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Index/Topics/Adverse event reporting

Adverse event reporting

The process of identifying, recording, and reporting adverse events in clinical trials.

Fact-Checks

2 results
Feb 3, 2026

What independent clinical trials or safety studies exist for Garaherb and what adverse events did they record?

No independent or safety studies for are identified in the supplied reporting; the sources provided discuss general principles and regulatory expectations for safety assessment in clinical research bu...

Jan 16, 2026

How can consumers report adverse reactions or request recalls for dietary supplements sold online?

Consumers who experience adverse reactions to dietary supplements should stop using the product, seek medical care, and report the event to the FDA through the Safety Reporting Portal or MedWatch so r...