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FDA ADE reports for Ezetimibe

ade_ezetimibe_adverse_events

ade en 2026-07-22

Ezetimibe 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. Ezetimibe is a active ingredient.

Total reports

Ezetimibe: 5

Reports by species (top entries)

  • Human 5

Top reported reactions (VEDDRA terms, top entries)

  • Abnormal radiograph finding 1
  • Accidental exposure 1
  • Burning mouth sensation 1
  • Dizziness 1
  • Dysphagia 1
  • Foaming at the mouth 1
  • Light headedness 1
  • Nasal irritation 1
  • Nerve pain NOS 1
  • Paronychia 1

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