Vetalog

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

1820.0%

Death Rate

Active Ingredients

Vetalog

Administration Routes

UnknownSubcutaneousIntramuscular

Species Affected

Dog 6

Cat 5

Most Affected Breeds

Retriever - Labrador 3

Siamese 1

American Wirehair 1

Domestic Longhair 1

Terrier - Bull 1

Cat (unknown) 1

Terrier - Bull - Staffordshire 1

Domestic Shorthair 1

Terrier (unspecified) 1

Most Reported Reactions

Weight loss 3

Agitation 2

Ataxia 2

Other abnormal test result NOS 2

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

Anorexia 2

Death 2

Muscle tremor 1

Abdominal pain 1

Diarrhoea 1

Appetite loss 1

Elevated total bilirubin 1

Outcome Breakdown

Ongoing

4 (36.4%)

Recovered/Normal

3 (27.3%)

Died

2 (18.2%)

Outcome Unknown

1 (9.1%)

Recovered with Sequela

1 (9.1%)

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