Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Regurgitation: reports listing this term

1,284reports listing the term, 1987–20260.1% of all reports
157reports, 12 months to March 2026133 in the 12 months before
61.6%classed serious, as reportedall reports: 38.6%
89.8%of these reports concern dogscat 6.7%

1,284 reports in FDA's animal adverse event database list the term "Regurgitation": 0.1% of all reports. It is a VeDDRA term, chosen by the person who coded the report to match what was described.

157 reports listed it in the 12 months to March 2026, up 18% from 133 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 maropitant, carprofen and gabapentin. 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.

89.8% of the reports concern dogs, 6.7% of the reports concern cats and 1.4% of the reports concern horses. Of reports listing this term that state seriousness, 61.6% were classed as serious; 18.5% 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
Maropitant2071.3%
Carprofen1290.2%
Gabapentin910.9%
Milbemycin Oxime + Spinosad890.1%
Deracoxib830.7%
Ivermectin + Pyrantel Pamoate720%
Butorphanol Tartrate700.9%
Fluralaner680.1%
Afoxolaner640.1%
Propofol561.2%
Metoclopramide538.1%
Midazolam522.6%
Moxidectin500.1%
Bedinvetmab490.3%
Isoflurane491%
Melarsomine Dihydrochloride480.2%
Tramadol481.3%
Buprenorphine470.6%
Oclacitinib450.2%
Enrofloxacin440.6%
Meloxicam420.2%
Famotidine411.4%
Ondansetron415%
Prednisone410.4%
Metronidazole391.1%

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
Maropitant2071.3%
Milbemycin Oxime1670.1%
Pyrantel Pamoate1430.1%
Carprofen1290.2%
Spinosad1190.1%
Ivermectin1010.1%
Gabapentin910.9%
Deracoxib830.7%
Moxidectin760.1%
Afoxolaner730.1%
Praziquantel730.1%
Butorphanol Tartrate710.9%
Fluralaner680.1%
Sarolaner600.1%
Propofol561.2%
Metoclopramide538.1%
Midazolam522.6%
Bedinvetmab490.3%
Isoflurane491%
Melarsomine Dihydrochloride480.2%
Tramadol481.3%
Buprenorphine470.6%
Oclacitinib450.2%
Enrofloxacin440.5%
Meloxicam420.2%

Species split

Dog89.8%1,153
Cat6.7%86
Horse1.4%18
Cattle0.3%4
Human exposure0.3%4
Pig0.3%4

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: 7May 2021: 9Jun 2021: 5Jul 2021: 8Aug 2021: 3Sep 2021: 4Oct 2021: 3Nov 2021: 2Dec 2021: 3Jan 2022: 12022Feb 2022: 8Mar 2022: 6Apr 2022: 5May 2022: 9Jun 2022: 5Jul 2022: 2Aug 2022: 9Sep 2022: 6Oct 2022: 4Nov 2022: 4Dec 2022: 2Jan 2023: 42023Feb 2023: 1Mar 2023: 3Apr 2023: 10May 2023: 12Jun 2023: 6Jul 2023: 9Aug 2023: 11Sep 2023: 5Oct 2023: 8Nov 2023: 7Dec 2023: 3Jan 2024: 82024Feb 2024: 12Mar 2024: 9Apr 2024: 13May 2024: 18Jun 2024: 9Jul 2024: 12Aug 2024: 11Sep 2024: 5Oct 2024: 14Nov 2024: 12Dec 2024: 11Jan 2025: 62025Feb 2025: 9Mar 2025: 13Apr 2025: 10May 2025: 15Jun 2025: 13Jul 2025: 14Aug 2025: 19Sep 2025: 21Oct 2025: 13Nov 2025: 13Dec 2025: 12Jan 2026: 82026Feb 2026: 11Mar 2026: 8

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.

0791581987: 219871994: 21995: 11997: 219971998: 21999: 102000: 120002001: 32002: 82003: 820032004: 202005: 132006: 820062007: 222008: 212009: 2620092010: 112011: 292012: 3220122013: 542014: 552015: 7120152016: 892017: 822018: 5720182019: 662020: 592021: 7120212022: 612023: 792024: 13420242025: 1582026: 27

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal27.3%351
Recovered with Sequela1.4%18
Ongoing22.4%288
Died8.8%113
Euthanized9.9%127
Outcome Unknown19.9%255

Age of the animal

Under 1 year9.1%117
1 to 3 years22.6%290
4 to 7 years26.2%336
8 to 11 years22.8%293
12 years and over12.9%165
Age not given6.5%83
MeasureReports listing this termAll reports
Reports1,2841,357,245
Classed serious, of reports stating it61.6%38.6%
Death or euthanasia recorded, per 1,000 reports184.663.8

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 "Regurgitation"

What does "Regurgitation" 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 regurgitation?

1,284 reports through March 2026 (0.1% of all reports), 157 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: maropitant (207), carprofen (129), gabapentin (91), milbemycin oxime + spinosad (89) and deracoxib (83). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (89.8%), cat (6.7%), horse (1.4%) and cattle (0.3%).

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.