YourLawyer.com® 1-800-LAW-INFO (1-800-529-4636)

FDA Issues Warning About Merck’s Rotavirus Vaccine

Feb 14, 2007 | NewsInferno.com

The U.S. Food and Drug Administration (FDA) is warning pediatric health-care professionals and consumers about potentially life-threatening side effects associated with Merck’s RotaTeq vaccine. According to the agency, several infants who’ve received the rotavirus vaccine have suffered from twisted or blocked intestines.

The FDA noted “28 post-marketing reports of intussusception following administration of Rotavirus, Live, Oral, Pentavalent vaccine (trade name RotaTeq), manufactured by Merck and Co. One portion of the intestine telescopes into a nearby portion, causing the intestinal obstruction. The most common site is where the small intestine joins the large intestine.”

At this point, it is unclear whether or not the vaccine is causing the intestinal problems, but the high incidence of this condition has led the FDA to issue an alert even though the number of cases hasn’t exceeded the “expected” rate.

“Approximately 3.5 million doses of RotaTeq have been distributed in the United States through February 1, 2007,” the FDA said. “Not all of these doses have been administered. Since its licensure on February 3, 2006 until January 31, 2007, 28 cases of intussusception have been reported in the U.S. in infants who received RotaTeq. The reported 28 cases occurred after dose 1, dose 2, and dose 3. Approximately half of the cases occurred 1 to 21 days after vaccination, with a range of 0 to 73 days. Sixteen of the 28 infants with intussusception required hospitalization and surgery on their intestine. The remaining 12 infants had reduction of the intussusception by contrast or air enema. No deaths due to intussusception were reported.”

In 1999, Wyeth was forced to pull its rotavirus vaccine from the market due to similar concerns about intussusception. Although rotavirus may cause fever, diarrhea, and vomiting, it is not usually fatal. However, the Centers for Disease Control and Prevention (CDC) still recommends that infants be vaccinated against it. Merck is currently in the midst of a large study of 44,000 children related to their vaccine, but they won’t have complete findings from the study until the end of next year.

RotaTeq had international sales of approximately $163 million in 2006, but that figure is expected to triple in the next three years.
Defective Drugs
* Denotes required field.

Title

* First Name

* Last Name

* Email Address

* Phone Number

Cell Phone Number

Office Phone Number

Street Address

Apartment/Suite

City

State

Zip Code

Please provide the best method and times to contact you:

Date of birth of person injured
(mm-dd-yyyy):

Name of drug:

Date you started taking the drug (mm-yyyy):

Date you stopped taking the drug (mm-yyyy):

Please describe any side effects:

Other Info:

No Yes, I agree to the Parker Waichman Alonso LLP disclaimers.Click here to review all.

Yes, I would like to receive the Parker Waichman Alonso LLP monthly newsletter, InjuryAlert.

please do not fill out the field below.

Bad Med
 
 

News Feeds

WE ALSO OFFER OUR FIRM NEWS AS RSS/XML FEEDS.
LEARN MORE ABOUT RSS

Home | Defective Drugs | Medical Devices | Toxic Substances | Accidents | Product Liability | Malpractice | Diseases
Nursing Home Negligence | Food Poisoning | Other Topics | Social Security Disability | Contact
Statement of Clients' Rights | Site Map | Drug Injury Search | Vioxx | Mesothelioma | Permax | Dostinex | Composix Kugel Mesh X Large Patch
Ortho Evra | Fosamax | Personal Injury Lawyer | Fusarium Keratitis | Stevens Johnson Syndrome | Florida Personal Injury Law Firm

© 2002-2009 YourLawyer.com®. All Rights Reserved.

Please note that you are not considered a client until you have signed a retainer agreement and your case has been accepted by us.
Prior results do not guarantee or predict a similar outcome with respect to any future matter.
Attorney Advertising

Parker Waichman Personal Injury News