Reaction profile

The FDA adverse-event record for skin necrosis

395 FDA reports name skin necrosis, a high-volume reaction in the CVM extract (VeDDRA 967). Plate stamps and neighbourhood peers follow.

#735 of 2,481
by report volume (all reactions)
395
reports citing this reaction
17.5%
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. Skin necrosis has 395 reports now versus 390 in that prior snapshot: 5 more (1.3%).

Report change
+5
Death-coded reports
+1
Death-coded share
+0.0 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 Skin necrosis changes

FDA AER · VeDDRA plate

Code 967 VOL-LOW

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

  • VOL-LOW 395 reports
  • DEATH-ELEV 17.5%
  • MID-PACK #735/2481
  • PHOTO-FINISH Corneal disorder NOS
  • SPECIES-DOG Dog · 311
  • DRUG-LEAD Carprofen · 84
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Corneal disorder NOS (±1 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 Skin necrosis

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

Vomiting · highest174348Corneal disorder NOS · near396Hearing decreased · near396Lumbar pain · near396Skin necrosis · this reaction395Mast cell tumour · near394Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Skin necrosis

What the FDA AER plate says about Skin necrosis

Signature read: 69 death-coded reports is a heavy tail count for Skin necrosis in the CVM extract. Report volume is upper-third scale: 395 named reports in the openFDA extract. 69 of 395 reports were death-coded (17.5% of named reports, not a population mortality rate). Nearest volume peer: Corneal disorder NOS (±1 reports). Lead species Dog (311). Lead co-reported drug Carprofen (84).

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 311
Cat 67
Horse 8
Pig 3
Cattle 2
Rabbit 2
Other 1
Chicken 1

Breeds Most Affected

Domestic Shorthair 32
Dog (unknown) 24
Retriever - Labrador 23
Crossbred Canine/dog 20
Chihuahua 15
Dachshund (unspecified) 13
Shepherd Dog - German 12
Boxer (German Boxer) 12
Retriever - Golden 8
Terrier - Boston 8

Associated Drugs

Carprofen 84
Tigilanol Tiglate 52
Cefovecin 48
Maropitant Citrate 47
Meloxicam 32
Enrofloxacin 27
Buprenorphine 27
Gabapentin 27
Isoflurane 23
Butorphanol 22
Prednisone 22
Dexmedetomidine Hydrochloride 18
Diphenhydramine 18
Tramadol 18
Propofol 17
Famotidine 15
Oclacitinib Maleate 15
Anesthetic 13
Moxidectin 12
Unspecified 12

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Skin necrosis, 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 (395 here).

Similar death-coded share

Nearest other reactions by death-coded share (17.5% 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 Skin necrosis (#735 of 2,481 by report volume); death-coded 17.5%. 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 →