Reaction profile

The FDA adverse-event record for ineffective, stomach worm nos

43 FDA adverse-event reports reference ineffective, stomach worm nos (VeDDRA 99149). See the species, breeds, and drugs most associated with it below.

43
reports citing this reaction
30.2%
death-coded share
Cattle
most-affected species
Doramectin
most-associated drug
Verify with FDA CVM →
43
Total Reports
13
Deaths
30.2%
Death Rate

Species Most Affected

Cattle 30
Sheep 6
Dog 5
Goat 1
Buffalo 1

Breeds Most Affected

Cattle (unknown) 7
Cattle (other) 7
Crossbred Bovine/Cattle 6
Aberdeen Angus 6
Sheep (unknown) 4
Retriever - Golden 2
Mixed (Cattle) 2
Katahdin 2
Boer 1
Unknown 1

Associated Drugs

Doramectin 7
Fenbendazole 7
Albendazole 5
Moxidectin 5
Ivermectin + Pyrantel As Pamoate Salt 4
Eprinomectin 2
Ivermectin(1%)/Clorsulon(10%) Injection 2
Fenbendazol Suspension 2
Ivermectin, Pyrantel 1
Clorsulon, Ivermectin 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
Oxfendazole 1
Lufenuron + Milbemycin Oxime 1
Eprinomectin 5% Injection 1
Doramectin; Phenol 1
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Mannheimia Haemolytica Toxoid 1
Fenbendazol Powder Mix 1
Eprinomectin 5 Mg/Ml Pour-On Solution 1
Portech App Gun 65 Ml Ivomec/Eprinex 1

INEFFECTIVE, STOMACH WORM NOS Reaction Insights

43 reports name INEFFECTIVE, STOMACH WORM NOS; 13 recorded a death outcome (30.2% of reported events, not a population-level mortality rate). VeDDRA code: 99149.

By species: Cattle (30 reports), Sheep (6 reports), Dog (5 reports). By breed: Cattle (unknown) (7), Cattle (other) (7), Crossbred Bovine/Cattle (6).

Most co-reported drugs: Doramectin (7 reports), Fenbendazole (7 reports), Albendazole (5 reports), Moxidectin (5 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.