Drug profile

The FDA adverse-event record for Vitamin And Mineral Supplement

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

29
adverse-event reports
27.6%
death-coded share
Dog
most-reported species
7
Lethargy (see also Central nervous system depression in 'Neurological') - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
29
Total Reports
8
Deaths Reported
27.6%
Death Rate

Active Ingredients

Vitamin And Mineral Supplement

Administration Routes

OralUnknownParenteral

Species Affected

Dog 17
Cattle 6
Cat 3
Human 2
Horse 1

Most Affected Breeds

Retriever - Labrador 3
Shih Tzu 2
Domestic Shorthair 2
Rottweiler 2
Siberian Husky 2
Unknown 2
Cattle (unknown) 2
Holstein-Friesian also known as Holstein 2
Lhasa Apso 1
Terrier - West Highland White 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in 'Neurological') 7
Death 5
Vomiting 4
Ataxia 4
Anorexia 4
Weight loss 4
Diarrhoea 4
Pain NOS 4
Lethargy (see also Central nervous system depression in Neurological) 4
Unable to stand 3
Emesis 3
Death by euthanasia 3

Outcome Breakdown

Outcome Unknown
9 (30.0%)
Recovered/Normal
8 (26.7%)
Died
5 (16.7%)
Ongoing
5 (16.7%)
Euthanized
3 (10.0%)

Vitamin And Mineral Supplement Adverse Event Insights

29 reports name Vitamin And Mineral Supplement; 8 recorded a death outcome (27.6% of reported events, not a population-level mortality rate). Active ingredient: Vitamin And Mineral Supplement. Administration routes: Oral, Unknown, Parenteral.

By species: Dog (17 reports), Cattle (6 reports), Cat (3 reports). By breed: Retriever - Labrador (3), Shih Tzu (2), Domestic Shorthair (2).

Leading clinical signs: Lethargy (see also Central nervous system depression in 'Neurological') (7), Death (5), Vomiting (4), Ataxia (4). Outcome, 30 coded reports: Outcome Unknown leads at 30.0%.

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.