Reaction profile

The FDA adverse-event record for facial swelling (see also skin)

1,517 FDA adverse-event reports reference facial swelling (see also skin) (VeDDRA 517). See the species, breeds, and drugs most associated with it below.

1,517
reports citing this reaction
2.1%
death-coded share
Dog
most-affected species
Moxidectin
most-associated drug
Verify with FDA CVM →
1,517
Total Reports
32
Deaths
2.1%
Death Rate

Species Most Affected

Dog 1,415
Cat 88
Human 5
Horse 4
Cattle 3
Ferret 1
Donkey 1

Breeds Most Affected

Retriever - Labrador 144
Terrier - Bull - American Pit 112
Chihuahua 96
Crossbred Canine/dog 89
Retriever - Golden 66
Bulldog - French 66
Domestic Shorthair 56
Boxer (German Boxer) 50
Dachshund (unspecified) 46
Terrier - Boston 43

Associated Drugs

Moxidectin 677
Rabies Virus, Kv 196
Leptospira Canicola L-15 Strain C-51;Leptospira Grippotyphosa 1550 Lot 10005 Str 131
Maropitant Citrate 129
Bordetella Bronchiseptica 92B 012992-7 Strain Boehringer Ingelheim 108
Diphenhydramine 94
Rabies Vaccine 91
Pyrantel Pamoate;Sarolaner 88
Anti-Il31 Mab Mcs Lot #1283563 77
Bedinvetmab 76
Canine Adenovirus Type 2, Strain Manhattan, 12-13-76;Canine Distemper Virus, Str 75
Oclacitinib Maleate 71
Canine Influenza Virus H3N2;Canine Influenza Virus H3N8 52
Carprofen 48
Prednisone 48
Lotilaner 48
Milbemycin Oxime + Praziquantel 47
Melarsomine Dihydrochloride 47
Bordetella Vaccine 44
Afoxolaner 41

Facial swelling (see also Skin) Reaction Insights

1,517 reports name Facial swelling (see also Skin); 32 recorded a death outcome (2.1% of reported events, not a population-level mortality rate). VeDDRA code: 517.

By species: Dog (1,415 reports), Cat (88 reports), Human (5 reports). By breed: Retriever - Labrador (144), Terrier - Bull - American Pit (112), Chihuahua (96).

Most co-reported drugs: Moxidectin (677 reports), Rabies Virus, Kv (196 reports), Leptospira Canicola L-15 Strain C-51;Leptospira Grippotyphosa 1550 Lot 10005 Str (131 reports), Maropitant Citrate (129 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.