FDA Investigation Finds Underreporting of Medical Device Problems
Under federal law, hospitals must report adverse events related to medical devices to the U.S. Food and Drug Administration (FDA), but an FDA investigation has revealed that many hospitals are likely underreporting these events. This reporting helps the FDA identify potentially defective medical devices and prevent additional … [Read more...] about FDA Investigation Finds Underreporting of Medical Device Problems
Teleflex Medical Recalls Tracheostomy Tube Set Due to Possible Disconnection During Use
Teleflex Medical has issued a recall for the Willy Rusch Tracheostomy Tube Set because the connector may disconnect from the tracheostomy tube during use on a ventilated patient. If the connector detaches from the tracheostomy tube shaft during use, the patient may not receive adequate ventilation and would need immediate medical … [Read more...] about Teleflex Medical Recalls Tracheostomy Tube Set Due to Possible Disconnection During Use
Federal Regulators Issue Warning Letter to Teva Pharmaceuticals
Teva Pharmaceuticals just received a “Warning Letter” from the U.S. Food and Drug Administration (FDA) due to the agency’s Current Good Manufacturing Practices (CGMP) inspection of Teva’s Gödöllő, Hungary’s manufacturing facility. Teva was also placed on Import Alert 66-40 on May 27, 2016. The agency’s warning letter notes … [Read more...] about Federal Regulators Issue Warning Letter to Teva Pharmaceuticals
Premature Battery Depletion of Defibrillator Caused Two Deaths
On October 11, 2016, the U.S. Food and Drug Administration (FDA) issued a safety warning for premature battery depletion of the St. Jude Medical Implanted Defibrillator. The St. Jude products in question were manufactured before May 2015 and are ICD and CRT-D models. A medical advisory has been released by St. Jude Medical. The … [Read more...] about Premature Battery Depletion of Defibrillator Caused Two Deaths
Fresh Express American Salad Voluntarily Recalled
A voluntary precautionary recall has been issued by Fresh Express Incorporated of 480 cases of 11-oz. Fresh Express American Salad with a Product Code of G264A12A and a Use-by-Date of October 5, 2016. The reason for the removal of the recalled product from store shelves was the possible exposure to undeclared allergens including … [Read more...] about Fresh Express American Salad Voluntarily Recalled
Hepatitis B Reactivation in Certain Patients Taking Hepatitis C Drugs
The U.S. Food and Drug Administration (FDA) has mandated that its most serious warning, the so-called “black box,” be placed on nine brand name hepatitis C virus (HCV) drugs. The call for the black box followed 24 reported cases of reactivation of HPV in patients who were being treated with direct acting antiviral (DAA) … [Read more...] about Hepatitis B Reactivation in Certain Patients Taking Hepatitis C Drugs
GAO Says FDA Information Systems Riddled with Cybersecurity Flaws
The Government Accountability Office (GAO) has found that the U.S. Food and Drug Administration’s (FDA) online information system has a number of weaknesses that make it vulnerable to cyberattacks. After conducting a review, GAO said it found over 80 weaknesses that make it easier for hackers to access confidential health … [Read more...] about GAO Says FDA Information Systems Riddled with Cybersecurity Flaws
DePuy Pinnacle MDL Status Update: Jury Selected, Motion to Quash Denied
A jury was selected last week in a case in the DePuy Pinnacle multidistrict litigation (MDL). The MDL—IN RE: DePuy Orthopaedics, Inc., Pinnacle Hip Implant Products Liability Litigation—(MDL 2244) is being heard in the Northern District Court, Northern District of Texas. A Second Mandamus was also filed this Saturday evening … [Read more...] about DePuy Pinnacle MDL Status Update: Jury Selected, Motion to Quash Denied
In Xarelto MDL, Judge Extends Deadline to File Complaints
Certain groups of plaintiffs in the Xarelto multidistrict litigation (MDL) have more time to file a lawsuit against manufacturers Janssen Pharmaceuticals and Bayer Healthcare. According to a recent order issued by Judge Eldon Fallon, who is overseeing the MDL in the Eastern District of Louisiana, the filing deadline has been extended … [Read more...] about In Xarelto MDL, Judge Extends Deadline to File Complaints
Final Rule for Antibacterial Soap Efficacy and Safety Released by Federal Regulators
