Reaction profile

The FDA adverse-event record for haematuria

2,473 FDA adverse-event reports reference haematuria (VeDDRA 1967). See the species, breeds, and drugs most associated with it below.

2,473
reports citing this reaction
20.3%
death-coded share
Dog
most-affected species
Carprofen
most-associated drug
Verify with FDA CVM →
2,473
Total Reports
503
Deaths
20.3%
Death Rate

Species Most Affected

Dog 2,023
Cat 432
Horse 11
Other 2
Human 1
Cattle 1
Guinea Pig 1
Sheep 1
Goat 1

Breeds Most Affected

Retriever - Labrador 310
Domestic Shorthair 233
Crossbred Canine/dog 175
Boxer (German Boxer) 82
Shepherd Dog - German 79
Domestic (unspecified) 74
Retriever - Golden 71
Chihuahua 61
Shih Tzu 61
Beagle 54

Associated Drugs

Carprofen 369
Bedinvetmab 239
Trilostane 201
Oclacitinib Maleate 186
Maropitant Citrate 143
Meloxicam 126
Afoxolaner 119
Gabapentin 112
Moxidectin 81
Milbemycin Oxime + Spinosad 78
Cefovecin 78
Fluralaner Chew Tablets 72
Deracoxib 69
Enrofloxacin 57
Cyclosporine 54
Tramadol 53
Frunevetmab 51
Prednisone 50
Spinosad 49
Firocoxib 49

Haematuria Reaction Insights

2,473 reports name Haematuria; 503 recorded a death outcome (20.3% of reported events, not a population-level mortality rate). VeDDRA code: 1967.

By species: Dog (2,023 reports), Cat (432 reports), Horse (11 reports). By breed: Retriever - Labrador (310), Domestic Shorthair (233), Crossbred Canine/dog (175).

Most co-reported drugs: Carprofen (369 reports), Bedinvetmab (239 reports), Trilostane (201 reports), Oclacitinib Maleate (186 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.