Reaction profile

The FDA adverse-event record for gastritis

447 FDA reports name gastritis, a high-volume reaction in the CVM extract (VeDDRA 341). Plate stamps and neighbourhood peers follow.

#688 of 2,481
by report volume (all reactions)
447
reports citing this reaction
26.0%
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. Gastritis has 447 reports now versus 437 in that prior snapshot: 10 more (2.3%).

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 Gastritis changes

FDA AER · VeDDRA plate

Code 341 VOL-LOW

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

  • VOL-LOW 447 reports
  • DEATH-HOT 26.0%
  • MID-PACK #688/2481
  • PHOTO-FINISH Application site grea…
  • SPECIES-DOG Dog · 396
  • DRUG-LEAD Carprofen · 88
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Application site greasy fur (±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 Gastritis

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

Vomiting · highest174348Application site grea… · near448Arched back · near448INEFFECTIVE, EUTHANAS… · near448Gastritis · this reaction447Gastric perforation · near445Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Gastritis

Gastritis: high death-coded share in the FDA AER plate

Signature read: 116 death-coded reports is a heavy tail count for Gastritis in the CVM extract. Report volume is upper-third scale: 447 named reports in the openFDA extract. Death-coded share is upper-third: 116 of 447 reports (26.0% of named reports). Nearest volume peer: Application site greasy fur (±1 reports). Lead species Dog (396). Lead co-reported drug Carprofen (88).

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 396
Cat 35
Horse 12
Cattle 1
Other Birds 1
Pig 1
Mouse 1

Breeds Most Affected

Retriever - Labrador 76
Crossbred Canine/dog 29
Retriever - Golden 20
Domestic Shorthair 18
Terrier (unspecified) 12
Terrier - Yorkshire 10
Dog (unknown) 9
Shih Tzu 9
Chihuahua 9
Pug 8

Associated Drugs

Carprofen 88
Maropitant Citrate 65
Milbemycin Oxime + Spinosad 63
Deracoxib 29
Gabapentin 29
Oclacitinib Maleate 24
Afoxolaner 19
Spinosad 18
Enrofloxacin 18
Grapiprant 18
Famotidine 16
Metronidazole 16
Bedinvetmab 16
Meloxicam 15
Ivermectin + Pyrantel As Pamoate Salt 15
Metoclopramide 14
Moxidectin 14
Firocoxib 13
Omeprazole 13
Prednisone 13

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Gastritis, 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 (447 here).

Similar death-coded share

Nearest other reactions by death-coded share (26.0% 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 Gastritis (#688 of 2,481 by report volume); death-coded 26.0%. PlainBreed reaction plate · death-coded report count stamp 116 · 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 →