Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Decreased haematocrit: reports listing this term

1,043reports listing the term, 2002–20260.1% of all reports
447reports, 12 months to March 2026308 in the 12 months before
75%classed serious, as reportedall reports: 38.6%
68.9%of these reports concern dogscat 30.8%

1,043 reports in FDA's animal adverse event database list the term "Decreased haematocrit": 0.1% of all reports. It is a VeDDRA term, chosen by the person who coded the report to match what was described.

447 reports listed it in the 12 months to March 2026, up 45% from 308 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, ilunocitinib and bedinvetmab. 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.

68.9% of the reports concern dogs, 30.8% of the reports concern cats and 0.3% of the reports concern horses. Of reports listing this term that state seriousness, 75% were classed as serious; 26.6% 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
Maropitant1681%
Ilunocitinib1327.4%
Bedinvetmab1170.6%
Gabapentin910.9%
Prednisone870.9%
Oclacitinib860.3%
Carprofen760.1%
Molidustat7111.3%
Fluralaner660.1%
Buprenorphine580.8%
Afoxolaner520.1%
Cefovecin sodium510.4%
Enrofloxacin510.6%
Metronidazole491.4%
Bexagliflozin461.2%
Frunevetmab450.6%
Mirtazapine451.6%
Capromorelin401.5%
Doxycycline390.9%
Trilostane390.3%
Cyclosporine370.2%
Famotidine331.1%
Ondansetron334.1%
Diphenhydramine310.6%
Insulin310.2%

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
Maropitant1681%
Ilunocitinib1327.4%
Bedinvetmab1170.6%
Pyrantel Pamoate990%
Gabapentin910.9%
Prednisone870.9%
Oclacitinib860.3%
Carprofen760.1%
Fluralaner760.1%
Molidustat7111.3%
Afoxolaner700.1%
Praziquantel700.1%
Moxidectin620.1%
Buprenorphine590.8%
Enrofloxacin520.6%
Cefovecin sodium510.4%
Clavulanate Potassium490.6%
Metronidazole491.4%
Milbemycin Oxime490%
Bexagliflozin461.2%
Frunevetmab450.6%
Mirtazapine451.6%
Sarolaner410.1%
Amoxicillin400.4%
Capromorelin401.5%

Species split

Dog68.9%719
Cat30.8%321
Horse0.3%3

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

03162Apr 2021: 0May 2021: 0Jun 2021: 0Jul 2021: 0Aug 2021: 0Sep 2021: 0Oct 2021: 1Nov 2021: 0Dec 2021: 1Jan 2022: 12022Feb 2022: 0Mar 2022: 0Apr 2022: 1May 2022: 1Jun 2022: 1Jul 2022: 3Aug 2022: 6Sep 2022: 6Oct 2022: 4Nov 2022: 8Dec 2022: 4Jan 2023: 92023Feb 2023: 11Mar 2023: 6Apr 2023: 14May 2023: 12Jun 2023: 12Jul 2023: 13Aug 2023: 24Sep 2023: 17Oct 2023: 21Nov 2023: 19Dec 2023: 24Jan 2024: 122024Feb 2024: 24Mar 2024: 26Apr 2024: 30May 2024: 28Jun 2024: 26Jul 2024: 22Aug 2024: 21Sep 2024: 22Oct 2024: 27Nov 2024: 25Dec 2024: 29Jan 2025: 282025Feb 2025: 24Mar 2025: 26Apr 2025: 28May 2025: 21Jun 2025: 39Jul 2025: 28Aug 2025: 40Sep 2025: 62Oct 2025: 50Nov 2025: 42Dec 2025: 32Jan 2026: 482026Feb 2026: 41Mar 2026: 16

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.

02104202002: 120022004: 120042006: 120062007: 120072020: 320202021: 220212022: 3520222023: 18220232024: 29220242025: 42020252026: 1052026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal7.7%80
Recovered with Sequela0.8%8
Ongoing40.9%427
Died6.8%71
Euthanized19.8%206
Outcome Unknown24.4%254

Age of the animal

Under 1 year9.1%95
1 to 3 years9.9%103
4 to 7 years22.8%238
8 to 11 years27.7%289
12 years and over28.9%301
Age not given1.6%17
MeasureReports listing this termAll reports
Reports1,0431,357,245
Classed serious, of reports stating it75%38.6%
Death or euthanasia recorded, per 1,000 reports265.663.8

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 "Decreased haematocrit"

What does "Decreased haematocrit" 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 decreased haematocrit?

1,043 reports through March 2026 (0.1% of all reports), 447 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: maropitant (168), ilunocitinib (132), bedinvetmab (117), gabapentin (91) and prednisone (87). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (68.9%), cat (30.8%) and horse (0.3%).

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.