PRESCRIPTION DRUG ALERT:  Pfizer's Arthritis Drug Bextra Withdrawn from Pharmaceutical Market Amid Health Concerns and Side Effects.
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Drug Alert Information on Valdecoxib / Bextra
 
BEXTRA ALERT! April 7, 2005

Arthritis Drugmaker Pfizer agrees to withdraw Bextra from U.S. and European markets at the request of the FDA. Citing dangerous health risks including heart attack, "life threatening" skin reactions, and additional cardiovascular events, sales of Bextra have been suspended.

If you or a loved one have taken Bextra and have experienced any serious side effects, please contact our lawyers today for a free claim evaluation.

Anyone who has taken an unsafe drug may be at risk for serious health problems. At Brown & Crouppen, we believe that drug companies who place profit above the health of our loved ones must be held accountable for their negligence and the damage they cause to innocent victim’s lives. Our lawyers, skills, credentials and resources have helped thousands of clients win millions of dollars from the manufacturers and suppliers of unsafe drugs and products.

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If you have been injured by Bextra or any other dangerous prescription drug, the manufacturer may have failed in its duty to design, make, inspect and label the product appropriately.

Contact our experienced injury attorneys today for a FREE claim evaluation. Contact Us Online, or call: 1(800)536-HELP
 

 
Bextra Information
  Bextra (valdecoxib) is in a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). It is also a COX-2 inhibitor like Vioxx, Merck & Co.’s blockbuster arthritis drug that was voluntarily withdrawn from the market because of the drug’s link to increased heart attack risk.

Like Vioxx, Bextra works by reducing substances in the body that cause inflammation, pain, and fever, and is used to reduce pain, inflammation, and stiffness caused by osteoarthritis and adult rheumatoid arthritis.

On April 7, 2005, Pfizer has agreed to suspend sales of the prescription drug Bextra. Amid health concerns, including heart attacks and other "life threatening" side effects, the FDA requested that the drug be withdrawn from the pharmaceutical market.

Bextra is also known to induce life-threatening skin and hypersensitivity reactions, conditions that appear in the form of inflammation of the mucous membranes of the mouth, throat, genitals, intestinal tract, and membrane lining the eyelids. This skin disorder is called Stevens-Johnson syndrome, and can lead to lesions and blisters causing intense pain and even death from infection.

» BEXTRA: DRUG DETAILS

 
Side Effects - Heart Attacks, Strokes, SJS
  Other serious, possible side effects of Bextra include:
  • Abdominal pain, tenderness, or discomfort
  • Bloody, black, or tarry stools
  • Nausea or heartburn
  • Bloody vomit
  • Unexplained weight gain
  • Swelling or water retention
  • Unusual fatigue or lethargy
  • Yellowing of the skin or eyes
  • Flu-like symptoms
  • Unusual bruising or bleeding

If you are experiencing any of the above listed side effects, and have taken Bextra, contact our experienced injury attorneys today for a FREE claim evaluation. Contact Us Online, or call: 1(800)536-HELP

Our firm has been building a reputation for success with personal injury clients for almost 25 years. Today, we are one of mid-America’s largest personal injury law firms with over 70 legal professionals and five offices throughout Missouri and Illinois. Brown & Crouppen has thrived because of our shared commitment to deliver the best possible service to clients throughout Missouri and the United States. A large area of our concentration is dangerous drug litigation involving manufacturers and suppliers of unsafe drugs and products.
 

 
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