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FDA ADE reports for Pravastatin

ade_pravastatin_adverse_events

ade en 2026-07-22

Pravastatin 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. Pravastatin is a active ingredient.

Total reports

Pravastatin: 6

Reports by species (top entries)

  • Human 6

Top reported reactions (VEDDRA terms, top entries)

  • Abdominal discomfort 1
  • Anxious state of mind 1
  • Application site blister 1
  • Application site burning sensation 1
  • Application site irritation 1
  • Injection site pain 1
  • Intentional misuse 1
  • Localised numbness (see also application site SOC) 1
  • Tiredness 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b31.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).