Vit E/ Selenite Inj Solution
121 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.
121
Total Reports
45
Deaths Reported
3720.0%
Death Rate
Active Ingredients
Vit E/ Selenite Inj Solution
Administration Routes
SubcutaneousUnknownIntramuscularIntravenousParenteralOral
Species Affected
Cattle 65
Horse 27
Unknown 10
Goat 8
Human 4
Sheep 3
Alpaca 2
Other Deer 1
Dog 1
Most Affected Breeds
Holstein-Friesian also known as Holstein 24
Unknown 16
Cattle (other) 12
Aberdeen Angus 9
Quarter Horse 9
Thoroughbred 7
Red Angus 5
Crossbred Bovine/Cattle 4
Charolais 3
Sheep (unknown) 3
Most Reported Reactions
Death 39
Anaphylaxis 20
Lack of efficacy - NOS 14
Recumbency 8
Injection site swelling 8
Increased respiratory rate 6
Laboured breathing 6
Anaphylactic-type reaction 6
Death by euthanasia 6
Injection site abscess 5
Foaming at the mouth 5
Ataxia 5
Outcome Breakdown
Recovered/Normal
46 (34.8%)
Died
40 (30.3%)
Outcome Unknown
21 (15.9%)
Ongoing
18 (13.6%)
Euthanized
6 (4.5%)
Recovered with Sequela
1 (0.8%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.