Reaction profile

The FDA adverse-event record for application site hair coat discolouration

198 FDA adverse-event reports reference application site hair coat discolouration (VeDDRA 2519). See the species, breeds, and drugs most associated with it below.

198
reports citing this reaction
1.0%
death-coded share
Cat
most-affected species
Selamectin
most-associated drug
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198
Total Reports
2
Deaths
1.0%
Death Rate

Species Most Affected

Cat 114
Dog 82
Hedgehog 1
Lynx 1

Breeds Most Affected

Domestic Shorthair 67
Domestic Longhair 12
Crossbred Canine/dog 6
Terrier - West Highland White 6
Cat (unknown) 6
Retriever - Golden 5
Retriever - Labrador 5
Dog (unknown) 5
Bichon Frise 4
Chihuahua 4

Associated Drugs

Selamectin 38
Fluralaner Spot-On Solution 29
Imidacloprid + Moxidectin 24
Selamectin;Sarolaner 20
Emodepside + Praziquantel 16
Chlorhexidine Gluconate + Ketoconazole + Phytosphingosine Salicyloyl 15
Eprinomectin + Praziquantel 13
Eprinomectin + Esafoxolaner + Praziquantel 11
Chlorhexidine Gluconate + Climbazole + Phytosphingosine Salicyloyl 7
Fluralaner/Moxidectin Spot-On 5
Ivermectin + Pyrantel As Pamoate Salt 3
Cefovecin Sodium 3
Fipronil + S-Methoprene 3
Phytosphingosine Hydrochloride 2
Chlorhexidine Gluconate + Phytosphingosine Salicyloyl 2
Shampoo 2
Imidacloprid, Flumethrin 2
Fipronil 10%/S Methoprene 9% Spot On 2
Milbemycin Oxime + Praziquantel 2
Chlorhexidine Gluconate + Hydrocortisone 1

Application site hair coat discolouration Reaction Insights

198 reports name Application site hair coat discolouration; 2 recorded a death outcome (1.0% of reported events, not a population-level mortality rate). VeDDRA code: 2519.

By species: Cat (114 reports), Dog (82 reports), Hedgehog (1 reports). By breed: Domestic Shorthair (67), Domestic Longhair (12), Crossbred Canine/dog (6).

Most co-reported drugs: Selamectin (38 reports), Fluralaner Spot-On Solution (29 reports), Imidacloprid + Moxidectin (24 reports), Selamectin;Sarolaner (20 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.