Reaction profile

The FDA adverse-event record for papilloma

521 FDA reports name papilloma, a high-volume reaction in the CVM extract (VeDDRA 920). Plate stamps and neighbourhood peers follow.

#633 of 2,481
by report volume (all reactions)
521
reports citing this reaction
2.1%
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. Papilloma has 521 reports now versus 515 in that prior snapshot: 6 more (1.2%).

Report change
+6
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 Papilloma changes

FDA AER · VeDDRA plate

Code 920 VOL-MID

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

  • VOL-MID 521 reports
  • DEATH-LOW 2.1%
  • MID-PACK #633/2481
  • PHOTO-FINISH Hypocortisolaemia
  • SPECIES-DOG Dog · 520
  • DRUG-LEAD Oclacitinib Malea… · 419
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hypocortisolaemia (±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 Papilloma

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

Vomiting · highest174348Hyposthenuria · near523Hypocortisolaemia · near521Papilloma · this reaction521Contamination NOS · near519Bumping into walls · near518Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Papilloma

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

Signature read: Papilloma's 2.1% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 521 named reports in the openFDA extract. Death-coded share is lower-third: 11 of 521 reports (2.1% of named reports). Nearest volume peer: Hypocortisolaemia (±0 reports). Lead species Dog (520). Lead co-reported drug Oclacitinib Maleate (419).

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 520
Cat 1

Breeds Most Affected

Retriever - Labrador 62
Retriever - Golden 58
Terrier - Bull - American Pit 39
Bulldog - French 39
Shepherd Dog - German 25
Crossbred Canine/dog 18
Dog (unknown) 17
Bulldog 16
Boxer (German Boxer) 16
Pug 14

Associated Drugs

Oclacitinib Maleate 419
Anti-Il31 Mab Mcs Lot #1283563 44
Cyclosporine A 36
Cyclosporine 19
Ilunocitinib 19
Carprofen 17
Prednisone 15
Milbemycin Oxime + Spinosad 14
Cephalexin 14
Afoxolaner 13
Immunotherapy 12
Gabapentin 12
Hydroxyzine 9
Azithromycin 9
Fluralaner 9
Trilostane 8
Ketoconazole 8
Cefpodoxime 7
Cefpodoxime Proxetil 7
Diphenhydramine Hcl 7

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Papilloma, 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 (521 here).

Similar death-coded share

Nearest other reactions by death-coded share (2.1% 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 Papilloma (#633 of 2,481 by report volume); death-coded 2.1%. PlainBreed reaction plate · death-coded share stamp 2.1% · 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 →