Supplement
141 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.
141
Total Reports
18
Deaths Reported
1280.0%
Death Rate
Active Ingredients
Supplement
Administration Routes
UnknownOral
Species Affected
Dog 112
Cat 20
Human 7
Cattle 2
Most Affected Breeds
Retriever - Labrador 12
Domestic Shorthair 11
Spitz - German Pomeranian 9
Spaniel - King Charles Cavalier 7
Retriever - Golden 7
Unknown 7
Pit Bull 7
Pug 6
Shepherd Dog - German 5
Collie - Border 5
Most Reported Reactions
Vomiting 22
Behavioural disorder NOS 20
Death by euthanasia 16
Diarrhoea 16
Lethargy (see also Central nervous system depression in Neurological) 13
Other abnormal test result NOS 11
Vocalisation 11
Lethargy (see also Central nervous system depression in 'Neurological') 10
Anorexia 10
Weight loss 10
Polydipsia 10
Seizure NOS 10
Outcome Breakdown
Outcome Unknown
51 (35.9%)
Ongoing
37 (26.1%)
Recovered/Normal
35 (24.6%)
Euthanized
16 (11.3%)
Died
3 (2.1%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.