Reaction profile

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

18 FDA adverse-event reports reference fibrinous (broncho) pneumonia/fibrinous pleuropneumonia (VeDDRA 2298). See the species, breeds, and drugs most associated with it below.

18
reports citing this reaction
100.0%
death-coded share
Cattle
most-affected species
Tulathromycin
most-associated drug
Verify with FDA CVM →
18
Total Reports
18
Deaths
100.0%
Death Rate

Species Most Affected

Cattle 16
Dog 2

Breeds Most Affected

Mixed (Cattle) 6
Aberdeen Angus 4
Cattle (other) 3
Cattle (unknown) 2
Red Angus 1
Crossbred Canine/dog 1
Terrier (unspecified) 1

Associated Drugs

Tulathromycin 8
Ceftiofur Crystalline Free Acid 6
Enrofloxacin 5
Florfenicol 4
Infectious Bovine Rhinotracheitis Virus(Ts), Rlb 106;Bovine Parainfluenza Virus 4
Ketoprofen;Tulathromycin 3
Bovine Parainfluenza 3, Pi3 Ebk-1/Ebht-1 Strain Al-Im;Bovine Respiratory Syncyti 3
Fenbendazol Suspension 2
Tulathromycin Inj Sol 2
Monensin Sodium 2
Ibr, Bvd1_2, Pi3,Brsv, Mh, Pm 2
Florfenicol And Flunixen Meglumine 2
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
Fenbendazole 1
Clostridium Chauvoei + Septicum + Haemolyticum + Novyi + Sordelli + Tetani + Perfringens Types C And D Bacterin-Toxoid 1
Clostr Perf*2/Clos Others*4 Kb 1
Ibr, Pi3, Bvd, Manheimia, Pasutrella 1
Pasteurella, Manheimia, Histophilus 1

Fibrinous (broncho) pneumonia/fibrinous pleuropneumonia Reaction Insights

18 reports name Fibrinous (broncho) pneumonia/fibrinous pleuropneumonia; 18 recorded a death outcome (100.0% of reported events, not a population-level mortality rate). VeDDRA code: 2298.

By species: Cattle (16 reports), Dog (2 reports). By breed: Mixed (Cattle) (6), Aberdeen Angus (4), Cattle (other) (3).

Most co-reported drugs: Tulathromycin (8 reports), Ceftiofur Crystalline Free Acid (6 reports), Enrofloxacin (5 reports), Florfenicol (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.