Reaction profile

The FDA adverse-event record for footpad disorder nos

53 FDA reports name footpad disorder nos, a lower-volume reaction in the CVM extract (VeDDRA 2880). Plate stamps and neighbourhood peers follow.

#1706 of 2,481
by report volume (all reactions)
53
reports citing this reaction
9.4%
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. Footpad disorder NOS has 53 reports now versus 50 in that prior snapshot: 3 more (6.0%).

Report change
+3
Death-coded reports
+1
Death-coded share
+1.4 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 Footpad disorder NOS changes

FDA AER · VeDDRA plate

Code 2880 VOL-LOW

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

  • VOL-LOW 53 reports
  • DEATH-PAR 9.4%
  • MID-PACK #1706/2481
  • PHOTO-FINISH Bloody foam in mouth…
  • SPECIES-DOG Dog · 40
  • DRUG-LEAD Bedinvetmab · 17
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Bloody foam in mouth and nose (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Lower-volume neighbourhood around Footpad disorder NOS

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

Vomiting · highest174348Bloody foam in mouth… · near53Decreased skin turgor · near53Easily startled · near53Footpad disorder NOS · this …53IGA Animal morbidity… · near53Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Footpad disorder NOS

What the FDA AER plate says about Footpad disorder NOS

Signature read: 5 death-coded reports is a thin tail count for Footpad disorder NOS in the CVM extract. Report volume is lower-third scale: 53 named reports in the openFDA extract. 5 of 53 reports were death-coded (9.4% of named reports, not a population mortality rate). Nearest volume peer: Bloody foam in mouth and nose (±0 reports). Lead species Dog (40). Lead co-reported drug Bedinvetmab (17).

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 40
Cat 11
Cattle 2

Breeds Most Affected

Domestic Shorthair 8
Retriever - Labrador 6
Dog (unknown) 3
Shepherd Dog - German 3
Pekingese 3
Retriever - Golden 3
Spaniel - King Charles Cavalier 3
Beagle 2
Crossbred Canine/dog 2
Bulldog - American 2

Associated Drugs

Bedinvetmab 17
Carprofen 8
Oclacitinib Maleate 7
Gabapentin 7
Frunevetmab 4
Amoxicillin 4
Trilostane 4
Fluralaner 13.64% 12-Week Chew 3
Buprenorphine 3
Incurin 3
Galliprant 3
Amantadine 3
Urinary Supplement 3
Cefpodoxime Proxetil 3
Amlodipine 3
Pyrantel Pamoate;Sarolaner 2
Imepitoin 2
Des 2
Adequan 2
Fatty Acids 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Footpad disorder 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 (9.4% 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 Footpad disorder NOS (#1706 of 2,481 by report volume); death-coded 9.4%. PlainBreed reaction plate · death-coded report count stamp 5 · 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 →