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Bextra Heart

Bextra heart safety has been the topic of controversy since the recall of a similar drug called Vioxx in September 2004. Bextra and Vioxx are both COX-2 selective non-steroidal anti inflammatory pain medications approved to treat osteoarthritis, rheumatoid arthritis and primary dysmenorrhea (menstrual cramps).

Vioxx was pulled from the market after studies found that taking Vioxx for eighteen months doubles a patient's chances of suffering from a heart attack or stroke. These findings have prompted Bextra heart safety scrutiny and worries that Bextra use may also cause an increased risk of heart problems or stroke in patients.

Bextra heart and stoke risks were discussed at an American Heart Association meeting in early November 2004. One study presented at the conference indicated that Bextra heart problems may be a possible side effect of taking this medication. Patients who were taking Bextra at the time they underwent cardiac bypass surgery had a higher risk of suffering heart complications than other surgery patients.

Pfizer, the manufacturers of Bextra, responded to these reports by claiming that these unsubstantiated findings have not been published in medical journals or confirmed by independent sources. The drug company has announced plans to conduct long term studies on Bextra heart problem and stroke risks. The FDA has also stated that they will be conducting studies on Bextra heart safety and the cardiovascular safety of all COX-2 selective pain medications.

It is still unclear whether Bextra heart problems and stroke are potential side effects of this medication. If you experience any symptoms of heart attack or stroke while taking Bextra, you should seek medical attention immediately. Symptoms of Bextra heart problems can include chest pains, shortness of breath or difficulty breathing, edema (tissue swelling), excessive fatigue or weakness, persistent coughing, appetite changes, and confusion. Symptoms of stroke may include sudden weakness of numbness to one side of the body, disorientation and confusion, loss of coordination, blurred vision, and troubles with walking, speaking and understanding others.

In addition to the possible risks associated with Bextra heart safety, Bextra is known to cause rare but serious side effects. Severe skin conditions, such as Stevens-Johnson syndrome and toxic epidermal necrolysis are possible Bextra side effects. Anaphylactic shock and allergic reactions are also possible side effects associated with Bextra use.

If you are taking Bextra and have experienced Bextra heart problems, stroke or any other adverse health conditions, you may be eligible to seek compensation for your damages in a product liability Bextra lawsuit. Recovery of medical expenses, loss of income, and pain and suffering may be possible through a civil claim. For more information on Bextra heart safety, you may wish to contact a qualified attorney who can advise you of your legal rights and options in a civil case.

Please contact a Bextra Lawyer if you would like more information on Bextra heart warnings and your legal rights and options.

More Bextra Resources

Bextra Consumer Information - Patient FAQ on Bextra, including side effects, warnings and drug information from the FDA.

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