Reaction profile

The FDA adverse-event record for nt - chronic (broncho)pneumonia/pleuropneumonia

20 FDA adverse-event reports reference nt - chronic (broncho)pneumonia/pleuropneumonia (VeDDRA 2296). See the species, breeds, and drugs most associated with it below.

20
reports citing this reaction
95.0%
death-coded share
Cattle
most-affected species
Gamithromycin
most-associated drug
Verify with FDA CVM →
20
Total Reports
19
Deaths
95.0%
Death Rate

Species Most Affected

Cattle 18
Cat 1
Dog 1

Breeds Most Affected

Cattle (unknown) 8
Cattle (other) 5
Mixed (Cattle) 3
Holstein-Friesian also known as Holstein 2
Domestic Shorthair 1
Retriever - Labrador 1

Associated Drugs

Gamithromycin 6
Ceftiofur Crystalline Free Acid 4
Tulathromycin 4
Oxfendazole 4
Tylosin Phosphate 4
Moxidectin 4
Bovine Respiratory Syncytial Virus, 597-10 10Th Psg Strain 375; Bovine Viral Dia 3
Monensin Sodium 3
Tilmicosin 3
Estradiol + Trenbolone 3
Dinoprost Tromethamine 3
Bovine Parainfluenza Virus 3 (Ts), Rlb103 (Nl-Bk-6), Mlv; Bovine Respiratory Syn 2
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine 2
Mannheimia Haemolytica Bacterial Extract-Toxoid 2
Clostridium Chauvoei, Strain F, Lot No. 2-84; Clostridium Novyi, 8296, Kb; Clost 1
Oxytetracycline Dihydrate (Oxytetracycline Amphoteric) 1
Multi-Vitamin 1
Bovine Parainfluenza Virus 3, Reisinger(Nl-Bk-6), Mlv; Bovine Respiratory Syncyt 1
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Mannheimia Haemolytica Toxoid 1
Clostridium Perfringens Types C And D Toxoid 1

NT - chronic (broncho)pneumonia/pleuropneumonia Reaction Insights

20 reports name NT - chronic (broncho)pneumonia/pleuropneumonia; 19 recorded a death outcome (95.0% of reported events, not a population-level mortality rate). VeDDRA code: 2296.

By species: Cattle (18 reports), Cat (1 reports), Dog (1 reports). By breed: Cattle (unknown) (8), Cattle (other) (5), Mixed (Cattle) (3).

Most co-reported drugs: Gamithromycin (6 reports), Ceftiofur Crystalline Free Acid (4 reports), Tulathromycin (4 reports), Oxfendazole (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.