FDA Supplement Safety Reports
Search the FDA's CAERS (Center for Food Safety and Applied Nutrition Adverse Event Reporting System) database for real adverse event reports filed about dietary supplements. This data helps you understand reported side effects and safety concerns.
Important: Adverse event reports do not prove that a product caused the reported reaction. These are unverified reports submitted by consumers, healthcare professionals, and manufacturers. The number of reports does not indicate the frequency of occurrence. Always consult a healthcare professional.
Data Source
This tool uses live data from the openFDA CAERS (Adverse Food Event) API, maintained by the U.S. Food and Drug Administration. The database contains adverse event reports for foods, dietary supplements, and cosmetics. Data is in the public domain.
Disclaimer: openFDA is not intended to be a definitive source for adverse event data. Reports do not establish causation. Always consult healthcare professionals for medical advice.