Pet Drug Reports

Reported signs

Reported sign · legacy FDA term

Ineffective, gastric ulcer(s): reports listing this term

In plain language: legacy FDA term: the product did not have the expected effect (gastric ulcer(s))

809reports listing the term, 2003–20260.1% of all reports
37reports, 12 months to March 202622 in the 12 months before
26.3%classed serious, as reportedall reports: 38.6%
100%of these reports concern horses

809 reports in FDA's animal adverse event database list the term "Ineffective, gastric ulcer(s)" (legacy FDA term: the product did not have the expected effect (gastric ulcer(s))): 0.1% of all reports. This is a legacy FDA term that predates the VeDDRA dictionary.

37 reports listed it in the 12 months to March 2026, up 68% from 22 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 omeprazole, sucralfate and misoprostol. 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.

100% of the reports concern horses. Of reports listing this term that state seriousness, 26.3% were classed as serious; 0.9% 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
Omeprazole80922.1%
Sucralfate1007.3%
Misoprostol2717.2%
Xylazine30.3%
Detomidine Hydrochloride20.2%
Doxycycline20%
Firocoxib20%
Flunixin20.9%
Metronidazole20.1%
Pergolide mesylate20.1%
Vitamin E20.2%
Acepromazine Maleate10%
Butorphanol Tartrate10%
Flunixin Meglumine10.1%
Gabapentin10%
Ivermectin10%
Ivermectin + Praziquantel10%
Methocarbamol10.1%

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
Omeprazole80922.1%
Sucralfate1007.2%
Misoprostol2717.1%
Xylazine30.3%
Detomidine Hydrochloride20.2%
Doxycycline20%
Firocoxib20%
Flunixin20.3%
Ivermectin20%
Metronidazole20.1%
Pergolide mesylate20.1%
Vitamin E20.2%
Acepromazine Maleate10%
Butorphanol Tartrate10%
Flunixin Meglumine10.1%
Gabapentin10%
Methocarbamol10.1%
Praziquantel10%

Species split

Horse100%809

Coloured bar: share of reports listing this term. Grey bar: the species' share of all reports. The term appears in 4.4% of all horse reports.

Trend

01020Apr 2021: 6May 2021: 5Jun 2021: 2Jul 2021: 1Aug 2021: 17Sep 2021: 12Oct 2021: 5Nov 2021: 7Dec 2021: 5Jan 2022: 82022Feb 2022: 6Mar 2022: 14Apr 2022: 15May 2022: 16Jun 2022: 12Jul 2022: 9Aug 2022: 14Sep 2022: 13Oct 2022: 10Nov 2022: 11Dec 2022: 8Jan 2023: 202023Feb 2023: 10Mar 2023: 9Apr 2023: 15May 2023: 20Jun 2023: 15Jul 2023: 13Aug 2023: 11Sep 2023: 0Oct 2023: 0Nov 2023: 1Dec 2023: 4Jan 2024: 52024Feb 2024: 4Mar 2024: 4Apr 2024: 0May 2024: 1Jun 2024: 2Jul 2024: 4Aug 2024: 0Sep 2024: 0Oct 2024: 4Nov 2024: 0Dec 2024: 6Jan 2025: 12025Feb 2025: 3Mar 2025: 1Apr 2025: 8May 2025: 1Jun 2025: 2Jul 2025: 0Aug 2025: 5Sep 2025: 2Oct 2025: 3Nov 2025: 0Dec 2025: 7Jan 2026: 82026Feb 2026: 1Mar 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. Legacy terms fade from recent years because new reports are coded in VeDDRA.

0681362003: 120032004: 62005: 320052006: 52007: 520072008: 62009: 1620092010: 132011: 1520112012: 172013: 2920132014: 372015: 2820152016: 372017: 5120172018: 322019: 5720192020: 622021: 6320212022: 1362023: 11820232024: 302025: 3320252026: 9

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal18.9%153
Recovered with Sequela0.2%2
Ongoing31.6%256
Died0%0
Euthanized0.9%7
Outcome Unknown39.7%321

Age of the animal

Under 1 year0.7%6
1 to 3 years4.9%40
4 to 7 years23.9%193
8 to 11 years25%202
12 years and over29.5%239
Age not given15.9%129
MeasureReports listing this termAll reports
Reports8091,357,245
Classed serious, of reports stating it26.3%38.6%
Death or euthanasia recorded, per 1,000 reports8.763.8

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 "Ineffective, gastric ulcer(s)"

What does "Ineffective, gastric ulcer(s)" mean in an adverse event report?

In plain language: legacy FDA term: the product did not have the expected effect (gastric ulcer(s)). It is a legacy FDA 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 ineffective, gastric ulcer(s)?

809 reports through March 2026 (0.1% of all reports), 37 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: omeprazole (809), sucralfate (100), misoprostol (27), xylazine (3) and detomidine hydrochloride (2). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

horse (100%).

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.