Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Polyphagia: reports listing this term

1,342reports listing the term, 1987–20260.1% of all reports
73reports, 12 months to March 202682 in the 12 months before
44.2%classed serious, as reportedall reports: 38.6%
81.4%of these reports concern dogscat 17.4%

1,342 reports in FDA's animal adverse event database list the term "Polyphagia": 0.1% of all reports. It is a VeDDRA term, chosen by the person who coded the report to match what was described.

73 reports listed it in the 12 months to March 2026, down 11% from 82 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 trilostane, dirlotapide 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.

81.4% of the reports concern dogs, 17.4% of the reports concern cats and 0.7% of the reports concern cattle. Of reports listing this term that state seriousness, 44.2% were classed as serious; 6% 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
Trilostane2251.9%
Dirlotapide1765.9%
Carprofen1070.2%
Insulin730.5%
Cyclosporine690.3%
Oclacitinib550.2%
Spinosad480.1%
Bexagliflozin461.2%
Velagliflozin461%
Prednisone440.5%
Milbemycin Oxime + Spinosad310%
Selegiline Hydrochloride300.7%
Desoxycorticosterone Pivalate281.1%
Meloxicam250.1%
Selamectin250%
Fluralaner240%
Ivermectin + Pyrantel Pamoate200%
Prednisolone + Trimeprazine Tartrate201%
Gabapentin190.2%
Afoxolaner170%
Bedinvetmab160.1%
Cefovecin sodium160.1%
Cefpodoxime proxetil160.4%
Deracoxib160.1%
Firocoxib160.2%

Ordered by number of reports, which mostly tracks how many reports a drug has overall. Across the whole database the term appears in 0.1% 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
Trilostane2251.9%
Dirlotapide1765.9%
Carprofen1070.2%
Spinosad760%
Insulin730.5%
Cyclosporine690.3%
Milbemycin Oxime600%
Oclacitinib550.2%
Bexagliflozin461.2%
Velagliflozin461%
Prednisone440.5%
Pyrantel Pamoate340%
Ivermectin300%
Selegiline Hydrochloride300.7%
Desoxycorticosterone Pivalate281.1%
Prednisolone270.5%
Praziquantel260%
Meloxicam250.1%
Selamectin250%
Fluralaner240%
Moxidectin230%
Afoxolaner200%
Trimeprazine Tartrate201%
Gabapentin190.2%
Bedinvetmab160.1%

Species split

Dog81.4%1,092
Cat17.4%234
Cattle0.7%9
Horse0.2%3
Turkey0.1%2
Pig0.1%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 0.2% of all cat reports.

Trend

0714Apr 2021: 2May 2021: 0Jun 2021: 2Jul 2021: 3Aug 2021: 3Sep 2021: 2Oct 2021: 3Nov 2021: 0Dec 2021: 3Jan 2022: 52022Feb 2022: 3Mar 2022: 1Apr 2022: 3May 2022: 0Jun 2022: 1Jul 2022: 2Aug 2022: 2Sep 2022: 1Oct 2022: 4Nov 2022: 5Dec 2022: 4Jan 2023: 32023Feb 2023: 4Mar 2023: 4Apr 2023: 5May 2023: 1Jun 2023: 1Jul 2023: 4Aug 2023: 5Sep 2023: 3Oct 2023: 5Nov 2023: 3Dec 2023: 6Jan 2024: 112024Feb 2024: 9Mar 2024: 2Apr 2024: 7May 2024: 1Jun 2024: 5Jul 2024: 3Aug 2024: 9Sep 2024: 9Oct 2024: 10Nov 2024: 1Dec 2024: 8Jan 2025: 102025Feb 2025: 14Mar 2025: 5Apr 2025: 4May 2025: 7Jun 2025: 5Jul 2025: 7Aug 2025: 6Sep 2025: 3Oct 2025: 7Nov 2025: 8Dec 2025: 9Jan 2026: 82026Feb 2026: 5Mar 2026: 4

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.

0631251987: 319871988: 21989: 11990: 11991: 119911992: 11995: 11996: 21997: 619971998: 181999: 302000: 122001: 920012002: 72003: 122004: 252005: 3220052006: 372007: 802008: 1102009: 12520092010: 872011: 422012: 612013: 5420132014: 612015: 422016: 682017: 3520172018: 392019: 312020: 282021: 2720212022: 312023: 442024: 752025: 8520252026: 17

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal7.2%96
Recovered with Sequela1.2%16
Ongoing15.7%211
Died4.1%55
Euthanized1.9%26
Outcome Unknown24.5%329

Age of the animal

Under 1 year3.3%44
1 to 3 years8.8%118
4 to 7 years24.4%327
8 to 11 years36.3%487
12 years and over22.2%298
Age not given5.1%68
MeasureReports listing this termAll reports
Reports1,3421,357,245
Classed serious, of reports stating it44.2%38.6%
Death or euthanasia recorded, per 1,000 reports60.463.8

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 "Polyphagia"

What does "Polyphagia" 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 polyphagia?

1,342 reports through March 2026 (0.1% of all reports), 73 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: trilostane (225), dirlotapide (176), carprofen (107), insulin (73) and cyclosporine (69). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (81.4%), cat (17.4%), cattle (0.7%) and horse (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.