Diltiazem

43 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

2090.0%

Death Rate

Active Ingredients

Diltiazem

Administration Routes

UnknownOral

Species Affected

Dog 29

Human 8

Cat 6

Most Affected Breeds

Unknown 9

Domestic Shorthair 4

Retriever - Labrador 4

Saint Bernard Dog 4

Shepherd Dog - Australian 2

Retriever - Golden 2

Rex - Devon 2

Corgi (unspecified) 2

Shepherd Dog - German 1

Bulldog 1

Most Reported Reactions

Death 6

Vomiting 5

Diarrhoea 4

Abnormal ultrasound finding 4

Decreased appetite 4

Urinary incontinence 4

Accidental exposure 4

Tachycardia 4

Musculoskeletal disorder NOS 3

Death by euthanasia 3

Anaemia NOS 3

Underdose 3

Outcome Breakdown

Ongoing

14 (32.6%)

Recovered/Normal

11 (25.6%)

Outcome Unknown

8 (18.6%)

Died

6 (14.0%)

Euthanized

3 (7.0%)

Recovered with Sequela

1 (2.3%)

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