Reaction profile

The FDA adverse-event record for renal insufficiency

376 FDA reports name renal insufficiency, a high-volume reaction in the CVM extract (VeDDRA 721). Plate stamps and neighbourhood peers follow.

#766 of 2,481
by report volume (all reactions)
376
reports citing this reaction
25.5%
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. Renal insufficiency has 376 reports now versus 368 in that prior snapshot: 8 more (2.2%).

Report change
+8
Death-coded reports
+1
Death-coded share
−0.3 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 Renal insufficiency changes

FDA AER · VeDDRA plate

Code 721 VOL-LOW

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

  • VOL-LOW 376 reports
  • DEATH-HOT 25.5%
  • MID-PACK #766/2481
  • PHOTO-FINISH Abnormal test result
  • SPECIES-DOG Dog · 277
  • DRUG-LEAD Deracoxib · 69
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Abnormal test result (±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 Renal insufficiency

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

Vomiting · highest174348Abnormal test result · near377Cellulitis · near377Renal insufficiency · this r…376Allergic pruritus · near375Hyperchloraemia · near375Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Renal insufficiency

Renal insufficiency: high death-coded share in the FDA AER plate

Signature read: 96 death-coded reports is a heavy tail count for Renal insufficiency in the CVM extract. Report volume is upper-third scale: 376 named reports in the openFDA extract. Death-coded share is upper-third: 96 of 376 reports (25.5% of named reports). Nearest volume peer: Abnormal test result (±1 reports). Lead species Dog (277). Lead co-reported drug Deracoxib (69).

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 277
Cat 90
Horse 8
Monkey 1

Breeds Most Affected

Domestic Shorthair 61
Retriever - Labrador 45
Crossbred Canine/dog 18
Terrier - Yorkshire 13
Retriever - Golden 11
Boxer (German Boxer) 9
Shepherd Dog - German 9
Dog (unknown) 9
Shih Tzu 8
Domestic Longhair 7

Associated Drugs

Deracoxib 69
Trilostane 43
Tramadol 30
Milbemycin Oxime + Spinosad 27
Robenacoxib 26
Bedinvetmab 24
Carprofen 20
Gabapentin 18
Grapiprant 17
Cyclosporine A 16
Prednisone 16
Frunevetmab 16
Meloxicam 14
Spinosad 13
Polysulfated Glycosaminoglycan 13
Maropitant Citrate 12
Enrofloxacin 11
Isoflurane 11
Oclacitinib Maleate 11
Milbemycin Oxime 9

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Renal insufficiency, 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 (376 here).

Similar death-coded share

Nearest other reactions by death-coded share (25.5% 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 Renal insufficiency (#766 of 2,481 by report volume); death-coded 25.5%. PlainBreed reaction plate · death-coded report count stamp 96 · 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 →