Reaction profile

The FDA adverse-event record for dermatitis

2,569 FDA reports name dermatitis, a high-volume reaction in the CVM extract (VeDDRA 932). Plate stamps and neighbourhood peers follow.

#184 of 2,481
by report volume (all reactions)
2,569
reports citing this reaction
7.0%
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. Dermatitis has 2,569 reports now versus 2,537 in that prior snapshot: 32 more (1.3%).

Report change
+32
Death-coded reports
+1
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 Dermatitis changes

FDA AER · VeDDRA plate

Code 932 VOL-MID

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

  • VOL-MID 2,569 reports
  • DEATH-PAR 7.0%
  • TOP-DECILE #184/2481
  • PHOTO-FINISH Blindness
  • SPECIES-DOG Dog · 1,829
  • DRUG-LEAD Frunevetmab · 302
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Blindness (±11 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 Dermatitis

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

Vomiting · highest174348Dermatitis · this reaction2569Blindness · near2558Application site eryt… · near2556Limping · near2549Systemic disorder NOS · near2540Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Dermatitis

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

Signature read: 2,569 reports place Dermatitis in the upper third of FDA AER volume (#184 of 2,481). Report volume is upper-third scale: 2,569 named reports in the openFDA extract. Death-coded share is lower-third: 179 of 2,569 reports (7.0% of named reports). Nearest volume peer: Blindness (±11 reports). Lead species Dog (1,829). Lead co-reported drug Frunevetmab (302).

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 1,829
Cat 627
Human 46
Horse 18
Chicken 16
Cattle 16
Unknown 6
Mouse 5
Pig 2
Ferret 2

Breeds Most Affected

Domestic Shorthair 316
Retriever - Labrador 198
Crossbred Canine/dog 178
Domestic (unspecified) 110
Retriever - Golden 89
Unknown 65
Shepherd Dog - German 62
Dog (unknown) 61
Shih Tzu 60
Chihuahua 58

Associated Drugs

Frunevetmab 302
Milbemycin Oxime + Spinosad 276
Oclacitinib Maleate 226
Selamectin 167
Bedinvetmab 158
Spinosad 143
Carprofen 126
Imidacloprid + Moxidectin 105
Afoxolaner 104
Prednisone 83
Fluralaner Chew Tablets 80
Cefovecin 78
Trilostane 70
Cyclosporine 68
Anti-Il31 Mab Mcs Lot #1283563 66
Gabapentin 62
Milbemycin Oxime + Praziquantel 61
Cephalexin 45
Maropitant Citrate 44
Cefpodoxime Proxetil 42

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for 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 (2,569 here).

Similar death-coded share

Nearest other reactions by death-coded share (7.0% 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 Dermatitis (#184 of 2,481 by report volume); death-coded 7.0%. PlainBreed reaction plate · report volume stamp 2,569 · 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 →