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FDA ADE reports for Atorvastatin

ade_atorvastatin_adverse_events

ade en 2026-07-22

Atorvastatin โ€” FDA Animal & Veterinary Adverse Event (ADE) Reports

Source: 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.

Total reports

Atorvastatin: 36

Reports by species (top entries)

  • Human 35
  • Monkey 1

Top reported reactions (VEDDRA terms, top entries)

  • Accidental exposure 24
  • Diarrhoea 3
  • Dizziness 3
  • Feeling anxious 3
  • Headache 3
  • Nausea 3
  • Administration error NOS 2
  • High blood pressure 2
  • Local swelling (not application site) 2
  • Nervousness 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).