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

ade_diltiazem_adverse_events

ade 200 tok en 2026-07-22

Diltiazem — 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. Diltiazem is a veterinary active ingredient.

Total reports

Diltiazem: 51

Reports by species (top entries)

  • Dog 33
  • Cat 10
  • Human 8

Top reported reactions (VEDDRA terms, top entries)

  • Death 8
  • Death by euthanasia 6
  • Lack of efficacy - NOS 6
  • Vomiting 6
  • Anorexia 5
  • Abnormal ultrasound finding 4
  • Accidental exposure 4
  • Decreased appetite 4
  • Diarrhoea 4
  • Lethargy (see also Central nervous system depression in Neurological) 4

"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