
According to the U.S. Food and Drug Administration (FDA) there have been 450,000 adverse event reports reported in pharmaceutical-related cases in the last 6 months. In comparison, there have only been 604 adverse event reports related to dietary supplements in the same six months.
Vice president of scientific and regulatory affairs of the Natural Products Association, Daniel Fabricant said, "As it stands now, the number of mandatory AERs (adverse event reports) is well within - and even a bit below - the normal range that the FDA expected to receive from dietary supplements based on last year's guidance," he said. "To put the number in perspective, the FDA received more than 450,000 mandatory AERs in 2007 from prescription pharmaceuticals."