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FDA ADE reports for Ciclesonide

ade_ciclesonide_adverse_events

ade en 2026-07-22

Ciclesonide — 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. Ciclesonide is a active ingredient.

Total reports

Ciclesonide: 301

Reports by species (top entries)

  • Horse 94
  • Human 3

Top reported reactions (VEDDRA terms, top entries)

  • Dispenser, Abnormal 88
  • Difficulty of Use 76
  • Lack of efficacy - NOS 42
  • Inhaler, malfunction 28
  • Product defect, product difficult to use/handle (see also 'Drug device difficult to use/handle') 26
  • Behavioural disorder NOS 20
  • Product problem 20
  • Circumstance or info capable of leading to medication error 12
  • Underfilling, Container 12
  • Administration device NOS, priming issue 7

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b16.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Ciclesonide (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_b16.json

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