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fda-database

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Query the openFDA API to retrieve FDA regulatory datasets (drugs, devices, adverse events, recalls, submissions, UNII) when you need programmatic safety/regulatory evidence for analysis or research.

scientific-skills/Evidence Insight/fda-database/SKILL.md

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> **Source**: [https://github.com/aipoch/medical-research-skills](https://github.com/aipoch/medical-research-skills)

## When to Use

1. **Pharmacovigilance / safety signal screening** when you need adverse event counts, common reactions, or serious-event rates for a drug.
2. **Medical device regulatory research** when you need 510(k)/PMA context, device classification, UDI lookups, or device adverse events/recalls.
3. **Recall and enforcement monitoring** when you need to track Class I/II/III recalls across drugs, devices, or foods.
4. **Substance identity resolution** when you need UNII/CAS/name-based lookups and basic substance relationship/structure retrieval.
5. **Veterinary safety analysis** when you need animal adverse events filtered by species/breed and product.

## Key Features

- Unified Python interface (`FDAQuery`) for multiple openFDA domains (drug, device, food, animalandveterinary, other).
- Convenience helpers for common tasks:
  - Drug events, labels, recalls, shortages
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