Reaction profile

The FDA adverse-event record for halitosis

458 FDA reports name halitosis, a high-volume reaction in the CVM extract (VeDDRA 291). Plate stamps and neighbourhood peers follow.

#675 of 2,481
by report volume (all reactions)
458
reports citing this reaction
15.1%
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. Halitosis has 458 reports now versus 453 in that prior snapshot: 5 more (1.1%).

Report change
+5
Death-coded reports
+0
Death-coded share
−0.2 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 Halitosis changes

FDA AER · VeDDRA plate

Code 291 VOL-LOW

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

  • VOL-LOW 458 reports
  • DEATH-ELEV 15.1%
  • MID-PACK #675/2481
  • PHOTO-FINISH Swollen vulva
  • SPECIES-DOG Dog · 413
  • DRUG-LEAD Imidacloprid + Mo… · 116
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Swollen vulva (±2 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Halitosis

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

Vomiting · highest174348Hepatitis · near463Red blood cell disord… · near463Swollen vulva · near460Halitosis · this reaction458Lack of response to o… · near454Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Halitosis

What the FDA AER plate says about Halitosis

Signature read: 69 death-coded reports is a heavy tail count for Halitosis in the CVM extract. Report volume is upper-third scale: 458 named reports in the openFDA extract. 69 of 458 reports were death-coded (15.1% of named reports, not a population mortality rate). Nearest volume peer: Swollen vulva (±2 reports). Lead species Dog (413). Lead co-reported drug Imidacloprid + Moxidectin (116).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Imidacloprid + Moxidectin 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 413
Cat 41
Human 2
Horse 1
Unknown 1

Breeds Most Affected

Retriever - Labrador 40
Crossbred Canine/dog 38
Retriever - Golden 25
Domestic Shorthair 23
Shepherd Dog - German 21
Chihuahua 18
Maltese 14
Dachshund (unspecified) 13
Shih Tzu 13
Terrier - Yorkshire 12

Associated Drugs

Imidacloprid + Moxidectin 116
Carprofen 27
Oclacitinib Maleate 26
Imidacloprid, Moxidectin 24
Milbemycin Oxime + Spinosad 22
Spinosad 20
Meloxicam 16
Fluralaner Chew Tablets 16
Trilostane 15
Afoxolaner 15
Gabapentin 15
Prednisone 14
Cyclosporine A 13
Bedinvetmab 13
Deracoxib 12
Cyclosporine 9
Imidacloprid And Moxidectin 9
Pimobendan 9
Maropitant Citrate 9
Cefovecin 8

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Halitosis, 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 (458 here).

Similar death-coded share

Nearest other reactions by death-coded share (15.1% 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 Halitosis (#675 of 2,481 by report volume); death-coded 15.1%. PlainBreed reaction plate · death-coded report count stamp 69 · 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 →