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A Bextra problem is any unfavorable side effect of this prescription medication that does harm to a Bextra user. Bextra is a COX-2 selective non-steroidal anti-inflammatory drug (NSAID) that was originally approved by the FDA in November 2001. Bextra is approved to treat osteoarthritis, rheumatoid arthritis, menstrual pain, and other pain conditions. The approval of Pfizer’s Bextra was based on clinical studies ranging between three and six months in duration. Bextra problem side effects often develop after a longer duration of use, though they can occur at any time.
Bextra problem reports began flooding in soon after this drug was approved for use in the United States. Bextra, and other drugs of its class, were originally developed to provide pain relief without the gastrointestinal problems associated with traditional NSAIDS. Some of the first Bextra problem reports involved unfavorable gastrointestinal side effects such as nausea, diarrhea, indigestion, and abdominal pain. In addition to these common Bextra problem side effects, patients also reported more serious side effects.
A very serious Bextra problem that has been known for years is the risk of serious allergic and skin reactions as a result of taking this medication. Patients who take Bextra are at an increased risk of suffering allergy related Bextra problems such as anaphylactic shock and angioedema. Bextra users are also at risk of suffering skin related Bextra problems.
A serious Bextra problem can cause a person to develop skin conditions like Stevens Johnson Syndrome and toxic epidermal necrolysis. Stevens Johnson Syndrome is a severe inflammatory skin condition characterized by an eruption of the skin and mucous membranes. Toxic epidermal necrolysis is a possible Bextra problem that causes large portions of the skin to become intensely red, blister, and peel off much as a second degree burn would. The risk of this serious Bextra problem has been known for years, yet the drug’s maker has failed to take the steps necessary to adequately inform or protect patients from this Bextra problem.
Another serious Bextra problem which has come to light though recent clinical trials is the increased risk of cardiovascular side effects associated with Bextra use. A major clinical trial found that certain patient populations are twice as likely to suffer from a heart attack or stroke compared to people not taking Bextra. News of this Bextra problem shortly follows the recall of a similar drug, Vioxx, for its cardiovascular risks. Again, Pfizer has failed to take the steps necessary to protect consumers from Bextra problem side effects.
If you, or a loved one, have suffered a Bextra problem side effect, you have the legal right to seek compensation for your losses. A Bextra problem lawsuit can help a victim of Bextra side effects seek compensation for related medical expenses, loss of income, and pain and suffering. If you would like to learn more about your legal rights and options after a Bextra problem, you may wish to speak with an experienced and highly qualified attorney who can protect and maximize your legal interests.
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