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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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