Drug profile

The FDA adverse-event record for Delmopinol 49 Mg Oral Chewable Tablet

29 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Delmopinol 49 Mg Oral Chewable Tablet. See the species affected, top reactions, and outcomes below.

29
adverse-event reports
0.0%
death-coded share
Dog
most-reported species
10
Diarrhoea - 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
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Delmopinol 49 Mg Oral Chewable Tablet

Administration Routes

OralUnknown

Species Affected

Dog 29

Most Affected Breeds

Retriever - Labrador 7
Retriever - Golden 4
Shepherd Dog - German 3
Boxer (German Boxer) 2
Beagle 2
Crossbred Canine/dog 2
Collie (unspecified) 1
Portuguese Water Dog 1
Irish Wolfhound 1
Alaskan Malamute 1

Most Reported Reactions

Diarrhoea 10
Vomiting 9
Loose stool 6
Abnormal stool colouration 5
Other abnormal test result NOS 5
Flatulence 2
Not eating 2
Stomach upset 2
Decreased appetite 2
HEMATOCRIT(HCT) HIGH, BLOOD 2
Hyperglycaemia 1
Inappropriate urination 1

Outcome Breakdown

Recovered/Normal
17 (58.6%)
Outcome Unknown
12 (41.4%)

Delmopinol 49 Mg Oral Chewable Tablet Adverse Event Insights

29 reports name Delmopinol 49 Mg Oral Chewable Tablet; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Delmopinol 49 Mg Oral Chewable Tablet. Administration routes: Oral, Unknown.

By species: Dog (29 reports). By breed: Retriever - Labrador (7), Retriever - Golden (4), Shepherd Dog - German (3).

Leading clinical signs: Diarrhoea (10), Vomiting (9), Loose stool (6), Abnormal stool colouration (5). Outcome, 29 coded reports: Recovered/Normal leads at 58.6%.

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.