date:Sep 22, 2012
nsumers or health professionals, she added.
As its resources permit, FDA also reviews product labels and other product information, such as package inserts, accompanying literature and internet promotion.
The FDA could take steps (via recalls, injunctions, etc.) to remove a product if it posed a safety issue, Ward said, and collected adverse event data relating to dietary supplements via its CAERS database.
One caveat though is that temporal associations between product use and reports of adv