Selenium, Vitamin E

54 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

3700.0%

Death Rate

Active Ingredients

Selenium, Vitamin E

Administration Routes

SubcutaneousUnknownIntramuscularIntravenous

Species Affected

Cattle 29

Horse 10

Sheep 5

Goat 4

Human 4

Unknown 2

Most Affected Breeds

Holstein-Friesian also known as Holstein 13

Unknown 6

Crossbred Bovine/Cattle 5

Aberdeen Angus 5

Quarter Horse 4

Cattle (unknown) 3

Sheep (unknown) 3

Tennessee Walking Horse 2

Sheep (other) 2

Thoroughbred 2

Most Reported Reactions

Anaphylaxis 25

Death 20

Hypersalivation 8

Collapse (see also 'Cardio-vascular' and 'Systemic disorders') 5

Dyspnoea 5

Injection site swelling 5

Unclassifiable adverse event 5

Recumbency 4

Respiratory distress 4

Tachypnoea 4

Accidental exposure 4

Abortion 3

Outcome Breakdown

Died

20 (90.9%)

Recovered/Normal

2 (9.1%)

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