Reaction profile

The FDA adverse-event record for lung sound

235 FDA adverse-event reports reference lung sound (VeDDRA 1175). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#966 of 2,481
by report volume (all reactions)
235
reports citing this reaction
41.7%
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. Lung sound has 235 reports now versus 235 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
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 Lung sound changes

FDA AER · VeDDRA plate

Code 1175 VOL-LOW

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

  • VOL-LOW 235 reports
  • DEATH-HOT 41.7%
  • MID-PACK #966/2481
  • PHOTO-FINISH Brain disorder NOS
  • SPECIES-DOG Dog · 183
  • DRUG-LEAD Milbemycin Oxime… · 51
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Brain disorder NOS (±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.

Report-volume neighbourhood around Lung sound

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

Vomiting · highest174348Blinking · near237Retinal disorder NOS · near236Lung sound · this reaction235Brain disorder NOS · near234Metastatic neoplasia · near234Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Lung sound

Lung sound: high death-coded share in the FDA AER plate

Signature read: Lung sound's 41.7% death-coded share is among the highest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is upper-third: 98 of 235 reports (41.7% of named reports). Nearest volume peer: Brain disorder NOS (±1 reports). Lead species Dog (183). Lead co-reported drug Milbemycin Oxime + Spinosad (51).

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 183
Cat 42
Horse 6
Cattle 4

Breeds Most Affected

Domestic Shorthair 23
Retriever - Labrador 19
Crossbred Canine/dog 13
Chihuahua 10
Domestic Longhair 10
Shih Tzu 8
Pug 7
Terrier - Yorkshire 7
Beagle 7
Maltese 6

Associated Drugs

Milbemycin Oxime + Spinosad 51
Maropitant Citrate 27
Spinosad 18
Cefovecin 17
Melarsomine Dihydrochloride Injection 17
Enrofloxacin 15
Carprofen 14
Furosemide 14
Prednisone 13
Dexamethasone 13
Oclacitinib Maleate 11
Buprenorphine 10
Butorphanol 9
Doxycycline 9
Metronidazole 9
Moxidectin 8
Diphenhydramine 8
Afoxolaner 8
Imidacloprid + Moxidectin 7
Famotidine 7

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Lung sound, 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 (235 here).

Similar death-coded share

Nearest other reactions by death-coded share (41.7% 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 Lung sound (#966 of 2,481 by report volume); death-coded 41.7%. PlainBreed reaction plate · death-coded share stamp 41.7% · 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 →