Reaction profile

The FDA adverse-event record for peripheral vestibular disorder

27 FDA adverse-event reports reference peripheral vestibular disorder (VeDDRA 2457). See the species, breeds, and drugs most associated with it below.

27
reports citing this reaction
11.1%
death-coded share
Dog
most-affected species
Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride
most-associated drug
Verify with FDA CVM →
27
Total Reports
3
Deaths
11.1%
Death Rate

Species Most Affected

Dog 20
Cat 7

Breeds Most Affected

Domestic Shorthair 6
Crossbred Canine/dog 3
Chihuahua 3
Retriever - Golden 2
Retriever - Labrador 2
Shih Tzu 2
Terrier - Bull - American Pit 2
Schnauzer - Miniature 1
Pug 1
Maine Coon 1

Associated Drugs

Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 6
Maropitant Citrate 4
Moxidectin 3
Florfenicol, Terbinafine, Betamethasone Acetate 3
Genta/Momet/Clotrim Ear Oint 2
Prednisone 2
Potassium Chloride 2
Trilostane 2
Deracoxib 2
Insulin Injectable Vial 2
Butorphanol 2
Maropitant 2
Dexamethasone Sodium Phosphate 2
Fluralaner 13.64% 12-Week Chew 2
Neomycin Sulfate, Dexamethasone, Thiabendazole Topical Ointment 2
Mirtazapine 2
Ondansetron 2
Bedinvetmab 2
Amoxicillin Trihydrate; Clavulanate Potassium ( K-Clavulanate) 1
Anesthetic 1

Peripheral vestibular disorder Reaction Insights

27 reports name Peripheral vestibular disorder; 3 recorded a death outcome (11.1% of reported events, not a population-level mortality rate). VeDDRA code: 2457.

By species: Dog (20 reports), Cat (7 reports). By breed: Domestic Shorthair (6), Crossbred Canine/dog (3), Chihuahua (3).

Most co-reported drugs: Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride (6 reports), Maropitant Citrate (4 reports), Moxidectin (3 reports), Florfenicol, Terbinafine, Betamethasone Acetate (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.