Flunixin
66 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.
66
Total Reports
15
Deaths Reported
2270.0%
Death Rate
Active Ingredients
Flunixin
Administration Routes
UnknownIntravenousIntramuscularOralParenteral
Species Affected
Horse 40
Cattle 11
Unknown 9
Dog 3
Sheep 1
Donkey 1
Pig 1
Most Affected Breeds
Quarter Horse 17
Unknown 10
Warmblood (unspecified) 4
Thoroughbred 4
Horse (unknown) 3
Holsteiner 3
Holstein-Friesian also known as Holstein 3
Simmental 3
Shepherd Dog - Australian 2
Hanovarian 2
Most Reported Reactions
Colic 12
Polyuria 11
Polydipsia 11
Other abnormal test result NOS 8
Elevated creatinine 7
Elevated blood urea nitrogen (BUN) 7
Contamination, Particulate Matter 6
Lethargy (see also Central nervous system depression in 'Neurological') 5
Depression 5
Lameness 4
Diarrhoea 4
Death 4
Outcome Breakdown
Recovered/Normal
29 (44.6%)
Died
12 (18.5%)
Ongoing
10 (15.4%)
Outcome Unknown
10 (15.4%)
Euthanized
4 (6.2%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.