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

ade_amlodipine_adverse_events

ade 200 tok en 2026-07-22

Amlodipine — 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. Amlodipine is a veterinary active ingredient.

Total reports

Amlodipine: 769

Reports by species (top entries)

  • Cat 378
  • Dog 354
  • Human 36

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 112
  • Diarrhoea 96
  • Death by euthanasia 82
  • Weight loss 80
  • Decreased appetite 69
  • Elevated blood urea nitrogen (BUN) 69
  • Lethargy (see also Central nervous system depression in 'Neurological') 69
  • Lethargy (see also Central nervous system depression in Neurological) 65
  • Anorexia 64
  • Lack of efficacy - NOS 62

"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