Reaction profile

The FDA adverse-event record for application site reddening

1,971 FDA adverse-event reports reference application site reddening (VeDDRA 1332). See the species, breeds, and drugs most associated with it below.

1,971
reports citing this reaction
0.7%
death-coded share
Cat
most-affected species
Selamectin
most-associated drug
Verify with FDA CVM →
1,971
Total Reports
13
Deaths
0.7%
Death Rate

Species Most Affected

Cat 1,595
Dog 300
Human 34
Horse 32
Cattle 4
Wolf 2
Bobcat 2
Rabbit 1
Other Birds 1

Breeds Most Affected

Domestic Shorthair 1,085
Domestic Longhair 125
Domestic Mediumhair 95
Cat (other) 62
Siamese 44
Maine Coon 44
Unknown 41
Cat (unknown) 33
Crossbred Canine/dog 29
Retriever - Labrador 26

Associated Drugs

Selamectin 483
Selamectin;Sarolaner 460
Fluralaner Spot-On Solution 342
Mirtazapine 139
Fluralaner/Moxidectin Spot-On 104
Eprinomectin + Esafoxolaner + Praziquantel 50
Ivermectin + Pyrantel As Pamoate Salt 39
Buprenorphine 37
Imidacloprid + Moxidectin 31
Fipronil 10%/S Methoprene 9% Spot On 21
Ivermectin(1.55%)/Praziquantel(7.75%) Paste 21
Emodepside + Praziquantel 21
Fipronil 9.8%/S-Methoprene 8.8%/Cyphenothrin 5.2% Squeeze-On 18
Imidacloprid, Flumethrin 18
Florfenicol, Terbinafine, Betamethasone Acetate 17
Maropitant Citrate 15
Chlorhexidine + Ophytrium 14
Prednisone 13
Chlorhexidine Gluconate + Climbazole + Phytosphingosine Salicyloyl 13
Eprinomectin + Praziquantel 13

Application site reddening Reaction Insights

1,971 reports name Application site reddening; 13 recorded a death outcome (0.7% of reported events, not a population-level mortality rate). VeDDRA code: 1332.

By species: Cat (1,595 reports), Dog (300 reports), Human (34 reports). By breed: Domestic Shorthair (1,085), Domestic Longhair (125), Domestic Mediumhair (95).

Most co-reported drugs: Selamectin (483 reports), Selamectin;Sarolaner (460 reports), Fluralaner Spot-On Solution (342 reports), Mirtazapine (139 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.