Adverse drug event reports from FDA's Adverse Event Reporting System (FAERS) — 9M+ records since 1968 covering serious adverse events, hospitalizations, deaths, and disabilities. Search by drug name (brand/generic/substance, all OR-matched) and optionally filter by MedDRA reaction term. Returns report ID, received date, seriousness flags, patient demographics, MedDRA-coded reactions, implicated drugs (up to 5 per report), and reporting country. Backed by OpenFDA; data is public-domain US government records.

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