Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Low thyroxine (T4): reports listing this term

656reports listing the term, 2004–20260.1% of all reports
124reports, 12 months to March 2026117 in the 12 months before
66.1%classed serious, as reportedall reports: 38.6%
89.3%of these reports concern dogscat 10.7%

656 reports in FDA's animal adverse event database list the term "Low thyroxine (T4)": 0.1% of all reports. It is a VeDDRA term, chosen by the person who coded the report to match what was described.

124 reports listed it in the 12 months to March 2026, close to the 117 of 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 trilostane, levothyroxine sodium 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.

89.3% of the reports concern dogs and 10.7% of the reports concern cats. Of reports listing this term that state seriousness, 66.1% were classed as serious; 18.3% 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
Trilostane1120.9%
Levothyroxine sodium872.8%
Bedinvetmab830.4%
Oclacitinib590.2%
Fluralaner580.1%
Gabapentin520.5%
Maropitant500.3%
Carprofen480.1%
Prednisone410.4%
Afoxolaner340.1%
Milbemycin Oxime + Spinosad310%
Pyrantel Pamoate + Sarolaner300.1%
Ivermectin + Pyrantel Pamoate270%
Grapiprant210.3%
Doxycycline200.5%
Ilunocitinib181%
Milbemycin Oxime + Praziquantel170.1%
Buprenorphine150.2%
Cefpodoxime proxetil150.4%
Moxidectin150%
Pimobendan150.2%
Enrofloxacin140.2%
Insulin140.1%
Metronidazole140.4%
Cefovecin sodium130.1%

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
Trilostane1120.9%
Levothyroxine sodium872.8%
Bedinvetmab830.4%
Pyrantel Pamoate680%
Milbemycin Oxime610%
Oclacitinib590.2%
Fluralaner580.1%
Gabapentin520.5%
Maropitant500.3%
Carprofen480.1%
Sarolaner430.1%
Prednisone410.4%
Afoxolaner370.1%
Spinosad350%
Ivermectin340%
Praziquantel270%
Moxidectin260%
Grapiprant210.3%
Clavulanate Potassium200.2%
Doxycycline200.5%
Ilunocitinib181%
Amoxicillin150.1%
Buprenorphine150.2%
Cefpodoxime proxetil150.4%
Pimobendan150.2%

Species split

Dog89.3%586
Cat10.7%70

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% of all cat reports.

Trend

0918Apr 2021: 4May 2021: 9Jun 2021: 4Jul 2021: 7Aug 2021: 5Sep 2021: 2Oct 2021: 7Nov 2021: 7Dec 2021: 2Jan 2022: 42022Feb 2022: 4Mar 2022: 2Apr 2022: 5May 2022: 8Jun 2022: 0Jul 2022: 3Aug 2022: 1Sep 2022: 6Oct 2022: 7Nov 2022: 5Dec 2022: 6Jan 2023: 52023Feb 2023: 5Mar 2023: 7Apr 2023: 6May 2023: 8Jun 2023: 3Jul 2023: 3Aug 2023: 12Sep 2023: 4Oct 2023: 1Nov 2023: 3Dec 2023: 6Jan 2024: 62024Feb 2024: 3Mar 2024: 5Apr 2024: 12May 2024: 12Jun 2024: 8Jul 2024: 4Aug 2024: 9Sep 2024: 10Oct 2024: 7Nov 2024: 11Dec 2024: 13Jan 2025: 122025Feb 2025: 9Mar 2025: 10Apr 2025: 11May 2025: 18Jun 2025: 9Jul 2025: 8Aug 2025: 6Sep 2025: 12Oct 2025: 8Nov 2025: 8Dec 2025: 12Jan 2026: 152026Feb 2026: 11Mar 2026: 6

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.

0621232004: 120042006: 12009: 120092012: 112013: 720132014: 82015: 720152016: 152017: 2220172018: 382019: 5920192020: 582021: 5920212022: 512023: 6320232024: 1002025: 12320252026: 32

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal6.4%42
Recovered with Sequela4.4%29
Ongoing37.8%248
Died4.6%30
Euthanized13.7%90
Outcome Unknown33.2%218

Age of the animal

Under 1 year1.1%7
1 to 3 years6.9%45
4 to 7 years21.3%140
8 to 11 years41.5%272
12 years and over28%184
Age not given1.2%8
MeasureReports listing this termAll reports
Reports6561,357,245
Classed serious, of reports stating it66.1%38.6%
Death or euthanasia recorded, per 1,000 reports182.963.8

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 "Low thyroxine (T4)"

What does "Low thyroxine (T4)" 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 low thyroxine (T4)?

656 reports through March 2026 (0.1% of all reports), 124 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: trilostane (112), levothyroxine sodium (87), bedinvetmab (83), oclacitinib (59) and fluralaner (58). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (89.3%) and cat (10.7%).

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.