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FDA ADE reports for Lovastatin

ade_lovastatin_adverse_events

ade en 2026-07-22

Lovastatin 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. Lovastatin is a active ingredient.

Total reports

Lovastatin: 4

Reports by species (top entries)

  • Human 4

Top reported reactions (VEDDRA terms, top entries)

  • Accidental exposure 2
  • Abdominal pain 1
  • Bad taste 1
  • Belching 1
  • Diverticular disorder 1
  • Itching 1
  • Lot # and /or Expiration date missing 1
  • Nausea 1
  • Odor, Abnormal 1
  • Weeping 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b32.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).