Reaction profile

The FDA adverse-event record for eructation

101 FDA adverse-event reports reference eructation (VeDDRA 336). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1389 of 2,481
by report volume (all reactions)
101
reports citing this reaction
5.9%
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. Eructation has 101 reports now versus 99 in that prior snapshot: 2 more (2.0%).

Report change
+2
Death-coded reports
+0
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 Eructation changes

FDA AER · VeDDRA plate

Code 336 VOL-LOW

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

  • VOL-LOW 101 reports
  • DEATH-PAR 5.9%
  • MID-PACK #1389/2481
  • PHOTO-FINISH Cachexia
  • SPECIES-DOG Dog · 92
  • DRUG-LEAD Maropitant Citrate · 9
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Cachexia (±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 Eructation

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

Vomiting · highest174348Cachexia · near101Elevated mean corpusc… · near101Eructation · this reaction101Idiopathic vestibular… · near101INEFFECTIVE, SARCOPTE… · near101Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Eructation

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

Signature read: Eructation's 5.9% 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: 6 of 101 reports (5.9% of named reports). Nearest volume peer: Cachexia (±0 reports). Lead species Dog (92). Lead co-reported drug Maropitant Citrate (9).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Maropitant Citrate 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 92
Cat 6
Horse 1
Human 1
Cattle 1

Breeds Most Affected

Retriever - Labrador 10
Crossbred Canine/dog 7
Chihuahua 5
Terrier - Boston 4
Retriever - Golden 4
Dog (unknown) 3
Shepherd Dog - German 3
Shepherd Dog - Australian 3
Beagle 3
Schnauzer - Miniature 3

Associated Drugs

Maropitant Citrate 9
Deracoxib 7
Milbemycin Oxime + Spinosad 7
Carprofen 7
Milbemycin 6
Oclacitinib Maleate 6
Ivermectin + Pyrantel As Pamoate Salt 5
Fluralaner Chew Tablets 5
Gabapentin 5
Fluralaner 13.64% 12-Week Chew 5
Famotidine 4
Meloxicam 4
Tramadol 4
Grapiprant 4
Probiotic (Unknown) 4
Pyrantel Pamoate;Sarolaner 4
Afoxolaner 3
Cephalexin 3
Tylosin Tartrate 3
Omeprazole 3

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Eructation, 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 (5.9% 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 Eructation (#1389 of 2,481 by report volume); death-coded 5.9%. PlainBreed reaction plate · death-coded share stamp 5.9% · 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 →