Reaction profile

The FDA adverse-event record for ineffective, strongyloids

49 FDA adverse-event reports reference ineffective, strongyloids (VeDDRA 99152). See the species, breeds, and drugs most associated with it below.

49
reports citing this reaction
6.1%
death-coded share
Dog
most-affected species
Ivermectin + Pyrantel As Pamoate Salt
most-associated drug
Verify with FDA CVM →
49
Total Reports
3
Deaths
6.1%
Death Rate

Species Most Affected

Dog 38
Cattle 6
Horse 3
Sheep 2

Breeds Most Affected

Retriever - Labrador 10
Shih Tzu 4
Quarter Horse 3
Crossbred Bovine/Cattle 3
Retriever - Golden 3
Cattle (other) 2
Sheep (unknown) 2
Dog (unknown) 2
Cattle (unknown) 1
Pug 1

Associated Drugs

Ivermectin + Pyrantel As Pamoate Salt 18
Lufenuron + Milbemycin Oxime 4
Ivermectin 3
Milbemycin Oxime + Praziquantel 3
Milbemycin 2
Moxidectin 2
Doramectin 2
Ivermectin/Pyrantel Pamoate Chewable 136Mcg/326Mg 2
Ivermectin, Pyrantel 1
Pyrantel Tartrate 1
Ivermectin/Pyrantel Pamoate Chewable 68Mcg/163Mg 1
Oxfendazole 1
Milbemycin Oxime + Spinosad 1
Bovine Respiratory Syncytial Virus, 597-10 10Th Psg Strain 375; Bovine Viral Dia 1
Bovine Parainfluenza Virus 3 (Ts), Rlb103 (Nl-Bk-6), Mlv; Bovine Respiratory Syn 1
Ivermectin/Pyrantel Pamoate Chewable 272Mcg/652Mg 1
Doramectin; Phenol 1
Milbemcyin Oxime, Lufenuron, Praziquantel 1
Ivermectin + Pyrantel 1
Milbemycin Oxime, Lufenuron 1

INEFFECTIVE, STRONGYLOIDS Reaction Insights

49 reports name INEFFECTIVE, STRONGYLOIDS; 3 recorded a death outcome (6.1% of reported events, not a population-level mortality rate). VeDDRA code: 99152.

By species: Dog (38 reports), Cattle (6 reports), Horse (3 reports). By breed: Retriever - Labrador (10), Shih Tzu (4), Quarter Horse (3).

Most co-reported drugs: Ivermectin + Pyrantel As Pamoate Salt (18 reports), Lufenuron + Milbemycin Oxime (4 reports), Ivermectin (3 reports), Milbemycin Oxime + Praziquantel (3 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.