The United States Food and Drug Administration (FDA) has begun daily publication of adverse event data from the FDA Adverse ...

W A S H I N G T O N, April 18 -- Tough new rules are needed to monitor the saleand use of dietary supplements, the vitamins and herbs now used byabout 60 percent of Americans, a government study says.

Officials say government found 604 'adverse events' from dietary supplements. Sept. 23, 2008— -- Serious side effects from the use of food supplements resulted in 604 "adverse-event" reports ...

The US Food and Drug Administration (FDA) began daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS). This represents a significant step forward in modernizing ...

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

The FDA's post-marketing responsibilities include monitoring safety (eg, voluntary dietary supplement adverse event reporting) and product information, such as labeling, claims, package inserts ...

A recent FDA study, the report said, estimated that the agency learns of fewer than 1 percent of adverse events involving dietary supplements, even though some, such as ephedrine alkaloids or ...

To date, Natural Dior LLC has not received any reports of adverse events related to this recall. The product is used as a state indication (s) and is packaged in 16.9 fl oz (1.06 pt) 500 mL ...

Dietary supplements are a big business. The industry made almost $39 billion in revenue in 2022, and with very little regulation and oversight, it stands to keep growing. The marketing of dietary ...