Reaction profile

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

17 FDA adverse-event reports reference lack of efficacy (virus) - coronavirus - nos (VeDDRA 2814). See the species, breeds, and drugs most associated with it below.

17
reports citing this reaction
47.1%
death-coded share
Cattle
most-affected species
Bovine Corona Des Lv
most-associated drug
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17
Total Reports
8
Deaths
47.1%
Death Rate

Species Most Affected

Cattle 14
Dog 3

Breeds Most Affected

Cattle (other) 8
Mixed (Cattle) 3
Aberdeen Angus 2
Bulldog - French 1
Shepherd Dog - Australian 1
Siberian Husky 1
Salers 1

Associated Drugs

Bovine Corona Des Lv 5
Clos P*2/Cl Oth*4/H.Somnus Kb 5
Ibr/Brsv/P13/Bvd T1, T2(Us) Lv 4
Bovine Virus*5/Past M+Mh Lv/Lb 4
Oxfendazole 4
Diflubenzuron And Permethrin 4
Infectious Bovine Rhinotracheitis Virus(Ts), Rlb 106;Bovine Parainfluenza Virus 4
Zeranol Implant 3
Mycoplasma Bovis 3
Fenbendazol Suspension 3
Trenbolone Acet/Estrad Sr Imp 2
Clostr Perf*2/Clos Others*6 Kb 2
Diflubenzuron Permethrin 2
Gamithromycin 2
Bovine Parainfluenza 3 Virus, Modified Live Virus + Bovine Respiratory Syncytial Virus, Modified Live Virus + Bovine Rhinotracheitis Virus, Modified Live Virus + Bovine Virus Diarrhea Type 1, Modified Live Virus + Bovine Virus Diarrhea Type 2, Modified Live Virus 2
Milbemycin Oxime + Praziquantel 2
Lotilaner 2
Bordetella Bronchiseptica Vaccine, Avirulent Live Culture 2
Bov.Virus*3/M Haem/Past Mult 2
Oxytetracycline 2

Lack of efficacy (virus) - coronavirus - NOS Reaction Insights

17 reports name Lack of efficacy (virus) - coronavirus - NOS; 8 recorded a death outcome (47.1% of reported events, not a population-level mortality rate). VeDDRA code: 2814.

By species: Cattle (14 reports), Dog (3 reports). By breed: Cattle (other) (8), Mixed (Cattle) (3), Aberdeen Angus (2).

Most co-reported drugs: Bovine Corona Des Lv (5 reports), Clos P*2/Cl Oth*4/H.Somnus Kb (5 reports), Ibr/Brsv/P13/Bvd T1, T2(Us) Lv (4 reports), Bovine Virus*5/Past M+Mh Lv/Lb (4 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.