Reaction profile

The FDA adverse-event record for pr-lung(s), edema

207 FDA adverse-event reports reference pr-lung(s), edema (VeDDRA 99630). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1018 of 2,481
by report volume (all reactions)
207
reports citing this reaction
100.0%
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. PR-LUNG(S), EDEMA has 207 reports now versus 207 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 PR-LUNG(S), EDEMA changes

FDA AER · VeDDRA plate

Code 99630 VOL-LOW

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

  • VOL-LOW 207 reports
  • DEATH-HOT 100.0%
  • MID-PACK #1018/2481
  • PHOTO-FINISH Administration device…
  • SPECIES-DOG Dog · 114
  • DRUG-LEAD Milbemycin Oxime… · 45
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Administration device NOS, abnormal (±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.

Report-volume neighbourhood around PR-LUNG, EDEMA

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

Vomiting · highest174348Application site hair… · near208Administration device… · near207Food allergy · near207PR-LUNG(S), EDEMA · this rea…207Gum disorder NOS · near206Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around PR-LUNG(S), EDEMA

PR-LUNG(S), EDEMA: high death-coded share in the FDA AER plate

Signature read: PR-LUNG(S), EDEMA's 100.0% 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: 207 of 207 reports (100.0% of named reports). Nearest volume peer: Administration device NOS, abnormal (±0 reports). Lead species Dog (114). Lead co-reported drug Milbemycin Oxime + Spinosad (45).

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 114
Cat 64
Cattle 25
Sheep 2
Horse 1
Ferret 1

Breeds Most Affected

Domestic Shorthair 27
Domestic (unspecified) 25
Crossbred Canine/dog 12
Retriever - Labrador 12
Shepherd Dog - German 9
Holstein-Friesian also known as Holstein 6
Dachshund (unspecified) 6
Crossbred Bovine/Cattle 6
Spaniel - King Charles Cavalier 5
Chihuahua 5

Associated Drugs

Milbemycin Oxime + Spinosad 45
Spinosad 24
Cefovecin 14
Cefovecin Sodium 13
Moxidectin 13
Maropitant Citrate 10
Dexmedetomidine Hydrochloride 9
Pyrantel Pamoate 6
Imidacloprid + Moxidectin 6
Fluralaner Chew Tablets 6
Tiletamine, Zolazepam 5
Carprofen 5
Rabies Vaccine 5
Dexamethasone 5
Meloxicam 5
Maropitant 4
Monensin 4
Enrofloxacin 4
Robenacoxib 4
Buprenorphine 4

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for PR-LUNG(S), EDEMA, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

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 PR-LUNG(S), EDEMA (#1018 of 2,481 by report volume); death-coded 100.0%. PlainBreed reaction plate · death-coded share stamp 100.0% · 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 →