Not Provided
16 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.
16
Total Reports
2
Deaths Reported
1250.0%
Death Rate
Active Ingredients
Not Provided
Administration Routes
UnknownOralTopicalIntravenous
Species Affected
Dog 14
Cat 2
Most Affected Breeds
Retriever - Labrador 5
Poodle - Toy 2
Terrier - Yorkshire 2
Domestic (unspecified) 2
Shih Tzu 1
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1
Spitz - German Pomeranian 1
Terrier - Jack Russell 1
Pekingese 1
Most Reported Reactions
Other abnormal test result NOS 6
Elevated serum alkaline phosphatase (SAP) 4
Elevated alanine aminotransferase (ALT) 3
Proteinuria 3
Skin inflammation NOS 3
Palpable mass NOS 3
Skin lesion NOS 3
Surgical site disorder 3
Pyoderma 2
Death 2
Lack of efficacy (ectoparasite) - flea 2
Thrombocytosis 1
Outcome Breakdown
Outcome Unknown
8 (50.0%)
Recovered/Normal
3 (18.8%)
Ongoing
3 (18.8%)
Died
2 (12.5%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.