Reaction profile

The FDA adverse-event record for emphysema nos (see 'respiratory' for pulmonary emphysema)

28 FDA reports name emphysema nos (see 'respiratory' for pulmonary emphysema), a lower-volume reaction in the CVM extract (VeDDRA 1010). Plate stamps and neighbourhood peers follow.

#2023 of 2,481
by report volume (all reactions)
28
reports citing this reaction
71.4%
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. Emphysema NOS (see 'Respiratory' for pulmonary emphysema) has 28 reports now versus 28 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 Emphysema NOS (see 'Respiratory' for pulmonary emphysema) changes

FDA AER · VeDDRA plate

Code 1010 VOL-TRACE

VOL-TRACE · DEATH-HOT · LOWER-Q · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-TRACE 28 reports
  • DEATH-HOT 71.4%
  • LOWER-Q #2023/2481
  • PHOTO-FINISH Absence seizure
  • SPECIES-DOG Dog · 12
  • DRUG-LEAD Meloxicam · 3
  • DESK-WIDE 15 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Absence seizure (±0 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.

Lower-volume neighbourhood around Emphysema NOS

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

Vomiting · highest174348Absence seizure · near28Application site brui… · near28BILIRUBIN(DIRECT) HIG… · near28Cholangitis · near28Emphysema NOS (see 'R… · thi…28Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Emphysema NOS (see 'Respiratory' for pulmonary emphysema)

Emphysema NOS (see 'Respiratory' for pulmonary emphysema): high death-coded share in the FDA AER plate

Signature read: Emphysema NOS (see 'Respiratory' for pulmonary emphysema)'s 71.4% death-coded share is among the highest in the openFDA reaction corpus. Report volume is lower-third scale: 28 named reports in the openFDA extract. Death-coded share is upper-third: 20 of 28 reports (71.4% of named reports). Nearest volume peer: Absence seizure (±0 reports). Lead species Dog (12). Lead co-reported drug Meloxicam (3).

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 12
Cat 9
Cattle 6
Human 1

Breeds Most Affected

Domestic (unspecified) 5
Holstein-Friesian also known as Holstein 5
Shih Tzu 3
Shepherd Dog - German 2
Retriever - Labrador 2
Domestic Shorthair 2
Ragdoll 1
Aberdeen Angus 1
Unknown 1
Schnauzer - Miniature 1

Associated Drugs

Meloxicam 3
Fluralaner Chew Tablets 3
Cefovecin Sodium 2
Propofol 2
Carprofen 2
Moxidectin 2
Ivermectin 2
Maropitant Citrate 2
Enrofloxacin 2
Isoflurane 2
Spinosad 2
Prednisone 2
Robenacoxib 2
Dinoprost Tromethamine 2
Dexmedetomidine Hydrochloride 1
Ketamine Hydrochloride 1
Cloprostenol Sodium 1
Ivermectin(1%)/Clorsulon(10%) Injection 1
Recombinant Human Insulin 1
Amoxicillin (As Trihydrate); Clavulanate Potassium ( K-Clavulanate) 1

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 Emphysema NOS (see 'Respiratory' for pulmonary emphysema) (#2023 of 2,481 by report volume); death-coded 71.4%. PlainBreed reaction plate · death-coded share stamp 71.4% · 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 →