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Bextra Drug Recall – Overview/Update

The FDA’s reasons to recall the popular painkiller Bextra from the marketplace were, in short, that the risks of cardiovascular (CV) events (e.g. – heart attack and stroke) and serious skin reactions were relatively high. The total number of people who experienced these serious side effects was small, but the percentage was high enough to outweigh the benefits of the pain-reliever drug. The risk of CV events for Bextra was high, but no higher than that of other nonsteroidal anti-inflammatory drugs (NSAIDs) – a problem which has prompted the FDA to instruct all makers of NSAIDs such as Advil, Aleve, etc., to post more detailed warnings about the risks on medicine labels. The risk of serious skin reactions, however, was greater than that of other NSAIDs. This increased risk coupled with the fact that Bextra’s positive effects were no more significant than those of any other NSAID, led to the assessment that the risk-benefit profile was unacceptable, which led to the Bextra drug recall.

Suffered harm from Bextra? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

The Bextra recall was based on several sets of data. Bextra’s increased CV event risk was established from two short-term trials in patients recovering from coronary artery bypass surgery. As for skin reactions, the FDA’s spontaneous reporting system for these skin reactions reported a much higher rate for Bextra than for other dugs in the same class. Lastly, as for the positive effects of Bextra, studies showed that its gastrointestinal (GI) safety, overall efficacy, and efficacy in patients who were resistant to other medications, all showed no advantage over any other NSAID.


The Bextra drug recall did not occur in a vacuum. Before Bextra, Vioxx, another COX-2 inhibitor NSAID that was also prescribed for arthritis-related pain and inflammation, was pulled from the market for unacceptable CV risk among other things. As more information about the risks and hazards of these COX-2 inhibitors is available and its users become injured, you can expect to see an influx of lawsuits. As with Vioxx, there are Bextra law firms that are knowledgeable in Bextra litigation. See the sections below on How to Find a Lawyer for more information about Bextra law firms and lawsuits.

Suffered harm from Bextra? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.


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What are the major legal issues involved with the prescription drug Bextra? Who can I sue if I was damaged from using it?

Are there any special considerations involved with Bextra that may be different from other product liability cases?

What defenses are Pfizer and/or my physician likely to use to defend themselves?

What kind of damages can I expect as a result of my Bextra injury?

What is the statute of limitations in a case alleging death or injury caused by Bextra?

I had a heart attack 8 years ago. I’ve been taking Bextra for rheumatoid arthritis for the past 6 months. I had a second heart attack a few weeks ago. What is the impact of pre-existing conditions on my Bextra claim?

I was taking Bextra for a year for my arthritis pain. Now it's been taken off the market and I don't know what I'm going to do. I stopped taking it and my pain is back. Can I sue the manufacturer?

My grandfather has an aneurysm in his iliac vein for which he will need to have surgery. He used to take Vioxx for arthritis pain, and when it went off the market, his doctor switched him to Bextra. The aneurysm was diagnosed about three months after beginning Bextra. Can he successfully sue the manufacturers of both drugs?

My 68-year-old mother has a history of ulcers, but she hadn’t had one in several years when her doctor prescribed Bextra for her osteoarthritis. She has since developed a bleeding ulcer and has had to be hospitalized. The label warned about possible ulcers, but my mother ignored it since she trusts her physician. Who is responsible for her pain and suffering?

I took Bextra for 4 months before it was pulled from the market. In the last few weeks while I was still taking it, I began suffering from blisters in my mouth and nose, swollen eyelids, and red splotches on my skin. My doctor thought it was allergy-related and told me to take Benadryl, but said nothing about Bextra. Now I read that Bextra can cause some severe skin problems that could even be fatal. Can I collect damages from the manufacturer? What is my doctor’s responsibility?

Can I handle my Bextra lawsuit myself without a Bextra attorney or should I join a Bextra class action?

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