Reaction profile

The FDA adverse-event record for eye haemorrhage

119 FDA adverse-event reports reference eye haemorrhage (VeDDRA 1099). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1308 of 2,481
by report volume (all reactions)
119
reports citing this reaction
33.6%
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. Eye haemorrhage has 119 reports now versus 119 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
Death-coded reports
+0
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 Eye haemorrhage changes

FDA AER · VeDDRA plate

Code 1099 VOL-LOW

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

  • VOL-LOW 119 reports
  • DEATH-HOT 33.6%
  • MID-PACK #1308/2481
  • PHOTO-FINISH Dry heaving
  • SPECIES-DOG Dog · 100
  • DRUG-LEAD Carprofen · 18
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Dry heaving (±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.

Report-volume neighbourhood around Eye haemorrhage

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

Vomiting · highest174348Dry heaving · near119Elevated betahydroxyb… · near119Eye haemorrhage · this react…119Mixed Product Strength · near119Papular rash · near119Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Eye haemorrhage

Eye haemorrhage: high death-coded share in the FDA AER plate

Signature read: Eye haemorrhage's 33.6% death-coded share is among the highest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is upper-third: 40 of 119 reports (33.6% of named reports). Nearest volume peer: Dry heaving (±0 reports). Lead species Dog (100). Lead co-reported drug Carprofen (18).

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 100
Cat 17
Cattle 1
Human 1

Breeds Most Affected

Retriever - Labrador 19
Crossbred Canine/dog 10
Domestic Shorthair 8
Retriever - Golden 6
Terrier - Rat 5
Domestic (unspecified) 4
Siberian Husky 4
Collie - Border 4
Spaniel - Cocker American 3
Boxer (German Boxer) 3

Associated Drugs

Carprofen 18
Maropitant Citrate 13
Enrofloxacin 12
Prednisone 10
Milbemycin Oxime + Spinosad 10
Tramadol 9
Cefovecin 9
Fluids 9
Spinosad 7
Moxidectin 7
Gabapentin 7
Cyclosporine 6
Buprenorphine 5
Atropine 5
Doxycycline 5
Famotidine 5
Oclacitinib Maleate 5
Ofloxacin 5
Cefpodoxime Proxetil 4
Dexamethasone 4

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Eye haemorrhage, 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 (119 here).

Similar death-coded share

Nearest other reactions by death-coded share (33.6% 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 Eye haemorrhage (#1308 of 2,481 by report volume); death-coded 33.6%. PlainBreed reaction plate · death-coded share stamp 33.6% · 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 →