Drug profile

The FDA adverse-event record for Delmopinol 35 Mg Oral Chewable Tablet

34 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Delmopinol 35 Mg Oral Chewable Tablet. See the species affected, top reactions, and outcomes below.

34
adverse-event reports
2.9%
death-coded share
Dog
most-reported species
12
Vomiting - 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.
34
Total Reports
1
Deaths Reported
2.9%
Death Rate

Active Ingredients

Delmopinol 35 Mg Oral Chewable Tablet

Administration Routes

OralUnknown

Species Affected

Dog 34

Most Affected Breeds

Beagle 3
Pointing Dog - Hungarian Short-haired (Vizsla) 2
Bulldog 2
Terrier - Scottish 2
Collie - Border 2
Terrier (unspecified) 2
Sheepdog - Shetland 2
Crossbred Canine/dog 2
Terrier - Bull - Staffordshire 1
Portuguese Water Dog 1

Most Reported Reactions

Vomiting 12
Loose stool 6
Diarrhoea 6
Abnormal stool colouration 5
Tracheal obstruction 3
Flatulence 2
Unusual stool colour 2
Weight gain 2
Emesis 2
Reluctant to move 2
Tooth disorder 1
Cough 1

Outcome Breakdown

Recovered/Normal
16 (47.1%)
Outcome Unknown
15 (44.1%)
Ongoing
2 (5.9%)
Euthanized
1 (2.9%)

Delmopinol 35 Mg Oral Chewable Tablet Adverse Event Insights

34 reports name Delmopinol 35 Mg Oral Chewable Tablet; 1 recorded a death outcome (2.9% of reported events, not a population-level mortality rate). Active ingredient: Delmopinol 35 Mg Oral Chewable Tablet. Administration routes: Oral, Unknown.

By species: Dog (34 reports). By breed: Beagle (3), Pointing Dog - Hungarian Short-haired (Vizsla) (2), Bulldog (2).

Leading clinical signs: Vomiting (12), Loose stool (6), Diarrhoea (6), Abnormal stool colouration (5). Outcome, 34 coded reports: Recovered/Normal leads at 47.1%.

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.