Reaction profile

The FDA adverse-event record for renal degeneration

71 FDA adverse-event reports reference renal degeneration (VeDDRA 2126). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1572 of 2,481
by report volume (all reactions)
71
reports citing this reaction
45.1%
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 degeneration has 71 reports now versus 69 in that prior snapshot: 2 more (2.9%).

Report change
+2
Death-coded reports
+1
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 Renal degeneration changes

FDA AER · VeDDRA plate

Code 2126 VOL-LOW

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

  • VOL-LOW 71 reports
  • DEATH-HOT 45.1%
  • MID-PACK #1572/2481
  • PHOTO-FINISH Administration device…
  • SPECIES-DOG Dog · 62
  • DRUG-LEAD Trilostane · 15
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Administration device NOS, missing component (±0 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.

Report-volume neighbourhood around Renal degeneration

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Administration device… · near71Application site thic… · near71Blotchy rash · near71Enlarged pupils · near71Renal degeneration · this re…71Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Renal degeneration

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

Signature read: Renal degeneration's 45.1% death-coded share is among the highest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is upper-third: 32 of 71 reports (45.1% of named reports). Nearest volume peer: Administration device NOS, missing component (±0 reports). Lead species Dog (62). Lead co-reported drug Trilostane (15).

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 62
Cat 8
Mouse 1

Breeds Most Affected

Retriever - Labrador 7
Domestic Shorthair 6
Chihuahua 5
Terrier - Yorkshire 4
Maltese 3
Spitz - German Pomeranian 3
Crossbred Canine/dog 3
Coton de Tuléar 3
Retriever - Golden 2
Beagle 2

Associated Drugs

Trilostane 15
Gabapentin 12
Maropitant Citrate 11
Bedinvetmab 11
Grapiprant 10
Carprofen 9
Prednisone 6
Oclacitinib Maleate 6
Tramadol 4
Cefovecin 4
Sucralfate 4
Doxycycline 4
Metronidazole 4
Milbemycin Oxime + Spinosad 3
Rattlesnake Vaccine 3
Metoclopramide 3
Fluralaner 3
Fluid Therapy 3
Leptospira Canicola L-15 Strain C-51;Leptospira Grippotyphosa 1550 Lot 10005 Str 3
Trazodone 3

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Renal degeneration, 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 (45.1% 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 degeneration (#1572 of 2,481 by report volume); death-coded 45.1%. PlainBreed reaction plate · death-coded share stamp 45.1% · 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 →