FDA Food & Supplement Adverse Event Reports (CAERS)
fda_openfda.safety.food_adverse_eventsSearch the FDA CAERS database of consumer-reported adverse events for foods and dietary supplements. Returns reported reactions, outcomes (hospitalization, death, etc.), implicated product names and industry, and consumer demographics (age, gender). Filter using Lucene syntax: products.industry_name:"Vit/Min/Prot/Unconv Diet(Human/Animal)" or reactions:"NAUSEA". Distinct from food recall enforcement (health.food_enforcement) — this covers consumer-reported illness/injury, not manufacturer recalls. Source: FDA CAERS database, US public domain.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| skip | No | Number of records to skip for pagination (default 0). | |
| limit | No | Number of records to return (1–99, default 10). | |
| search | No | OpenFDA search expression using Lucene syntax. Single field: brand_name:"tylenol" or classification:"Class I". Combined: generic_name:"ibuprofen"+AND+dosage_form:"TABLET". Omit to return recent records sorted by date. |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| error | No | Present only when the call failed. Includes error code, message, request_id, and any provider-specific extras. | |
| result | No | Tool response payload. Shape varies per tool — consult the tool description and inputSchema. May be an object, array, string, or number depending on the upstream provider response. |