Reaction profile

The FDA adverse-event record for positive tracheal pinch

14 FDA adverse-event reports reference positive tracheal pinch (VeDDRA 2585). See the species, breeds, and drugs most associated with it below.

14
reports citing this reaction
7.1%
death-coded share
Dog
most-affected species
Maropitant Citrate
most-associated drug
Verify with FDA CVM →
14
Total Reports
1
Deaths
7.1%
Death Rate

Species Most Affected

Dog 14

Breeds Most Affected

Retriever - Labrador 2
Poodle - Toy 2
Maltese 2
Collie - Border 1
Spaniel - Cocker American 1
Crossbred Canine/dog 1
Shepherd Dog - Australian 1
Beagle 1
Retriever - Golden 1
Terrier - Yorkshire 1

Associated Drugs

Maropitant Citrate 2
Milbemycin Oxime, Lufenuron 2
Fluralaner Chew Tablets 2
Bordetella Bronchiseptica Vaccine, Avirulent Live Culture 2
Doxycycline 2
Rabies Virus, Kv 1
Cefpodoxime Proxetil 1
Bordetella Bronchiseptica, Strain 78-9159, Kb 1
Bordetella Bronchiseptica 92B 012992-7 Strain Boehringer Ingelheim 1
Oclacitinib Maleate 1
Milbemycin Oxime + Spinosad 1
Milbemycin Oxime 1
Spinosad 1
Canine Distemper-Adenovirus Type 2-Parvovirus Vaccine, Modified Live Virus, Leptospira Canicola-Grippotyphosa-Icterohaemorrhagiae-Pomona Bacterial Extract 1
Canine Distemper-Adenovirus Type 2-Parvovirus Vaccine, Modified Live Virus 1
Deracoxib 1
Afoxolaner 1
Milbemycin Oxime + Lufenuron + Praziquantel 1
Trimeprazine Tartrate;Prednisolone 1
Amoxicillin Trihydrate;Clavulanate Potassium ( K-Clavulanate) 1

Positive tracheal pinch Reaction Insights

14 reports name Positive tracheal pinch; 1 recorded a death outcome (7.1% of reported events, not a population-level mortality rate). VeDDRA code: 2585.

By species: Dog (14 reports). By breed: Retriever - Labrador (2), Poodle - Toy (2), Maltese (2).

Most co-reported drugs: Maropitant Citrate (2 reports), Milbemycin Oxime, Lufenuron (2 reports), Fluralaner Chew Tablets (2 reports), Bordetella Bronchiseptica Vaccine, Avirulent Live Culture (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.