Reaction profile

The FDA adverse-event record for acute renal failure

643 FDA reports name acute renal failure, a high-volume reaction in the CVM extract (VeDDRA 1159). Plate stamps and neighbourhood peers follow.

#546 of 2,481
by report volume (all reactions)
643
reports citing this reaction
44.8%
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. Acute renal failure has 643 reports now versus 633 in that prior snapshot: 10 more (1.6%).

Report change
+10
Death-coded reports
+4
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 Acute renal failure changes

FDA AER · VeDDRA plate

Code 1159 VOL-MID

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

  • VOL-MID 643 reports
  • DEATH-HOT 44.8%
  • UPPER-Q #546/2481
  • PHOTO-FINISH Hyperpigmentation
  • SPECIES-DOG Dog · 412
  • DRUG-LEAD Meloxicam · 151
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hyperpigmentation (±1 reports)

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

High-volume neighbourhood around Acute renal failure

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

Vomiting · highest174348Difficulty standing · near645Hyperpigmentation · near644Pinnal reddening · near644Acute renal failure · this r…643Urinary bladder disor… · near641Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Acute renal failure

Acute renal failure: high death-coded share in the FDA AER plate

Signature read: 288 death-coded reports is a heavy tail count for Acute renal failure in the CVM extract. Report volume is upper-third scale: 643 named reports in the openFDA extract. Death-coded share is upper-third: 288 of 643 reports (44.8% of named reports). Nearest volume peer: Hyperpigmentation (±1 reports). Lead species Dog (412). Lead co-reported drug Meloxicam (151).

Read these counts as reporting volume, not risk: per our methodology, A high death-coded share in FDA filings does not prove causation; co-reporting is voluntary temporal association only. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 412
Cat 207
Horse 19
Human 2
Primate 1
Gerbil 1
Donkey 1

Breeds Most Affected

Domestic Shorthair 124
Retriever - Labrador 55
Chihuahua 23
Crossbred Canine/dog 20
Terrier - Yorkshire 19
Dog (unknown) 19
Shepherd Dog - German 16
Retriever - Golden 16
Quarter Horse 15
Domestic Mediumhair 14

Associated Drugs

Meloxicam 151
Carprofen 75
Deracoxib 60
Maropitant Citrate 56
Robenacoxib 47
Gabapentin 37
Bedinvetmab 36
Tramadol 34
Propofol 33
Isoflurane 31
Oclacitinib Maleate 29
Butorphanol 25
Buprenorphine 25
Trilostane 24
Grapiprant 24
Milbemycin Oxime + Spinosad 22
Firocoxib 22
Famotidine 20
Cefovecin 20
Frunevetmab 18

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Acute renal failure, 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 (643 here).

Similar death-coded share

Nearest other reactions by death-coded share (44.8% 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 Acute renal failure (#546 of 2,481 by report volume); death-coded 44.8%. PlainBreed reaction plate · death-coded report count stamp 288 · 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 →