Unspecified
336 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.
336
Total Reports
31
Deaths Reported
920.0%
Death Rate
Active Ingredients
Unspecified
Administration Routes
UnknownOralTopicalNasalIntravenousParenteralSubcutaneousAuricular (Otic)IntramuscularIntra-Articular
Species Affected
Dog 265
Cat 56
Cattle 8
Unknown 4
Chicken 1
Pig 1
Horse 1
Most Affected Breeds
Retriever - Labrador 41
Domestic Shorthair 38
Crossbred Canine/dog 34
Beagle 17
Chihuahua 13
Terrier - Bull - American Pit 12
Dachshund (unspecified) 12
Shih Tzu 11
Dog (unknown) 9
Shepherd Dog - German 9
Most Reported Reactions
Vomiting 56
Not eating 33
Lethargy (see also Central nervous system depression in 'Neurological') 32
Quiet 29
Behavioural disorder NOS 28
Lack of efficacy - NOS 26
Vocalisation 25
Polydipsia 23
Diarrhoea 23
Panting 22
Bruising 22
Elevated serum alkaline phosphatase (ALP) 22
Outcome Breakdown
Outcome Unknown
130 (38.6%)
Ongoing
105 (31.2%)
Recovered/Normal
65 (19.3%)
Died
22 (6.5%)
Euthanized
9 (2.7%)
Recovered with Sequela
6 (1.8%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.