Reaction profile

The FDA adverse-event record for haemothorax

68 FDA adverse-event reports reference haemothorax (VeDDRA 889). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1587 of 2,481
by report volume (all reactions)
68
reports citing this reaction
89.7%
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. Haemothorax has 68 reports now versus 67 in that prior snapshot: 1 more (1.5%).

Report change
+1
Death-coded reports
+0
Death-coded share
−1.3 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 Haemothorax changes

FDA AER · VeDDRA plate

Code 889 VOL-LOW

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

  • VOL-LOW 68 reports
  • DEATH-HOT 89.7%
  • MID-PACK #1587/2481
  • PHOTO-FINISH Chewing disorder
  • SPECIES-DOG Dog · 60
  • DRUG-LEAD Milbemycin Oxime… · 13
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Chewing disorder (±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 Haemothorax

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

Vomiting · highest174348Chewing disorder · near68Device failure · near68Elevated lactic acid… · near68Haemothorax · this reaction68Hypopigmentation · near68Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Haemothorax

Haemothorax: high death-coded share in the FDA AER plate

Signature read: Haemothorax's 89.7% 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: 61 of 68 reports (89.7% of named reports). Nearest volume peer: Chewing disorder (±0 reports). Lead species Dog (60). Lead co-reported drug Milbemycin Oxime + Spinosad (13).

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 60
Cat 5
Cattle 2
Bison 1

Breeds Most Affected

Retriever - Labrador 4
Pit Bull 4
Crossbred Canine/dog 3
Shih Tzu 3
Chihuahua 3
Beagle 3
Boxer (German Boxer) 3
Siberian Husky 2
Pug 2
Terrier - Jack Russell 2

Associated Drugs

Milbemycin Oxime + Spinosad 13
Oclacitinib Maleate 6
Milbemycin Oxime + Praziquantel 6
Carprofen 5
Rabies Vaccine 5
Ivermectin 3
Moxidectin 3
Butorphanol 3
Furosemide 3
Cyclosporine A 3
Famotidine 3
Afoxolaner 3
Spinosad 2
Firocoxib 2
Bordetella Vaccine 2
Maropitant Citrate 2
Rabies Virus, Kv 2
Diphenhydramine Hcl 2
Fentanyl 2
Cefpodoxime 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Haemothorax, 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 (68 here).

Similar death-coded share

Nearest other reactions by death-coded share (89.7% 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 Haemothorax (#1587 of 2,481 by report volume); death-coded 89.7%. PlainBreed reaction plate · death-coded share stamp 89.7% · 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 →