Sam-E
51 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 | 51 |
| Reports involving death | 4 |
| Case-fatality rate (reported events) | 780.0% |
| Distinct species in reports | 2 |
| 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.
Sam-E Adverse Event Insights
The FDA Center for Veterinary Medicine database currently holds 51 adverse event reports referencing Sam-E, including 4 reports in which the animal died — a 780.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Sam-E. Reported administration routes include Oral, Unknown. 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 Sam-E reports are Dog (49 reports), Cat (2 reports), with Dog accounting for the largest share. Within those species, Retriever - Labrador (6), Crossbred Canine/dog (6), Chihuahua (3) 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 Sam-E are Decreased appetite (10), Lethargy (see also Central nervous system depression in 'Neurological') (10), Elevated alanine aminotransferase (ALT) (10), Elevated serum alkaline phosphatase (SAP) (9). Of the 51 reports with a coded outcome, Outcome Unknown is the leading category at 58.8%. 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 Sam-E.
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.