Reaction profile

The FDA adverse-event record for dysuria

94 FDA adverse-event reports reference dysuria (VeDDRA 727). See the species, breeds, and drugs most associated with it below.

94
reports citing this reaction
16.0%
death-coded share
Dog
most-affected species
Milbemycin Oxime + Spinosad
most-associated drug
Verify with FDA CVM →
94
Total Reports
15
Deaths
16.0%
Death Rate

Species Most Affected

Dog 65
Cat 23
Horse 5
Guinea Pig 1

Breeds Most Affected

Domestic Shorthair 9
Domestic (unspecified) 8
Retriever - Labrador 6
Crossbred Canine/dog 6
Terrier - Yorkshire 4
Dachshund (unspecified) 3
Dog (unknown) 3
Deutsche Dogge, Great Dane 3
Boxer (German Boxer) 3
Retriever - Golden 2

Associated Drugs

Milbemycin Oxime + Spinosad 7
Meloxicam 6
Buprenorphine 6
Fluralaner Chew Tablets 6
Enrofloxacin 5
Spinosad 5
Frunevetmab 5
Bedinvetmab 5
Carprofen 4
Butorphanol 4
Imidacloprid + Moxidectin 3
Melarsomine Dihydrochloride Injection 3
Isoflurane 3
Oclacitinib Maleate 3
Melarsomine Dihydrochloride 3
Ivermectin, Pyrantel 2
Selamectin 2
Prednisone 2
Ivermectin 2
Insulin Injectable Vial 2

Dysuria Reaction Insights

94 reports name Dysuria; 15 recorded a death outcome (16.0% of reported events, not a population-level mortality rate). VeDDRA code: 727.

By species: Dog (65 reports), Cat (23 reports), Horse (5 reports). By breed: Domestic Shorthair (9), Domestic (unspecified) (8), Retriever - Labrador (6).

Most co-reported drugs: Milbemycin Oxime + Spinosad (7 reports), Meloxicam (6 reports), Buprenorphine (6 reports), Fluralaner Chew Tablets (6 reports).

Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.

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.