Reaction profile

The FDA adverse-event record for pleuritis

31 FDA adverse-event reports reference pleuritis (VeDDRA 892). See the species, breeds, and drugs most associated with it below.

31
reports citing this reaction
100.0%
death-coded share
Cattle
most-affected species
Tulathromycin
most-associated drug
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31
Total Reports
31
Deaths
100.0%
Death Rate

Species Most Affected

Cattle 18
Pig 4
Cat 4
Dog 4
Mouse 1

Breeds Most Affected

Cattle (other) 9
Domestic Shorthair 4
Crossbred Bovine/Cattle 2
Aberdeen Angus 2
Mixed (Cattle) 2
Pig (unknown) 2
Holstein-Friesian also known as Holstein 2
Commercial hybrid 1
Boxer (German Boxer) 1
Cattle (unknown) 1

Associated Drugs

Tulathromycin 8
Monensin Sodium 5
Moxidectin 5
Bovine Respiratory Syncytial Virus, 597-10 10Th Psg Strain 375; Bovine Viral Dia 4
Bovine Parainfluenza Virus 3 (Ts), Rlb103 (Nl-Bk-6), Mlv; Bovine Respiratory Syn 3
Ceftiofur Crystalline Free Acid 3
Meloxicam 3
Tylosin Phosphate 2
Bovine Parainfluenza Virus 3, Reisinger(Nl-Bk-6), Mlv; Bovine Respiratory Syncyt 2
Cefovecin 2
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Mannheimia Haemolytica Toxoid 2
Narasin 2
Isoflurane 2
Buprenorphine 2
Tilmicosin Phosphate 1
Tiamulin Hydrogen Fumarate 1
Pasteurella Multocida Bacterial Extract, Mannheimia Haemolytica Toxoid 1
Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C & D-Haemophilus Somnus Bacterin-Toxoid 1
Bovine Rhinotracheitis Virus Diarrhea Pi3 Rsv Vaccine, Ml & Kv 1
Doramectin 1

Pleuritis Reaction Insights

31 reports name Pleuritis; 31 recorded a death outcome (100.0% of reported events, not a population-level mortality rate). VeDDRA code: 892.

By species: Cattle (18 reports), Pig (4 reports), Cat (4 reports). By breed: Cattle (other) (9), Domestic Shorthair (4), Crossbred Bovine/Cattle (2).

Most co-reported drugs: Tulathromycin (8 reports), Monensin Sodium (5 reports), Moxidectin (5 reports), Bovine Respiratory Syncytial Virus, 597-10 10Th Psg Strain 375; Bovine Viral Dia (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.