Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Papilloma: reports listing this term

517reports listing the term, 2011–20260% of all reports
35reports, 12 months to March 202629 in the 12 months before
36.5%classed serious, as reportedall reports: 38.6%
99.8%of these reports concern dogscat 0.2%

"Papilloma" is a coded term listed in 517 adverse event reports received by FDA, 0% of the database. Terms come from VeDDRA, the veterinary dictionary that FDA and drug companies use to code what a reporter describes.

35 reports listed it in the 12 months to March 2026, up 21% from 29 in the 12 months before. FDA posts reports quarterly with a delay of three to six months, so the newest months are incomplete and usually grow in later releases.

By active ingredient, the drugs named most often in those reports are oclacitinib, cyclosporine and carprofen. That order mostly follows how many reports each has overall; the table gives the term's share within each drug's own reports as well.

99.8% of the reports concern dogs and 0.2% of the reports concern cats. Of reports listing this term that state seriousness, 36.5% were classed as serious; 2.1% record a death or euthanasia among the outcomes.

Drugs named most often in these reports, by active ingredient

Active ingredients recorded for the drugReports listing the termShare of that drug's own reports
Oclacitinib4171.4%
Cyclosporine470.2%
Carprofen170%
Cefpodoxime proxetil160.4%
Ilunocitinib160.9%
Prednisone150.2%
Cephalexin140.5%
Fluralaner140%
Afoxolaner130%
Ivermectin + Pyrantel Pamoate130%
Milbemycin Oxime + Spinosad130%
Gabapentin110.1%
Ketoconazole110.5%
Hydroxyzine90.8%
Azithromycin85.3%
Lufenuron + Milbemycin Oxime80%
Diphenhydramine70.1%
Prednisolone + Trimeprazine Tartrate70.3%
Amoxicillin Trihydrate + Clavulanate Potassium60.1%
Ivermectin60%
Prednisolone60.2%
Sarolaner60%
Amoxicillin50.1%
Bedinvetmab50%
Famotidine50.2%

Ordered by number of reports, which mostly tracks how many reports a drug has overall. Across the whole database the term appears in 0% of reports. A drug's presence in a report means the animal received it, not that it produced the sign; FDA states that these data cannot be used to compare one product with another. openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand.

Single ingredients, pooled across combinations

Active ingredientReports listing the termShare of the ingredient's own reports
Oclacitinib4171.4%
Cyclosporine470.2%
Milbemycin Oxime250%
Pyrantel Pamoate240%
Ivermectin190%
Carprofen170%
Cefpodoxime proxetil160.4%
Ilunocitinib160.9%
Afoxolaner150%
Prednisone150.2%
Cephalexin140.5%
Fluralaner140%
Moxidectin130%
Prednisolone130.2%
Spinosad130%
Sarolaner120%
Gabapentin110.1%
Ketoconazole110.4%
Lufenuron100%
Hydroxyzine90.8%
Azithromycin85.3%
Clavulanate Potassium80.1%
Diphenhydramine70.1%
Trimeprazine Tartrate70.3%
Amoxicillin60.1%

Species split

Dog99.8%516
Cat0.2%1

Coloured bar: share of reports listing this term. Grey bar: the species' share of all reports. The term appears in 0.1% of all dog reports; The term appears in 0% of all cat reports.

Trend

059Apr 2021: 2May 2021: 2Jun 2021: 2Jul 2021: 4Aug 2021: 4Sep 2021: 1Oct 2021: 1Nov 2021: 4Dec 2021: 1Jan 2022: 32022Feb 2022: 2Mar 2022: 4Apr 2022: 2May 2022: 1Jun 2022: 2Jul 2022: 2Aug 2022: 3Sep 2022: 2Oct 2022: 4Nov 2022: 3Dec 2022: 1Jan 2023: 32023Feb 2023: 3Mar 2023: 3Apr 2023: 3May 2023: 2Jun 2023: 1Jul 2023: 3Aug 2023: 2Sep 2023: 0Oct 2023: 2Nov 2023: 2Dec 2023: 1Jan 2024: 22024Feb 2024: 1Mar 2024: 5Apr 2024: 3May 2024: 2Jun 2024: 2Jul 2024: 3Aug 2024: 4Sep 2024: 3Oct 2024: 5Nov 2024: 1Dec 2024: 1Jan 2025: 12025Feb 2025: 3Mar 2025: 1Apr 2025: 1May 2025: 4Jun 2025: 3Jul 2025: 5Aug 2025: 1Sep 2025: 1Oct 2025: 4Nov 2025: 9Dec 2025: 1Jan 2026: 22026Feb 2026: 3Mar 2026: 1

Reports by month FDA received them, five years to March 2026. The newest months are incomplete because FDA posts reports with a delay of three to six months.

036722011: 220112012: 1520122013: 920132014: 3320142015: 4920152016: 7020162017: 7220172018: 5520182019: 3920192020: 2420202021: 2320212022: 2920222023: 2520232024: 3220242025: 3420252026: 62026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal14.1%73
Recovered with Sequela0.6%3
Ongoing72.1%373
Died0.8%4
Euthanized1.4%7
Outcome Unknown11%57

Age of the animal

Under 1 year2.5%13
1 to 3 years38.7%200
4 to 7 years30.6%158
8 to 11 years19.3%100
12 years and over4.6%24
Age not given4.3%22
MeasureReports listing this termAll reports
Reports5171,357,245
Classed serious, of reports stating it36.5%38.6%
Death or euthanasia recorded, per 1,000 reports21.363.8

Grey bars and the right-hand column are the whole database. Outcomes are as stated by the reporter and describe the report as a whole, not this term alone.

Questions about "Papilloma"

What does "Papilloma" mean in an adverse event report?

It is a VeDDRA dictionary term picked to code what the reporter described. The report's free-text description is not published by FDA and is not shown here.

How many reports list papilloma?

517 reports through March 2026 (0% of all reports), 35 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: oclacitinib (417), cyclosporine (47), carprofen (17), cefpodoxime proxetil (16) and ilunocitinib (16). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (99.8%) and cat (0.2%).

Does a drug appearing here mean it produced this sign?

No such conclusion can be drawn. FDA states that "there is no certainty that the reported drug or device caused the adverse event" and that the event "may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources."

My animal shows this sign. What now?

This site cannot assess an animal. A veterinarian can; for an emergency, contact a veterinary emergency clinic. See the guide on when to call a vet.

Where this comes from. Counts are built from the openFDA Animal & Veterinary adverse event bulk files released 28 Sep 2026, which hold reports FDA's Center for Veterinary Medicine received through 31 Mar 2026. openFDA masks brand and manufacturer names in these files, so drugs are counted by the active ingredients each record discloses and no figure is attributed to a brand, application or company. Ingredient names, and the separate reference lists of approved products, follow the FDA Green Book as of 1 Oct 2026. Spelling variants of the same VeDDRA term (for example with and without a cross-reference note) are pooled. No report text, lot numbers or reporter details are published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.