{"topic_id":"ade_atorvastatin_adverse_events","category":"ade","context":"---\ntopic_id: ade_atorvastatin_adverse_events\ncategory: ade\ntitle: \"FDA ADE reports for Atorvastatin (active ingredient) — total reports, species & reaction breakdown\"\nlang: en\nsource: \"openFDA animalandveterinary/event.json (FDA CVM adverse event reports), pulled 2026-07-22\"\nsource_file: pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json\ndate_parsed: 2026-07-22\ntokens_estimated: 328\nverification:\n  method: substring_match\n  claims: 26\n  passed: 26\n  date: 2026-07-22\n---\n\n# Atorvastatin — FDA Animal & Veterinary Adverse Event (ADE) Reports\n\nSource: openFDA `animalandveterinary/event.json`, the FDA Center for Veterinary Medicine (CVM) adverse event report database. Data pulled 2026-07-22. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. Atorvastatin is a active ingredient.\n\n## Total reports\nAtorvastatin: 36\n\n## Reports by species (top entries)\n- Human 35\n- Monkey 1\n\n## Top reported reactions (VEDDRA terms, top entries)\n- Accidental exposure 24\n- Diarrhoea 3\n- Dizziness 3\n- Feeling anxious 3\n- Headache 3\n- Nausea 3\n- Administration error NOS 2\n- High blood pressure 2\n- Local swelling (not application site) 2\n- Nervousness 2\n\nSource JSON: `pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json` (openFDA animalandveterinary/event.json, pulled 2026-07-22).\n","sources":[],"tokens_estimated":227,"generated_at":null,"tip":"Use /api/v1/topics to discover more topics. /api/v1/nutrient for precise single-point queries. /api/v1/cross_compare for 2-3 standard comparisons."}