Reaction profile

The FDA adverse-event record for wound

1,048 FDA reports name wound, a high-volume reaction in the CVM extract (VeDDRA 2593). Plate stamps and neighbourhood peers follow.

#382 of 2,481
by report volume (all reactions)
1,048
reports citing this reaction
8.6%
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. Wound has 1,048 reports now versus 1,005 in that prior snapshot: 43 more (4.3%).

Report change
+43
Death-coded reports
+1
Death-coded share
−0.3 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 Wound changes

FDA AER · VeDDRA plate

Code 2593 VOL-MID

VOL-MID · DEATH-PAR · UPPER-Q · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-MID 1,048 reports
  • DEATH-PAR 8.6%
  • UPPER-Q #382/2481
  • PHOTO-FINISH Licking at applicatio…
  • SPECIES-DOG Dog · 759
  • DRUG-LEAD Tigilanol Tiglate · 401
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Licking at application site (±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 Wound

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

Vomiting · highest174348Elevated creatine-kin… · near1053Discoloured urine · near1051Eye redness · near1050Licking at applicatio… · near1049Wound · this reaction1048Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Wound

What the FDA AER plate says about Wound

Signature read: 1,048 reports place Wound in the upper third of FDA AER volume (#382 of 2,481). Report volume is upper-third scale: 1,048 named reports in the openFDA extract. 90 of 1,048 reports were death-coded (8.6% of named reports, not a population mortality rate). Nearest volume peer: Licking at application site (±1 reports). Lead species Dog (759). Lead co-reported drug Tigilanol Tiglate (401).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Tigilanol Tiglate 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 759
Cat 256
Human 18
Horse 6
Cattle 3
Pig 2
Other Rodents 1
Other 1
Unknown 1
Chicken 1

Breeds Most Affected

Domestic Shorthair 163
Retriever - Labrador 85
Dog (unknown) 62
Boxer (German Boxer) 58
Pit Bull 55
Retriever - Golden 37
Shepherd Dog - German 33
Crossbred Canine/dog 32
Bulldog - French 28
Domestic Longhair 26

Associated Drugs

Tigilanol Tiglate 401
Frunevetmab 127
Gabapentin 106
Diphenhydramine 93
Prednisone 83
Maropitant Citrate 72
Famotidine 72
Butorphanol 70
Dexmedetomidine 60
Carprofen 46
Oclacitinib Maleate 44
Milbemycin Oxime + Praziquantel 42
Bedinvetmab 42
Atipamezole 41
Cefovecin 36
Propofol 36
Buprenorphine 34
Trilostane 29
Isoflurane 29
Milbemycin Oxime + Spinosad 28

Nationwide reactions with similar profiles

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

Similar death-coded share

Nearest other reactions by death-coded share (8.6% 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 Wound (#382 of 2,481 by report volume); death-coded 8.6%. PlainBreed reaction plate · report volume stamp 1,048 · 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 →