: Daily Aspirin Regimen Not Safe for Everyone, FDA Warns
Posted May 8, 2014
TUESDAY, May 6, 2014 (HealthDay News) -- Taking an aspirin a day can help prevent heart attack and stroke in people who have suffered such health crises in the past, but not in people who have never had heart problems, according to the U.S. Food and Drug Administration.
"Since the 1990s, clinical data have shown that in people who have experienced a heart attack, stroke or who have a disease of the blood vessels in the heart, a daily low dose of aspirin can help prevent a reoccurrence," Dr. Robert Temple, deputy director for clinical science at the FDA, said in an agency news release.
A low-dose tablet contains 80 milligrams (mg) of aspirin, compared with 325 mg in a regular strength tablet.
However, an analysis of data from major studies does not support the use of aspirin as a preventive medicine in people who have not had a heart attack, stroke or heart problems. In these people, aspirin provides no benefits and puts them at risk for side effects such as dangerous bleeding in the brain or stomach, the FDA said.
Also, there's no evidence that taking aspirin every day is safe and effective for people who have not had heart problems or a stroke but have a family history of heart attack or stroke, or have evidence of arterial disease, Temple said.
He noted that a number of large studies are being conducted to assess the use of aspirin in preventing heart attack and stroke in people with no previous history of heart problems, and that the FDA is monitoring those clinical trials.
Anyone thinking about taking low-dose aspirin needs to discuss the risks and benefits with their doctor, Temple emphasized. It's also important to have your doctor determine the dose and frequency that's appropriate for you.
If your doctor does recommend daily aspirin to reduce your risk of heart attack and stroke, closely examine drug labels. Some drugs combine aspirin with other pain relievers or ingredients and should not be used for long-term aspirin therapy, the FDA said in the news release.
-- Robert Preidt
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