Drug profile

The FDA adverse-event record for Vitamin

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

22
adverse-event reports
0.0%
death-coded share
Dog
most-reported species
5
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.
22
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Vitamin

Administration Routes

OralUnknown

Species Affected

Dog 19
Cat 3

Most Affected Breeds

Spitz - German Pomeranian 3
Shih Tzu 3
Terrier - Yorkshire 2
Shepherd Dog - German 2
Crossbred Canine/dog 2
Domestic Shorthair 1
Bulldog 1
Hound - Basset 1
Spaniel - Cocker American 1
Domestic Mediumhair 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in 'Neurological') 5
Behavioural disorder NOS 5
Overdose 4
Panting 3
Vomiting 3
Hyperactivity 3
Vocalisation 3
Anxiety 3
Excessive thirst 3
Polyphagia 3
Blindness 2
Abnormal radiograph finding 2

Outcome Breakdown

Ongoing
10 (45.5%)
Recovered/Normal
6 (27.3%)
Outcome Unknown
5 (22.7%)
Recovered with Sequela
1 (4.5%)

Vitamin Adverse Event Insights

22 reports name Vitamin; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Vitamin. Administration routes: Oral, Unknown.

By species: Dog (19 reports), Cat (3 reports). By breed: Spitz - German Pomeranian (3), Shih Tzu (3), Terrier - Yorkshire (2).

Leading clinical signs: Lethargy (see also Central nervous system depression in 'Neurological') (5), Behavioural disorder NOS (5), Overdose (4), Panting (3). Outcome, 22 coded reports: Ongoing leads at 45.5%.

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.