Budesonide
174 adverse event reports submitted to the FDA
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
174
Total Reports
19
Deaths Reported
1090.0%
Death Rate
Active Ingredients
Budesonide
Administration Routes
UnknownOralRespiratory (Inhalation)
Species Affected
Cat 88
Dog 84
Horse 1
Human 1
Most Affected Breeds
Domestic Shorthair 53
Retriever - Labrador 13
Shih Tzu 7
Cat (unknown) 6
Domestic Mediumhair 6
Siamese 5
Dog (unknown) 4
Domestic Longhair 4
Persian 4
Crossbred Canine/dog 3
Most Reported Reactions
Diarrhoea 38
Vomiting 33
Not eating 20
Lack of efficacy - NOS 19
Weight loss 18
Death by euthanasia 17
Lethargy (see also Central nervous system depression in 'Neurological') 15
Lethargy (see also Central nervous system depression in Neurological) 14
Decreased appetite 13
Behavioural disorder NOS 12
Elevated blood urea nitrogen (BUN) 12
Polyuria 12
Outcome Breakdown
Ongoing
73 (42.0%)
Outcome Unknown
53 (30.5%)
Recovered/Normal
28 (16.1%)
Euthanized
18 (10.3%)
Recovered with Sequela
1 (0.6%)
Died
1 (0.6%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.