Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Eosinopenia: reports listing this term

722reports listing the term, 2004–20260.1% of all reports
315reports, 12 months to March 2026196 in the 12 months before
76.6%classed serious, as reportedall reports: 38.6%
73.4%of these reports concern dogscat 26.5%

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

315 reports listed it in the 12 months to March 2026, up 61% from 196 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 maropitant, oclacitinib and ilunocitinib. 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.

73.4% of the reports concern dogs, 26.5% of the reports concern cats and 0.1% of the reports concern goats. Of reports listing this term that state seriousness, 76.6% were classed as serious; 26.5% 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
Maropitant1551%
Oclacitinib820.3%
Ilunocitinib804.5%
Gabapentin770.7%
Prednisone640.7%
Carprofen570.1%
Buprenorphine540.7%
Bedinvetmab490.3%
Fluralaner490.1%
Cefovecin sodium480.4%
Afoxolaner390.1%
Doxycycline390.9%
Diphenhydramine380.8%
Frunevetmab380.5%
Metronidazole381.1%
Robenacoxib381%
Famotidine371.2%
Butorphanol Tartrate350.5%
Ondansetron334.1%
Moxidectin320.1%
Propofol300.6%
Pyrantel Pamoate + Sarolaner300.1%
Dexamethasone291%
Ivermectin + Pyrantel Pamoate290%
Lotilaner280.2%

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
Maropitant1551%
Pyrantel Pamoate1050%
Moxidectin830.1%
Oclacitinib820.3%
Ilunocitinib804.5%
Gabapentin770.7%
Praziquantel720.1%
Afoxolaner660.1%
Prednisone640.7%
Sarolaner580.1%
Carprofen570.1%
Fluralaner570.1%
Buprenorphine540.7%
Bedinvetmab490.3%
Cefovecin sodium480.4%
Milbemycin Oxime440%
Doxycycline390.9%
Butorphanol Tartrate380.5%
Diphenhydramine380.8%
Famotidine381.3%
Frunevetmab380.5%
Ivermectin380%
Metronidazole381.1%
Robenacoxib381%
Dexamethasone360.7%

Species split

Dog73.4%530
Cat26.5%191
Goat0.1%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 0.1% of all cat reports.

Trend

01836Apr 2021: 0May 2021: 0Jun 2021: 0Jul 2021: 0Aug 2021: 0Sep 2021: 1Oct 2021: 2Nov 2021: 1Dec 2021: 1Jan 2022: 22022Feb 2022: 1Mar 2022: 5Apr 2022: 5May 2022: 0Jun 2022: 2Jul 2022: 3Aug 2022: 3Sep 2022: 9Oct 2022: 6Nov 2022: 9Dec 2022: 10Jan 2023: 52023Feb 2023: 9Mar 2023: 11Apr 2023: 12May 2023: 8Jun 2023: 6Jul 2023: 9Aug 2023: 16Sep 2023: 13Oct 2023: 7Nov 2023: 10Dec 2023: 11Jan 2024: 82024Feb 2024: 11Mar 2024: 11Apr 2024: 11May 2024: 14Jun 2024: 14Jul 2024: 12Aug 2024: 14Sep 2024: 18Oct 2024: 24Nov 2024: 17Dec 2024: 17Jan 2025: 152025Feb 2025: 21Mar 2025: 19Apr 2025: 24May 2025: 18Jun 2025: 22Jul 2025: 22Aug 2025: 32Sep 2025: 28Oct 2025: 29Nov 2025: 31Dec 2025: 36Jan 2026: 312026Feb 2026: 34Mar 2026: 8

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.

01492972004: 120042006: 120062020: 220202021: 520212022: 5520222023: 11720232024: 17120242025: 29720252026: 732026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal9.7%70
Recovered with Sequela0.8%6
Ongoing40.4%292
Died8.9%64
Euthanized17.6%127
Outcome Unknown22.6%163

Age of the animal

Under 1 year9.1%66
1 to 3 years15.7%113
4 to 7 years29.5%213
8 to 11 years29.1%210
12 years and over15.9%115
Age not given0.7%5
MeasureReports listing this termAll reports
Reports7221,357,245
Classed serious, of reports stating it76.6%38.6%
Death or euthanasia recorded, per 1,000 reports264.563.8

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 "Eosinopenia"

What does "Eosinopenia" 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 eosinopenia?

722 reports through March 2026 (0.1% of all reports), 315 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: maropitant (155), oclacitinib (82), ilunocitinib (80), gabapentin (77) and prednisone (64). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (73.4%), cat (26.5%) and goat (0.1%).

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.