About Vioxx
Approved by the FDA on May 21, 1999, Vioxx is prescribed to treat signs and symptoms of osteoarthritis, acute pain, and pain associated with menstruation. Vioxx is a classification of medication called “NSAID”, or non-steroidal anti-inflammatory drug ( other NSAIDs include ibuprofen and naproxen.) Although Vioxx makers claim it carries less risk of stomach ulcers and GI problems, the drug is being blamed for causing blood clots, hearts attacks and strokes and other serious side effects. And recent reports reveal that original claims of less stomach related side effects may be false.
Vioxx promises effective pain relief without the potentially serious side effects associated with NSAIDs. Millions of arthritis sufferers and others who live with chronic pain were prescribed the “miracle drug” after heavy advertising and promotion from the manufacturer ( Merck). Although Vioxx was more expensive than other NSAIDs, and did not offer a generic equivalent, the drug was highly prescribed based on the shaky claims of “safe” pain relief. It is estimated that Americans spend $6 billion a year on Vioxx and Celebrex (a similar medication).
Vioxx and Celebrex were marketed as being free of the side effects commonly associated with nonsteroidal anti-inflammatory drugs (NSAIDs). However, studies conducted after Vioxx was already on the market found that many of the same side effects that had been associated with other NSAIDs were also associated with these medications, that the risk increases the longer the medication is used , and that users of these NSAIDs may actually be at greater risk of heart attack and stroke.
Vioxx side effects began to be reported in 2002. Common side effects include upset stomach, vomiting, constipation, and dizziness. Some arthritis patients may be at a higher risk for suffering serious, life-threatening Vioxx side effects including heart attack and stroke. A March 2002 FDA report on Vioxx side effects indicated Vioxx might also be associated to nonbacterial meningitis.
Serious problems associated with the long-term use of NSAIDs include bleeding stomach ulcers, intestinal bleeding, heart problems, and damage to the liver and kidneys. These complications can occur with or without warning symptoms and can lead to hospitalization or death.
FDA Warning Letter to Merck & Co.
Vioxx Contraindications
Vioxx Side Effects
Vioxx Study Results
September, 2001
The American Heart Association, the National Stroke Association and the Arthritis Foundation asked the Vioxx manufacturer, Merck & Co., to test whether Vioxx increases the risk of heart attack and stroke.
September 17, 2001
The U.S. Food and Drug Administration sends Merck & Co. a Warning Letter requiring Merck to cease certain promotional activities for Vioxx.
It called Merck promotions for Vioxx “false, lacking in fair balance or otherwise misleading.”
April, 2002
The FDA orders a change in the Vioxx label information to include warnings based on the newly available information. The updated label says, "Serious problems from stomach ulcers, such as bleeding, are well-known complications in people treated with NSAIDs." The FDA also concluded that the Vioxx label should include warnings of possible liver and kidney damage.
If you or someone you know suffered injury after taking Vioxx, call or
e-mail our experienced Texas Vioxx attorneys at 1-800-683-8383 and find out your legal rights.