Officials with the U.S. Food and Drug Administration (FDA) just released the agency’s final rule concerning over-the-counter (OTC) consumer antiseptic hand soap products that are made with specific active ingredients, including triclocarban and triclosan. These soaps are no longer marketable and firms that make these products will … [Read more...] about Final Rule for Antibacterial Soap Efficacy and Safety Released by Federal Regulators
Boston Scientific Plaintiff Wins Appeal, Gets New Trial
A woman who lost her case in the Boston Scientific transvaginal mesh litigation more than two years ago is getting another opportunity in court. Previously, she filed a lawsuit alleging that she suffered injuries caused by the Pinnacle Pelvic Floor Repair Kit, which was implanted in 2010 to treat an anterior pelvic organ prolapse, or … [Read more...] about Boston Scientific Plaintiff Wins Appeal, Gets New Trial
Hepatitis A Outbreak Linked to Strawberry Smoothies
The Centers for Disease Control and Prevention (CDC) said 89 people from seven states have been sickened in an outbreak of the liver disease hepatitis A linked to strawberries at a smoothie chain. Investigators have interviewed 54 of the people who became ill and all of them said they drank a smoothie containing strawberries … [Read more...] about Hepatitis A Outbreak Linked to Strawberry Smoothies
Illinois Woman Alleges Essure Complications Led to Removal of Uterus, Fallopian Tubes
Another lawsuit has been filed against Bayer over Essure, the permanent birth control device for women. An Illinois woman alleges that Essure implantation led to serious complications, ultimately leading to the removal of her uterus and fallopian tubes. Essure consists of metal coils inserted into the fallopian tubes as a permanent … [Read more...] about Illinois Woman Alleges Essure Complications Led to Removal of Uterus, Fallopian Tubes
FDA Scrutinizes Pfizer Study Evaluating Chantix Suicide Risks
The U.S. Food and Drug Administration (FDA) is questioning whether or not Pfizer’s study of neuropsychiatric effects of Chantix, the smoking cessation drug, accurately reflects the risks. Pfizer conducted the clinical trial upon request from the FDA, following a high rate of suicidal thoughts linked to Chantix. The study also … [Read more...] about FDA Scrutinizes Pfizer Study Evaluating Chantix Suicide Risks
Mississippi Woman Files Benicar Lawsuit Alleging Drug Caused Colitis
A lawsuit filed recently on behalf of a Mississippi woman alleges that the blood-pressure drug Benicar HCT caused her colitis and other gastrointestinal complications. This lawsuit is part of a multidistrict litigation (MDL) in progress in federal court in New Jersey, Top Class Actions reports. … [Read more...] about Mississippi Woman Files Benicar Lawsuit Alleging Drug Caused Colitis
FDA Orders Antibacterial Ingredients Removed from Consumer Soaps
The U.S. Food and Drug Administration (FDA) has issued a rule ordering the removal of antibacterial ingredients from soaps and body washes, saying there is not enough scientific evidence that antibacterial soaps are better than plain soaps at preventing illness. Health officials have raised questions about potential negative … [Read more...] about FDA Orders Antibacterial Ingredients Removed from Consumer Soaps
Vaginal Mesh Associated with Inflammation Revealed in New Study
Surgical vaginal mesh is used in the treatment of pelvic organ prolapse (POP) and stress urinary incontinence in women. The University of Pittsburgh has revealed a significant connection between vaginal mesh and inflammation in patients. POP, common in older women, or those who have been pregnant or given birth, is when organs … [Read more...] about Vaginal Mesh Associated with Inflammation Revealed in New Study
Lawsuit Alleges Benicar HCT Led to Colitis
A new lawsuit has been filed over Benicar HCT (olmesartan medoxomil and hydrochlorothiazide), a hypertension medication manufactured by Daiichi-Sankyo and Forest Laboratories. The plaintiff is a Mississippi woman who began taking the drug in 2005. She developed colitis and other gastrointestinal symptoms, allegedly due to Benicar … [Read more...] about Lawsuit Alleges Benicar HCT Led to Colitis
Island Soups Co. Issues Recall Due to Botulism Risk
Island Soups Co. is recalling six flavors of soup due to the risk of botulism poisoning. The U.S. Food and Drug Administration (FDA) conducted an inspection and found that company records do not show that the soups were processed adequately to stop the growth of Clostridium botulinum. Botulism poisoning can be fatal. Foodborne … [Read more...] about Island Soups Co. Issues Recall Due to Botulism Risk
What is Stevens-Johnson Syndrome and How is it Related to Zithromax?
