Reaction profile

The FDA adverse-event record for crust

1,615 FDA reports name crust, a high-volume reaction in the CVM extract (VeDDRA 1189). Plate stamps and neighbourhood peers follow.

#270 of 2,481
by report volume (all reactions)
1,615
reports citing this reaction
6.6%
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. Crust has 1,615 reports now versus 1,572 in that prior snapshot: 43 more (2.7%).

Report change
+43
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 Crust changes

FDA AER · VeDDRA plate

Code 1189 VOL-MID

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

  • VOL-MID 1,615 reports
  • DEATH-PAR 6.6%
  • UPPER-Q #270/2481
  • PHOTO-FINISH Unsteady gait
  • SPECIES-DOG Dog · 1,183
  • DRUG-LEAD Oclacitinib Malea… · 178
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Unsteady gait (±8 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 Crust

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

Vomiting · highest174348Crust · this reaction1615Unsteady gait · near1607Skin sore · near1606Hot spot (pyotraumati… · near1604Hyperproteinaemia · near1597Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Crust

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

Signature read: 1,615 reports place Crust in the upper third of FDA AER volume (#270 of 2,481). Report volume is upper-third scale: 1,615 named reports in the openFDA extract. Death-coded share is lower-third: 107 of 1,615 reports (6.6% of named reports). Nearest volume peer: Unsteady gait (±8 reports). Lead species Dog (1,183). Lead co-reported drug Oclacitinib Maleate (178).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Oclacitinib Maleate 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 1,183
Cat 408
Cattle 15
Horse 8
Ferret 1

Breeds Most Affected

Domestic Shorthair 264
Retriever - Labrador 121
Crossbred Canine/dog 94
Retriever - Golden 62
Shepherd Dog - German 62
Chihuahua 54
Domestic Longhair 39
Shih Tzu 37
Dog (unknown) 34
Terrier - Yorkshire 25

Associated Drugs

Oclacitinib Maleate 178
Frunevetmab 138
Cefovecin 111
Carprofen 110
Milbemycin Oxime + Spinosad 96
Afoxolaner 92
Prednisone 89
Bedinvetmab 84
Selamectin 76
Anti-Il31 Mab Mcs Lot #1283563 76
Maropitant Citrate 74
Trilostane 74
Gabapentin 67
Fluralaner Chew Tablets 63
Spinosad 51
Pyrantel Pamoate;Sarolaner 50
Florfenicol + Mometasone Furoate + Terbinafine Hydrochloride 48
Cyclosporine 47
Imidacloprid + Moxidectin 47
Moxidectin 47

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Crust, 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 (1,615 here).

Similar death-coded share

Nearest other reactions by death-coded share (6.6% 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 Crust (#270 of 2,481 by report volume); death-coded 6.6%. PlainBreed reaction plate · report volume stamp 1,615 · 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 →