Drug profile

The FDA adverse-event record for Budesonide

199 FDA reports name Budesonide, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#532 of 2,679
by report volume (all drugs)
199
adverse-event reports
10.1%
death-coded share
Cat
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Budesonide ranks #532 of 2679 by total reports (199) and #545 of 1130 by death-coded share (10.1%). National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#532
This drug, reports of 2679
#545
This drug, death share of 1130

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Budesonide has 199 reports now versus 190 in that prior snapshot: 9 more (4.7%).

Report change
+9
Death-coded reports
+0
Death-coded share
−0.5 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Budesonide changes

Signature read: 199 reports place Budesonide in the upper third of FDA AER volume (#532 of 2,679).

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
199
Total Reports
20
Deaths Reported
10.1%
Death-coded share of reports

Active Ingredients

Budesonide

Administration Routes

UnknownOralRespiratory (Inhalation)

Species Affected

Cat 103
Dog 94
Horse 1
Human 1

Most Affected Breeds

Domestic Shorthair 63
Retriever - Labrador 14
Shih Tzu 8
Domestic Mediumhair 7
Cat (unknown) 6
Siamese 6
Dog (unknown) 5
Crossbred Canine/dog 4
Domestic Longhair 4
Cat (other) 4

Most Reported Reactions

Diarrhoea 44
Vomiting 40
Lack of efficacy - NOS 22
Weight loss 21
Not eating 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
Elevated blood urea nitrogen (BUN) 13
Polyuria 13
Behavioural disorder NOS 12

Outcome Breakdown

Ongoing
88 (44.2%)
Outcome Unknown
57 (28.6%)
Recovered/Normal
33 (16.6%)
Euthanized
19 (9.5%)
Recovered with Sequela
1 (0.5%)
Died
1 (0.5%)

Budesonide: high report volume in the FDA AER row

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Budesonide, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Budesonide (#532 of 2,679 by report volume); death-coded 10.1%. PlainBreed drug row · report volume stamp 199 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →