaundice. Periodic assessment of transaminases is recommended in patients with significant hepatic disease. <br /><br />Prescribing should be consistent with the need to minimize the risk of neuroleptic malignant syndrome, tardive dyskinesia, seizures, and orthostatic hypotension. Full prescribing information is available at www.zyprexa.com. <br /><br />This press release contains statements about potential label changes for Zyprexa and other atypical anti-psychotic drugs, and forward-looking statements about future research involving Zyprexa. <br /><br />These statements reflect management's current beliefs, however, as with any commercial pharmaceutical product, there are risks and uncertainties in the process of commercialization and regulatory review. <br /><br />There are no guarantees that the potential label changes will occur or that the product will continue to be commercially successful. For further discussion of these and other risks and uncertainties, see Lilly's filings with the United States Securities and Exchange Commission. Lilly undertakes no duty to update forward-looking statements.]]></content:encoded>
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		<title>Atypical Antipsychotics May Cause Pancreatitis</title>
		<link>http://www.yourlawyer.com/articles/read/10442</link>		
		<pubDate>Tue, 02 Sep 2003 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/10442</guid>
		<description><![CDATA[A class of widely prescribed antipsychotic medicines called atypical antipsychotics, already under suspicion for causing diabetes, may also precipitate a dangerous inflammation of the pancreas, researchers say.An analysis of adverse reactions to the medicines reported to the government and in medical journals showed that there were more cases of pancreatitis, an uncommon but potentially fatal condition, among patients taking the newer medicines...]]></description>
			<content:encoded><![CDATA[A class of widely prescribed antipsychotic medicines called atypical antipsychotics, already under suspicion for causing diabetes, may also precipitate a dangerous inflammation of the pancreas, researchers say.<br /><br />An analysis of adverse reactions to the medicines reported to the government and in medical journals showed that there were more cases of pancreatitis, an uncommon but potentially fatal condition, among patients taking the newer medicines than those taking haloperidol, an older antipsychotic drug on the U.S. market since 1969.<br /><br />The difference is provocative, the researchers say, because the 68 million prescriptions written for haloperidol during the study period are more than double the number for any of the newer medicines, the first of which became available in 1991 in the U.S. The report is part of growing body of scientific work suggesting a link between the &quot;atypical&quot; antipsychotic medicines and disorders of the pancreas, including diabetes.<br /><br />The researchers analyzed reports of adverse reactions from antipsychotic medicines during a 21-year period ending in February 2002. Only six cases of pancreatitis were reported for patients taking only haloperidol, sold as Haldol by Johnson &amp; Johnson. In contrast, there were 53 documented cases of pancreatitis reported for patients taking only Clozapine, the first of the atypical antipsychotics, sold under the brand name Clozaril by Novartis AG.<br /><br />Among patients taking only Zyprexa, made by Eli Lilly &amp; Co., there were 40 documented pancreatitis cases, and patients taking only Risperdal, also sold by Johnson &amp; Johnson, accounted for 17 documented cases.<br /><br />A spokesman for Eli Lilly said: &quot;Zyprexa has been used successfully by millions of patients and has a dependable safety and effectiveness profile.&quot; He reserved specific comment on the study of pancreatitis until company researchers could review it.<br /><br />The results appear in the current issue of the medical journal Pharmacotherapy.<br /><br />The researchers stressed that the risk of an inflamed pancreas from taking any of the antipsychotic medicines is very small. &quot;Nothing in this report should discourage people from appropriate use of atypical antipsychotics, which can be lifesaving for many patients,&quot; said P. Murali Doraiswamy, a Duke University psychiatrist and co-author of the study.<br /><br />Nonetheless, he said the results should alert doctors to a potential difference between haloperidol and the newer antipsychotics.<br /><br />A Johnson &amp; Johnson spokeswoman said the company agrees with the study's authors that the risks of pancreatitis appear to be quite small, particularly for Risperdal, but agree that further investigation is warranted.<br /><br />The study was limited by its historical look at reports made voluntarily to the Food and Drug Administration and in the medical literature. Dr. Doraiswamy said doctors may have been more likely to report problems with the atypical antipsychotics because they were newer and less familiar than haloperidol. Also, difficult-to-treat patients are more likely to receive the newer drugs, he said, and some of these people may be more predisposed to pancreatitis due to complicating conditions, such as alcoholism.<br /><br />&quot;There is a need for more rigorous studies to look for a cause-and-effect relationship,&quot; Dr. Doraiswamy said.]]></content:encoded>
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		<title>Risperdal (Risperidone) Associated With Cerebrovascular</title>
		<link>http://www.yourlawyer.com/articles/read/5630</link>		
