Reaction profile

The FDA adverse-event record for moist dermatitis

692 FDA reports name moist dermatitis, a high-volume reaction in the CVM extract (VeDDRA 937). Plate stamps and neighbourhood peers follow.

#521 of 2,481
by report volume (all reactions)
692
reports citing this reaction
6.1%
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. Moist dermatitis has 692 reports now versus 686 in that prior snapshot: 6 more (0.9%).

Report change
+6
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 Moist dermatitis changes

FDA AER · VeDDRA plate

Code 937 VOL-MID

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

  • VOL-MID 692 reports
  • DEATH-PAR 6.1%
  • UPPER-Q #521/2481
  • PHOTO-FINISH Dysphoria
  • SPECIES-DOG Dog · 523
  • DRUG-LEAD Frunevetmab · 75
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Dysphoria (±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 Moist dermatitis

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

Vomiting · highest174348Dysphoria · near693Warm feeling to the t… · near693Moist dermatitis · this reac…692Increased packed cell… · near691Reduced globulins · near690Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Moist dermatitis

Moist dermatitis: low death-coded share in the FDA AER plate

Signature read: 692 reports place Moist dermatitis in the upper third of FDA AER volume (#521 of 2,481). Report volume is upper-third scale: 692 named reports in the openFDA extract. Death-coded share is lower-third: 42 of 692 reports (6.1% of named reports). Nearest volume peer: Dysphoria (±1 reports). Lead species Dog (523). Lead co-reported drug Frunevetmab (75).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Frunevetmab 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 523
Cat 164
Horse 4
Cattle 1

Breeds Most Affected

Domestic Shorthair 107
Retriever - Labrador 73
Crossbred Canine/dog 47
Shepherd Dog - German 41
Retriever - Golden 34
Domestic (unspecified) 19
Chihuahua 18
Shih Tzu 18
Domestic Longhair 16
Dog (unknown) 15

Associated Drugs

Frunevetmab 75
Oclacitinib Maleate 60
Carprofen 51
Selamectin 49
Milbemycin Oxime + Spinosad 39
Spinosad 38
Cefovecin 38
Gabapentin 34
Fluralaner Chew Tablets 34
Maropitant Citrate 33
Trilostane 31
Afoxolaner 27
Anti-Il31 Mab Mcs Lot #1283563 27
Bedinvetmab 25
Prednisone 24
Enrofloxacin 24
Fluralaner Spot-On Solution 21
Deracoxib 20
Moxidectin 20
Cefpodoxime Proxetil 20

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Moist dermatitis, 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 (692 here).

Similar death-coded share

Nearest other reactions by death-coded share (6.1% 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 Moist dermatitis (#521 of 2,481 by report volume); death-coded 6.1%. PlainBreed reaction plate · report volume stamp 692 · 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 →