Stevens-Johnson Syndrome is a severe reaction that affects the skin and mucous membranes. It causes a rash that spreads and blisters, ultimately causing the top layer of the skin to shed and die. When SJS affects more than 30 percent of the body, it is referred to as toxic epidermal necrolysis (TEN). SJS can be caused by viral … [Read more...] about What is Stevens-Johnson Syndrome and How is it Related to Zithromax?
Jeni’s Splendid Ice Creams get FDA Warning Letter due to Listeria
For the second time, Listeria contamination is a problem for Jeni’s Splendid Ice Creams’ manufacturers. The first recall of Jeni's Splendid Ice Creams was in 2015 after the bacteria was found in Jeni’s production facility. Jeni’s issued a voluntary recall and was out of business for some time. This recent concern began in January … [Read more...] about Jeni’s Splendid Ice Creams get FDA Warning Letter due to Listeria
Investigation of St. Jude Medical Devices Now Includes FDA
The U.S. Food and Drug Administration (FDA) has now joined the investigation into security claims that devices made by St. Jude Medical can be hacked remotely. These claims are still being defended by St. Jude. Muddy Waters Capital, an investment group, says that St. Jude Medical pacemakers and defibrillators are particularly … [Read more...] about Investigation of St. Jude Medical Devices Now Includes FDA
Quality of Xarelto Clinical Trials Expected to be an Issue in 2017 Court Cases
When the first lawsuits involving the blood-thinning drug Xarelto go to trial in 2017, attorneys expect the quality of the clinical trials involved in the drug’s approval to be a major issue. Xarelto lawsuits have been filed in both federal courts and in state court in Pennsylvania. In both state and federal cases, plaintiffs who … [Read more...] about Quality of Xarelto Clinical Trials Expected to be an Issue in 2017 Court Cases
Power Morcellator Use Drops in Light of FDA Warning
The use of power morcellators in gynecologic procedures has decreased substantially after the U.S. Food and Drug Administration (FDA) warned in 2014 that the devices could spread undetected uterine cancers. A study published in JAMA examined trends in power morcellation among women undergoing a hysterectomy. Researchers found that in … [Read more...] about Power Morcellator Use Drops in Light of FDA Warning
Honeywell Issues Recall for Possibly Contaminated Eyesaline Eyewash
In cooperation with the Food and Drug Administration, Honeywell has recalled one lot of Eyesaline Eyewash solution. The eyewash is used for emergency eye rinsing after an injury. The product has been recalled as a precaution because of the risk of Klebsiella pneumoniae contamination. According to the Centers for Disease Control … [Read more...] about Honeywell Issues Recall for Possibly Contaminated Eyesaline Eyewash
Biomet Faces New Lawsuit over Metal-on-Metal Hip Implant
Biomet is facing a new lawsuit alleging that its metal-on-metal hip implant is to blame for a New York woman’s injuries. The plaintiff is a 61-year-old woman who was implanted with the Biomet M2a Magnum Hip Replacement System in her right hip six years ago. As the name implies, the implant is a metal-on-metal hip device where all … [Read more...] about Biomet Faces New Lawsuit over Metal-on-Metal Hip Implant
Cipro Linked to the Serious Allergic Reaction Stevens-Johnson Syndrome
The fluoroquinolone antibiotic Cipro (ciprofloxacin) is one the medications linked to the extreme allergic reaction Stevens-Johnson syndrome (SJS). Though Stevens-Johnson is not common, it can be fatal if not treated quickly, according to Top Class Actions. … [Read more...] about Cipro Linked to the Serious Allergic Reaction Stevens-Johnson Syndrome
Import of Laxachem Products Halted by FDA due to Inspection Issues
Laxachem manufactures active pharmaceutical ingredients (API) for repackers, labelers, and wholesale drug distributors, some of which do business with manufacturing facilities in the United States. One of the drugs Laxachem manufactures is Docusate Sodium USP, a stool softener that is often prescribed by doctors for the treatment of … [Read more...] about Import of Laxachem Products Halted by FDA due to Inspection Issues
11-Year-Old Girl Goes Nearly Bald After Using Wen Hair Product
An 11-year-old girl suffered hair loss and went nearly bald after using Wen cleansing conditioner, but she isn’t the only one. More than 21,000 complaints have been filed over celebrity hairstylist Chaz Dean’s line of Wen hair products alleging hair loss, hair breakage and other issues. In the young girl’s case, she noticed large … [Read more...] about 11-Year-Old Girl Goes Nearly Bald After Using Wen Hair Product
