Reaction profile

The FDA adverse-event record for cellulitis

377 FDA reports name cellulitis, a high-volume reaction in the CVM extract (VeDDRA 970). Plate stamps and neighbourhood peers follow.

#763 of 2,481
by report volume (all reactions)
377
reports citing this reaction
18.3%
death-coded share
Dog
most-affected species

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Cellulitis has 377 reports now versus 367 in that prior snapshot: 10 more (2.7%).

Report change
+10
Death-coded reports
+1
Death-coded share
−0.2 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Cellulitis changes

FDA AER · VeDDRA plate

Code 970 VOL-LOW

VOL-LOW · DEATH-ELEV · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-LOW 377 reports
  • DEATH-ELEV 18.3%
  • MID-PACK #763/2481
  • PHOTO-FINISH Abnormal test result
  • SPECIES-DOG Dog · 267
  • DRUG-LEAD Carprofen · 59
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Abnormal test result (±0 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Cellulitis

Upper-third volume poles plus nearest peers, not a full reaction corpus board reprint.

Vomiting · highest174348Increased drinking · near378Abnormal test result · near377Cellulitis · this reaction377Residues in milk · near377Weight fluctuation · near377Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Cellulitis

What the FDA AER plate says about Cellulitis

Signature read: 69 death-coded reports is a heavy tail count for Cellulitis in the CVM extract. Report volume is upper-third scale: 377 named reports in the openFDA extract. 69 of 377 reports were death-coded (18.3% of named reports, not a population mortality rate). Nearest volume peer: Abnormal test result (±0 reports). Lead species Dog (267). Lead co-reported drug Carprofen (59).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Carprofen appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 267
Cat 40
Horse 38
Cattle 18
Human 6
Rabbit 5
Goat 1
Sheep 1
Other 1

Breeds Most Affected

Retriever - Labrador 47
Domestic Shorthair 23
Terrier - Bull - American Pit 14
Boxer (German Boxer) 12
Shepherd Dog - German 12
Retriever - Golden 12
Bulldog - French 12
Pit Bull 11
Unknown 11
Crossbred Canine/dog 10

Associated Drugs

Carprofen 59
Maropitant Citrate 43
Tigilanol Tiglate 39
Gabapentin 37
Moxidectin 33
Prednisone 30
Oclacitinib Maleate 29
Buprenorphine 25
Meloxicam 22
Cefovecin 22
Famotidine 22
Diphenhydramine 20
Enrofloxacin 18
Butorphanol 17
Bedinvetmab 17
Dexamethasone 15
Dexmedetomidine Hydrochloride 14
Diphenhydramine Hcl 13
Ceftiofur Crystalline Free Acid 12
Ketamine 12

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Cellulitis, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

Similar report volume

Nearest other reactions by FDA report count (377 here).

Similar death-coded share

Nearest other reactions by death-coded share (18.3% here), distinct from the volume row.

What to do with this reaction

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Cellulitis (#763 of 2,481 by report volume); death-coded 18.3%. PlainBreed reaction plate · death-coded report count stamp 69 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →