Kenalog

19 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.

Total Reports

Deaths Reported

530.0%

Death Rate

Active Ingredients

Kenalog

Administration Routes

UnknownIntra-ArticularParenteralIntramuscular

Species Affected

Dog 10

Horse 5

Cat 4

Most Affected Breeds

Quarter Horse 4

Domestic Shorthair 3

Crossbred Canine/dog 2

Retriever - Golden 2

Warmblood - Dutch 1

Great Pyrenees 1

Spitz - American Eskimo Dog 1

Dog (unknown) 1

Chihuahua 1

Maine Coon 1

Most Reported Reactions

Emesis (multiple) 4

Weight loss 3

Aural haematoma 3

Lethargy (see also Central nervous system depression in 'Neurological') 2

Pale mucous membrane 2

Fever 2

Elevated creatinine 2

Injection site swelling 2

Vomiting 2

Diarrhoea 2

Ataxia 2

Lethargy (see also Central nervous system depression in Neurological) 2

Outcome Breakdown

Ongoing

10 (52.6%)

Recovered/Normal

4 (21.1%)

Outcome Unknown

4 (21.1%)

Died

1 (5.3%)

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