Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Diabetic ketoacidosis: reports listing this term

630reports listing the term, 2012–20260.1% of all reports
130reports, 12 months to March 2026210 in the 12 months before
97.1%classed serious, as reportedall reports: 38.6%
73.5%of these reports concern catsdog 26.5%

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

130 reports listed it in the 12 months to March 2026, down 38% from 210 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 bexagliflozin, velagliflozin and insulin. 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.

73.5% of the reports concern cats and 26.5% of the reports concern dogs. Of reports listing this term that state seriousness, 97.1% were classed as serious; 42.1% 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
Bexagliflozin2677%
Velagliflozin1683.7%
Insulin1000.8%
Maropitant500.3%
Trilostane480.4%
Cefovecin sodium250.2%
Dextrose258.5%
Gabapentin250.2%
Capromorelin170.6%
Bedinvetmab160.1%
Milbemycin Oxime + Spinosad150%
Mirtazapine140.5%
Buprenorphine120.2%
Carprofen120%
Prednisone120.1%
Famotidine110.4%
Insulin Glargine1116.2%
Ampicillin Sodium103.1%
Cyclosporine100%
Moxidectin90%
Ondansetron91.1%
Afoxolaner80%
Amoxicillin + Clavulanate Potassium80.3%
Metronidazole80.2%
Oclacitinib80%

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
Bexagliflozin2677%
Velagliflozin1683.7%
Insulin1000.8%
Maropitant500.3%
Trilostane480.4%
Cefovecin sodium250.2%
Dextrose256.2%
Gabapentin250.2%
Capromorelin170.6%
Milbemycin Oxime170%
Bedinvetmab160.1%
Spinosad150%
Mirtazapine140.5%
Moxidectin130%
Buprenorphine120.2%
Carprofen120%
Prednisone120.1%
Famotidine110.4%
Insulin Glargine1116.2%
Ampicillin Sodium103.1%
Clavulanate Potassium100.1%
Cyclosporine100%
Ondansetron91.1%
Afoxolaner80%
Amoxicillin80.1%

Species split

Cat73.5%463
Dog26.5%167

Coloured bar: share of reports listing this term. Grey bar: the species' share of all reports. The term appears in 0.3% of all cat reports; The term appears in 0% of all dog reports.

Trend

01428Apr 2021: 1May 2021: 1Jun 2021: 1Jul 2021: 0Aug 2021: 0Sep 2021: 0Oct 2021: 1Nov 2021: 3Dec 2021: 0Jan 2022: 02022Feb 2022: 0Mar 2022: 2Apr 2022: 1May 2022: 2Jun 2022: 0Jul 2022: 1Aug 2022: 0Sep 2022: 0Oct 2022: 1Nov 2022: 1Dec 2022: 0Jan 2023: 02023Feb 2023: 0Mar 2023: 2Apr 2023: 3May 2023: 5Jun 2023: 10Jul 2023: 7Aug 2023: 6Sep 2023: 8Oct 2023: 9Nov 2023: 18Dec 2023: 16Jan 2024: 282024Feb 2024: 14Mar 2024: 22Apr 2024: 17May 2024: 16Jun 2024: 15Jul 2024: 19Aug 2024: 17Sep 2024: 17Oct 2024: 17Nov 2024: 20Dec 2024: 16Jan 2025: 232025Feb 2025: 22Mar 2025: 11Apr 2025: 19May 2025: 11Jun 2025: 13Jul 2025: 13Aug 2025: 17Sep 2025: 10Oct 2025: 7Nov 2025: 10Dec 2025: 8Jan 2026: 82026Feb 2026: 9Mar 2026: 5

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.

01092182012: 720122013: 1320132014: 2420142015: 1920152016: 2420162017: 1020172018: 820182019: 820192020: 920202021: 1220212022: 820222023: 8420232024: 21820242025: 16420252026: 222026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal11.3%71
Recovered with Sequela1%6
Ongoing26%164
Died8.7%55
Euthanized33.3%210
Outcome Unknown20%126

Age of the animal

Under 1 year0%0
1 to 3 years1.7%11
4 to 7 years20.3%128
8 to 11 years44.4%280
12 years and over26.5%167
Age not given7%44
MeasureReports listing this termAll reports
Reports6301,357,245
Classed serious, of reports stating it97.1%38.6%
Death or euthanasia recorded, per 1,000 reports420.663.8

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 "Diabetic ketoacidosis"

What does "Diabetic ketoacidosis" 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 diabetic ketoacidosis?

630 reports through March 2026 (0.1% of all reports), 130 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: bexagliflozin (267), velagliflozin (168), insulin (100), maropitant (50) and trilostane (48). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

cat (73.5%) and dog (26.5%).

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.