Reaction profile

The FDA adverse-event record for lipoma

363 FDA reports name lipoma, a high-volume reaction in the CVM extract (VeDDRA 2062). Plate stamps and neighbourhood peers follow.

#789 of 2,481
by report volume (all reactions)
363
reports citing this reaction
15.4%
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. Lipoma has 363 reports now versus 353 in that prior snapshot: 10 more (2.8%).

Report change
+10
Death-coded reports
+2
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 Lipoma changes

FDA AER · VeDDRA plate

Code 2062 VOL-LOW

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

  • VOL-LOW 363 reports
  • DEATH-ELEV 15.4%
  • MID-PACK #789/2481
  • PHOTO-FINISH Gut sounds increased
  • SPECIES-DOG Dog · 353
  • DRUG-LEAD Oclacitinib Malea… · 82
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Gut sounds increased (±0 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 Lipoma

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

Vomiting · highest174348Gut sounds increased · near363Head pressing · near363Increased urine conce… · near363Lipoma · this reaction363Paralysis NOS · near363Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Lipoma

What the FDA AER plate says about Lipoma

Signature read: 56 death-coded reports is a heavy tail count for Lipoma in the CVM extract. Report volume is upper-third scale: 363 named reports in the openFDA extract. 56 of 363 reports were death-coded (15.4% of named reports, not a population mortality rate). Nearest volume peer: Gut sounds increased (±0 reports). Lead species Dog (353). Lead co-reported drug Oclacitinib Maleate (82).

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 353
Cat 7
Horse 3

Breeds Most Affected

Retriever - Labrador 74
Crossbred Canine/dog 20
Dog (unknown) 19
Shepherd Dog - Australian 15
Pit Bull 14
Retriever - Golden 13
Beagle 12
Schnauzer - Miniature 12
Terrier - Bull - American Pit 11
Chihuahua 8

Associated Drugs

Oclacitinib Maleate 82
Milbemycin Oxime + Spinosad 63
Gabapentin 28
Afoxolaner 23
Spinosad 19
Trilostane 19
Bedinvetmab 19
Unspecified 19
Prednisone 16
Carprofen 15
Milbemycin Oxime + Praziquantel 15
Milbemycin Oxime 14
Fluralaner Chew Tablets 14
Moxidectin 14
Recombinant Human Insulin 13
Ivermectin 12
Maropitant Citrate 12
Famotidine 11
Grapiprant 10
Diphenhydramine 10

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Lipoma, 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 (363 here).

Similar death-coded share

Nearest other reactions by death-coded share (15.4% 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 Lipoma (#789 of 2,481 by report volume); death-coded 15.4%. PlainBreed reaction plate · death-coded report count stamp 56 · 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 →