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FDA ADE reports for Simvastatin

ade_simvastatin_adverse_events

ade en 2026-07-22

Simvastatin 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. Simvastatin is a active ingredient.

Total reports

Simvastatin: 16

Reports by species (top entries)

  • Human 16

Top reported reactions (VEDDRA terms, top entries)

  • Accidental exposure 7
  • Bad taste 5
  • Diarrhoea 3
  • Eye pain 2
  • High blood pressure 2
  • Nausea 2
  • Stomach upset 2
  • Abdominal cramp 1
  • Abdominal pain 1
  • Agitated state of mind 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b28.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).