Drug profile

The FDA adverse-event record for Anti-Nausea Medication (Unknown)

28 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Anti-Nausea Medication (Unknown). See the species affected, top reactions, and outcomes below.

28
adverse-event reports
21.4%
death-coded share
Dog
most-reported species
13
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.
28
Total Reports
6
Deaths Reported
21.4%
Death Rate

Active Ingredients

Anti-Nausea Medication (Unknown)

Administration Routes

UnknownParenteralOral

Species Affected

Dog 17
Cat 11

Most Affected Breeds

Domestic Shorthair 4
Shepherd Dog - German 4
Cat (unknown) 2
Retriever - Golden 2
Doberman Pinscher 2
Dalmatian 1
Terrier - Yorkshire 1
Stephen's Stock Cur 1
Pinscher - Miniature 1
Siberian Husky 1

Most Reported Reactions

Vomiting 13
Diarrhoea 9
Lethargy (see also Central nervous system depression in Neurological) 9
Not eating 7
Weight loss 6
Dehydration 4
Bloody diarrhoea 4
Anorexia 4
Death 4
Lack of efficacy - NOS 3
Nausea 3
Behavioural disorder NOS 3

Outcome Breakdown

Ongoing
9 (32.1%)
Outcome Unknown
9 (32.1%)
Recovered/Normal
4 (14.3%)
Died
4 (14.3%)
Euthanized
2 (7.1%)

Anti-Nausea Medication (Unknown) Adverse Event Insights

28 reports name Anti-Nausea Medication (Unknown); 6 recorded a death outcome (21.4% of reported events, not a population-level mortality rate). Active ingredient: Anti-Nausea Medication (Unknown). Administration routes: Unknown, Parenteral, Oral.

By species: Dog (17 reports), Cat (11 reports). By breed: Domestic Shorthair (4), Shepherd Dog - German (4), Cat (unknown) (2).

Leading clinical signs: Vomiting (13), Diarrhoea (9), Lethargy (see also Central nervous system depression in Neurological) (9), Not eating (7). Outcome, 28 coded reports: Ongoing leads at 32.1%.

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.