Reaction profile

The FDA adverse-event record for sleep disturbance nos

551 FDA reports name sleep disturbance nos, a high-volume reaction in the CVM extract (VeDDRA 141). Plate stamps and neighbourhood peers follow.

#605 of 2,481
by report volume (all reactions)
551
reports citing this reaction
8.7%
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. Sleep disturbance NOS has 551 reports now versus 537 in that prior snapshot: 14 more (2.6%).

Report change
+14
Death-coded reports
+2
Death-coded share
+0.1 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 Sleep disturbance NOS changes

FDA AER · VeDDRA plate

Code 141 VOL-MID

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

  • VOL-MID 551 reports
  • DEATH-PAR 8.7%
  • UPPER-Q #605/2481
  • PHOTO-FINISH Gastric ulcer
  • SPECIES-DOG Dog · 487
  • DRUG-LEAD Trilostane · 70
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Gastric ulcer (±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 Sleep disturbance NOS

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

Vomiting · highest174348Gastric ulcer · near551Sleep disturbance NOS · this…551Fly biting behaviour · near550Increased borborygmus · near550Pallor · near550Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Sleep disturbance NOS

What the FDA AER plate says about Sleep disturbance NOS

Signature read: 551 reports place Sleep disturbance NOS in the upper third of FDA AER volume (#605 of 2,481). Report volume is upper-third scale: 551 named reports in the openFDA extract. 48 of 551 reports were death-coded (8.7% of named reports, not a population mortality rate). Nearest volume peer: Gastric ulcer (±0 reports). Lead species Dog (487). Lead co-reported drug Trilostane (70).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Trilostane 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 487
Cat 62
Cattle 1
Horse 1

Breeds Most Affected

Retriever - Labrador 41
Domestic Shorthair 36
Crossbred Canine/dog 30
Chihuahua 23
Shih Tzu 23
Retriever - Golden 21
Shepherd Dog - German 19
Dog (unknown) 15
Terrier - Yorkshire 14
Pug 13

Associated Drugs

Trilostane 70
Bedinvetmab 53
Milbemycin Oxime + Spinosad 45
Afoxolaner 40
Buprenorphine 39
Pyrantel Pamoate;Sarolaner 37
Oclacitinib Maleate 33
Gabapentin 30
Carprofen 20
Maropitant Citrate 20
Sarolaner 20
Ivermectin + Pyrantel As Pamoate Salt 18
Grapiprant 16
Spinosad 14
Nitenpyram 14
Prednisone 13
Ivermectin 13
Imidacloprid + Moxidectin 13
Fluralaner 13.64% 12-Week Chew 13
Meloxicam 12

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Sleep disturbance 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 report volume

Nearest other reactions by FDA report count (551 here).

Similar death-coded share

Nearest other reactions by death-coded share (8.7% 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 Sleep disturbance NOS (#605 of 2,481 by report volume); death-coded 8.7%. PlainBreed reaction plate · report volume stamp 551 · 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 →