About Vioxx

FDA approved Vioxx in 1999 for the reduction of pain and inflammation caused by osteoarthritis, as well as for acute pain in adults and for the treatment of menstrual pain. It was the second of a new kind of NSAID (Cox-2 selective) approved by FDA. Subsequently, FDA approved Vioxx to treat the signs and symptoms of rheumatoid arthritis in adults and children.

Vioxx was distributed to more than 30,000 pharmacies only eleven days after it's approval by the FDA.

Vioxx (rofecoxib) was removed from the U.S. and worldwide market due to an increased risk of cardiovascular events (including heart attack and stroke) in patients on Vioxx. Vioxx is a prescription COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) that was approved by FDA in May 1999 for the relief of the signs and symptoms of osteoarthritis, for the management of acute pain in adults, and for the treatment of menstrual symptoms. Vioxx was later approved for the relief of the signs and symptoms of rheumatoid arthritis in adults and children.

Vioxx has been shown to triple patient risk for heart attacks and sudden cardiac death in recent tests. By November 2004, Merck faces 300 lawsuits related to Vioxx, and hundreds more are expected.

Vioxx Recall News

November 4, 2004 - Vioxx withdrawal could cost Merck billions

Disclaimer: The information contained in this website does not constitute legal advice. We make no promises, claims or guarantees about the completeness, accuracy, or adequacy of the information contained in or linked to this web site and websites it we link to. Legal advice is specific to each case, current laws and must be addressed by an experienced lawyer.

Trademark Notice: "Vioxx" is a registered trademark of Merck. VioxxLawsuits.info is in no way affiliated with Merck, and the Vioxx trademark is used solely for informational purposes.