Reaction profile

The FDA adverse-event record for pulmonary metastases

26 FDA adverse-event reports reference pulmonary metastases (VeDDRA 2369). See the species, breeds, and drugs most associated with it below.

26
reports citing this reaction
65.4%
death-coded share
Dog
most-affected species
Bedinvetmab
most-associated drug
Verify with FDA CVM →
26
Total Reports
17
Deaths
65.4%
Death Rate

Species Most Affected

Dog 19
Cat 7

Breeds Most Affected

Crossbred Canine/dog 4
Domestic Shorthair 3
Spaniel - King Charles Cavalier 2
Spaniel - Springer English 2
Domestic Mediumhair 2
Maltese 2
Collie (unspecified) 1
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1
Coonhound - Treeing Walker 1
Beagle 1

Associated Drugs

Bedinvetmab 9
Gabapentin 8
Cefovecin 5
Grapiprant 4
Pimobendan 4
Maropitant Citrate 4
Liver Supplement 4
Oclacitinib Maleate 3
Toceranib Phosphate 3
Hydromorphone 3
Ropivacaine 3
Trilostane 3
Cosyntropin 3
Spironolactone 3
Furosemide 3
Codeine 2
Joint Supplement 2
Melarsomine Dihydrochloride 2
Galliprant 2
Feline Leukemia Virus, Kawakami-Theilen 2

Pulmonary metastases Reaction Insights

26 reports name Pulmonary metastases; 17 recorded a death outcome (65.4% of reported events, not a population-level mortality rate). VeDDRA code: 2369.

By species: Dog (19 reports), Cat (7 reports). By breed: Crossbred Canine/dog (4), Domestic Shorthair (3), Spaniel - King Charles Cavalier (2).

Most co-reported drugs: Bedinvetmab (9 reports), Gabapentin (8 reports), Cefovecin (5 reports), Grapiprant (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.