Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Elevated triglyceride: reports listing this term

983reports listing the term, 1997–20260.1% of all reports
121reports, 12 months to March 202687 in the 12 months before
56.5%classed serious, as reportedall reports: 38.6%
82.7%of these reports concern dogscat 14.8%

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

121 reports listed it in the 12 months to March 2026, up 39% from 87 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, trilostane and oclacitinib. 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.

82.7% of the reports concern dogs, 14.8% of the reports concern cats and 2.3% of the reports concern horses. Of reports listing this term that state seriousness, 56.5% were classed as serious; 14.1% 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
Carprofen1370.3%
Trilostane1211%
Oclacitinib610.2%
Cyclosporine530.2%
Fluralaner510.1%
Bexagliflozin471.2%
Gabapentin390.4%
Velagliflozin390.8%
Deracoxib370.3%
Insulin370.3%
Milbemycin Oxime + Spinosad360%
Afoxolaner330.1%
Ivermectin + Pyrantel Pamoate330%
Cefovecin sodium310.2%
Prednisone290.3%
Maropitant280.2%
Bedinvetmab270.1%
Moxidectin250%
Grapiprant190.2%
Selamectin190%
Dirlotapide180.6%
Spinosad180%
Amoxicillin160.2%
Selegiline Hydrochloride140.3%
Meloxicam130.1%

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
Carprofen1370.3%
Trilostane1211%
Milbemycin Oxime640%
Oclacitinib610.2%
Pyrantel Pamoate570%
Cyclosporine530.2%
Spinosad530%
Fluralaner520.1%
Bexagliflozin471.2%
Ivermectin460%
Moxidectin420%
Gabapentin390.4%
Velagliflozin390.8%
Afoxolaner370.1%
Deracoxib370.3%
Insulin370.3%
Cefovecin sodium310.2%
Prednisone290.3%
Maropitant280.2%
Bedinvetmab270.1%
Amoxicillin240.2%
Sarolaner230%
Praziquantel220%
Grapiprant190.2%
Selamectin190%

Species split

Dog82.7%813
Cat14.8%145
Horse2.3%23
Ferret0.1%1
Human exposure0.1%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

01121Apr 2021: 5May 2021: 1Jun 2021: 4Jul 2021: 2Aug 2021: 5Sep 2021: 2Oct 2021: 5Nov 2021: 5Dec 2021: 0Jan 2022: 22022Feb 2022: 0Mar 2022: 3Apr 2022: 4May 2022: 2Jun 2022: 0Jul 2022: 4Aug 2022: 0Sep 2022: 2Oct 2022: 6Nov 2022: 2Dec 2022: 5Jan 2023: 02023Feb 2023: 5Mar 2023: 2Apr 2023: 3May 2023: 3Jun 2023: 4Jul 2023: 1Aug 2023: 2Sep 2023: 3Oct 2023: 2Nov 2023: 3Dec 2023: 4Jan 2024: 32024Feb 2024: 4Mar 2024: 9Apr 2024: 7May 2024: 4Jun 2024: 7Jul 2024: 6Aug 2024: 16Sep 2024: 6Oct 2024: 8Nov 2024: 7Dec 2024: 6Jan 2025: 42025Feb 2025: 7Mar 2025: 9Apr 2025: 6May 2025: 9Jun 2025: 9Jul 2025: 7Aug 2025: 9Sep 2025: 11Oct 2025: 10Nov 2025: 10Dec 2025: 13Jan 2026: 212026Feb 2026: 11Mar 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.

0521041997: 119971998: 121999: 152000: 1420002001: 122002: 92003: 1320032004: 352005: 362006: 3020062007: 342008: 322009: 2220092010: 292011: 242012: 3220122013: 212014: 232015: 2520152016: 502017: 562018: 4920182019: 482020: 382021: 3720212022: 302023: 322024: 8320242025: 1042026: 37

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal5.1%50
Recovered with Sequela2.3%23
Ongoing25.7%253
Died7.3%72
Euthanized6.8%67
Outcome Unknown24.9%245

Age of the animal

Under 1 year1.4%14
1 to 3 years4.9%48
4 to 7 years21.4%210
8 to 11 years39.2%385
12 years and over31.8%313
Age not given1.3%13
MeasureReports listing this termAll reports
Reports9831,357,245
Classed serious, of reports stating it56.5%38.6%
Death or euthanasia recorded, per 1,000 reports141.463.8

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 "Elevated triglyceride"

What does "Elevated triglyceride" 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 elevated triglyceride?

983 reports through March 2026 (0.1% of all reports), 121 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: carprofen (137), trilostane (121), oclacitinib (61), cyclosporine (53) and fluralaner (51). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (82.7%), cat (14.8%), horse (2.3%) and ferret (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.