		<pubDate>Fri, 25 Apr 2003 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/5630</guid>
		<description><![CDATA[Janssen Pharmaceutica and FDA revised the WARNINGS section of the prescribing information for Risperdal (risperidone), indicated for thetreatment of schizophrenia. Cerebrovascular adverse events (e.g., stroke,transient ischemic attack), including fatalities, were reported in patients in trials of risperidone in elderly patients with dementia-related psychosis. In placebo-controlled trials, there was a significantly higher incidence of...]]></description>
			<content:encoded><![CDATA[Janssen Pharmaceutica and FDA revised the WARNINGS section of the prescribing information for Risperdal (risperidone), indicated for the<br />treatment of schizophrenia. <br /><br />Cerebrovascular adverse events (e.g., stroke,<br />transient ischemic attack), including fatalities, were reported in patients in trials of risperidone in elderly patients with dementia-related psychosis. <br /><br />In placebo-controlled trials, there was a significantly higher incidence of cerebrovascular adverse events in patients treated with<br />risperidone compared to patients treated with placebo. <br /><br />RISPERDAL has not been shown to be safe or effective in the treatment of patients with<br />dementia-related psychosis.<br />]]></content:encoded>
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		<title>Medications Can Fan Children's Emotional Flames</title>
		<link>http://www.yourlawyer.com/articles/read/5395</link>		
		<pubDate>Tue, 08 Apr 2003 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
		<guid isPermaLink="false">http://www.yourlawyer.com/articles/read/5395</guid>
		<description><![CDATA[Lee thrashed in her father's arms, a raging 60-pound girl. She had been agitated all day, jumping around and threatening to kill herself. When she stuck her fingers into the electrical outlet, saying she was going to electrocute herself, her parents decided they had to get her to the hospital. Maybe someone there could help her, they thought. But her admission to a crisis center under Florida's Baker Act was only one step in a two- month journey...]]></description>
			<content:encoded><![CDATA[Lee thrashed in her father's arms, a raging 60-pound girl. She had been agitated all day, jumping around and threatening to kill herself. <br /><br />When she stuck her fingers into the electrical outlet, saying she was going to electrocute herself, her parents decided they had to get her to the hospital. Maybe someone there could help her, they thought. <br /><br />But her admission to a crisis center under Florida's Baker Act was only one step in a two- month journey through emotional bedlam. <br /><br />Lee, 9, had been diagnosed a year earlier with bipolar disorder and prescribed psychiatric medication, including Seroquel and Risperdal. About September, when she developed an obsessive fear of germs, the psychiatrist suggested Paxil, used for anxiety and depression. <br /><br />Within weeks, Lee's mother noticed a surge in her aggression. She told the doctor, but he said it was an acceptable side effect and she would be fine. If he had taken her more seriously, Lee's mother says, her daughter might have been spared four wrenching trips to crisis units. <br /><br />The family has seen the worst of the Baker Act system, Lee's father says. <br /><br />In roughly a fourth of Baker Act cases involving children, there are references to psychiatric drugs, a study by The Tampa Tribune shows. <br /><br />The analysis involved nearly 600 sheriff's reports in Hillsborough and Pinellas counties and was part of a five-month Tribune investigation into the rising number of child Baker Act incidents statewide. <br /><br />In at least 10 percent of the cases, the child had refused to take a prescribed psychiatric drug, often because of unpleasant side effects. Several other reports listed a recent medication change as a factor in the crisis. <br /><br />Prescribing In The Blind <br /><br />For years, parents and mental health experts have debated the use of medications to calm disruptive children. <br /><br />Many say the drugs ease the symptoms of brain dysfunctions such as attention deficit disorder and bipolar disorder. <br /><br />Others, however, say insurance systems that won't pay the cost of proper diagnoses and family counseling force parents to give their children potentially dangerous medications, which they may not need. <br /><br />The debate flared anew in January when a medical journal, Archives of Pediatrics and Adolescent Medicine, reported the number of children taking psychiatric drugs nationwide has at least doubled in the past decade, rising to more than 6 percent. <br /><br />Local pharmacist Bob Bobo has noticed the jump. Better diagnosis of children's problems is causing some of the increase, Bobo says, but he also has heard alarming stories from parents. <br /><br />``They're telling me teachers won't let their kids back in class until they're on a drug,'' says Bobo, of Davis Islands Pharmacy. ``It's scary. It's like they just want to sedate them.'' <br /><br />Many of the drugs in the national study, among them Seroquel and Risperdal, were created for psychotic adults. That disturbs the study's lead author, Julie Magno Zito, a University of Maryland associate professor of pharmacy. There is very little research on how these compounds affect the young. <br /><br />Nevertheless, psychiatrists are prescribing them to uncounted children in office visits and during Baker Act stays in crisis centers. The drugs, in turn, sometimes