Reaction profile

The FDA adverse-event record for decubitus

27 FDA adverse-event reports reference decubitus (VeDDRA 2024). See the species, breeds, and drugs most associated with it below.

27
reports citing this reaction
25.9%
death-coded share
Dog
most-affected species
Meloxicam
most-associated drug
Verify with FDA CVM →
27
Total Reports
7
Deaths
25.9%
Death Rate

Species Most Affected

Dog 17
Cat 6
Rabbit 2
Pig 1
Sheep 1

Breeds Most Affected

Domestic Shorthair 4
Poodle - Standard 2
Retriever - Labrador 2
Crossbred rabbit 2
European 1
Hound (unspecified) 1
Collie - Border 1
Crossbred Porcine/Pig 1
Chihuahua 1
Sheep (unknown) 1

Associated Drugs

Meloxicam 6
Pimobendan 5
Afoxolaner 4
Ketamine Hydrochloride 3
Protamine Zinc Recombinant Human Insulin 3
Afoxolaner 11.3 Mg Chewable Tablets 2
Eurican Chppi2Lr-Nf 2
Midazolam 2
Ivermectin 1
Firocoxib 1
Ivermectin/Pyrantel Pamoate Chewable 136Mcg/326Mg 1
Gamithromycin 15% Solution For Injection 1
Ivermectin 10 Mg/Ml Solution For Injection 1
Afoxolaner 28.3 Mg Chewable Tablets 1
Dolthene Oral Solution 1
Afoxolaner 68 Mg Chewable Tablets 1
Ivermectin/Pyrantel Pamoate Chewable 272Mcg/652Mg 1
Melarsomine Dihydrochloride 1
Acepromazine Maleate 1
Ivermectin + Pyrantel As Pamoate Salt 1

Decubitus Reaction Insights

27 reports name Decubitus; 7 recorded a death outcome (25.9% of reported events, not a population-level mortality rate). VeDDRA code: 2024.

By species: Dog (17 reports), Cat (6 reports), Rabbit (2 reports). By breed: Domestic Shorthair (4), Poodle - Standard (2), Retriever - Labrador (2).

Most co-reported drugs: Meloxicam (6 reports), Pimobendan (5 reports), Afoxolaner (4 reports), Ketamine Hydrochloride (3 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.