Adverse events associated with use of DMAA

To monitor the safety of dietary supplements on the market, the Food and Drug Administration collects reports of health-related adverse effects, such as serious illness and death, that occurred after taking the product. Manufacturers, packers and distributors are required to report such events, and the public, patients, health care providers and others also can submit reports. The FDA then analyzes them to try to determine if the health problem was caused by the product.

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