Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Hypoadrenocorticism: reports listing this term

865reports listing the term, 1997–20250.1% of all reports
5reports, 12 months to March 20269 in the 12 months before
57.4%classed serious, as reportedall reports: 38.6%
99.5%of these reports concern dogscat 0.3%

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

5 reports listed it in the 12 months to March 2026, down 44% from 9 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 trilostane, carprofen 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.

99.5% of the reports concern dogs, 0.3% of the reports concern cats and 0.1% of the reports concern exposed people. Of reports listing this term that state seriousness, 57.4% were classed as serious; 8.9% 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
Trilostane6915.8%
Carprofen610.1%
Oclacitinib240.1%
Levothyroxine sodium230.7%
Insulin200.2%
Milbemycin Oxime + Spinosad180%
Gabapentin160.2%
Cyclosporine150.1%
Deracoxib120.1%
Prednisone110.1%
Ursodiol111.5%
Grapiprant100.1%
Moxidectin100%
Enalapril Maleate90.4%
Maropitant90.1%
Amlodipine81.1%
Metronidazole80.2%
Selegiline Hydrochloride80.2%
Pimobendan70.1%
Polysulfated Glycosaminoglycan70.1%
Benazepril61.1%
Meloxicam60%
Firocoxib50.1%
Fluralaner50%
Spinosad50%

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
Trilostane6915.8%
Carprofen610.1%
Milbemycin Oxime250%
Oclacitinib240.1%
Levothyroxine sodium230.7%
Spinosad230%
Insulin200.2%
Gabapentin160.2%
Cyclosporine150.1%
Deracoxib120.1%
Moxidectin110%
Prednisone110.1%
Ursodiol111.5%
Grapiprant100.1%
Enalapril Maleate90.4%
Maropitant90.1%
Amlodipine81.1%
Metronidazole80.2%
Selegiline Hydrochloride80.2%
Ivermectin70%
Pimobendan70.1%
Polysulfated Glycosaminoglycan70.1%
Benazepril61.1%
Meloxicam60%
Amoxicillin50%

Species split

Dog99.5%861
Cat0.3%3
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% of all cat reports.

Trend

0611Apr 2021: 7May 2021: 4Jun 2021: 6Jul 2021: 2Aug 2021: 10Sep 2021: 10Oct 2021: 8Nov 2021: 2Dec 2021: 6Jan 2022: 72022Feb 2022: 6Mar 2022: 6Apr 2022: 6May 2022: 5Jun 2022: 4Jul 2022: 7Aug 2022: 10Sep 2022: 11Oct 2022: 9Nov 2022: 11Dec 2022: 7Jan 2023: 102023Feb 2023: 11Mar 2023: 5Apr 2023: 5May 2023: 1Jun 2023: 0Jul 2023: 0Aug 2023: 4Sep 2023: 2Oct 2023: 0Nov 2023: 0Dec 2023: 1Jan 2024: 12024Feb 2024: 0Mar 2024: 1Apr 2024: 1May 2024: 0Jun 2024: 1Jul 2024: 2Aug 2024: 2Sep 2024: 1Oct 2024: 1Nov 2024: 0Dec 2024: 0Jan 2025: 02025Feb 2025: 0Mar 2025: 1Apr 2025: 1May 2025: 0Jun 2025: 0Jul 2025: 1Aug 2025: 2Sep 2025: 1Oct 2025: 0Nov 2025: 0Dec 2025: 0Jan 2026: 02026Feb 2026: 0Mar 2026: 0

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.

0501001997: 219971998: 31999: 132000: 420002001: 52002: 92003: 420032004: 72005: 92006: 1020062007: 82008: 112009: 1120092010: 152011: 202012: 4920122013: 392014: 102015: 2320152016: 712017: 912018: 3920182019: 1002020: 942021: 7420212022: 892023: 392024: 1020242025: 6

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal7.6%66
Recovered with Sequela1.4%12
Ongoing17.3%150
Died4%35
Euthanized4.9%42
Outcome Unknown51.9%449

Age of the animal

Under 1 year1.3%11
1 to 3 years4.6%40
4 to 7 years12.4%107
8 to 11 years42.7%369
12 years and over36.3%314
Age not given2.8%24
MeasureReports listing this termAll reports
Reports8651,357,245
Classed serious, of reports stating it57.4%38.6%
Death or euthanasia recorded, per 1,000 reports8963.8

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 "Hypoadrenocorticism"

What does "Hypoadrenocorticism" 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 hypoadrenocorticism?

865 reports through March 2026 (0.1% of all reports), 5 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: trilostane (691), carprofen (61), oclacitinib (24), levothyroxine sodium (23) and insulin (20). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (99.5%), cat (0.3%) and human exposure (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.