Reaction profile

The FDA adverse-event record for application site warmth

63 FDA adverse-event reports reference application site warmth (VeDDRA 2406). See the species, breeds, and drugs most associated with it below.

63
reports citing this reaction
0.0%
death-coded share
Cat
most-affected species
Mirtazapine
most-associated drug
Verify with FDA CVM →
63
Total Reports
0
Deaths
0.0%
Death Rate

Species Most Affected

Cat 51
Dog 10
Human 2

Breeds Most Affected

Domestic Shorthair 31
Domestic Longhair 6
Cat (unknown) 5
Domestic Mediumhair 3
Unknown 2
Crossbred Canine/dog 2
Maine Coon 1
Coonhound - Black and Tan 1
Retriever - Labrador 1
Hound (unspecified) 1

Associated Drugs

Mirtazapine 31
Fluralaner Spot-On Solution 6
Selamectin 5
Emodepside + Praziquantel 4
Fluralaner/Moxidectin Spot-On 4
Phytosphingosine Hydrochloride 2
Phytosphingosine Salicyloyl 2
Cefovecin 2
Buprenorphine 2
Prednisolone 2
Gabapentin 2
Tresaderm Dermatological Solution 1
Imidacloprid + Moxidectin 1
Florfenicol/Terbinafine Hydrochloride/Mometasone Furoate 1
Deionized Water, Propylene Glycol, Aloe Vera Gel, Sd Alcohol 40, Lactic Acid, Glycerin, Dioctyl Sodium Sulfosuccinate, Salicylic Acid, Fragrance, Benzoic Acid, Benzyl Alcohol. 1
Topical Flea Solution 1
Bupivacaine Lipsome Injectable Suspension 1
Betamethasone + Florfenicol + Terbinafine 1
Phytosphingosine 1
Feline Viral Rhinotracheitis, Calicivirus And Panleukopenia Vaccine 1

Application site warmth Reaction Insights

63 reports name Application site warmth; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). VeDDRA code: 2406.

By species: Cat (51 reports), Dog (10 reports), Human (2 reports). By breed: Domestic Shorthair (31), Domestic Longhair (6), Cat (unknown) (5).

Most co-reported drugs: Mirtazapine (31 reports), Fluralaner Spot-On Solution (6 reports), Selamectin (5 reports), Emodepside + Praziquantel (4 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.