Reaction profile

The FDA adverse-event record for hyperpigmentation

644 FDA reports name hyperpigmentation, a high-volume reaction in the CVM extract (VeDDRA 913). Plate stamps and neighbourhood peers follow.

#544 of 2,481
by report volume (all reactions)
644
reports citing this reaction
3.4%
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. Hyperpigmentation has 644 reports now versus 634 in that prior snapshot: 10 more (1.6%).

Report change
+10
Death-coded reports
+3
Death-coded share
+0.4 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 Hyperpigmentation changes

FDA AER · VeDDRA plate

Code 913 VOL-MID

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

  • VOL-MID 644 reports
  • DEATH-LOW 3.4%
  • UPPER-Q #544/2481
  • PHOTO-FINISH Pinnal reddening
  • SPECIES-DOG Dog · 590
  • DRUG-LEAD Oclacitinib Malea… · 127
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Pinnal reddening (±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 Hyperpigmentation

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

Vomiting · highest174348Patient instructions… · near647Difficulty standing · near645Hyperpigmentation · this rea…644Pinnal reddening · near644Acute renal failure · near643Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Hyperpigmentation

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

Signature read: Hyperpigmentation's 3.4% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 644 named reports in the openFDA extract. Death-coded share is lower-third: 22 of 644 reports (3.4% of named reports). Nearest volume peer: Pinnal reddening (±0 reports). Lead species Dog (590). Lead co-reported drug Oclacitinib Maleate (127).

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 590
Cat 49
Ferret 2
Human 1
Rabbit 1
Cattle 1

Breeds Most Affected

Retriever - Labrador 47
Chihuahua 38
Crossbred Canine/dog 37
Retriever - Golden 32
Shepherd Dog - German 31
Terrier - Yorkshire 26
Dog (unknown) 22
Boxer (German Boxer) 20
Domestic Shorthair 19
Dachshund (unspecified) 18

Associated Drugs

Oclacitinib Maleate 127
Afoxolaner 48
Milbemycin Oxime + Spinosad 47
Spinosad 38
Imidacloprid + Moxidectin 29
Cyclosporine 27
Prednisone 26
Trilostane 25
Estriol Tablets 23
Rabacfosadine Succinate 23
Selamectin 19
Ivermectin + Pyrantel As Pamoate Salt 19
Unspecified 19
Carprofen 18
Fluralaner Chew Tablets 15
Moxidectin 13
Bedinvetmab 13
Levothyroxine Sodium 12
Cyclosporine A 12
Rabacfosadine 12

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Hyperpigmentation, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

Similar death-coded share

Nearest other reactions by death-coded share (3.4% 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 Hyperpigmentation (#544 of 2,481 by report volume); death-coded 3.4%. PlainBreed reaction plate · death-coded share stamp 3.4% · 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 →