Drug profile

The FDA adverse-event record for Vitamin-Mineral

48 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Vitamin-Mineral. See the species affected, top reactions, and outcomes below.

48
adverse-event reports
10.4%
death-coded share
Dog
most-reported species
7
Lethargy (see also Central nervous system depression in 'Neurological') - top reaction
Verify with FDA CVM →
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
48
Total Reports
5
Deaths Reported
10.4%
Death Rate

Active Ingredients

Vitamin-Mineral

Administration Routes

UnknownOralSubcutaneousIntravenous

Species Affected

Dog 36
Cat 9
Cattle 2
Human 1

Most Affected Breeds

Domestic Shorthair 7
Retriever - Golden 4
Shih Tzu 4
Retriever - Labrador 3
Dog (unknown) 3
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 2
Terrier - Yorkshire 2
Shepherd Dog - German 2
Spaniel - King Charles Cavalier 2
Domestic Longhair 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in 'Neurological') 7
Vomiting 6
Behavioural disorder NOS 6
Diarrhoea 5
Decreased appetite 5
Anorexia 4
Loose stool 4
Lack of efficacy - NOS 4
Anaemia NOS 3
Not eating 3
Death by euthanasia 3
Ataxia 3

Outcome Breakdown

Outcome Unknown
24 (50.0%)
Ongoing
16 (33.3%)
Euthanized
3 (6.3%)
Recovered/Normal
3 (6.3%)
Died
2 (4.2%)

Vitamin-Mineral Adverse Event Insights

48 reports name Vitamin-Mineral; 5 recorded a death outcome (10.4% of reported events, not a population-level mortality rate). Active ingredient: Vitamin-Mineral. Administration routes: Unknown, Oral, Subcutaneous, Intravenous.

By species: Dog (36 reports), Cat (9 reports), Cattle (2 reports). By breed: Domestic Shorthair (7), Retriever - Golden (4), Shih Tzu (4).

Leading clinical signs: Lethargy (see also Central nervous system depression in 'Neurological') (7), Vomiting (6), Behavioural disorder NOS (6), Diarrhoea (5). Outcome, 48 coded reports: Outcome Unknown leads at 50.0%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.