Reaction profile

The FDA adverse-event record for peripheral vascular disorder

Name: Peripheral vascular disorder - FDA Animal Adverse Reaction
Creator: PlainBreed
License: https://open.fda.gov/license/

20 FDA reports name peripheral vascular disorder, a lower-volume reaction in the CVM extract (VeDDRA 1690). Plate stamps and neighbourhood peers follow.

#2171 of 2,481
by report volume (all reactions): 20
reports citing this reaction: 20.0%
death-coded share: Dog
most-affected species

Compiled by PlainBreed

Verify with FDA CVM →

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. Peripheral vascular disorder has 20 reports now versus 19 in that prior snapshot: 1 more (5.3%).

Report change: +1
Death-coded reports: +0
Death-coded share: −1.1 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 Peripheral vascular disorder changes

FDA AER · VeDDRA plate

Code 1690 VOL-TRACE

VOL-TRACE · DEATH-HOT · LOWER-Q · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

VOL-TRACE 20 reports
DEATH-HOT 20.0%
LOWER-Q #2171/2481
PHOTO-FINISH Agalactia
SPECIES-DOG Dog · 12
DRUG-LEAD Noinformationsupp… · 11
DESK-WIDE 15 breeds
BOOK-FULL 8/8 fields

Nearest volume peer: Agalactia (±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 Peripheral vascular disorder

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

FDA AER report volume · neighbourhood around Peripheral vascular disorder

What the FDA AER plate says about Peripheral vascular disorder

Signature read: 20 reports place Peripheral vascular disorder in the lower third of FDA AER volume (#2171 of 2,481). Report volume is lower-third scale: 20 named reports in the openFDA extract. 4 of 20 reports were death-coded (20.0% of named reports, not a population mortality rate). Nearest volume peer: Agalactia (±0 reports). Lead species Dog (12). Lead co-reported drug Noinformationsupplied (11).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Noinformationsupplied 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 12

Horse 3

Cat 2

Pig 1

Cattle 1

Human 1

Breeds Most Affected

Dog (unknown) 3

Terrier - Jack Russell 2

Thoroughbred 2

Domestic Shorthair 2

Schnauzer - Miniature 1

Collie - Border 1

Pug 1

Spitz - German Pomeranian 1

Pig (unknown) 1

Charolais 1

Associated Drugs

Noinformationsupplied 11

Dexmedetomidine Hydrochloride 5

Trilostane 3

Moxidectin 2

Ampicillin Sodium & Sulbactam Sodium 2

Milbemycin Oxime + Spinosad 1

Nitenpyram 1

Afoxolaner 1

Device: Cardiovascular 1

Eprinomectin 5 Mg/Ml Pour-On Solution 1

Rabies Virus, 1

Hetastarch 1

Maropitant Citrate 1

Anti-Il31 Mab Mcs Lot #1283563 1

Famotidine 1

Ondansetron Hcl 1

Enrofloxacin 1

Diphenhydramine Hcl 1

Ceftiofur Sodium 1

Ceftiofur Crystalline Free Acid 1

What to do with this reaction

Read how death-coded share differs from a mortality rate before drawing conclusions. Understanding adverse events
Browse the full reaction directory to compare report counts across reaction types. All reactions

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 Peripheral vascular disorder (#2171 of 2,481 by report volume); death-coded 20.0%. PlainBreed reaction plate · report volume stamp 20 · 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 →