Asit
58 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.
58
Total Reports
1
Deaths Reported
170.0%
Death Rate
Active Ingredients
Asit
Administration Routes
UnknownSubcutaneousSublingualParenteral
Species Affected
Dog 53
Cat 5
Most Affected Breeds
Retriever - Labrador 6
Crossbred Canine/dog 5
Domestic Shorthair 3
Shepherd Dog - German 3
Terrier - West Highland White 2
Retriever - Golden 2
Terrier - Jack Russell 2
Terrier - Boston 2
Terrier - Bull 2
Bulldog - French 2
Most Reported Reactions
Emesis 11
Diarrhoea 10
Lethargy (see also Central nervous system depression in 'Neurological') 10
Anxiety 5
Other abnormal test result NOS 5
INEFFECTIVE, ATOPY CONTROL 5
Decreased appetite 4
Panting 4
Emesis (multiple) 4
Erythema (for urticaria see Immune SOC) 4
Gingival hyperplasia 4
Hair shedding 4
Outcome Breakdown
Ongoing
23 (39.7%)
Recovered/Normal
23 (39.7%)
Outcome Unknown
11 (19.0%)
Euthanized
1 (1.7%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.