cause new problems that lead to more Baker Act commitments. <br /><br />Such was Lee's case, her parents say. <br /><br />Tripping On A Diagnosis <br /><br />When Lee's symptoms began years ago, her parents say, they tried it all. Lee's mother was home with Lee and her two siblings, and she spent her free time researching child disorders and how to handle them. <br /><br />Nothing worked. When the psychiatrist recommended medication, the parents didn't question it. <br /><br />``We felt like she was a guinea pig'' because he tried one drug after another, says Lee's father, who works for the state. ``But it seems like that's the only way of finding out what works.'' <br /><br />Bipolar disorder can be confounding in children. It is characterized by severe mood swings. But children can cycle through the extremes so fast they are continuously irritated and anxious and often appear to have other disorders. Some researchers say bipolar disorder coexists with others. <br /><br />Some of these maladies, such as obsessive-compulsive disorder, improve when patients take Paxil. But with bipolar disorder, the drug can trigger mania. <br /><br />Lee's parents believe that is what happened to her. <br /><br />Despite her psychiatrist's assurances that she would adjust to Paxil, her hostility and aggression grew, they say. She stomped around, kicking at walls, saying repeatedly she wanted to kill herself. <br /><br />In a frenzy one afternoon, she grabbed a knife and threatened her younger sister. Her parents took her to Community Hospital of New Port Richey, and she was sent to a crisis center at Morton Plant Hospital in Clearwater. <br /><br />One problem, a unit doctor said, was Paxil. The dose was too low. So the hospital increased it and, after four days, released Lee. On the way home with her parents, she threw a fit. <br /><br />The Rules Cause Delay <br /><br />At rest, Lee is a frail-looking girl with plaintive blue eyes. But she can turn ferocious in an instant. <br /><br />Soon she was back at Morton Plant, where she was treated and sent home a second time only to unravel within hours, threatening that night to electrocute herself. <br /><br />This time, the parents called a crisis center in New Port Richey, The Harbor Behavioral Health Care Institute. They were assured there was an open bed, but they arrived to learn they had to wait for a social worker to come in to write the Baker Act order. <br /><br />Because disturbed children often are most aggressive toward family members, attendants separated Lee from her parents. Dressed in pajamas, she sat in the waiting area with an unkempt older man and later with a teenager in handcuffs. <br /><br />Attendants could see Lee through a window, but reaching her would have required them to run around a counter, down a short hallway and through a door. <br /><br />Her parents waited, sick with apprehension. Then, after the counselor arrived and signed the Baker Act form, they learned another patient had arrived and the 10-bed unit was full. <br /><br />The staff offered to send Lee back to Morton Plant. Her parents said no, worried that she would end up home again in three or four days with the same problems. <br /><br />(Morton Plant officials say they can't comment on Lee's case but are bound by the Baker Act to discharge patients when they cease to be dangerous to themselves and others. Each discharge, they say, is approved by a board-certified psychiatrist.) <br /><br />Workers found an opening at a crisis center in Tampa, run by Mental Health Care Inc. <br /><br />The Crises Continue <br /><br />The Tampa center found reason to keep Lee for five days, and therapists took that time to work with the family. But that ended at discharge. <br /><br />And although the doctor agreed to change Lee's medication, she was prescribed Zoloft, a relative of Paxil. On her fourth day home, Lee tried to run away. <br /><br />Lee's father took her to work with him the next day. That usually calmed her, but this time she became more agitated. <br /><br />He got her into the family van to take her to the hospital. She jumped out. <br /><br />Emergency workers cornered her behind the office and tied her to a gurney. She screamed and thrashed the whole way to the Community Hospital emergency room and screamed throughout the afternoon as nurses tried to sedate her. They finally succeeded by giving her a shot of Thorazine. <br /><br />The family refused a transfer to Morton Plant. The crisis units in New Port Richey and Tampa were full. But there was a bed at a crisis center run by Coastal Behavioral Health Care in Sarasota. That turned out to be the break Lee needed. <br /><br />A doctor there took a special interest in Lee. He kept her for 10 days, stopping the antidepressants. Lee responded. <br /><br />Insurers Prefer Drugs <br /><br />Lee's case is extreme, but thousands of parents feel the same confusion and frustration over giving their children psychiatric drugs. <br /><br />Massachusetts psychiatrist Michael Jellinek, responding to the University of Maryland study, says the findings point to a weakness in public and private insurance health plans: They would rather pay for drugs than for costly and time- consuming counseling. <br /><br />Another Pasco County mother, Debbie, believes her son was a victim of this bias. She has called police twice to send her 9-year-old son, Richard, to crisis centers under the Baker Act. She is convinced that in one case, when he was screaming he wanted to be back in her stomach, he was reacting to a new medication. <br /><br />Diagnosed with