Reaction profile

The FDA adverse-event record for hepatic failure

41 FDA adverse-event reports reference hepatic failure (VeDDRA 497). See the species, breeds, and drugs most associated with it below.

41
reports citing this reaction
75.6%
death-coded share
Dog
most-affected species
Carprofen
most-associated drug
Verify with FDA CVM →
41
Total Reports
31
Deaths
75.6%
Death Rate

Species Most Affected

Dog 35
Cat 6

Breeds Most Affected

Retriever - Labrador 11
Collie - Border 3
Crossbred Canine/dog 3
Terrier - Jack Russell 2
Spaniel - Cocker American 2
Domestic Shorthair 2
Cat (unknown) 2
Unknown 2
Maine Coon 1
Schnauzer - Miniature 1

Associated Drugs

Carprofen 11
Cyclosporine A 4
Fluralaner Chew Tablets 3
Firocoxib 57 Mg Chewable 2
Spinosad 2
Ivermectin 2
Pradofloxacin 2
Maropitant Citrate 2
Famotidine 2
Gabapentin 2
Cyclosporine 1
Allergy Injections 1
Melarsomine Dihydrochloride Injection 1
Ivermectin + Pyrantel 1
Ivermectin/Pyrantel Pamoate Chewable 136Mcg/326Mg 1
Firocoxib 227 Mg Chewable 1
Lufenuron + Milbemycin Oxime 1
Cephalexin 1
Glucoasmine Supplement 1
Deracoxib 1

Hepatic failure Reaction Insights

41 reports name Hepatic failure; 31 recorded a death outcome (75.6% of reported events, not a population-level mortality rate). VeDDRA code: 497.

By species: Dog (35 reports), Cat (6 reports). By breed: Retriever - Labrador (11), Collie - Border (3), Crossbred Canine/dog (3).

Most co-reported drugs: Carprofen (11 reports), Cyclosporine A (4 reports), Fluralaner Chew Tablets (3 reports), Firocoxib 57 Mg Chewable (2 reports).

Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.