Reaction profile

The FDA adverse-event record for skin slough

695 FDA reports name skin slough, a high-volume reaction in the CVM extract (VeDDRA 943). Plate stamps and neighbourhood peers follow.

#517 of 2,481
by report volume (all reactions)
695
reports citing this reaction
12.9%
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 slough has 695 reports now versus 695 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
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 slough changes

FDA AER · VeDDRA plate

Code 943 VOL-MID

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

  • VOL-MID 695 reports
  • DEATH-ELEV 12.9%
  • UPPER-Q #517/2481
  • PHOTO-FINISH Expired drug administ…
  • SPECIES-DOG Dog · 522
  • DRUG-LEAD Tigilanol Tiglate · 133
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Expired drug administered (±0 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 slough

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

Vomiting · highest174348Expired drug administ… · near695Pleural effusion · near695Skin slough · this reaction695Unwell · near694Dysphoria · near693Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Skin slough

What the FDA AER plate says about Skin slough

Signature read: 695 reports place Skin slough in the upper third of FDA AER volume (#517 of 2,481). Report volume is upper-third scale: 695 named reports in the openFDA extract. 90 of 695 reports were death-coded (12.9% of named reports, not a population mortality rate). Nearest volume peer: Expired drug administered (±0 reports). Lead species Dog (522). Lead co-reported drug Tigilanol Tiglate (133).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Tigilanol Tiglate 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 522
Cat 91
Horse 59
Cattle 8
Human 6
Fish 2
Pig 2
Goat 2
Guinea Pig 1
Mouse 1

Breeds Most Affected

Domestic Shorthair 53
Retriever - Labrador 47
Dog (unknown) 36
Chihuahua 32
Crossbred Canine/dog 23
Retriever - Golden 22
Boxer (German Boxer) 22
Pit Bull 21
Terrier - Boston 16
Domestic (unspecified) 13

Associated Drugs

Tigilanol Tiglate 133
Carprofen 116
Cefovecin 67
Maropitant Citrate 55
Prednisone 38
Meloxicam 34
Gabapentin 33
Famotidine 32
Selamectin 31
Buprenorphine 28
Butorphanol 27
Anesthetic 26
Enrofloxacin 24
Diphenhydramine 22
Milbemycin Oxime + Spinosad 20
Oclacitinib Maleate 20
Melarsomine Dihydrochloride 19
Ceftiofur Crystalline Free Acid 19
Propofol 17
Moxidectin 17

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Skin slough, 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 (695 here).

Similar death-coded share

Nearest other reactions by death-coded share (12.9% 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 Skin slough (#517 of 2,481 by report volume); death-coded 12.9%. PlainBreed reaction plate · report volume stamp 695 · 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 →