Frozen Corn Products Recalled for Possible Listeria Contamination
Cambridge Farms, LLC of Lancaster, Pennsylvania has recalled three brands of frozen corn products because they may be contaminated with listeria monocytogenes. The organism can cause serious and sometimes fatal infections in young children, the elderly and people with weakened immune systems. To date, no illnesses have been … [Read more...] about Frozen Corn Products Recalled for Possible Listeria Contamination
Bill Proposes to Give FDA More Authority on Cosmetics
Compared to drugs and medical devices, there are few regulations in place to assure the safety of a cosmetic product. A new bill, introduced by senators Dianne Feinstein (D-CA) and Susan Collins (R-ME), seeks change. The proposed legislation would require the U.S. Food and Drug Administration (FDA) to assess the safety of at least 5 … [Read more...] about Bill Proposes to Give FDA More Authority on Cosmetics
FDA Places Laxachem Organics on Important Alert, Prohibits Products from Entering US
Laxachem Organics of Ahmednagar, Maharashtra, India has been placed on “important alert” by the U.S. Food and Drug Administration (FDA), legally stopping all of the company’s pharmaceutical products from entering the United States. According to an update posted on the FDA website Aug. 15, the important alert was placed on August 11, … [Read more...] about FDA Places Laxachem Organics on Important Alert, Prohibits Products from Entering US
No Settlement Reached in IVC Filter MDL Conference
The U.S. Judicial Panel on Multidistrict Litigation (JPML) consolidated Cook IVC filter lawsuits, in October 2014, into the U.S. District Court for the Southern District of Indiana. Over 500 plaintiffs have joined the litigation, all alleging to have been injured by Cook Celect and Gunther Tulip IVC filters. A settlement … [Read more...] about No Settlement Reached in IVC Filter MDL Conference
FDA Investigates Wen Hair Care Products
A class-action lawsuit has been filed against Wen Hair Care products and their distributor, Guehy-Renker, for allegedly causing hair loss (alopecia). More than 21,000 complaints have been received against Wen, sold by Hollywood hairstylist Chaz Dean. The U.S. Food and Drug Administration (FDA) is investigating claims ranging from … [Read more...] about FDA Investigates Wen Hair Care Products
Medtronic Issues Warning for Heart Valve Delivery System
Medtronic PLC has issued a warning regarding its minimally invasive EnVeo R delivery system, which is used to implant the Evolut R aortic valve in the heart. The company is urging doctors to take extra precautions when inserting the device, which is used to treat aortic stenosis, a narrowing of heart valves that can lead to heart … [Read more...] about Medtronic Issues Warning for Heart Valve Delivery System
Sanofi Faces Another Lawsuit over Taxotere
Sanofi-Aventis faces another lawsuit alleging that its chemotherapy drug Taxotere led to permanent hair loss, or alopecia. The suit accuses the drug maker of failing to adequately warn about the risk of irreversible hair loss. The plaintiff is a California woman who was diagnosed with Stage II breast cancer in 2010. She underwent six … [Read more...] about Sanofi Faces Another Lawsuit over Taxotere
Kentucky Attorney General Files Lawsuit Against Johnson & Johnson Over Transvaginal Mesh
Kentucky Attorney General Andy Beshear announced on August 16, 2016 that his office was filing a civil lawsuit against Johnson & Johnson and its medical device unit, Ethicon, over surgical mesh devices used in gynecological surgery. The lawsuit alleges the companies used deceptive marketing for transvaginal mesh devices, … [Read more...] about Kentucky Attorney General Files Lawsuit Against Johnson & Johnson Over Transvaginal Mesh
Oriental Packing Co. Curry Powders Recalled for Lead Contamination
Oriental Packing Co., Inc., of Miami, Florida has recalled approximately 377,000 lbs. of blended curry seasoning products because the products are contaminated with lead. Lead can accumulate in the body over time and can cause serious and sometimes permanent adverse health consequences, the Food and Drug Administration (FDA) … [Read more...] about Oriental Packing Co. Curry Powders Recalled for Lead Contamination
Hospira Recalls Lot of Injectable Anesthetic Due to Particulate Contamination
Hospira is recalling one lot of an injectable anesthetic due to contamination with particulate matter, which was identified in a single vial. The voluntary recall affects one lot of 0.25% Bupivacaine Hydrochloride Injection, USP (NDC: 0409-1159-02, Lot 59-064- DK, Expiry 1NOV2017). Hospira, a Pfizer company, learned of the … [Read more...] about Hospira Recalls Lot of Injectable Anesthetic Due to Particulate Contamination
