Reaction profile

The FDA adverse-event record for polyuria

7,747 FDA reports name polyuria, a high-volume reaction in the CVM extract (VeDDRA 718). Plate stamps and neighbourhood peers follow.

#61 of 2,481
by report volume (all reactions)
7,747
reports citing this reaction
9.8%
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. Polyuria has 7,747 reports now versus 7,578 in that prior snapshot: 169 more (2.2%).

Report change
+169
Death-coded reports
+10
Death-coded share
−0.1 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 Polyuria changes

FDA AER · VeDDRA plate

Code 718 VOL-HIGH

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

  • VOL-HIGH 7,747 reports
  • DEATH-PAR 9.8%
  • TOP-DECILE #61/2481
  • PHOTO-FINISH Dehydration
  • SPECIES-DOG Dog · 6,827
  • DRUG-LEAD Bedinvetmab · 1,517
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Dehydration (±96 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 Polyuria

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

Vomiting · highest174348Tremor · near8033Drooling · near7886Polyuria · this reaction7747Dehydration · near7651Elevated creatinine · near7526Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Polyuria

What the FDA AER plate says about Polyuria

Signature read: 7,747 reports place Polyuria in the upper third of FDA AER volume (#61 of 2,481). Report volume is upper-third scale: 7,747 named reports in the openFDA extract. 757 of 7,747 reports were death-coded (9.8% of named reports, not a population mortality rate). Nearest volume peer: Dehydration (±96 reports). Lead species Dog (6,827). Lead co-reported drug Bedinvetmab (1,517).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Bedinvetmab 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 6,827
Cat 801
Horse 111
Cattle 2
Human 2
Pig 1
Monkey 1
Goat 1
Ferret 1

Breeds Most Affected

Retriever - Labrador 812
Crossbred Canine/dog 482
Domestic Shorthair 474
Retriever - Golden 282
Shepherd Dog - German 261
Boxer (German Boxer) 225
Dog (unknown) 197
Terrier - Yorkshire 172
Chihuahua 166
Shih Tzu 158

Associated Drugs

Bedinvetmab 1,517
Trilostane 1,130
Carprofen 700
Oclacitinib Maleate 628
Prednisone 464
Gabapentin 383
Milbemycin Oxime + Spinosad 277
Maropitant Citrate 259
Fluralaner Chew Tablets 247
Pyrantel Pamoate;Sarolaner 234
Bexagliflozin 227
Desoxycorticosterone Pivalate 197
Afoxolaner 181
Deracoxib 179
Meloxicam 170
Grapiprant 167
Cyclosporine 166
Moxidectin 166
Anti-Il31 Mab Mcs Lot #1283563 165
Lotilaner 152

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Polyuria, 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 (7,747 here).

Similar death-coded share

Nearest other reactions by death-coded share (9.8% 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 Polyuria (#61 of 2,481 by report volume); death-coded 9.8%. PlainBreed reaction plate · report volume stamp 7,747 · 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 →