Reaction profile

The FDA adverse-event record for taste disorder

Name: Taste disorder - FDA Animal Adverse Reaction
Creator: PlainBreed
License: https://creativecommons.org/publicdomain/zero/1.0/

32 FDA adverse-event reports reference taste disorder (VeDDRA 1824). See the species, breeds, and drugs most associated with it below.

32
reports citing this reaction: 0.0%
death-coded share: Human
most-affected species: Selamectin
most-associated drug

Compiled by PlainBreed Editorial, Pet Health Editorial Team

Verify with FDA CVM →

Total Reports

Deaths

0.0%

Death Rate

Species Most Affected

Human 32

Breeds Most Affected

Unknown 32

Associated Drugs

Selamectin 4

Tilmicosin Phosphate 3

Copper Naphthenate 3

Milbemycin Oxime + Spinosad 2

Toceranib Phosphate 2

Tylosin Tartrate 2

Imidacloprid + Moxidectin 1

Flumethrin-Imidacloprid 1

Vancomycin 1

Ivermectin 10 Mg/Ml Solution For Injection 1

Nitenpyram 1

Atorvastatin 1

Sertraline 1

Amlodipine + Hydrochlorothiazide + Olmesartan 1

Maropitant Citrate 1

Dimethyl Sulfoxide;Fluocinolone Acetonide 1

Neomycin Sulfate;Tetracaine Hydrochloride 1

Mupirocin 1

Eprinomectin 1

Cyclosporine 1

Taste disorder Reaction Insights

32 reports name Taste disorder; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). VeDDRA code: 1824.

By species: Human (32 reports). By breed: Unknown (32).

Most co-reported drugs: Selamectin (4 reports), Tilmicosin Phosphate (3 reports), Copper Naphthenate (3 reports), Milbemycin Oxime + Spinosad (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.