Reaction profile

The FDA adverse-event record for sticky eye

Name: Sticky eye - FDA Animal Adverse Reaction
Creator: PlainBreed
License: https://open.fda.gov/license/

20 FDA reports name sticky eye, a lower-volume reaction in the CVM extract (VeDDRA 1791). Plate stamps and neighbourhood peers follow.

#2174 of 2,481
by report volume (all reactions): 20
reports citing this reaction: 15.0%
death-coded share: Dog
most-affected species

Compiled by PlainBreed

Verify with FDA CVM →

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. Sticky eye has 20 reports now versus 19 in that prior snapshot: 1 more (5.3%).

Report change: +1
Death-coded reports: +0
Death-coded share: −0.8 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 Sticky eye changes

FDA AER · VeDDRA plate

Code 1791 VOL-TRACE

VOL-TRACE · DEATH-ELEV · LOWER-Q · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

VOL-TRACE 20 reports
DEATH-ELEV 15.0%
LOWER-Q #2174/2481
PHOTO-FINISH Agalactia
SPECIES-DOG Dog · 15
DRUG-LEAD Enrofloxacin · 5
DESK-WIDE 16 breeds
BOOK-FULL 8/8 fields

Nearest volume peer: Agalactia (±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.

Lower-volume neighbourhood around Sticky eye

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

FDA AER report volume · neighbourhood around Sticky eye

What the FDA AER plate says about Sticky eye

Signature read: 20 reports place Sticky eye in the lower third of FDA AER volume (#2174 of 2,481). Report volume is lower-third scale: 20 named reports in the openFDA extract. 3 of 20 reports were death-coded (15.0% of named reports, not a population mortality rate). Nearest volume peer: Agalactia (±0 reports). Lead species Dog (15). Lead co-reported drug Enrofloxacin (5).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Enrofloxacin 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 15

Cat 3

Pig 2

Breeds Most Affected

Shih Tzu 2

Cat (unknown) 2

Spaniel (unspecified) 2

Dog (other) 2

Siberian Husky 1

Domestic Longhair 1

Poodle - Standard 1

Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1

Terrier - Yorkshire 1

Poodle - Toy 1

Associated Drugs

Enrofloxacin 5

Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 4

Doxycycline 3

Milbemycin/Lufenuron Tablets 3

Cefovecin 2

Grapiprant 2

Bordetella Vaccine 2

Canine Leptospirosis Vaccine 2

Ear Cleanser 2

Dexamethasone Sodium Phosphate 2

Cefpodoxime 2

Carprofen 2

Tacrolimus Ointment 2

Eye Medication (Unknown) 2

Ofloxacin 2

Tobramycin 2

Tylosin 2

Porcine Reproductive And Respiratory Syndrome Virus, Sd11-21 Strain 2

Bordetella Bronchiseptica, Field Strain,Erysipelothrix Rhusiopathiae, Se-9 Strain,Pasteurella Multocida, 169 Strain,Pasteurella Multocida, Type D, Atcc 12948 Strain 2

Iron 2

What to do with this reaction

Read how death-coded share differs from a mortality rate before drawing conclusions. Understanding adverse events
Browse the full reaction directory to compare report counts across reaction types. All reactions

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 Sticky eye (#2174 of 2,481 by report volume); death-coded 15.0%. PlainBreed reaction plate · report volume stamp 20 · 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 →