Adverse Event Report Labeling for Supplements — the Controversy Continues

In 2006, AAHF took a stand against the proposed Dietary Supplement and Non-Prescription Drug Consumer Protection legislation, now law, because we felt the bill was not in the public’s best interest. The Food, Drug, and Cosmetic Act had already been amended to require reporting of serious adverse events for both over-the-counter and dietary supplements to […]

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Adverse Event Reporting—New FDA Report Puts Things in Perspective

Research published in the October 2008 issue of Pediatrics says that some of free prescription drug samples being distributed to pediatric patients may be unsafe. The researchers found that one in twenty American children received free drug samples in 2004—and that the most frequently distributed samples were unsafe to children. Four of the 15 most […]

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Surviving Cardiac Arrest May Depend on Where You Live

Conventional Medicine Ignores the Science behind Preventing Sudden Cardiac Death with Fish Oil The U.S. has waged a five-decade war on heart disease thanks to the information gleaned  from the Framingham Study and the studies that followed it. That war has been dominated by the use of prescription drugs, surgery, and procedures that include angioplasty […]

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