FDA Issues Safety Warning On Aleve / Naproxen Safety
December 21, 2004
Aleve News Alerts and Lawyer Updates
Aleve, the popular over-the-counter pain reliever made by Bayer, is
now linked to an increased risk of heart attack and stroke, and the
National Institutes of Health has ceased giving the drug to study
participants, the agency announced Monday, December 20, 2004.
The NIH had been investigating whether Aleve or the pain reliever
Celebrex could prevent Alzheimer's disease. Instead, it found a 50
percent increased risk of heart attacks and strokes in those on
Aleve than those on a placebo. Aleve has been on the market since
1994. Naprosyn, the prescription version of Aleve, has been on the
market since 1976.
John Breitner of the University of Washington, the lead scientist on
the NIH study, said researchers will continue to follow the Aleve
participants, some of whom had been taking the drug for nearly three
years.
Aleve is the first non-prescription product to join a growing list
of pain relievers linked to heart attacks and strokes. An FDA
warning advises patients not to take naproxen for more than 10 days
unless directed by a doctor, and only in the amounts specified on
its label: No more than two pills a day.
TO REACH
ALEVE / NAPROXEN LAWYERS / ATTORNEYS
If you or a loved one have
suffered from the dangerous side effects of Aleve / Naproxen, you should
consider receiving a free legal evaluation from an experienced
Aleve / Naproxen lawyer. For a free evaluation of your situation please
complete the following form and an attorney will contact you
promptly - free of charge.
Study Raises More Questions on Painkillers, Including Aleve
ABC News - 04/19/04
FDA Issues Aleve Safety Warning
NBC5.com - 12/21/2004
Aleve Is Facing Safety Questions
USA Today - 12/21/2004
Painkiller Aleve Faces Questions on Safety
Seattle Times -
12/21/2004
Another Pain Medicine, Naproxen / Aleve, Could Cause Drug Problems
WNDU-TV - 12/21/2004
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