Reaction profile

The FDA adverse-event record for proteinuria

3,907 FDA reports name proteinuria, a high-volume reaction in the CVM extract (VeDDRA 1961). Plate stamps and neighbourhood peers follow.

#122 of 2,481
by report volume (all reactions)
3,907
reports citing this reaction
17.5%
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. Proteinuria has 3,907 reports now versus 3,784 in that prior snapshot: 123 more (3.3%).

Report change
+123
Death-coded reports
+14
Death-coded share
−0.2 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 Proteinuria changes

FDA AER · VeDDRA plate

Code 1961 VOL-MID

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

  • VOL-MID 3,907 reports
  • DEATH-ELEV 17.5%
  • TOP-DECILE #122/2481
  • PHOTO-FINISH Lameness
  • SPECIES-DOG Dog · 3,250
  • DRUG-LEAD Trilostane · 802
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Lameness (±12 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 Proteinuria

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

Vomiting · highest174348Injection site pain · near3968Drug dose omission · near3948Lameness · near3919Proteinuria · this reaction3907Lack of efficacy (bac… · near3861Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Proteinuria

What the FDA AER plate says about Proteinuria

Signature read: 684 death-coded reports is a heavy tail count for Proteinuria in the CVM extract. Report volume is upper-third scale: 3,907 named reports in the openFDA extract. 684 of 3,907 reports were death-coded (17.5% of named reports, not a population mortality rate). Nearest volume peer: Lameness (±12 reports). Lead species Dog (3,250). Lead co-reported drug Trilostane (802).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Trilostane 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 3,250
Cat 646
Horse 9
Human 1
Cattle 1

Breeds Most Affected

Retriever - Labrador 489
Domestic Shorthair 411
Crossbred Canine/dog 230
Retriever - Golden 158
Terrier - Yorkshire 114
Shih Tzu 98
Chihuahua 97
Beagle 95
Boxer (German Boxer) 85
Maltese 85

Associated Drugs

Trilostane 802
Carprofen 503
Bedinvetmab 396
Oclacitinib Maleate 359
Maropitant Citrate 288
Gabapentin 224
Milbemycin Oxime + Spinosad 181
Afoxolaner 153
Meloxicam 147
Prednisone 122
Fluralaner Chew Tablets 117
Grapiprant 117
Cefovecin 115
Velagliflozin Proline Monohydrate 112
Famotidine 92
Bexagliflozin 91
Spinosad 88
Ivermectin + Pyrantel As Pamoate Salt 82
Cyclosporine 81
Deracoxib 75

Nationwide reactions with similar profiles

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

Similar death-coded share

Nearest other reactions by death-coded share (17.5% 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 Proteinuria (#122 of 2,481 by report volume); death-coded 17.5%. PlainBreed reaction plate · death-coded report count stamp 684 · 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 →