Reaction profile

The FDA adverse-event record for haematuria

2,626 FDA reports name haematuria, a high-volume reaction in the CVM extract (VeDDRA 1967). Plate stamps and neighbourhood peers follow.

#182 of 2,481
by report volume (all reactions)
2,626
reports citing this reaction
20.3%
death-coded share
Dog
most-affected species

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Haematuria has 2,626 reports now versus 2,578 in that prior snapshot: 48 more (1.9%).

Report change
+48
Death-coded reports
+3
Death-coded share
−0.3 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Haematuria changes

FDA AER · VeDDRA plate

Code 1967 VOL-MID

VOL-MID · DEATH-HOT · TOP-DECILE · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-MID 2,626 reports
  • DEATH-HOT 20.3%
  • TOP-DECILE #182/2481
  • PHOTO-FINISH Laboured breathing
  • SPECIES-DOG Dog · 2,121
  • DRUG-LEAD Carprofen · 383
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Laboured breathing (±3 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Haematuria

Upper-third volume poles plus nearest peers, not a full reaction corpus board reprint.

Vomiting · highest174348Bradycardia · near2681Application site scab · near2645Breathing difficulty · near2640Haematuria · this reaction2626Laboured breathing · near2623Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Haematuria

What the FDA AER plate says about Haematuria

Signature read: 534 death-coded reports is a heavy tail count for Haematuria in the CVM extract. Report volume is upper-third scale: 2,626 named reports in the openFDA extract. 534 of 2,626 reports were death-coded (20.3% of named reports, not a population mortality rate). Nearest volume peer: Laboured breathing (±3 reports). Lead species Dog (2,121). Lead co-reported drug Carprofen (383).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Carprofen appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 2,121
Cat 484
Horse 14
Other 2
Cattle 1
Human 1
Guinea Pig 1
Sheep 1
Goat 1

Breeds Most Affected

Retriever - Labrador 321
Domestic Shorthair 275
Crossbred Canine/dog 181
Boxer (German Boxer) 83
Shepherd Dog - German 80
Retriever - Golden 75
Domestic (unspecified) 74
Chihuahua 63
Shih Tzu 61
Beagle 59

Associated Drugs

Carprofen 383
Bedinvetmab 271
Trilostane 206
Oclacitinib Maleate 205
Maropitant Citrate 164
Gabapentin 136
Meloxicam 129
Afoxolaner 123
Cefovecin 84
Moxidectin 82
Milbemycin Oxime + Spinosad 78
Fluralaner Chew Tablets 72
Deracoxib 70
Frunevetmab 63
Enrofloxacin 60
Cyclosporine 56
Prednisone 56
Velagliflozin Proline Monohydrate 55
Tramadol 53
Grapiprant 53

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Haematuria, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

Similar report volume

Nearest other reactions by FDA report count (2,626 here).

Similar death-coded share

Nearest other reactions by death-coded share (20.3% here), distinct from the volume row.

What to do with this reaction

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Haematuria (#182 of 2,481 by report volume); death-coded 20.3%. PlainBreed reaction plate · death-coded report count stamp 534 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →