Reaction profile

The FDA adverse-event record for skin irritation

1,098 FDA reports name skin irritation, a high-volume reaction in the CVM extract (VeDDRA 1760). Plate stamps and neighbourhood peers follow.

#369 of 2,481
by report volume (all reactions)
1,098
reports citing this reaction
2.3%
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. Skin irritation has 1,098 reports now versus 1,080 in that prior snapshot: 18 more (1.7%).

Report change
+18
Death-coded reports
+0
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 Skin irritation changes

FDA AER · VeDDRA plate

Code 1760 VOL-MID

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

  • VOL-MID 1,098 reports
  • DEATH-LOW 2.3%
  • UPPER-Q #369/2481
  • PHOTO-FINISH Flaking skin
  • SPECIES-DOG Dog · 790
  • DRUG-LEAD Milbemycin Oxime… · 137
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Flaking skin (±4 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 Skin irritation

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

Vomiting · highest174348Faecal incontinence · near1107Electrolyte disorder · near1105Flaking skin · near1102Skin irritation · this react…1098Dry skin · near1091Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Skin irritation

Skin irritation: low death-coded share in the FDA AER plate

Signature read: 1,098 reports place Skin irritation in the upper third of FDA AER volume (#369 of 2,481). Report volume is upper-third scale: 1,098 named reports in the openFDA extract. Death-coded share is lower-third: 25 of 1,098 reports (2.3% of named reports). Nearest volume peer: Flaking skin (±4 reports). Lead species Dog (790). Lead co-reported drug Milbemycin Oxime + Spinosad (137).

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 790
Cat 182
Human 111
Cattle 7
Horse 6
Other Birds 1
Donkey 1

Breeds Most Affected

Unknown 117
Domestic Shorthair 105
Retriever - Labrador 67
Crossbred Canine/dog 65
Chihuahua 46
Retriever - Golden 39
Dog (unknown) 35
Pit Bull 30
Shih Tzu 28
Shepherd Dog - German 28

Associated Drugs

Milbemycin Oxime + Spinosad 137
Selamectin 105
Afoxolaner 97
Imidacloprid + Moxidectin 66
Fluralaner Chew Tablets 59
Nitenpyram 55
Oclacitinib Maleate 41
Ivermectin + Pyrantel As Pamoate Salt 40
Spinosad 36
Selamectin;Sarolaner 33
Fluralaner 13.64% 12-Week Chew 26
Frunevetmab 24
Pyrantel Pamoate;Sarolaner 22
Moxidectin 20
Fluralaner Spot-On Solution 20
Milbemycin Oxime + Praziquantel 20
Trilostane 19
Carprofen 19
Diphenhydramine 18
Prednisone 18

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Skin irritation, 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 (1,098 here).

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 Skin irritation (#369 of 2,481 by report volume); death-coded 2.3%. PlainBreed reaction plate · report volume stamp 1,098 · 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 →