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FDA ADE reports for Mometasone Furoate

ade_mometasone_furoate_adverse_events

ade en 2026-07-22

Mometasone Furoate 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. Mometasone Furoate is a active ingredient.

Total reports

Mometasone Furoate: 3894

Reports by species (top entries)

  • Dog 2580
  • Cat 529
  • Human 96
  • Rabbit 1

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 613
  • Ataxia 528
  • Head tilt - ear disorder 395
  • Vomiting 352
  • Nystagmus 303
  • Head shake - ear disorder 251
  • Corneal ulcer 248
  • Vestibular disorder NOS 247
  • Behavioural disorder NOS 238
  • Ear discharge 224

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b9.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).