Reaction profile

The FDA adverse-event record for respiratory tract irritation

16 FDA adverse-event reports reference respiratory tract irritation (VeDDRA 1728). See the species, breeds, and drugs most associated with it below.

16
reports citing this reaction
0.0%
death-coded share
Human
most-affected species
Imidacloprid + Moxidectin
most-associated drug
Verify with FDA CVM →
16
Total Reports
0
Deaths
0.0%
Death Rate

Species Most Affected

Human 10
Dog 4
Turkey 1
Cat 1

Breeds Most Affected

Unknown 10
Turkey (unknown) 1
Retriever - Chesapeake Bay 1
Himalayan 1
Dog (unknown) 1
Bulldog 1
Crossbred Canine/dog 1

Associated Drugs

Imidacloprid + Moxidectin 5
Tylosin 1
Phenylpropanolamine Hcl 1
Maropitant Citrate 1
Marbofloxacin 1
Amoxicillin Trihydrate; Clavulanate Potassium ( K-Clavulanate) 1
Selamectin 1
Glycerol + Nicotine + Propylene Glycol 1
Copper Naphthenate 1
Fluralaner Spot-On Solution 1
Fluralaner Chew Tablets 1
Moxidectin 1
Grapiprant 1
Milbemycin Oxime + Lufenuron 1
Neomycin Sulfate;Tetracaine Hydrochloride 1
Pimobendan 1

Respiratory tract irritation Reaction Insights

16 reports name Respiratory tract irritation; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). VeDDRA code: 1728.

By species: Human (10 reports), Dog (4 reports), Turkey (1 reports). By breed: Unknown (10), Turkey (unknown) (1), Retriever - Chesapeake Bay (1).

Most co-reported drugs: Imidacloprid + Moxidectin (5 reports), Tylosin (1 reports), Phenylpropanolamine Hcl (1 reports), Maropitant Citrate (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.