Reaction profile

The FDA adverse-event record for abdominal mass

633 FDA reports name abdominal mass, a high-volume reaction in the CVM extract (VeDDRA 2277). Plate stamps and neighbourhood peers follow.

#555 of 2,481
by report volume (all reactions)
633
reports citing this reaction
57.7%
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. Abdominal mass has 633 reports now versus 625 in that prior snapshot: 8 more (1.3%).

Report change
+8
Death-coded reports
+3
Death-coded share
−0.3 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 Abdominal mass changes

FDA AER · VeDDRA plate

Code 2277 VOL-MID

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

  • VOL-MID 633 reports
  • DEATH-HOT 57.7%
  • UPPER-Q #555/2481
  • PHOTO-FINISH Vials, Abnormal
  • SPECIES-DOG Dog · 524
  • DRUG-LEAD Oclacitinib Malea… · 79
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Vials, Abnormal (±1 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.

High-volume neighbourhood around Abdominal mass

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

Vomiting · highest174348Circulatory collapse… · near636Weak pulse · near635Abdominal mass · this reacti…633Vials, Abnormal · near632Diabetic ketoacidosis · near631Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Abdominal mass

Abdominal mass: high death-coded share in the FDA AER plate

Signature read: 365 death-coded reports is a heavy tail count for Abdominal mass in the CVM extract. Report volume is upper-third scale: 633 named reports in the openFDA extract. Death-coded share is upper-third: 365 of 633 reports (57.7% of named reports). Nearest volume peer: Vials, Abnormal (±1 reports). Lead species Dog (524). Lead co-reported drug Oclacitinib Maleate (79).

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 524
Cat 104
Horse 2
Ferret 2
Fish 1

Breeds Most Affected

Retriever - Labrador 77
Domestic Shorthair 41
Crossbred Canine/dog 38
Retriever - Golden 35
Beagle 20
Terrier - Yorkshire 18
Shepherd Dog - German 18
Chihuahua 14
Shepherd Dog - Australian 13
Rottweiler 11

Associated Drugs

Oclacitinib Maleate 79
Trilostane 68
Milbemycin Oxime + Spinosad 57
Carprofen 56
Bedinvetmab 55
Maropitant Citrate 44
Fluralaner Chew Tablets 40
Gabapentin 34
Afoxolaner 33
Grapiprant 31
Prednisone 24
Ivermectin + Pyrantel As Pamoate Salt 24
Fluralaner 13.64% 12-Week Chew 19
Metronidazole 18
Spinosad 16
Frunevetmab 16
Cefovecin 15
Polysulfated Glycosaminoglycan 14
Moxidectin 14
Fluralaner Spot-On Solution 13

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Abdominal mass, 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 (57.7% 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 Abdominal mass (#555 of 2,481 by report volume); death-coded 57.7%. PlainBreed reaction plate · death-coded report count stamp 365 · 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 →