Reaction profile

The FDA adverse-event record for isosthenuria

356 FDA reports name isosthenuria, a high-volume reaction in the CVM extract (VeDDRA 2254). Plate stamps and neighbourhood peers follow.

#801 of 2,481
by report volume (all reactions)
356
reports citing this reaction
14.9%
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. Isosthenuria has 356 reports now versus 336 in that prior snapshot: 20 more (6.0%).

Report change
+20
Death-coded reports
+3
Death-coded share
+0.0 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 Isosthenuria changes

FDA AER · VeDDRA plate

Code 2254 VOL-LOW

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

  • VOL-LOW 356 reports
  • DEATH-ELEV 14.9%
  • MID-PACK #801/2481
  • PHOTO-FINISH Closed eyelid
  • SPECIES-DOG Dog · 311
  • DRUG-LEAD Trilostane · 107
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Closed eyelid (±0 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 Isosthenuria

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

Vomiting · highest174348Closed eyelid · near356Isosthenuria · this reaction356Lip smacking · near356Vasculitis · near356Skin tumour NOS · near355Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Isosthenuria

What the FDA AER plate says about Isosthenuria

Signature read: 53 death-coded reports is a heavy tail count for Isosthenuria in the CVM extract. Report volume is upper-third scale: 356 named reports in the openFDA extract. 53 of 356 reports were death-coded (14.9% of named reports, not a population mortality rate). Nearest volume peer: Closed eyelid (±0 reports). Lead species Dog (311). Lead co-reported drug Trilostane (107).

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 311
Cat 40
Horse 5

Breeds Most Affected

Retriever - Labrador 45
Domestic Shorthair 28
Crossbred Canine/dog 19
Shepherd Dog - German 18
Chihuahua 14
Terrier - Bull - American Pit 14
Boxer (German Boxer) 13
Retriever - Golden 13
Beagle 9
Shepherd Dog - Australian 8

Associated Drugs

Trilostane 107
Bedinvetmab 92
Carprofen 41
Gabapentin 32
Maropitant Citrate 22
Meloxicam 21
Grapiprant 20
Oclacitinib Maleate 15
Anti-Il31 Mab Mcs Lot #1283563 14
Fluralaner Chew Tablets 13
Frunevetmab 13
Pyrantel Pamoate;Sarolaner 11
Famotidine 10
Deracoxib 9
Cefovecin 8
Milbemycin Oxime + Spinosad 8
Prednisone 8
Firocoxib 7
Butorphanol 7
Fluralaner 13.64% 12-Week Chew 7

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Isosthenuria, 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 (356 here).

Similar death-coded share

Nearest other reactions by death-coded share (14.9% 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 Isosthenuria (#801 of 2,481 by report volume); death-coded 14.9%. PlainBreed reaction plate · death-coded report count stamp 53 · 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 →