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Prescription Drug
Manufacturer Pfizer Withdraws Bextra from Market
April 7, 2005
Citing concerns regarding the risk of
heart attacks, strokes, "life threatening" skin reactions, and other
cardiovascular events the FDA requested that drugmaker Pfizer withdraw
Bextra from U.S. and European pharmaceutical markets.
The FDA stated that Bextra's dangerous side effects outweigh the benefits of
the medication.
"For now, patients should stop taking Bextra and contact their physicians
about appropriate treatment options," Pfizer said in a statement Thursday. |
More About Bextra:
Bextra has been linked to Stevens
Johnson Syndrome and other skin hypersensitivity disorders and side effects.
Bextra is used to treat osteoarthritis and adult rheumatoid arthritis, pain
associated with menstrual cramping, and for the treatment of primary
dysmenorrhera.
Stevens Johnson Syndrome is an
extreme allergic reaction to chemicals. Common causes are the drugs including
Arava (leflunomide), painkillers, and antibiotics. Bextra has now been linked to
this potentially life threatening syndrome.
Symptoms of Stevens Johnson Syndrome
are skin rash, swelling or blistering of skin, difficulty breathing, fever,
cough, malaise, swelling of face, swelling and lesions of gums, tongue or lips,
excessive tearing or stickiness of eyes and sores in the genital tract
causing painful urination.
Patients who have
severe allergies to antibiotics should not use Bextra. If you develop any of the
above symptoms consult your doctor immediately.
Bextra is a COX-2 inhibitor,
marketed by Pharmacia Corporation and Pfizer, Inc. in the United States.
Celebrex was the first of Pharmacia's COX-2 inhibitors.
Individuals that have experienced
adverse effects from taking Bextra should contact us to learn your legal rights
and options.
FDA Drug Safety Report
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