FDA CAERS Supplement Adverse Events 2014-2024: Classified Decade Aggregates

This dataset is MODELED, not a live FDA extract. A modeled ten-year audit of US dietary supplement adverse events, organized against the FDA CFSAN Adverse Event Reporting System (CAERS) framework, 2014–2024. The figures (per-category counts, severity percentages, trends; nominal scale ~78,000 supplement-attributable reports) are analyzed aggregates calibrated against published CAERS-derived literature (e.g., Geller et al., NEJM 2015, and FDA/CFSAN summary analyses) applied through a 14-category supplement taxonomy. They are directional estimates, not exact counts extracted from raw CAERS files, and must not be quoted as exact FDA record counts. For the official raw quarterly CAERS data, see the FDA CFSAN CAERS page (fda.gov). CC-BY 4.0. Informational and research use only; not medical advice. CAERS is voluntary and captures an FDA-estimated 1–10% of true events; reports do not establish causation.