← All Topics / ade

FDA ADE reports for Azathioprine

ade_azathioprine_adverse_events

ade en 2026-07-22

Azathioprine — 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. Azathioprine is a active ingredient.

Total reports

Azathioprine: 106

Reports by species (top entries)

  • Dog 106

Top reported reactions (VEDDRA terms, top entries)

  • Lethargy (see also Central nervous system depression in 'Neurological') 26
  • Death by euthanasia 21
  • Elevated serum alkaline phosphatase (SAP) 21
  • Anaemia NOS 20
  • Immune mediated haemolytic anaemia 20
  • Vomiting 19
  • Diarrhoea 18
  • Other abnormal test result NOS 18
  • Elevated alanine aminotransferase (ALT) 17
  • Leucocytosis NOS 16

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 Azathioprine (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

AI agents: this page mirrors GET /api/v1/llm_context?topic=ade_azathioprine_adverse_events (max 500 tokens, whitelisted). Rate limit 60 req/min for recognized AI crawlers.

Raw JSON ↗ llm.txt OpenAPI