Reaction profile

The FDA adverse-event record for drug device use error

Name: Drug device use error - FDA Animal Adverse Reaction
Creator: PlainBreed
License: https://open.fda.gov/license/

10 FDA reports name drug device use error, a lower-volume reaction in the CVM extract (VeDDRA 93091). Plate stamps and neighbourhood peers follow.

#2451 of 2,481
by report volume (all reactions): 10
reports citing this reaction: 10.0%
death-coded share: Unknown
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. Drug device use error has 10 reports now versus 10 in that prior snapshot: 0 the same number of (0.0%).

Report change: +0
Death-coded reports: +0
Death-coded share: +0.0 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 Drug device use error changes

FDA AER · VeDDRA plate

Code 93091 VOL-TRACE

VOL-TRACE · DEATH-ELEV · BOTTOM-DECILE · PHOTO-FINISH · SPECIES-UNKNOWN · DRUG-LEAD · DESK-MID · BOOK-FULL

VOL-TRACE 10 reports
DEATH-ELEV 10.0%
BOTTOM-DECILE #2451/2481
PHOTO-FINISH Anoxia
SPECIES-UNKNOWN Unknown · 4
DRUG-LEAD Imidacloprid + Mo… · 3
DESK-MID 5 breeds
BOOK-FULL 8/8 fields

Nearest volume peer: Anoxia (±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 Drug device use error

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

FDA AER report volume · neighbourhood around Drug device use error

What the FDA AER plate says about Drug device use error

Signature read: 10 reports place Drug device use error in the lower third of FDA AER volume (#2451 of 2,481). Report volume is lower-third scale: 10 named reports in the openFDA extract. 1 of 10 reports were death-coded (10.0% of named reports, not a population mortality rate). Nearest volume peer: Anoxia (±0 reports). Lead species Unknown (4). Lead co-reported drug Imidacloprid + Moxidectin (3).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Imidacloprid + Moxidectin 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

Unknown 4

Dog 3

Cat 3

Breeds Most Affected

Unknown 4

Crossbred Canine/dog 2

Domestic Shorthair 2

Retriever - Golden 1

Siamese 1

Associated Drugs

Imidacloprid + Moxidectin 3

Insulin Injectable Vial 2

Protamine Zinc Recombinant Human Insulin 2

Device: Syringe 1

Velagliflozin Proline Monohydrate 1

Selamectin 1

Selamectin To Note, Strength Of Selamectin Not Known As Customer Did Not Report Package Weight Or Lot. 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 Drug device use error (#2451 of 2,481 by report volume); death-coded 10.0%. PlainBreed reaction plate · report volume stamp 10 · 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 →