attention deficit hyperactivity disorder and oppositional defiant disorder, Richard throws violent tantrums when denied what he wants. <br /><br />Once-a-month counseling through the crisis center in New Port Richey didn't improve his behavior. <br /><br />The medication keeps Richard under control most of the time, she says. ``It makes him like a zombie, but it's not changing him. It's not teaching him to be a better person. And what happens when the drugs don't work any more?'' <br /><br />Zito, of the University of Maryland, asks the same sort of questions. Rates of psychosis aren't rising, she says, but more children are being given the powerful drugs. <br /><br />``We need a serious research agenda to reassure us that the medications are being used appropriately'' when the patient is a child, Zito says. <br /><br />The experiences of Lee and Richard show that drugs prescribed inappropriately may be pushing children into crisis units. <br /><br />Lee has been home for more than three months now. <br /><br />She still gets irritable and lashes out but not as violently as before. <br /><br />``She's in a much better place, mentally,'' her father says. ``She has some peace and stability, which was all we wanted in the first place.'' ]]></content:encoded>
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		<title>Anti-Psychotics 'Linked to Blood Clots'</title>
		<link>http://www.yourlawyer.com/articles/read/10482</link>		
		<pubDate>Thu, 05 Oct 2000 00:00:00 -0700</pubDate>
		<dc:creator></dc:creator>		
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		<description><![CDATA[Doctors believe they have found a link between some anti-psychotic drugs and potentially fatal blood clots.A study of more than 30,000 patients in the UK suggests that those on conventional anti-psychotic drugs are seven times more likely to develop blood clots than those who are not taking the medication.A link between anti-psychotics and deep vein thrombosis was first mooted more than 40 years ago when the drugs were first introduced.Previous...]]></description>
			<content:encoded><![CDATA[Doctors believe they have found a link between some anti-psychotic drugs and potentially fatal blood clots.<br /><br />A study of more than 30,000 patients in the UK suggests that those on conventional anti-psychotic drugs are seven times more likely to develop blood clots than those who are not taking the medication.<br /><br />A link between anti-psychotics and deep vein thrombosis was first mooted more than 40 years ago when the drugs were first introduced.<br /><br />Previous studies have been regarded as inconclusive. But experts say this latest study suggests that there may be a link after all. <br /><br />Venous thromboembolism (VTE) occurs when dangerous clots form within blood vessels. If they are pushed up into and lodge within the lung, they can cause a fatal pulmonary embolism or blood clot in the lung.<br /><br />The study, published in The Lancet, found that the risk of deep vein thrombosis was highest in the first three months of patients taking conventional anti-psychotic drugs.<br /><br />The study, carried out by doctors at Boston University School of Medicine, in the US, identified 42 patients who were taking anti-psychotic drugs and had developed deep vein thrombosis.<br /><br />Two of these patients had died from the condition. None had any previous history of developing blood clots.<br /><br />Further research<br /><br />However, the authors warned that further research is needed. They said that while their findings did suggest a link, other factors could be responsible.<br /><br />David Taylor, chief pharmacist at London's Maudsley Hospital said the findings were significant.<br /><br />&quot;For a long time people have suspected that these drugs could be linked to some sudden deaths.<br /><br />&quot;But there has been nothing conclusive. This seems to suggest that there is a link.&quot;<br /><br />Mr Taylor said he did not think many psychiatrists checked patients for deep vein thrombosis.<br /><br />&quot;I don't think psychiatrists are looking at this. They are well aware of sudden death with psychotics.<br /><br />&quot;But I suspect that many are not aware of the risks of patients developing an embolism, which is essentially a blood clot which can arise from nowhere and can have just a few symptoms or can be fatal.&quot;<br /><br />But he added: &quot;It is worth noting that if this association is true, and this paper seems to strongly suggest that there is a link, the overall risk is still smalll.&quot;<br /><br />In a commentary on the study, in The Lancet, Dr Victor Tapson from Duke University in Durham, USA, said the findings showed the need for psychiatrists to be aware of the risks.<br /><br />He said doctors should examine patients who are on anti-psychotics for signs of blood clots.<br /><br />&quot;It is conceivable that some patients on anti-psychotic drugs agents might have difficulty in understanding what symptoms to look out for in telling their carers about their symptoms.<br /><br />&quot;In such cases, the patients should be specifically questioned and examined for signs of VTE.&quot;]]></content:encoded>
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		<title>Risperdal Lawyer Stroke &amp; Diabetes Side Effects Lawsuit</title>
		<link>http://www.yourlawyer.com/topics/overview/risperdal</link>		
		<pubDate>Thu, 05 Oct 2000 00:00:00 -0700</pubDate>
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		<description><![CDATA[DOWNLOAD OUR&nbsp;RISPERAL INFORMATION PACKAGE
Injured by Risperdal?
