Reaction profile

The FDA adverse-event record for ecchymosis

430 FDA reports name ecchymosis, a high-volume reaction in the CVM extract (VeDDRA 2038). Plate stamps and neighbourhood peers follow.

#696 of 2,481
by report volume (all reactions)
430
reports citing this reaction
33.7%
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. Ecchymosis has 430 reports now versus 423 in that prior snapshot: 7 more (1.7%).

Report change
+7
Death-coded reports
+3
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 Ecchymosis changes

FDA AER · VeDDRA plate

Code 2038 VOL-LOW

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

  • VOL-LOW 430 reports
  • DEATH-HOT 33.7%
  • MID-PACK #696/2481
  • PHOTO-FINISH External ear disorder…
  • SPECIES-DOG Dog · 363
  • DRUG-LEAD Carprofen · 74
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: External ear disorder NOS (±0 reports)

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

High-volume neighbourhood around Ecchymosis

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

Vomiting · highest174348Dermal cyst(s) · near433Erythematous rash · near432Food refusal · near431Ecchymosis · this reaction430External ear disorder… · near430Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Ecchymosis

Ecchymosis: high death-coded share in the FDA AER plate

Signature read: 145 death-coded reports is a heavy tail count for Ecchymosis in the CVM extract. Report volume is upper-third scale: 430 named reports in the openFDA extract. Death-coded share is upper-third: 145 of 430 reports (33.7% of named reports). Nearest volume peer: External ear disorder NOS (±0 reports). Lead species Dog (363). Lead co-reported drug Carprofen (74).

Read these counts as reporting volume, not risk: per our methodology, A high death-coded share in FDA filings does not prove causation; co-reporting is voluntary temporal association only. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 363
Cat 34
Human 29
Cattle 2
Horse 1
Other Birds 1

Breeds Most Affected

Crossbred Canine/dog 37
Retriever - Labrador 31
Unknown 30
Chihuahua 18
Maltese 18
Retriever - Golden 15
Domestic (unspecified) 13
Dachshund (unspecified) 13
Poodle (unspecified) 12
Terrier - Yorkshire 10

Associated Drugs

Carprofen 74
Maropitant Citrate 35
Meloxicam 31
Moxidectin 30
Prednisone 24
Doxycycline 21
Bedinvetmab 20
Milbemycin Oxime + Spinosad 19
Cefovecin 18
Deracoxib 15
Cefpodoxime Proxetil 15
Oclacitinib Maleate 15
Cefovecin Sodium 14
Metronidazole 14
Dexamethasone 13
Enrofloxacin 13
Trilostane 11
Sucralfate 11
Famotidine 11
Diphenhydramine 11

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Ecchymosis, 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 (430 here).

Similar death-coded share

Nearest other reactions by death-coded share (33.7% 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 Ecchymosis (#696 of 2,481 by report volume); death-coded 33.7%. PlainBreed reaction plate · death-coded report count stamp 145 · 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 →