Reaction profile

The FDA adverse-event record for lack of efficacy (ectoparasite) - nos

2,119 FDA adverse-event reports reference lack of efficacy (ectoparasite) - nos (VeDDRA 2492). See the species, breeds, and drugs most associated with it below.

2,119
reports citing this reaction
0.2%
death-coded share
Dog
most-affected species
Fluralaner Chew Tablets
most-associated drug
Verify with FDA CVM →
2,119
Total Reports
5
Deaths
0.2%
Death Rate

Species Most Affected

Dog 1,835
Cattle 186
Cat 86
Unknown 2
Horse 2
Other 2
Rabbit 1
Hamster 1
Alpaca 1
Sheep 1

Breeds Most Affected

Dog (unknown) 300
Crossbred Canine/dog 211
Retriever - Labrador 125
Chihuahua 90
Shih Tzu 80
Terrier - Yorkshire 73
Shepherd Dog - German 56
Retriever - Golden 56
Pit Bull 49
Cattle (other) 47

Associated Drugs

Fluralaner Chew Tablets 1,042
Afoxolaner 292
Afoxolaner 28.3 Mg Chewable Tablets 86
Fluralaner 13.64% 12-Week Chew 61
Afoxolaner 11.3 Mg Chewable Tablets 57
Lotilaner 56
Imidacloprid 50
Afoxolaner 68 Mg Chewable Tablets 48
Eprinomectin 47
Selamectin 42
Afoxolaner 136 Mg Chewable Tablets 39
Portech App Gun 65 Ml Ivomec/Eprinex 38
Pyrantel Pamoate;Sarolaner 35
Ivermectin 33
Moxidectin 31
Fluralaner Spot-On Solution 30
Eprinomectin 5 Mg/Ml Pour-On Solution 29
Nitenpyram 23
Doramectin 21
Ivermectin 0.5% Pour-On Topical Solution 21

Lack of efficacy (ectoparasite) - NOS Reaction Insights

2,119 reports name Lack of efficacy (ectoparasite) - NOS; 5 recorded a death outcome (0.2% of reported events, not a population-level mortality rate). VeDDRA code: 2492.

By species: Dog (1,835 reports), Cattle (186 reports), Cat (86 reports). By breed: Dog (unknown) (300), Crossbred Canine/dog (211), Retriever - Labrador (125).

Most co-reported drugs: Fluralaner Chew Tablets (1,042 reports), Afoxolaner (292 reports), Afoxolaner 28.3 Mg Chewable Tablets (86 reports), Fluralaner 13.64% 12-Week Chew (61 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.