Reaction profile

The FDA adverse-event record for belching

160 FDA adverse-event reports reference belching (VeDDRA 337). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1152 of 2,481
by report volume (all reactions)
160
reports citing this reaction
5.6%
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. Belching has 160 reports now versus 159 in that prior snapshot: 1 more (0.6%).

Report change
+1
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 Belching changes

FDA AER · VeDDRA plate

Code 337 VOL-LOW

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

  • VOL-LOW 160 reports
  • DEATH-PAR 5.6%
  • MID-PACK #1152/2481
  • PHOTO-FINISH Mouth pain
  • SPECIES-DOG Dog · 146
  • DRUG-LEAD Milbemycin Oxime… · 41
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Mouth pain (±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.

Report-volume neighbourhood around Belching

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Increased lung sounds · near161Lack of efficacy · near161Belching · this reaction160Mouth pain · near160Blood clot · near159Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Belching

Belching: low death-coded share in the FDA AER plate

Signature read: Belching's 5.6% death-coded share is among the lowest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is lower-third: 9 of 160 reports (5.6% of named reports). Nearest volume peer: Mouth pain (±0 reports). Lead species Dog (146). Lead co-reported drug Milbemycin Oxime + Spinosad (41).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Milbemycin Oxime + Spinosad 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 146
Human 7
Cat 6
Horse 1

Breeds Most Affected

Retriever - Labrador 16
Crossbred Canine/dog 12
Retriever - Golden 11
Chihuahua 7
Unknown 7
Shih Tzu 6
Pit Bull 6
Shepherd Dog - German 5
Dog (unknown) 5
Maltese 4

Associated Drugs

Milbemycin Oxime + Spinosad 41
Maropitant Citrate 20
Spinosad 14
Famotidine 10
Oclacitinib Maleate 10
Carprofen 10
Tramadol 8
Prednisone 8
Fluralaner Chew Tablets 8
Deracoxib 7
Enrofloxacin 7
Afoxolaner 7
Milbemycin Oxime + Praziquantel 6
Cyclosporine A 5
Buprenorphine 5
Selamectin 5
Metoclopramide 5
Sucralfate 5
Polysulfated Glycosaminoglycan 4
Trazodone 4

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Belching, 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 (160 here).

Similar death-coded share

Nearest other reactions by death-coded share (5.6% 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 Belching (#1152 of 2,481 by report volume); death-coded 5.6%. PlainBreed reaction plate · death-coded share stamp 5.6% · 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 →