Lawmakers Propose Bill in Effort to Better Detect Medical Device Issues
New legislation seeks to identify medical device problems as early as possible. Under the Medical Device Guardians Act of 2016, introduced by U.S. Reps. Louise Slaughter, D-N.Y. and Michael Fitzpatrick, R-Pa., physicians would be required to report medical device injuries and complications to the U.S. Food and Drug Administration … [Read more...] about Lawmakers Propose Bill in Effort to Better Detect Medical Device Issues
Fluoroquinolones and Peripheral Neuropathy
Fluoroquinolones are a class of antibiotics that include ciprofloxacin (brand names: Cipro, Cetraxal and Proquin), levofloxacin (Levaquin, Quixin and Iquix), moxifloxacin (brand name: Avelox), gemifloxacin (brand name: Factive) and ofloxacin (brand name: Ofloxacin). One potential side effect that may occur after using Levaquin or … [Read more...] about Fluoroquinolones and Peripheral Neuropathy
Fluoroquinolone Injuries are Among the Most Frequently Reported Drug Side Effects
According to a new report, antibiotics in the same class as Avelox (moxifloxacin) were the drugs most frequently associated with reports of persistent adverse effects in 2015. The report appeared in QuarterWatch, a publication of the Institute for Safe Medication Practices. QuarterWatch reviews reports made to the Food and Drug … [Read more...] about Fluoroquinolone Injuries are Among the Most Frequently Reported Drug Side Effects
Zithromax may Lead to Serious Kidney Side Effects
Zithromax (Azithromycin) is among the most popular antibiotics prescribed in the United States; however, the drug has been tied to a variety of serious side effects, including those involving the kidneys. Zithromax, manufactured by Pfizer Inc., received U.S. Food and Drug Administration (FDA) clearance in 1992 and is prescribed to … [Read more...] about Zithromax may Lead to Serious Kidney Side Effects
Cook IVC Filter Bellwether Trials Slated for 2017
Trials dates have been set by the judge presiding over the Cook inferior vena cava (IVC) multidistrict litigation (MDL) in Indiana to begin 2017. Hundreds of additional lawsuits have been filed by people alleging that Cook Medical’s devices tend to break in the vein causing serious injury. IVC filters are meant to prevent blood … [Read more...] about Cook IVC Filter Bellwether Trials Slated for 2017
Pradaxa Linked to Brain Bleeds
Researchers report that they have found a possible link between the anticoagulant drug Pradaxa and intracerebral hemorrhage (brain bleeding). When a blood vessel wall or vein is damaged, the vessel can leak blood into tissues, causing a hematoma, a swelling of clotted blood within the tissues. The hematoma can be cause swelling … [Read more...] about Pradaxa Linked to Brain Bleeds
Power Morcellators can Worsen Uterine Cancers
A few years ago, the use of power morcellators in minimally invasive gynecologic surgeries did not arouse much concern. The tool, which cuts up large masses of tissue into smaller pieces, make it easier for surgeons to remove through small incisions. Laparoscopic procedures with power morcellators were also sometimes preferred due to … [Read more...] about Power Morcellators can Worsen Uterine Cancers
New Legislation Introduced in Light of Morcellator Risks
Safety concerns surrounding power morcellators have prompted lawmakers to team up with patient advocates and introduce new legislation. The Medical Device Guardians Act of 2016, which was introduced by U.S. Reps. Louise Slaughter, D-N.Y. and Michael Fitzpatrick, R-Pa., would require physicians to report any medical device problems to … [Read more...] about New Legislation Introduced in Light of Morcellator Risks
Taxotere and the Risk of Alopecia
The U.S. Food and Drug Administration (FDA) approved Taxotere as a chemotherapy drug in 1996. Taxotere is manufactured by Sanofi-Aventis and is commonly used to treat breast cancer, as well as other cancers. Some patients taking Taxotere have reported experiencing permanent hair loss, or alopecia. In December 2015, the FDA warned … [Read more...] about Taxotere and the Risk of Alopecia
Zithromax: An Overview of Potential Side Effects
Zithromax, known generically as azithromycin, is an antibiotic manufactured by Pfizer. It is used to treat bacterial infections such as pneumonia, sexually transmitted diseases (STDs) and infections of the ears, lungs, sinuses, skin, throat and reproductive organs. Azithromycin is classified as a macrolide antibiotic and works by … [Read more...] about Zithromax: An Overview of Potential Side Effects
Monsanto Faces Growing Litigation over Roundup Herbicide
Litigation is mounting against multinational agrochemical manufacturer Monsanto Co. alleging that an ingredient in its Roundup herbicide increases the risk of cancer. Madison Record reports that a growing litigation in Illinois could become a class action lawsuit. Plaintiff's lawsuits have sprung up more frequently ever since the … [Read more...] about Monsanto Faces Growing Litigation over Roundup Herbicide
Medtronic Infuse Recipients Receive $8.45 Million in Settlements
The University of California, Los Angeles has agreed to pay a combined $8.45 million to two patients who received Medtronic's controversial Infuse bone graft product. These individuals filed lawsuits alleging that the product caused unwanted bone growth. They also claimed that the implanting surgeon had a conflict of interest because … [Read more...] about Medtronic Infuse Recipients Receive $8.45 Million in Settlements
Case Study Examines Long-Term Inferior Vena Cava (IVC) Filter Retrieval
Inferior vena cava (IVC) filters are umbrella-shaped devices that are implanted into a patient's inferior vena cava, a major vein carrying blood from the lower part of the body to the heart. They are used when patients are at risk for a pulmonary embolism, a potentially life-threatening condition where a piece of a blood clot can … [Read more...] about Case Study Examines Long-Term Inferior Vena Cava (IVC) Filter Retrieval
FDA Approval of Transvaginal Mesh is Questioned by Victims
A study by Northwestern University, published May 4, 2016 in Obstetrics and Gynecology criticized the U.S. Food and Drug Administation (FDA) for approving a number of high-risk health devices based on unsubstantiated clinical studies, including transvaginal mesh. Dr. Steve Xu, lead researcher said, “Although it is impossible to … [Read more...] about FDA Approval of Transvaginal Mesh is Questioned by Victims
FDA Says to Beware of Skin Care Products Containing Mercury
In a recently updated statement, the U.S. Food and Drug Administration (FDA) is warning consumers to beware of skin care products containing mercury. Exposure to mercury is hazardous, and can damage the brain, lungs and kidneys. It is especially harmful to pregnant women as well as infants and young children, whose brains are still … [Read more...] about FDA Says to Beware of Skin Care Products Containing Mercury
Wen Conditioner Hair Loss Complaints Prompt FDA Safety Alert
Numerous complaints of hair loss, bald spots, rashes, and itching after using Wen hair cleansing conditioner prompted the U.S. Food and Drug Administration (FDA) to issue a safety alert. As of July 7, 2016, the agency has received 127 direct complaints from consumers, the most ever concerning a cosmetic hair product. Also, the FDA … [Read more...] about Wen Conditioner Hair Loss Complaints Prompt FDA Safety Alert
Schumer Slams FDA for Sluggish Dangerous Food Recall Process
Senator Chuck Schumer criticized the U.S. Food and Drug Administration (FDA) for being too slow in recalling potentially dangerous food. The Senator is calling for a top-to-bottom review of the agency’s process. “Delays in getting bad food off shelves is just a recipe for disaster,” said Schumer in a recent press release. “That’s … [Read more...] about Schumer Slams FDA for Sluggish Dangerous Food Recall Process
Cerebellar Atrophy Reported in Dilantin Patients
The U.S. Food and Drug Administration (FDA) has approved labeling changes stating that cerebellar atrophy has been reported in patients taking phenytoin. This nervous system adverse reaction appears to occur more frequently when drug levels are elevated or when it is used long-term. Phenytoin is sold by Pfizer under the brand name … [Read more...] about Cerebellar Atrophy Reported in Dilantin Patients
Lawsuit Alleges Benicar HCT Makers Failed to Warn about Risk of Intestinal Side Effects
Daiichi Sankyo and Forest Laboratories are facing a new lawsuit alleging the companies failed to warn about the risk of gastrointestinal injuries with Benicar HCT, a high blood pressure medication. The plaintiff began taking the drug in April 2006, and alleges that it caused her to suffer gastrointestinal injuries and kidney failure. … [Read more...] about Lawsuit Alleges Benicar HCT Makers Failed to Warn about Risk of Intestinal Side Effects
Chicago fertility clinic cited for failing to screen eggs for STDs
A Chicago fertility doctor has been accepting egg donors without screening women donating them for sexually transmitted diseases. According to an Associated Press report this week, Dr. Martin Balin has received a formal warning letter from the Food and Drug Administration following an agency inspection of his clinic earlier this … [Read more...] about Chicago fertility clinic cited for failing to screen eggs for STDs
