Antisedan

20 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

3000.0%

Death Rate

Active Ingredients

Antisedan

Administration Routes

UnknownIntramuscular

Species Affected

Dog 17

Cat 3

Most Affected Breeds

Crossbred Canine/dog 2

Domestic Shorthair 2

Maltese 2

Retriever - Labrador 2

Retriever (unspecified) 1

Terrier - Bull - Staffordshire 1

Alaskan Malamute 1

Bulldog 1

Domestic Mediumhair 1

Greyhound 1

Most Reported Reactions

Vomiting 4

Diarrhoea 4

Lethargy (see also Central nervous system depression in 'Neurological') 4

Death 4

Wound 4

Weight loss 3

Pain NOS 3

Injection site swelling 3

Swollen limb 3

Elevated creatinine 2

Anorexia 2

Ataxia 2

Outcome Breakdown

Outcome Unknown

7 (35.0%)

Recovered/Normal

5 (25.0%)

Died

4 (20.0%)

Ongoing

2 (10.0%)

Euthanized

2 (10.0%)

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