Reaction profile

The FDA adverse-event record for cellulitis

355 FDA adverse-event reports reference cellulitis (VeDDRA 970). See the species, breeds, and drugs most associated with it below.

355
reports citing this reaction
18.6%
death-coded share
Dog
most-affected species
Carprofen
most-associated drug
Verify with FDA CVM →
355
Total Reports
66
Deaths
18.6%
Death Rate

Species Most Affected

Dog 254
Cat 38
Horse 33
Cattle 16
Human 6
Rabbit 5
Goat 1
Sheep 1
Other 1

Breeds Most Affected

Retriever - Labrador 44
Domestic Shorthair 23
Terrier - Bull - American Pit 14
Boxer (German Boxer) 11
Pit Bull 11
Retriever - Golden 11
Bulldog - French 11
Shepherd Dog - German 10
Unknown 10
Crossbred Canine/dog 10

Associated Drugs

Carprofen 55
Tigilanol Tiglate 37
Maropitant Citrate 36
Moxidectin 33
Gabapentin 29
Prednisone 26
Oclacitinib Maleate 25
Meloxicam 22
Buprenorphine 22
Cefovecin 21
Diphenhydramine 18
Famotidine 17
Bedinvetmab 17
Enrofloxacin 16
Dexamethasone 15
Butorphanol 14
Diphenhydramine Hcl 13
Dexmedetomidine Hydrochloride 12
Tramadol 10
Ketamine 10

Cellulitis Reaction Insights

355 reports name Cellulitis; 66 recorded a death outcome (18.6% of reported events, not a population-level mortality rate). VeDDRA code: 970.

By species: Dog (254 reports), Cat (38 reports), Horse (33 reports). By breed: Retriever - Labrador (44), Domestic Shorthair (23), Terrier - Bull - American Pit (14).

Most co-reported drugs: Carprofen (55 reports), Tigilanol Tiglate (37 reports), Maropitant Citrate (36 reports), Moxidectin (33 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.