Reaction profile
The FDA adverse-event record for abdominal cavity hernia
66 FDA adverse-event reports reference abdominal cavity hernia (VeDDRA 252). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.
- #1600 of 2,481
- by report volume (all reactions)
- 66
- reports citing this reaction
- 30.3%
- 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 cavity hernia has 66 reports now versus 66 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 Abdominal cavity hernia changesFDA AER · VeDDRA plate
Code 252 VOL-LOW
VOL-LOW · DEATH-HOT · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-LOW 66 reports
- DEATH-HOT 30.3%
- MID-PACK #1600/2481
- PHOTO-FINISH Administration device…
- SPECIES-DOG Dog · 25
- DRUG-LEAD Device: Suture · 24
- DESK-WIDE 20 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Administration device NOS, leaking (±0 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.
Report-volume neighbourhood around Abdominal cavity hernia
Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.
Abdominal cavity hernia: high death-coded share in the FDA AER plate
Signature read: Abdominal cavity hernia's 30.3% death-coded share is among the highest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is upper-third: 20 of 66 reports (30.3% of named reports). Nearest volume peer: Administration device NOS, leaking (±0 reports). Lead species Dog (25). Lead co-reported drug Device: Suture (24).
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
Breeds Most Affected
Associated Drugs
Nationwide reactions with similar profiles
Two openFDA-derived peer sets for Abdominal cavity hernia, 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 (66 here).
Similar death-coded share
Nearest other reactions by death-coded share (30.3% here), distinct from the volume row.
What to do with this reaction
- Compare Abdominal cavity hernia's report profile against similar reactions nationwide. See similar reactions
- 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
Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →