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

ade_budesonide_adverse_events

ade 200 tok en 2026-07-22

Budesonide — 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. Budesonide is a veterinary active ingredient.

Total reports

Budesonide: 201

Reports by species (top entries)

  • Cat 103
  • Dog 95
  • Human 2
  • Horse 1

Top reported reactions (VEDDRA terms, top entries)

  • Diarrhoea 44
  • Vomiting 41
  • Lack of efficacy - NOS 22
  • Not eating 21
  • Weight loss 21
  • Death by euthanasia 18
  • Decreased appetite 16
  • Lethargy (see also Central nervous system depression in 'Neurological') 15
  • Lethargy (see also Central nervous system depression in Neurological) 14
  • Polyuria 13

"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