Vit E/ Selenite Inj Solution
121 adverse event reports submitted to the FDA
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Data Summary
| Metric | Value |
|---|---|
| Total adverse event reports | 121 |
| Reports involving death | 45 |
| Case-fatality rate (reported events) | 3720.0% |
| Distinct species in reports | 9 |
| Distinct breeds in reports | 20 |
| Distinct reactions reported | 20 |
| Active ingredients on file | 1 |
Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.
Vit E/ Selenite Inj Solution Adverse Event Insights
The FDA Center for Veterinary Medicine database currently holds 121 adverse event reports referencing Vit E/ Selenite Inj Solution, including 45 reports in which the animal died — a 3720.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Vit E/ Selenite Inj Solution. Reported administration routes include Subcutaneous, Unknown, Intramuscular, Intravenous. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.
The species most frequently named in Vit E/ Selenite Inj Solution reports are Cattle (65 reports), Horse (27 reports), Unknown (10 reports), with Cattle accounting for the largest share. Within those species, Holstein-Friesian also known as Holstein (24), Unknown (16), Cattle (other) (12) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.
The most commonly reported clinical signs associated with Vit E/ Selenite Inj Solution are Death (39), Anaphylaxis (20), Lack of efficacy - NOS (14), Recumbency (8). Of the 132 reports with a coded outcome, Recovered/Normal is the leading category at 34.8%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Vit E/ Selenite Inj Solution.
Source: FDA Center for Veterinary Medicine — Adverse Event Reports FDA Center for Veterinary Medicine — Adverse Event Reports Data reflects voluntary submissions and may not represent actual incidence rates
Read our methodology — how this data is sourced, computed, and verified.