Reaction profile

The FDA adverse-event record for eye redness

1,050 FDA reports name eye redness, a high-volume reaction in the CVM extract (VeDDRA 457). Plate stamps and neighbourhood peers follow.

#380 of 2,481
by report volume (all reactions)
1,050
reports citing this reaction
3.9%
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 redness has 1,050 reports now versus 1,038 in that prior snapshot: 12 more (1.2%).

Report change
+12
Death-coded reports
+1
Death-coded share
+0.1 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 redness changes

FDA AER · VeDDRA plate

Code 457 VOL-MID

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

  • VOL-MID 1,050 reports
  • DEATH-LOW 3.9%
  • UPPER-Q #380/2481
  • PHOTO-FINISH Discoloured urine
  • SPECIES-DOG Dog · 748
  • DRUG-LEAD Milbemycin Oxime… · 128
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Discoloured urine (±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 Eye redness

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

Vomiting · highest174348Elevated creatine-kin… · near1053Discoloured urine · near1051Eye redness · this reaction1050Licking at applicatio… · near1049Wound · near1048Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Eye redness

Eye redness: low death-coded share in the FDA AER plate

Signature read: 1,050 reports place Eye redness in the upper third of FDA AER volume (#380 of 2,481). Report volume is upper-third scale: 1,050 named reports in the openFDA extract. Death-coded share is lower-third: 41 of 1,050 reports (3.9% of named reports). Nearest volume peer: Discoloured urine (±1 reports). Lead species Dog (748). Lead co-reported drug Milbemycin Oxime + Spinosad (128).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Milbemycin Oxime + Spinosad 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 748
Human 209
Cat 88
Horse 2
Cattle 2
Goat 1

Breeds Most Affected

Unknown 210
Retriever - Labrador 59
Crossbred Canine/dog 59
Domestic Shorthair 43
Boxer (German Boxer) 40
Shih Tzu 35
Chihuahua 31
Pit Bull 27
Retriever - Golden 26
Dachshund (unspecified) 23

Associated Drugs

Milbemycin Oxime + Spinosad 128
Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 77
Moxidectin 68
Imidacloprid + Moxidectin 47
Selamectin 41
Carprofen 40
Spinosad 38
Maropitant Citrate 38
Meloxicam 27
Enrofloxacin 26
Oclacitinib Maleate 26
Cyclosporine 22
Prednisone 22
Pyrantel Pamoate;Sarolaner 22
Afoxolaner 20
Cefovecin 17
Pilocarpine 15
Buprenorphine 14
Ivermectin 13
Trilostane 13

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Eye redness, 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 (1,050 here).

Similar death-coded share

Nearest other reactions by death-coded share (3.9% 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 redness (#380 of 2,481 by report volume); death-coded 3.9%. PlainBreed reaction plate · report volume stamp 1,050 · 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 →