Vioxx®, also know as rofecoxib, has been voluntarily removed from the market.

Increased risk of:

  • Heart Attacks
  • Strokes

The FDA has stated that they have "acknowledged the voluntary withdrawal from the market of Vioxx (chemical name rofecoxib), a non-steroidal anti-inflammatory drug (NSAID) manufactured by Merck & Co. FDA today also issued a Public Health Advisory to inform patients of this action and to advise them to consult with a physician about alternative medications."

Vioxx is a NSAID (Non-Steroidal Anti-Inflammatory Drug) It is prescribed for the relief of symptoms of the following:

  • osteoarthritis
  • management of acute pain in adults
  • treatment of menstrual symptoms
  • relief of rheumatoid arthritis symptoms (adults and children)

If you have taken Vioxx® and have had a heart attack, stroke or blood clots, learn more about your options and get an instant answer to your questions. Call today and speak with an Attorney: 1.800.838.0800.


We currently represent a young woman who took this drug for pain management. Prior to taking the drug she was a healthy person. After taking Vioxx she suffered a heart attack as a result of a blood clot.

If this sounds like your situation or you had other problems from this drug, then please contact us. Use our Instant Answer Form.



$1.5 Million: Over the counter Pharmacy cases.  Two cases involving an over the counter drug. 2004

$5+ Million: Multiple pharmacy cases.  Involving damage caused by a prescription drug. 2004


"I was amazed at how the team at Burke and Eisner was able to cut through it all, and successfully obtain the highest possible compensation for my losses."
(NH Client)


FDA: FDA Issues Public Health Advisory Recommending Limited Use of Cox-2 Inhibitors

FDA: Public Health Advisory Non-Steroidal Anti-Inflammatory Drug Products (NSAIDS)

Yahoo: FDA Urges Limited Use of Pfizer's Celebrex, Bextra

FDA: Vioxx Voluntarily Withdrawn; Health Advisory Issued

Additional FDA Information regarding Vioxx

FDA health advisory

FDA Vioxx press release

The FDA has created a question and answer page. You can get basic information here.

Brief Forbes Article from August 2004

 

 

 

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