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

ade_spironolactone_adverse_events

ade 200 tok en 2026-07-22

Spironolactone — 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. Spironolactone is a veterinary active ingredient.

Total reports

Spironolactone: 297

Reports by species (top entries)

  • Dog 248
  • Cat 22
  • Human 4

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 64
  • Diarrhoea 37
  • Elevated blood urea nitrogen (BUN) 34
  • Death by euthanasia 33
  • Lethargy (see also Central nervous system depression in 'Neurological') 33
  • Anorexia 27
  • Lack of efficacy - NOS 27
  • Death 25
  • Elevated creatinine 24
  • Decreased appetite 21

"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