Reaction profile

The FDA adverse-event record for papillomatosis

83 FDA adverse-event reports reference papillomatosis (VeDDRA 952). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1487 of 2,481
by report volume (all reactions)
83
reports citing this reaction
0.0%
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. Papillomatosis has 83 reports now versus 83 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 Papillomatosis changes

FDA AER · VeDDRA plate

Code 952 VOL-LOW

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

  • VOL-LOW 83 reports
  • DEATH-RARE 0.0%
  • MID-PACK #1487/2481
  • PHOTO-FINISH Destructive behaviour
  • SPECIES-DOG Dog · 82
  • DRUG-LEAD Cyclosporine A · 51
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Destructive behaviour (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Report-volume neighbourhood around Papillomatosis

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Destructive behaviour · near83Elevated mean corpusc… · near83Erosion · near83Haemoglobinuria · near83Papillomatosis · this reacti…83Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Papillomatosis

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

Signature read: Papillomatosis's 0.0% death-coded share is among the lowest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is lower-third: 0 of 83 reports (0.0% of named reports). Nearest volume peer: Destructive behaviour (±0 reports). Lead species Dog (82). Lead co-reported drug Cyclosporine A (51).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Cyclosporine A 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 82
Cat 1

Breeds Most Affected

Retriever - Golden 7
Retriever - Labrador 7
Boxer (German Boxer) 6
Pit Bull 4
Terrier - West Highland White 4
Bulldog 4
Dog (unknown) 4
Terrier - Bull - American Pit 4
Terrier - Boston 3
Poodle (unspecified) 3

Associated Drugs

Cyclosporine A 51
Oclacitinib Maleate 32
Ketoconazole 12
Cyclosporine 5
Milbemycin Oxime + Spinosad 4
Ivermectin/Pyrantel 3
Prednisone 3
Ilunocitinib 3
Phenylpropanolamine 2
Tramadol 2
Chlorhexidine 2
Cephalexin 2
Fluconazole 2
Selamectin 1
Lufenuron + Milbemycin Oxime 1
Amoxicillin 1
Cefpodoxime 1
Spinosad 1
Diphenhydramine Topical Spray 1
Triamcinolone Acetonide 1

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Papillomatosis, 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 (0.0% 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 Papillomatosis (#1487 of 2,481 by report volume); death-coded 0.0%. PlainBreed reaction plate · death-coded share stamp 0.0% · 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 →