Drug profile

The FDA adverse-event record for Dental Supplement

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

16
adverse-event reports
0.0%
death-coded share
Dog
most-reported species
3
Vomiting - 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.
16
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Dental Supplement

Administration Routes

UnknownOral

Species Affected

Dog 13
Cat 3

Most Affected Breeds

Retriever - Labrador 2
Domestic Shorthair 2
Samoyed 2
Terrier - Cairn 1
Chihuahua 1
Rex - Cornish 1
Retriever - Golden 1
Spaniel - Springer English 1
Sheepdog - Shetland 1
Shepherd (unspecified) 1

Most Reported Reactions

Vomiting 3
Elevated alanine aminotransferase (ALT) 3
Other abnormal test result NOS 2
Elevated aspartate aminotransferase (AST) 2
Not eating 2
Abnormal ultrasound finding 2
Decreased appetite 2
Dysphoria 2
Emesis 1
Lack of efficacy - NOS 1
Haemorrhagic gastroenteritis 1
INEFFECTIVE, HEARTWORM LARVAE 1

Outcome Breakdown

Recovered/Normal
8 (50.0%)
Ongoing
5 (31.3%)
Outcome Unknown
3 (18.8%)

Dental Supplement Adverse Event Insights

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

By species: Dog (13 reports), Cat (3 reports). By breed: Retriever - Labrador (2), Domestic Shorthair (2), Samoyed (2).

Leading clinical signs: Vomiting (3), Elevated alanine aminotransferase (ALT) (3), Other abnormal test result NOS (2), Elevated aspartate aminotransferase (AST) (2). Outcome, 16 coded reports: Recovered/Normal 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.