Reaction profile

The FDA adverse-event record for hepatopathy

774 FDA reports name hepatopathy, a high-volume reaction in the CVM extract (VeDDRA 496). Plate stamps and neighbourhood peers follow.

#470 of 2,481
by report volume (all reactions)
774
reports citing this reaction
32.2%
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. Hepatopathy has 774 reports now versus 759 in that prior snapshot: 15 more (2.0%).

Report change
+15
Death-coded reports
+7
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 Hepatopathy changes

FDA AER · VeDDRA plate

Code 496 VOL-MID

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

  • VOL-MID 774 reports
  • DEATH-HOT 32.2%
  • UPPER-Q #470/2481
  • PHOTO-FINISH Hair shedding
  • SPECIES-DOG Dog · 676
  • DRUG-LEAD Carprofen · 227
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hair shedding (±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.

High-volume neighbourhood around Hepatopathy

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

Vomiting · highest174348Diabetes · near777Skin and tissue infec… · near777Hair shedding · near774Hepatopathy · this reaction774PR-LIVER, LESION(S) · near772Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Hepatopathy

Hepatopathy: high death-coded share in the FDA AER plate

Signature read: 249 death-coded reports is a heavy tail count for Hepatopathy in the CVM extract. Report volume is upper-third scale: 774 named reports in the openFDA extract. Death-coded share is upper-third: 249 of 774 reports (32.2% of named reports). Nearest volume peer: Hair shedding (±0 reports). Lead species Dog (676). Lead co-reported drug Carprofen (227).

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 676
Cat 85
Cattle 9
Turkey 1
Rabbit 1
Snake 1
Goat 1

Breeds Most Affected

Retriever - Labrador 127
Crossbred Canine/dog 57
Domestic Shorthair 30
Retriever - Golden 27
Domestic (unspecified) 26
Chihuahua 26
Shih Tzu 25
Maltese 20
Dog (unknown) 18
Shepherd Dog - Australian 15

Associated Drugs

Carprofen 227
Maropitant Citrate 78
Trilostane 60
Cefovecin Sodium 44
Milbemycin Oxime + Spinosad 38
Gabapentin 36
Oclacitinib Maleate 31
Famotidine 29
Bedinvetmab 28
Meloxicam 26
Spinosad 25
Fluralaner Chew Tablets 25
Enrofloxacin 24
Afoxolaner 24
Moxidectin 22
Doxycycline 22
Sam-E, Silybin, Vitamin E, Zinc 21
Deracoxib 20
Tramadol 20
Prednisone 20

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Hepatopathy, 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 (774 here).

Similar death-coded share

Nearest other reactions by death-coded share (32.2% 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 Hepatopathy (#470 of 2,481 by report volume); death-coded 32.2%. PlainBreed reaction plate · death-coded report count stamp 249 · 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 →