Percorten

12 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

2500.0%

Death Rate

Active Ingredients

Percorten

Administration Routes

UnknownSubcutaneousIntramuscularOral

Species Affected

Dog 12

Most Affected Breeds

Poodle - Standard 3

Retriever - Golden 2

Retriever - Labrador 2

Beagle 1

Terrier - Yorkshire 1

Crossbred Canine/dog 1

Chihuahua 1

Mixed (Dog) 1

Most Reported Reactions

Other abnormal test result NOS 3

Death by euthanasia 3

Shaking 2

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

Fever 2

Panting 2

Polyuria 2

Azotaemia 2

Anorexia 2

Dehydration 2

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

Weakness 2

Outcome Breakdown

Recovered/Normal

4 (33.3%)

Outcome Unknown

3 (25.0%)

Euthanized

3 (25.0%)

Recovered with Sequela

1 (8.3%)

Ongoing

1 (8.3%)

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