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FDA ADE reports for Famotidine — total reports, species & reaction breakdown

ade_famotidine_adverse_events

ade 200 tok en 2026-07-22

Famotidine — 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. Famotidine is a veterinary active ingredient.

Total reports

Famotidine: 2995

Reports by species (top entries)

  • Dog 2577
  • Cat 402
  • Human 9
  • Goat 2
  • Parrot 2
  • Ferret 1

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 874
  • Lethargy (see also Central nervous system depression in 'Neurological') 656
  • Diarrhoea 520
  • Anorexia 487
  • Death by euthanasia 425
  • Other abnormal test result NOS 395
  • Elevated alanine aminotransferase (ALT) 347
  • Weight loss 284
  • Death 281
  • Decreased appetite 278

"Lack of efficacy" terms denote product-performance reports, not adverse reactions.

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b6.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

  • openFDA animalandveterinary/event.json (FDA CVM adverse event reports), pulled 2026-07-22