Manufacturers, packers, and distributors of dietary supplements in the United States are required to report information about serious adverse effects associated with the use of these supplements to the Food and Drug Administration (FDA). The FDA carefully considers all the available safety information submitted to the agency before a product is approved. However, unexpected and sometimes serious safety problems can emerge once a product goes to market and is used by mil...
[PDF.sh25] Dietary Supplements and FDA Use of Adverse Event Reports (Public Health in the 21st Century) Rating: 4.59 (517 Votes)
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