Reaction profile

The FDA adverse-event record for eyelid lump

57 FDA reports name eyelid lump, a lower-volume reaction in the CVM extract (VeDDRA 2461). Plate stamps and neighbourhood peers follow.

#1673 of 2,481
by report volume (all reactions)
57
reports citing this reaction
7.0%
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. Eyelid lump has 57 reports now versus 57 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 Eyelid lump changes

FDA AER · VeDDRA plate

Code 2461 VOL-LOW

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

  • VOL-LOW 57 reports
  • DEATH-PAR 7.0%
  • MID-PACK #1673/2481
  • PHOTO-FINISH Atrial fibrillation
  • SPECIES-DOG Dog · 55
  • DRUG-LEAD Oclacitinib Malea… · 14
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Atrial fibrillation (±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 Eyelid lump

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

Vomiting · highest174348Atrial fibrillation · near57Epistaxis (unilateral) · near57Eyelid lump · this reaction57Lack of efficacy (bac… · near57Leucocytosis · near57Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Eyelid lump

Eyelid lump: low death-coded share in the FDA AER plate

Signature read: 4 death-coded reports is a thin tail count for Eyelid lump in the CVM extract. Report volume is lower-third scale: 57 named reports in the openFDA extract. Death-coded share is lower-third: 4 of 57 reports (7.0% of named reports). Nearest volume peer: Atrial fibrillation (±0 reports). Lead species Dog (55). Lead co-reported drug Oclacitinib Maleate (14).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Oclacitinib Maleate 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 55
Cat 2

Breeds Most Affected

Retriever - Labrador 8
Retriever - Golden 4
Beagle 4
Shih Tzu 2
Terrier (unspecified) 2
Terrier - Yorkshire 2
Dog (unknown) 2
Terrier - Bull - American Pit 2
Shepherd Dog - German 2
Terrier - West Highland White 2

Associated Drugs

Oclacitinib Maleate 14
Milbemycin Oxime + Praziquantel 8
Trilostane 6
Carprofen 6
Milbemycin Oxime + Spinosad 5
Fluralaner Chew Tablets 5
Doxycycline 4
Fluralaner 4
Prednisone 3
Insulin Injectable Vial 3
Afoxolaner 3
Canine Distemper-Adenovirus Type 2-Parainfluenza-Parvovirus Vaccine, Modified Live Virus 3
Rabies Vaccine 3
Butorphanol 3
Diphenhydramine Hcl 2
Propofol 2
Anesthetic 2
Cefazolin 2
Microchip 2
Ivermectin + Pyrantel As Pamoate Salt 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Eyelid lump, 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 (7.0% 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 Eyelid lump (#1673 of 2,481 by report volume); death-coded 7.0%. PlainBreed reaction plate · death-coded report count stamp 4 · 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 →