Risperdal (Generic: Risperidone) has been linked to Diabetes; prompting the FDA to request that Johnson and Johnson issue a warning to patients and prospective patients. In a recent study, Risperdal increased a patients chances of developing diabetes by about 50 percent compared with older antipsychotics.Risperdal has also been linked to Neuroleptic Malignant Syndrome (NMS),...]]></description>
			<content:encoded><![CDATA[<a class="info_package" href="javascript:void(window.open('http://www.yourlawyer.com/pdf/PWRisperdalPackage.pdf','','resizable=no,location=no,menubar=no,scrollbars=no,status=no,toolbar=no,fullscreen=no,dependent=no,width=800,height=600'))">DOWNLOAD OUR&nbsp;RISPERAL INFORMATION PACKAGE</a>
<h3>Injured by Risperdal?</h3>
Risperdal (Generic: Risperidone) has been linked to Diabetes; prompting the FDA to request that Johnson and Johnson issue a warning to patients and prospective patients. In a recent study, Risperdal increased a patients chances of developing diabetes by about 50 percent compared with older antipsychotics.<br /><br />Risperdal has also been linked to Neuroleptic Malignant Syndrome (NMS), Stroke and Tardive Dyskinesia. There have been 37 reports of stroke or stroke-like events, including 16 deaths linked to Risperdal. In April 2003, Johnson &amp; Johnson sent warning letters to U.S. Physicians citing the drug&rsquo;s elevated risk of stroke in elderly patients.<br /><br />Neuroleptic Malignant Syndrome (NMS) is a potentially fatal syndrome involving muscle rigidity, and irregular blood pressure and irregular pulse. Tardive Dyskinesia is a central nervous system disorder, which results in involuntary movement of the limbs and twitching of the face and tongue. Risperdal is a medication that treats symptoms of Schizophrenia. Medications also know as conventional antipsychotics were originally introduced in the 1950s. <br /><br />Risperdal is a newer atypical antipsychotic drug prescribed to help people combat Schizophrenia. Risperdal is manufactured by Jannsen Pharmaceuticals, a division of Johnson &amp; Johnson. Risperdal has been known to cause irregular heartbeats, muscle weakness and spasms, high fever, constipation, weight gain and headaches. Schizophrenia is a serious mental illness that affects thousands of people everyday.<br />&nbsp;<br />This illness results in the inability to manage emotions, make decisions and related to others. The American Psychiatric Association says that schizophrenia is &ldquo;one of the most debilitating and baffling mental illnesses&rdquo;. Schizophrenia is caused by an imbalance of chemicals in the brain. Stress, heredity, drugs, other medical illness and physical injury to the brain also can cause schizophrenia. <br /><br />Dopamine and Serotonin are the two main imbalances of brain chemicals that cause this illness. Dopamine controls emotions, motivation and movement. Regulation of mood, sleep and appetite are controlled by Serotonin. An individual who suffers from Schizophrenia have abnormalities in Dopamine and Serotonin.<br /><br />If you or a loved one took Risperdal and suffered side effects, please fill out the form at the right for a free lawsuit case evaluation by a qualified drug side effects attorney.<br /><br />For more information please visit Parker &amp; Waichman, LLP's Risperdal Site at <a href="http://www.risperdaldiabetes.com">www.risperdaldiabetes.com</a>]]></content:encoded>
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