Reaction profile

The FDA adverse-event record for arthropathy nos

54 FDA reports name arthropathy nos, a lower-volume reaction in the CVM extract (VeDDRA 1335). Plate stamps and neighbourhood peers follow.

#1697 of 2,481
by report volume (all reactions)
54
reports citing this reaction
25.9%
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. Arthropathy NOS has 54 reports now versus 51 in that prior snapshot: 3 more (5.9%).

Report change
+3
Death-coded reports
+0
Death-coded share
−1.5 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 Arthropathy NOS changes

FDA AER · VeDDRA plate

Code 1335 VOL-LOW

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

  • VOL-LOW 54 reports
  • DEATH-HOT 25.9%
  • MID-PACK #1697/2481
  • PHOTO-FINISH Acute mastitis
  • SPECIES-DOG Dog · 44
  • DRUG-LEAD Bedinvetmab · 18
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Acute mastitis (±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 Arthropathy NOS

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

Vomiting · highest174348Acute mastitis · near54Arthropathy NOS · this react…54Exophthalmia · near54Hypovolaemic shock · near54INEFFECTIVE, COGNITIV… · near54Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Arthropathy NOS

Arthropathy NOS: high death-coded share in the FDA AER plate

Signature read: Arthropathy NOS's 25.9% death-coded share is among the highest in the openFDA reaction corpus. Report volume is lower-third scale: 54 named reports in the openFDA extract. Death-coded share is upper-third: 14 of 54 reports (25.9% of named reports). Nearest volume peer: Acute mastitis (±0 reports). Lead species Dog (44). Lead co-reported drug Bedinvetmab (18).

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 44
Cat 8
Sheep 1
Cattle 1

Breeds Most Affected

Retriever - Labrador 12
Crossbred Canine/dog 4
Shepherd Dog - German 3
Siberian Husky 3
Domestic Mediumhair 3
Shih Tzu 2
Retriever - Golden 2
Dog (unknown) 2
Terrier - Bull - American Pit 2
Spaniel - King Charles Cavalier 2

Associated Drugs

Bedinvetmab 18
Carprofen 11
Gabapentin 9
Trilostane 7
Frunevetmab 6
Milbemycin Oxime + Spinosad 4
Grapiprant 4
Buprenorphine 4
Meloxicam 3
Fluralaner 13.64% 12-Week Chew 3
Amantadine 3
Polysulfated Glycosaminoglycan 3
Pyrantel Pamoate;Sarolaner 3
Unspecified Ketamine 3
Oclacitinib Maleate 2
Cefpodoxime 2
Tramadol 2
Lotilaner 2
Fluralaner 2
Maropitant Citrate 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Arthropathy NOS, 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 (54 here).

Similar death-coded share

Nearest other reactions by death-coded share (25.9% 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 Arthropathy NOS (#1697 of 2,481 by report volume); death-coded 25.9%. PlainBreed reaction plate · death-coded share stamp 25.9% · 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 →