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Vioxx Information

Las Vegas Lawyer -- Vioxx Information

Vioxx Alert FDA Advisory Vioxx Hearings
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Vioxx Alert
September 30, 2004 -- Merck & Co., Inc. announced a voluntary withdrawal of Vioxx (rofecoxib) from the U.S. and worldwide market due to safety concerns of 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 Info | Drug Index | Home Page

This information came from an FDA online article.


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