Device: Collection, Blood

13 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

770.0%

Death Rate

Active Ingredients

Device: Collection, Blood

Administration Routes

Unknown

Species Affected

Unknown 11

Primate 1

Dog 1

Most Affected Breeds

Unknown 12

Primate (unknown) 1

Most Reported Reactions

Device Defective NOS 13

Death 1

Disseminated intravascular coagulation 1

Acute renal failure 1

Complications of device insertion 1

Contamination NOS 1

Expired drug administered 1

Outcome Breakdown

Died

1 (50.0%)

Ongoing

1 (50.0%)

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