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Welcome to Vioxx Lawsuits

We provide news and legal information about the Vioxx litigation, Vioxx class action and FDA announcements.

Vioxx Recall

On September 30, 2004, Merck & Co., Inc. announced a voluntary withdrawal of Vioxx from the U.S. market due to safety concerns. Vioxx has been linked to serious cardiovascular events, including heart attacks and strokes.

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. It is also approved for the relief of the signs and symptoms of rheumatoid arthritis in adults and children.

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Vioxx Legal News

» Vioxx on 60 Minutes
»Vioxx Lawsuits Stack Up
»Vioxx Side Effects Report
»Vioxx Recall Leads to Regulatory Changes
»More Vioxx News

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