Reaction profile

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

10 FDA adverse-event reports reference suppurative (broncho) pneumonia/pleuropneumonia (VeDDRA 2300). See the species, breeds, and drugs most associated with it below.

10
reports citing this reaction
100.0%
death-coded share
Cattle
most-affected species
Tulathromycin
most-associated drug
Verify with FDA CVM →
10
Total Reports
10
Deaths
100.0%
Death Rate

Species Most Affected

Cattle 10

Breeds Most Affected

Mixed (Cattle) 6
Aberdeen Angus 2
Red Angus 1
Cattle (other) 1

Associated Drugs

Tulathromycin 7
Bovine Parainfluenza 3, Pi3 Ebk-1/Ebht-1 Strain Al-Im;Bovine Respiratory Syncyti 4
Infectious Bovine Rhinotracheitis Virus(Ts), Rlb 106;Bovine Parainfluenza Virus 2
Florfenicol/Flunixin Inj-Triac 1
Dexamethasone 1
Enrofloxacin 1
Ibr, Bvd Cp Type1, Ncp Type 1 And 2, Pi3, Brsv, Killed Virus 1
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine 1
Mannheimia Haemolytica Bacterial Extract-Toxoid 1
Florfenicol 1
Fenbendazole 1
Clostridium Chauvoei + Septicum + Haemolyticum + Novyi + Sordelli + Tetani + Perfringens Types C And D Bacterin-Toxoid 1
Ketoprofen;Tulathromycin 1
Ceftiofur Crystalline Free Acid 1
Monensin Sodium 1
Lubabegron Fumarate 1
Clostridium Chauvoei, Strain F, Lot No. 2-84;Clostridium Novyi, 8296 1
Bovine Viral Diarrhea Virus, Type 1, Strain Nadl-Sbvd, Msvx+1;Bovine Viral Diarr 1

Suppurative (broncho) pneumonia/pleuropneumonia Reaction Insights

10 reports name Suppurative (broncho) pneumonia/pleuropneumonia; 10 recorded a death outcome (100.0% of reported events, not a population-level mortality rate). VeDDRA code: 2300.

By species: Cattle (10 reports). By breed: Mixed (Cattle) (6), Aberdeen Angus (2), Red Angus (1).

Most co-reported drugs: Tulathromycin (7 reports), Bovine Parainfluenza 3, Pi3 Ebk-1/Ebht-1 Strain Al-Im;Bovine Respiratory Syncyti (4 reports), Infectious Bovine Rhinotracheitis Virus(Ts), Rlb 106;Bovine Parainfluenza Virus (2 reports), Florfenicol/Flunixin Inj-Triac (1 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.