Reaction profile

The FDA adverse-event record for skin oedema

196 FDA adverse-event reports reference skin oedema (VeDDRA 968). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1050 of 2,481
by report volume (all reactions)
196
reports citing this reaction
18.4%
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 oedema has 196 reports now versus 195 in that prior snapshot: 1 more (0.5%).

Report change
+1
Death-coded reports
+1
Death-coded share
+0.4 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 oedema changes

FDA AER · VeDDRA plate

Code 968 VOL-LOW

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

  • VOL-LOW 196 reports
  • DEATH-ELEV 18.4%
  • MID-PACK #1050/2481
  • PHOTO-FINISH Burning sensation of…
  • SPECIES-DOG Dog · 143
  • DRUG-LEAD Carprofen · 28
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Burning sensation of eye (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Report-volume neighbourhood around Skin oedema

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Less social · near197Burning sensation of… · near196Localised skin reacti… · near196Skin oedema · this reaction196Disseminated intravas… · near195Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Skin oedema

What the FDA AER plate says about Skin oedema

Signature read: 36 death-coded reports is the most distinctive absolute-outcome stamp on Skin oedema. Report volume sits in the middle third of the reaction corpus. 36 of 196 reports were death-coded (18.4% of named reports, not a population mortality rate). Nearest volume peer: Burning sensation of eye (±0 reports). Lead species Dog (143). Lead co-reported drug Carprofen (28).

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 143
Cat 22
Human 11
Horse 10
Rabbit 8
Cattle 1
Chicken 1

Breeds Most Affected

Retriever - Labrador 20
Domestic Shorthair 14
Unknown 13
Pit Bull 9
Chihuahua 9
Crossbred Canine/dog 8
Boxer (German Boxer) 8
Retriever - Golden 8
Shepherd Dog - German 6
Crossbred rabbit 6

Associated Drugs

Carprofen 28
Meloxicam 21
Tigilanol Tiglate 18
Milbemycin Oxime + Spinosad 16
Maropitant Citrate 16
Prednisone 15
Cefovecin 11
Isoflurane 10
Fluralaner Chew Tablets 10
Unspecified 10
Oclacitinib Maleate 9
Moxidectin 9
Midazolam 9
Butorphanol 8
Gabapentin 8
Dexmedetomidine Hydrochloride 7
Buprenorphine 7
Ketamine Hydrochloride 7
Enrofloxacin 7
Diphenhydramine 7

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Skin oedema, 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 (18.4% 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 oedema (#1050 of 2,481 by report volume); death-coded 18.4%. PlainBreed reaction plate · death-coded report count stamp 36 · 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 →