Duralactin

14 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

1430.0%

Death Rate

Active Ingredients

Duralactin

Administration Routes

OralUnknown

Species Affected

Dog 8

Cat 6

Most Affected Breeds

Domestic Shorthair 5

Crossbred Canine/dog 3

Rottweiler 1

Terrier (unspecified) 1

Sphynx 1

Newfoundland 1

Shepherd Dog - Australian 1

Retriever - Labrador 1

Most Reported Reactions

Weakness 3

Lack of efficacy - NOS 3

Anorexia 2

Urinary tract infection 2

Death by euthanasia 2

Vomiting 2

Not eating 2

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

Ataxia 2

Hypoadrenocorticism 1

Elevated blood urea nitrogen (BUN) 1

Hypercalcaemia 1

Outcome Breakdown

Ongoing

6 (42.9%)

Outcome Unknown

3 (21.4%)

Recovered/Normal

3 (21.4%)

Euthanized

2 (14.3%)

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