Ketoprofen

120 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.

120

Total Reports

Deaths Reported

2750.0%

Death Rate

Active Ingredients

Ketoprofen

Administration Routes

UnknownSubcutaneousParenteralIntravenousIntramuscularOralOther

Species Affected

Dog 74

Cat 30

Unknown 6

Mouse 2

Human 2

Horse 2

Goat 1

Other Birds 1

Rabbit 1

Cattle 1

Most Affected Breeds

Domestic Shorthair 24

Retriever - Labrador 22

Unknown 10

Retriever - Golden 5

Crossbred Canine/dog 4

Shepherd Dog - German 4

Shepherd Dog - Australian 3

Poodle - Standard 3

Domestic (unspecified) 2

Chihuahua 2

Most Reported Reactions

Vomiting 32

Death 22

Lethargy (see also Central nervous system depression in 'Neurological') 22

Elevated blood urea nitrogen (BUN) 19

Anorexia 18

Leucocytosis NOS 18

Fever 17

Elevated creatinine 15

Hyperglycaemia 15

Polydipsia 14

Other abnormal test result NOS 14

Dehydration 13

Outcome Breakdown

Ongoing

30 (28.3%)

Recovered/Normal

29 (27.4%)

Died

25 (23.6%)

Outcome Unknown

13 (12.3%)

Euthanized

8 (7.5%)

Recovered with Sequela

1 (0.9%)

Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.