Drug profile

The FDA adverse-event record for Emodepside And Praziquantel

36 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Emodepside And Praziquantel. See the species affected, top reactions, and outcomes below.

36
adverse-event reports
2.8%
death-coded share
Cat
most-reported species
15
Emesis - 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.
36
Total Reports
1
Deaths Reported
2.8%
Death Rate

Active Ingredients

Emodepside And Praziquantel

Administration Routes

TopicalUnknownOralParenteralSubcutaneous

Species Affected

Cat 34
Dog 2

Most Affected Breeds

Domestic Shorthair 23
Domestic Mediumhair 6
Domestic Longhair 3
Siamese 1
Persian 1
Shepherd Dog - German 1
Retriever - Labrador 1

Most Reported Reactions

Emesis 15
Vomiting 8
Lethargy (see also Central nervous system depression in 'Neurological') 7
Fever 3
Ataxia 3
Diarrhoea 3
Lymphopenia 2
Inappetence 2
Other abnormal test result NOS 2
Urinary tract infection 2
UNPALATABLE 2
Polyuria 2

Outcome Breakdown

Recovered/Normal
24 (66.7%)
Ongoing
6 (16.7%)
Outcome Unknown
4 (11.1%)
Recovered with Sequela
1 (2.8%)
Died
1 (2.8%)

Emodepside And Praziquantel Adverse Event Insights

36 reports name Emodepside And Praziquantel; 1 recorded a death outcome (2.8% of reported events, not a population-level mortality rate). Active ingredient: Emodepside And Praziquantel. Administration routes: Topical, Unknown, Oral, Parenteral.

By species: Cat (34 reports), Dog (2 reports). By breed: Domestic Shorthair (23), Domestic Mediumhair (6), Domestic Longhair (3).

Leading clinical signs: Emesis (15), Vomiting (8), Lethargy (see also Central nervous system depression in 'Neurological') (7), Fever (3). Outcome, 36 coded reports: Recovered/Normal leads at 66.7%.

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.