Reaction profile

The FDA adverse-event record for lumbar pain

396 FDA reports name lumbar pain, a high-volume reaction in the CVM extract (VeDDRA 2390). Plate stamps and neighbourhood peers follow.

#734 of 2,481
by report volume (all reactions)
396
reports citing this reaction
16.2%
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. Lumbar pain has 396 reports now versus 389 in that prior snapshot: 7 more (1.8%).

Report change
+7
Death-coded reports
+0
Death-coded share
−0.3 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 Lumbar pain changes

FDA AER · VeDDRA plate

Code 2390 VOL-LOW

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

  • VOL-LOW 396 reports
  • DEATH-ELEV 16.2%
  • MID-PACK #734/2481
  • PHOTO-FINISH Corneal disorder NOS
  • SPECIES-DOG Dog · 350
  • DRUG-LEAD Bedinvetmab · 75
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Corneal disorder NOS (±0 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Lumbar pain

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

Vomiting · highest174348Elevated protein:crea… · near397Polycythaemia · near397Corneal disorder NOS · near396Hearing decreased · near396Lumbar pain · this reaction396Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Lumbar pain

What the FDA AER plate says about Lumbar pain

Signature read: 64 death-coded reports is a heavy tail count for Lumbar pain in the CVM extract. Report volume is upper-third scale: 396 named reports in the openFDA extract. 64 of 396 reports were death-coded (16.2% of named reports, not a population mortality rate). Nearest volume peer: Corneal disorder NOS (±0 reports). Lead species Dog (350). Lead co-reported drug Bedinvetmab (75).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Bedinvetmab appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 350
Cat 40
Human 5
Horse 1

Breeds Most Affected

Retriever - Labrador 30
Domestic Shorthair 30
Crossbred Canine/dog 24
Chihuahua 17
Dog (unknown) 15
Shih Tzu 15
Retriever - Golden 12
Maltese 11
Terrier - Bull - American Pit 11
Dachshund (unspecified) 8

Associated Drugs

Bedinvetmab 75
Gabapentin 64
Trilostane 57
Carprofen 55
Maropitant Citrate 37
Fluralaner Chew Tablets 25
Afoxolaner 23
Fluralaner 13.64% 12-Week Chew 23
Moxidectin 22
Prednisone 21
Melarsomine Dihydrochloride 20
Meloxicam 18
Cefovecin 17
Oclacitinib Maleate 17
Pyrantel Pamoate;Sarolaner 17
Doxycycline 14
Frunevetmab 14
Tramadol 13
Grapiprant 13
Buprenorphine 11

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Lumbar pain, 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 (396 here).

Similar death-coded share

Nearest other reactions by death-coded share (16.2% 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 Lumbar pain (#734 of 2,481 by report volume); death-coded 16.2%. PlainBreed reaction plate · death-coded report count stamp 64 · 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 →