Vioxx Claims Attorney
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Vioxx is a rofecoxib-based drug manufactured by Merck and Co. Taken orally, Vioxx is used to treat:
- Osteoarthritis
- Rheumatoid Arthritis
- Acute pain
- Dysmenorrhea
Vioxx was approved in the late 1990s and was touted as a wonder drug. Unlike traditional NSADs, such as aspirin and Aleve, Vioxx did not cause such side effects as stomach ulcers and other gastrointestinal side effects. Unfortunately, it was eventually discovered that Vioxx heightens the risk of heart attacks and sudden cardiac events. These Vioxx side effects may result in death or serious long-term complications.
After a long-term study proved the severity of these side effects, the U.S. Food and Drug Administration issued a warning letter about Vioxx in 2001. This warning told Merck that its review of the company's promotional activities and materials for Vioxx were "false, lacking in fair balance or otherwise misleading." The FDA also criticized Merck for minimizing and omitting important risk information about the use of Vioxx in combination with other drugs. However, Merck chose not to remove Vioxx from the market.
On Sept. 30, 2004, Merck voluntary removed Vioxx from the market. Vioxx's withdrawal came upon the results of Merck's own study that suggested Vioxx users face twice the risk of suffering a heart attack.
Vioxx Lawyers across the country are bringing individual and class action lawsuits against Merck. If you have ever taken Vioxx and have subsequently suffered a heart attack, stroke, or any cardiovascular event, contact us for a free evaluation of your claim.
