Firocoxib 57 Mg
61 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.
61
Total Reports
7
Deaths Reported
1150.0%
Death Rate
Active Ingredients
Firocoxib 57 Mg
Administration Routes
OralUnknown
Species Affected
Dog 35
Unknown 23
Human 2
Horse 1
Most Affected Breeds
Unknown 25
Dog (other) 4
Spitz - German Pomeranian 4
Chihuahua 3
Dog (unknown) 3
Dachshund (unspecified) 3
Poodle - Miniature 3
Schnauzer - Miniature 2
Beagle 2
Shepherd Dog - Australian 1
Most Reported Reactions
Uncoded sign 23
Tablets, Abnormal 12
Vomiting 10
Death 5
Elevated serum alkaline phosphatase (SAP) 4
Lethargy (see also Central nervous system depression in 'Neurological') 4
Underfilling, Bottles 3
Underfilling, Container 3
Ataxia 3
Diarrhoea 3
Containers, Damaged 2
Underfilling, Package 2
Outcome Breakdown
Outcome Unknown
23 (60.5%)
Died
7 (18.4%)
Recovered/Normal
6 (15.8%)
Ongoing
2 (5.3%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.