Reaction profile

The FDA adverse-event record for nose swelling

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

18 FDA adverse-event reports reference nose swelling (VeDDRA 3016). See the species, breeds, and drugs most associated with it below.

18
reports citing this reaction: 0.0%
death-coded share: Dog
most-affected species: Gentamicin + Mometasone + Clotrimazole
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

Dog 14

Cat 3

Horse 1

Breeds Most Affected

Chihuahua 4

Domestic Shorthair 2

Pug 1

Domestic Longhair 1

Bulldog - English 1

Dog (other) 1

Dachshund - Standard Long-haired 1

Maltese 1

Chinese Crested Dog – Hairless 1

Retriever - Labrador 1

Associated Drugs

Gentamicin + Mometasone + Clotrimazole 3

Oclacitinib Maleate 3

Trilostane 2

Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 2

Ketoconazole,Hydrocortisone 2

Carprofen 2

Cefpodoxime Proxetil 2

Diphenhydramine 2

Bupivacaine 2

Leptospira Canicola L-15 Strain C-51;Leptospira Grippotyphosa 1550 Lot 10005 Str 2

Diclofenac 1% Ophthalmic Solution 1

Cyclosporine Eye Ointment 1

Florfenicol, Terbinafine, Betamethasone Acetate 1

Adrenal Tincture 1

Melatonin 1

Tramadol 1

Clindamycin Drops 1

Alprazolam 1

Milbemycin Oxime + Praziquantel 1

Lotilaner 1

Nose swelling Reaction Insights

18 reports name Nose swelling; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). VeDDRA code: 3016.

By species: Dog (14 reports), Cat (3 reports), Horse (1 reports). By breed: Chihuahua (4), Domestic Shorthair (2), Pug (1).

Most co-reported drugs: Gentamicin + Mometasone + Clotrimazole (3 reports), Oclacitinib Maleate (3 reports), Trilostane (2 reports), Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride (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.