Reaction profile

The FDA adverse-event record for trace element disorder

15 FDA adverse-event reports reference trace element disorder (VeDDRA 549). See the species, breeds, and drugs most associated with it below.

15
reports citing this reaction
80.0%
death-coded share
Cattle
most-affected species
Ceftiofur Crystalline Free Acid
most-associated drug
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15
Total Reports
12
Deaths
80.0%
Death Rate

Species Most Affected

Cattle 12
Pig 2
Dog 1

Breeds Most Affected

Mixed (Cattle) 5
Cattle (other) 4
Pig (unknown) 2
Holstein-Friesian also known as Holstein 1
Brangus 1
Siberian Husky 1
Aberdeen Angus 1

Associated Drugs

Ceftiofur Crystalline Free Acid 4
Oxytetracycline 2
Bovine Parainfluenza Virus 3 (Ts), Rlb103 (Nl-Bk-6), Mlv; Bovine Respiratory Syn 2
Moxidectin 2
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Mannheimia Haemolytica Toxoid 2
Doramectin 2
Tiamulin 1
Narasin 1
Chlortetracycline Hcl 1
Neomycin 1
Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D-Haemophilus Somnus Bacterin-Toxoid 1
Bovine Respiratory Syncytial Virus, 597-10 10Th Psg Strain 375; Bovine Viral Dia 1
Iron Dextran 1
Fenbendazol Suspension 1
Past Mult / M Haem Cattle Lb 1
Ibr / Pi3 (Orig S-P Us) Lv 1
Ibr/Brsv/P13/Bvd T1, T2(Us) Lv 1
Decoquinate 1
Infectious Bovine Rhinotracheitis Virus(Ts), Rlb 106;Bovine Parainfluenza Virus 1
Bovine Viral Diarrhea Virus, Type 2, Strain 53637, Lot Bvd2Mlv-D;Bovine Viral Di 1

Trace element disorder Reaction Insights

15 reports name Trace element disorder; 12 recorded a death outcome (80.0% of reported events, not a population-level mortality rate). VeDDRA code: 549.

By species: Cattle (12 reports), Pig (2 reports), Dog (1 reports). By breed: Mixed (Cattle) (5), Cattle (other) (4), Pig (unknown) (2).

Most co-reported drugs: Ceftiofur Crystalline Free Acid (4 reports), Oxytetracycline (2 reports), Bovine Parainfluenza Virus 3 (Ts), Rlb103 (Nl-Bk-6), Mlv; Bovine Respiratory Syn (2 reports), Moxidectin (2 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.