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FDA ADE reports for Fenofibrate

ade_fenofibrate_adverse_events

ade en 2026-07-22

Fenofibrate 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. Fenofibrate is a active ingredient.

Total reports

Fenofibrate: 17

Reports by species (top entries)

  • Dog 12
  • Human 5

Top reported reactions (VEDDRA terms, top entries)

  • Death 5
  • Accidental exposure 4
  • Elevated protein:creatinine ratio 4
  • Diarrhoea 3
  • Hyperglycaemia 3
  • Hypochloraemia 3
  • Hyponatremia 3
  • Lack of efficacy (bacteria) - Leptospira 3
  • Nausea 3
  • Proteinuria 3

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