Reaction profile

The FDA adverse-event record for heart murmur

2,328 FDA reports name heart murmur, a high-volume reaction in the CVM extract (VeDDRA 213). Plate stamps and neighbourhood peers follow.

#200 of 2,481
by report volume (all reactions)
2,328
reports citing this reaction
22.8%
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. Heart murmur has 2,328 reports now versus 2,261 in that prior snapshot: 67 more (3.0%).

Report change
+67
Death-coded reports
+14
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 Heart murmur changes

FDA AER · VeDDRA plate

Code 213 VOL-MID

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

  • VOL-MID 2,328 reports
  • DEATH-HOT 22.8%
  • TOP-DECILE #200/2481
  • PHOTO-FINISH Rash
  • SPECIES-DOG Dog · 1,807
  • DRUG-LEAD Milbemycin Oxime… · 366
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Rash (±11 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 Heart murmur

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

Vomiting · highest174348Neutropenia · near2374Dispenser, Abnormal · near2350Rash · near2339Heart murmur · this reaction2328Blood in faeces · near2312Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Heart murmur

What the FDA AER plate says about Heart murmur

Signature read: 530 death-coded reports is a heavy tail count for Heart murmur in the CVM extract. Report volume is upper-third scale: 2,328 named reports in the openFDA extract. 530 of 2,328 reports were death-coded (22.8% of named reports, not a population mortality rate). Nearest volume peer: Rash (±11 reports). Lead species Dog (1,807). Lead co-reported drug Milbemycin Oxime + Spinosad (366).

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 1,807
Cat 501
Horse 17
Unknown 1
Other Equids 1
Guinea Pig 1

Breeds Most Affected

Domestic Shorthair 326
Chihuahua 170
Crossbred Canine/dog 135
Shih Tzu 95
Maltese 82
Retriever - Labrador 77
Dachshund (unspecified) 60
Beagle 55
Boxer (German Boxer) 48
Terrier (unspecified) 47

Associated Drugs

Milbemycin Oxime + Spinosad 366
Trilostane 228
Maropitant Citrate 175
Bedinvetmab 141
Oclacitinib Maleate 121
Carprofen 105
Milbemycin Oxime + Praziquantel 102
Gabapentin 101
Prednisone 96
Spinosad 87
Fluralaner 13.64% 12-Week Chew 86
Cefovecin 84
Frunevetmab 82
Afoxolaner 79
Buprenorphine 77
Fluralaner Chew Tablets 75
Moxidectin 71
Ivermectin + Pyrantel As Pamoate Salt 65
Pimobendan 51
Selamectin 48

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Heart murmur, 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 (2,328 here).

Similar death-coded share

Nearest other reactions by death-coded share (22.8% 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 Heart murmur (#200 of 2,481 by report volume); death-coded 22.8%. PlainBreed reaction plate · death-coded report count stamp 530 · 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 →