Drug profile

The FDA adverse-event record for Loperamide

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

31
adverse-event reports
9.7%
death-coded share
Dog
most-reported species
16
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.
31
Total Reports
3
Deaths Reported
9.7%
Death Rate

Active Ingredients

Loperamide

Administration Routes

OralUnknownOther

Species Affected

Dog 26
Cat 5

Most Affected Breeds

Retriever - Labrador 6
Doberman Pinscher 3
Brittany 2
Shepherd Dog - German 2
Spaniel - King Charles 1
Pug 1
Bengal 1
Collie - Border 1
Pit Bull 1
Siamese 1

Most Reported Reactions

Diarrhoea 16
Vomiting 10
Lethargy (see also Central nervous system depression in 'Neurological') 7
Weight loss 6
Emesis 5
Anorexia 5
Not eating 4
Lack of efficacy - NOS 3
Other abnormal test result NOS 3
Decreased appetite 3
Hypothermia 2
Urinary tract infection 2

Outcome Breakdown

Outcome Unknown
13 (41.9%)
Recovered/Normal
11 (35.5%)
Ongoing
4 (12.9%)
Euthanized
2 (6.5%)
Died
1 (3.2%)

Loperamide Adverse Event Insights

31 reports name Loperamide; 3 recorded a death outcome (9.7% of reported events, not a population-level mortality rate). Active ingredient: Loperamide. Administration routes: Oral, Unknown, Other.

By species: Dog (26 reports), Cat (5 reports). By breed: Retriever - Labrador (6), Doberman Pinscher (3), Brittany (2).

Leading clinical signs: Diarrhoea (16), Vomiting (10), Lethargy (see also Central nervous system depression in 'Neurological') (7), Weight loss (6). Outcome, 31 coded reports: Outcome Unknown leads at 41.9%.

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.