Reaction profile

The FDA adverse-event record for ketonuria

719 FDA reports name ketonuria, a high-volume reaction in the CVM extract (VeDDRA 2910). Plate stamps and neighbourhood peers follow.

#503 of 2,481
by report volume (all reactions)
719
reports citing this reaction
20.4%
death-coded share
Cat
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. Ketonuria has 719 reports now versus 667 in that prior snapshot: 52 more (7.8%).

Report change
+52
Death-coded reports
+6
Death-coded share
−0.7 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 Ketonuria changes

FDA AER · VeDDRA plate

Code 2910 VOL-MID

VOL-MID · DEATH-HOT · UPPER-Q · PHOTO-FINISH · SPECIES-CAT · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-MID 719 reports
  • DEATH-HOT 20.4%
  • UPPER-Q #503/2481
  • PHOTO-FINISH Underfilling, Vials
  • SPECIES-CAT Cat · 657
  • DRUG-LEAD Velagliflozin Pro… · 504
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Underfilling, Vials (±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 Ketonuria

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

Vomiting · highest174348Solution/Suspension,… · near722Application site skin… · near720Ketonuria · this reaction719Underfilling, Vials · near719Localised itching · near718Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Ketonuria

What the FDA AER plate says about Ketonuria

Signature read: 147 death-coded reports is a heavy tail count for Ketonuria in the CVM extract. Report volume is upper-third scale: 719 named reports in the openFDA extract. 147 of 719 reports were death-coded (20.4% of named reports, not a population mortality rate). Nearest volume peer: Underfilling, Vials (±0 reports). Lead species Cat (657). Lead co-reported drug Velagliflozin Proline Monohydrate (504).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Velagliflozin Proline Monohydrate 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

Cat 657
Dog 62

Breeds Most Affected

Domestic Shorthair 474
Domestic Longhair 57
Domestic Mediumhair 42
Cat (unknown) 35
Maine Coon 10
Ragdoll 8
Chihuahua 7
Siamese 7
Retriever - Labrador 7
Shepherd Dog - Australian 4

Associated Drugs

Velagliflozin Proline Monohydrate 504
Bexagliflozin 122
Maropitant Citrate 25
Trilostane 23
Fluid Therapy 21
Insulin 19
Bedinvetmab 19
Senvelgo Velagliflozin Oral Solution 16
Gabapentin 13
Dextrose 11
Sc Fluids 10
Cefovecin Sodium 9
Cefovecin 9
Prescription Diet 8
Potassium Chloride 6
Metoclopramide 6
Prednisone 6
Amoxicillin + Clavulanic Acid 6
Buprenorphine 6
Enrofloxacin 5

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Ketonuria, 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 (20.4% 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 Ketonuria (#503 of 2,481 by report volume); death-coded 20.4%. PlainBreed reaction plate · death-coded report count stamp 147 · 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 →