Reaction profile

The FDA adverse-event record for spinal pain nos

105 FDA adverse-event reports reference spinal pain nos (VeDDRA 3104). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1371 of 2,481
by report volume (all reactions)
105
reports citing this reaction
28.6%
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. Spinal pain NOS has 105 reports now versus 97 in that prior snapshot: 8 more (8.2%).

Report change
+8
Death-coded reports
+1
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 Spinal pain NOS changes

FDA AER · VeDDRA plate

Code 3104 VOL-LOW

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

  • VOL-LOW 105 reports
  • DEATH-HOT 28.6%
  • MID-PACK #1371/2481
  • PHOTO-FINISH Decreased mean corpus…
  • SPECIES-DOG Dog · 91
  • DRUG-LEAD Bedinvetmab · 54
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Decreased mean corpuscular haemoglobin concentration (MCHC) (±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 Spinal pain NOS

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

Vomiting · highest174348Decreased mean corpus… · near105Hyperaemia · near105Injection site stiffn… · near105Lack of efficacy (neo… · near105Spinal pain NOS · this react…105Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Spinal pain NOS

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

Signature read: Spinal pain NOS's 28.6% 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: 30 of 105 reports (28.6% of named reports). Nearest volume peer: Decreased mean corpuscular haemoglobin concentration (MCHC) (±0 reports). Lead species Dog (91). Lead co-reported drug Bedinvetmab (54).

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 91
Cat 14

Breeds Most Affected

Retriever - Labrador 14
Crossbred Canine/dog 10
Domestic Shorthair 8
Chihuahua 5
Shepherd Dog - German 3
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 3
Shih Tzu 3
Dog (unknown) 3
Retriever - Golden 3
Beagle 2

Associated Drugs

Bedinvetmab 54
Gabapentin 26
Carprofen 25
Maropitant Citrate 15
Frunevetmab 9
Metronidazole 7
Methocarbamol 7
Buprenorphine 6
Moxidectin 6
Capromorelin 6
Cefpodoxime 5
Grapiprant 5
Oclacitinib Maleate 5
Probiotics 4
Prednisone 4
Lotilaner 4
Tramadol 4
Methadone 4
Pyrantel Pamoate;Sarolaner 4
Doxycycline 3

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Spinal pain 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 death-coded share

Nearest other reactions by death-coded share (28.6% 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 Spinal pain NOS (#1371 of 2,481 by report volume); death-coded 28.6%. PlainBreed reaction plate · death-coded share stamp 28.6% · 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 →