Polyflex

11 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

910.0%

Death Rate

Active Ingredients

Polyflex

Administration Routes

UnknownSubcutaneousIntramuscular

Species Affected

Dog 6

Cattle 4

Cat 1

Most Affected Breeds

Retriever - Labrador 2

Holstein-Friesian also known as Holstein 2

Cattle (other) 2

Terrier (unspecified) 2

Terrier - Boston 1

Ragdoll 1

Pug 1

Most Reported Reactions

Residues in meat/offal 4

Fever 3

Diarrhoea 2

Leucocytosis NOS 2

Neutropenia 2

Abnormal radiograph finding 2

Monocytosis 2

Regurgitation 2

Lethargy (see also Central nervous system depression in 'Neurological') 1

Decreased appetite 1

Weight loss 1

Depression 1

Outcome Breakdown

Ongoing

5 (45.5%)

Outcome Unknown

4 (36.4%)

Euthanized

1 (9.1%)

Recovered/Normal

1 (9.1%)

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