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FDA ADE reports for Aminopentamide

ade_aminopentamide_adverse_events

ade en 2026-07-22

Aminopentamide — 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. Aminopentamide is a active ingredient.

Total reports

Aminopentamide: 120

Reports by species (top entries)

  • Dog 74
  • Cat 23

Top reported reactions (VEDDRA terms, top entries)

  • Death 20
  • Elevated alanine aminotransferase (ALT) 16
  • INEFFECTIVE, ANTIEMETIC 13
  • Anorexia 11
  • Mydriasis 11
  • Elevated blood urea nitrogen (BUN) 10
  • Elevated serum alkaline phosphatase (SAP) 10
  • Vomiting 10
  • Hypoalbuminaemia 9
  • Anaemia NOS 8

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b20.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Aminopentamide (active ingredient) — total reports, species & reaction breakdown
Source document: FDA FAERS / openFDA Animal & Veterinary Event Reports
US FDA Center for Veterinary Medicine (openFDA animal & veterinary event database)retrieved 2026-07-22

Verification file: pdf-raw/ade/ade_active_ingredients_2026-07-22_b20.json

Link points to the issuing authority's site; a direct document link is still being verified.

Machine access

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Raw JSON ↗ llm.txt OpenAPI