Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Hypophosphataemia: reports listing this term

930reports listing the term, 1987–20260.1% of all reports
123reports, 12 months to March 2026102 in the 12 months before
76.9%classed serious, as reportedall reports: 38.6%
72%of these reports concern dogscat 23.8%

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

123 reports listed it in the 12 months to March 2026, up 21% from 102 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 carprofen, fluralaner and maropitant. 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.

72% of the reports concern dogs, 23.8% of the reports concern cats and 2.2% of the reports concern horses. Of reports listing this term that state seriousness, 76.9% were classed as serious; 22% 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
Carprofen960.2%
Fluralaner880.1%
Maropitant840.5%
Afoxolaner500.1%
Moxidectin500.1%
Oclacitinib470.2%
Milbemycin Oxime + Spinosad460%
Velagliflozin461%
Ivermectin + Pyrantel Pamoate440%
Cefovecin sodium330.2%
Deracoxib300.3%
Spinosad270%
Bexagliflozin260.7%
Insulin260.2%
Bedinvetmab250.1%
Selamectin250%
Gabapentin240.2%
Buprenorphine230.3%
Pyrantel Pamoate + Sarolaner220%
Diphenhydramine180.4%
Milbemycin Oxime + Praziquantel180.1%
Ivermectin170.1%
Robenacoxib170.5%
Sarolaner170.1%
Trilostane170.1%

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
Carprofen960.2%
Pyrantel Pamoate950%
Fluralaner930.1%
Milbemycin Oxime890%
Maropitant840.5%
Moxidectin780.1%
Spinosad730%
Ivermectin650%
Praziquantel600.1%
Afoxolaner580.1%
Oclacitinib470.2%
Velagliflozin461%
Sarolaner450.1%
Cefovecin sodium330.2%
Deracoxib300.3%
Selamectin280%
Bexagliflozin260.7%
Insulin260.2%
Bedinvetmab250.1%
Gabapentin240.2%
Buprenorphine230.3%
Lufenuron210.1%
Diphenhydramine180.4%
Amoxicillin170.2%
Robenacoxib170.5%

Species split

Dog72%670
Cat23.8%221
Horse2.2%20
Cattle1.9%18
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 0.1% of all cat reports.

Trend

0816Apr 2021: 4May 2021: 0Jun 2021: 3Jul 2021: 7Aug 2021: 4Sep 2021: 2Oct 2021: 4Nov 2021: 4Dec 2021: 5Jan 2022: 12022Feb 2022: 1Mar 2022: 3Apr 2022: 3May 2022: 3Jun 2022: 2Jul 2022: 2Aug 2022: 3Sep 2022: 3Oct 2022: 1Nov 2022: 4Dec 2022: 4Jan 2023: 32023Feb 2023: 3Mar 2023: 4Apr 2023: 1May 2023: 6Jun 2023: 7Jul 2023: 1Aug 2023: 2Sep 2023: 1Oct 2023: 3Nov 2023: 6Dec 2023: 3Jan 2024: 82024Feb 2024: 5Mar 2024: 9Apr 2024: 6May 2024: 11Jun 2024: 5Jul 2024: 2Aug 2024: 14Sep 2024: 12Oct 2024: 8Nov 2024: 5Dec 2024: 8Jan 2025: 112025Feb 2025: 13Mar 2025: 7Apr 2025: 9May 2025: 10Jun 2025: 8Jul 2025: 6Aug 2025: 12Sep 2025: 10Oct 2025: 16Nov 2025: 9Dec 2025: 9Jan 2026: 122026Feb 2026: 10Mar 2026: 12

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.

0601201987: 119871988: 11989: 11995: 519951996: 21997: 11998: 619981999: 62000: 82001: 920012002: 32003: 92004: 2120042005: 162006: 172007: 2520072008: 172009: 212010: 2620102011: 282012: 212013: 1420132014: 302015: 472016: 4720162017: 522018: 652019: 3620192020: 352021: 432022: 3020222023: 402024: 932025: 12020252026: 34

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal9.6%89
Recovered with Sequela2.3%21
Ongoing30.2%281
Died11.3%105
Euthanized10.8%100
Outcome Unknown18.7%174

Age of the animal

Under 1 year3.8%35
1 to 3 years18.7%174
4 to 7 years33.4%311
8 to 11 years26.9%250
12 years and over15.4%143
Age not given1.8%17
MeasureReports listing this termAll reports
Reports9301,357,245
Classed serious, of reports stating it76.9%38.6%
Death or euthanasia recorded, per 1,000 reports220.463.8

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 "Hypophosphataemia"

What does "Hypophosphataemia" 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 hypophosphataemia?

930 reports through March 2026 (0.1% of all reports), 123 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: carprofen (96), fluralaner (88), maropitant (84), afoxolaner (50) and moxidectin (50). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (72%), cat (23.8%), horse (2.2%) and cattle (1.9%).

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 30 Sep 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.