• Bextra®
• Alert
• Alternative
• Attorney
• Claim
• Class Action
• Complications
• Danger
• Depression
• Dosage
• Effects
• Heart
• Information
• Injury
• Lawsuit
• Litigation
• Medication
• Problems
• Reaction
• Recall
• Risks
• Safety
• Stroke
• Warnings
• Contact a Lawyer

Find a Lawyer in Your State

Need Help?

• Accutane®
• Cerebral Palsy
• Darvocet®
• Denture Cream
• Depuy ASR™ Hip Implant
• Fosamax® Femur Fracture
• MiniMed Insulin Pump
• Multaq®
• Nephrogenic Systemic Fibrosis
• Paxil® Birth Defects
• Propecia®
• Shoulder Pain Pump
• Topamax®
• Truck Accident Lawyer
• Wellbutrin®
• Yaz® Birth Control

A Bextra® attorney is a legal professional who can help a Bextra® victim seek compensation for their losses. A Bextra® attorney is trained in the area of personal injury law and knows the laws pertaining to strict liability and defective drug lawsuits. A Bextra® attorney can evaluate your Bextra® injury case to determine your legal rights and options with regards to filing a personal injury lawsuit. Through a personal injury lawsuit, a Bextra® attorney can help you receive compensation for your losses, including medical expenses, loss of income, pain and suffering, and more.

A Bextra® attorney stays abreast of the current legal actions surrounding this popular pain reliever. Bextra® is a COX-2 selective non-steroidal anti-inflammatory drug (NSAID) which was approved by the FDA in 2001. Pfizer’s Bextra® was approved to treat the pain associated with osteoarthritis, rheumatoid arthritis, menstrual cramps, and other pain conditions. Since this drug was introduced on the US market, Bextra® has been associated with numerous life threatening side effects.

Bextra® has been proven to cause serious skin and cardiovascular side effects. Stevens Johnson syndrome and toxic epidermal necrolysis are two potentially fatal skin conditions that a person taking Bextra® can develop. These conditions are physically devastating and can lead to fatal complications if not promptly and properly treated. Bextra® can also increase a patient’s risk of developing serious cardiovascular complications, such as heart attack or stroke. One study found that those taking Bextra® were twice as likely as the control group to suffer a heart attack, stroke, blood clot, or other cardiovascular injury.

A Bextra® attorney is familiar with the details of these findings and the subsequent legal and medical actions taken by the government and the pharmaceutical company. Concern about Bextra®’s cardiovascular safety first began after the Vioxx® recall in September 2004. Pfizer consistently maintained that cardiovascular side effects were Vioxx® and that Bextra® was safe for consumer use. Less than three months later, Pfizer announced findings that suggested Bextra® posed similar cardiovascular risks.

A Bextra® attorney is familiar with the numerous occasions where Pfizer has failed to adequately inform or protect consumers from serious Bextra® risks. Pfizer has consistently downplayed or denied the risks associated with its dangerous drug. Pfizer has failed to acknowledge or investigate the risks associated with Bextra®. In April 2005, the FDA prompted Pfizer to pull Bextra® off the shelves, stating that its risks far exceeded its intended benefits. Pfizer complied with the government request but stated that they will continue to look for ways to market their defective drug.

A Bextra® attorney knows the legal ramifications of Pfizer’s gross negligence and can use these facts to build a strong personal injury lawsuit for you. If you or a loved one has taken Bextra®, you may wish to contact a Bextra® attorney who can determine your legal rights and options.

"Bextra Suit Filed"

Bextra , the popular cox-2 inhibitor recalled by Pfizer, is the subject of another lawsuit.

Rita Fohne has filed her lawsuit against Pfizer in Madison County, Illinois, seeking ...

» Read More

"FDA issues drug warnings on its Web site"

The U.S. Food and Drug Administration has started issuing alerts to patients and doctors on its new site Drug Watch. Including emerging drug-safety concerns, as well as dangers presented by drugs prescribed for unapproved uses, the new site is in resp...

» Read More

"FDA to listen to outside advisers in hopes of improving drug-monitoring system"

After a controversial year of drug recalls, the FDA was under attack for failing to adequately protect consumers from dangerous drugs. Currently, the FDA has the Adverse Event Reporting System, or AERS, to collect voluntary reports of possible reactio...

» Read More

• Accutane® |
• Acetaminophen |
• Actavis Information |
• Actos® |
• Amiodarone |
• Trasylol® - Aprotinin Injection |
• Avandia® |
• Baycol® |
• Bextra® |
• Botox |
• Byetta® |
• Celebrex |
• Cellcept |
• Chantix® |
• Cipro Side Effects |
• Crestor |
• Darvocet |
• Darvon® |
• Defective Drug FAQ |
• Common Defective Drugs |
• Depakote® |
• Drug Company Information |
• Defective Drug Side Effects |
• Duragesic Patch |
• Exjade |
• Fentanyl |
• Fen Phen |
• Fleet Phospho Soda |
• Fluoroquinolone Antibiotics |
• Fosamax |
• Gadolinium |
• Gardasil |
• Gleevec |
• Heparin |
• Humira and Remicade |
• Hydroquinone |
• Hydroxycut |
• Januvia® and Janumet® Information |
• Kava Kava |
• Ketek |
• Lariam |
• Levaquin |
• Lupron (Leuprolide) |
• Meridia |
• Multaq® |
• Naproxen (Aleve) |
• Natrecor |
• Neurontin |
• Nexium® (Esomeprazole Magnesium) Heartburn Relief |
• NuvaRing® |
• Ocella Information |
• Osteonecrosis and Fosamax |
• Oxycontin |
• Palladone |
• Paxil |
• Permax |
• Plavix |
• PPA |
• Pradaxa® |
• Prevacid® |
• Prilosec® |
• Procrit |
• Propecia® (Finasteride) |
• Propoxyphene |
• Protonix® |
• Protopic |
• Prozac |
• What is Quinine? |
• Rapamune® Lawyer |
• Raptiva |
• Reglan |
• Remicade Lawsuit |
• Rezulin |
• Risperdal |
• Ritalin |
• Serevent |
• Seroquel |
• Serzone |
• Tequin |
• Thimerosal |
• Topamax® (Topiramate) |
• Viagra® |
• Wellbutrin® |
• Xenical |
• Yasmin® |
• Yaz Birth Control Lawyer |
• Zelnorm |
• Zocor® Medication Information |
• Zoloft |
• Zyprexa |