Reaction profile

The FDA adverse-event record for tiredness

1,456 FDA reports name tiredness, a high-volume reaction in the CVM extract (VeDDRA 1844). Plate stamps and neighbourhood peers follow.

#291 of 2,481
by report volume (all reactions)
1,456
reports citing this reaction
7.8%
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. Tiredness has 1,456 reports now versus 1,430 in that prior snapshot: 26 more (1.8%).

Report change
+26
Death-coded reports
+1
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 Tiredness changes

FDA AER · VeDDRA plate

Code 1844 VOL-MID

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

  • VOL-MID 1,456 reports
  • DEATH-PAR 7.8%
  • UPPER-Q #291/2481
  • PHOTO-FINISH Immune mediated haemo…
  • SPECIES-DOG Dog · 1,223
  • DRUG-LEAD Milbemycin Oxime… · 319
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Immune mediated haemolytic anaemia (±1 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 Tiredness

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

Vomiting · highest174348Vestibular disorder N… · near1471Head bobbing · near1461Tiredness · this reaction1456Immune mediated haemo… · near1455Frequent urination · near1445Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Tiredness

Tiredness: low death-coded share in the FDA AER plate

Signature read: 1,456 reports place Tiredness in the upper third of FDA AER volume (#291 of 2,481). Report volume is upper-third scale: 1,456 named reports in the openFDA extract. Death-coded share is lower-third: 113 of 1,456 reports (7.8% of named reports). Nearest volume peer: Immune mediated haemolytic anaemia (±1 reports). Lead species Dog (1,223). Lead co-reported drug Milbemycin Oxime + Spinosad (319).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Milbemycin Oxime + Spinosad 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 1,223
Cat 162
Human 58
Horse 6
Cattle 4
Rat 2
Pig 1

Breeds Most Affected

Retriever - Labrador 114
Crossbred Canine/dog 97
Domestic Shorthair 87
Chihuahua 78
Unknown 62
Retriever - Golden 58
Shih Tzu 50
Dog (unknown) 49
Shepherd Dog - German 47
Terrier - Yorkshire 42

Associated Drugs

Milbemycin Oxime + Spinosad 319
Afoxolaner 93
Spinosad 91
Milbemycin Oxime + Praziquantel 74
Ivermectin + Pyrantel As Pamoate Salt 68
Pyrantel Pamoate;Sarolaner 68
Nitenpyram 57
Trilostane 56
Lotilaner 51
Fluralaner Chew Tablets 46
Oclacitinib Maleate 44
Fluralaner 13.64% 12-Week Chew 44
Gabapentin 40
Carprofen 40
Maropitant Citrate 38
Bedinvetmab 38
Prednisone 32
Moxidectin 29
Buprenorphine 29
Ivermectin 27

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Tiredness, 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 (7.8% 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 Tiredness (#291 of 2,481 by report volume); death-coded 7.8%. PlainBreed reaction plate · report volume stamp 1,456 · 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 →