Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Bad taste: reports listing this term

281reports listing the term, 2009–20260% of all reports
17reports, 12 months to March 20268 in the 12 months before
46.7%classed serious, as reportedall reports: 38.6%
99.6%of these reports concern exposed people

"Bad taste" is a coded term listed in 281 adverse event reports received by FDA, 0% of the database. Terms come from VeDDRA, the veterinary dictionary that FDA and drug companies use to code what a reporter describes.

17 reports listed it in the 12 months to March 2026, up 113% from 8 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 fluralaner, selamectin and imidacloprid + moxidectin. 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.

99.6% of the reports concern exposed people. Of reports listing this term that state seriousness, 46.7% were classed as serious; 0% 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
Fluralaner290%
Selamectin290%
Imidacloprid + Moxidectin260.1%
Tilmicosin234.6%
Milbemycin Oxime + Spinosad190%
Tilmicosin Phosphate180.5%
Tylosin Tartrate112.1%
Ivermectin100%
Emodepside + Praziquantel80.1%
Spinosad80%
Capromorelin70.3%
Levothyroxine sodium60.2%
Aspirin51.9%
Moxidectin50%
Cyclosporine40%
Enrofloxacin40.1%
Fluralaner + Moxidectin40.1%
Milbemycin Oxime + Praziquantel40%
Omeprazole40.1%
Amlodipine30.4%
Florfenicol30.3%
Furosemide30.1%
Mirtazapine30.1%
Nitenpyram30%
Pentobarbital Sodium + Phenytoin Sodium30.5%

Ordered by number of reports, which mostly tracks how many reports a drug has overall. Across the whole database the term appears in 0% 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
Moxidectin360%
Fluralaner330%
Selamectin310%
Spinosad270%
Imidacloprid260.1%
Milbemycin Oxime240%
Tilmicosin234.6%
Praziquantel210%
Tilmicosin Phosphate180.5%
Ivermectin120%
Tylosin Tartrate111.8%
Emodepside80.1%
Capromorelin70.3%
Levothyroxine sodium60.2%
Aspirin51.9%
Eprinomectin50.1%
Pyrantel Pamoate50%
Cyclosporine40%
Enrofloxacin40%
Omeprazole40.1%
Amlodipine30.4%
Florfenicol30%
Furosemide30.1%
Lotilaner30%
Mirtazapine30.1%

Species split

Human exposure99.6%280

Coloured bar: share of reports listing this term. Grey bar: the species' share of all reports. The term appears in 1.7% of all human exposure reports.

Trend

024Apr 2021: 1May 2021: 0Jun 2021: 2Jul 2021: 1Aug 2021: 4Sep 2021: 1Oct 2021: 2Nov 2021: 2Dec 2021: 1Jan 2022: 02022Feb 2022: 1Mar 2022: 2Apr 2022: 0May 2022: 1Jun 2022: 2Jul 2022: 0Aug 2022: 0Sep 2022: 1Oct 2022: 0Nov 2022: 2Dec 2022: 1Jan 2023: 22023Feb 2023: 0Mar 2023: 0Apr 2023: 1May 2023: 3Jun 2023: 1Jul 2023: 3Aug 2023: 1Sep 2023: 1Oct 2023: 0Nov 2023: 1Dec 2023: 0Jan 2024: 12024Feb 2024: 0Mar 2024: 0Apr 2024: 0May 2024: 0Jun 2024: 0Jul 2024: 3Aug 2024: 1Sep 2024: 0Oct 2024: 2Nov 2024: 1Dec 2024: 0Jan 2025: 02025Feb 2025: 0Mar 2025: 1Apr 2025: 1May 2025: 1Jun 2025: 2Jul 2025: 2Aug 2025: 0Sep 2025: 1Oct 2025: 3Nov 2025: 1Dec 2025: 2Jan 2026: 12026Feb 2026: 2Mar 2026: 1

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.

014282009: 220092011: 72012: 1820122013: 252014: 2420142015: 212016: 2820162017: 242018: 2520182019: 192020: 2020202021: 192022: 1020222023: 132024: 820242025: 142026: 42026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal49.5%139
Recovered with Sequela0.4%1
Ongoing12.1%34
Died0%0
Euthanized0%0
Outcome Unknown37%104

Age of the animal

Under 1 year0%0
1 to 3 years2.8%8
4 to 7 years0.4%1
8 to 11 years1.1%3
12 years and over59.8%168
Age not given35.9%101
MeasureReports listing this termAll reports
Reports2811,357,245
Classed serious, of reports stating it46.7%38.6%
Death or euthanasia recorded, per 1,000 reports063.8

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 "Bad taste"

What does "Bad taste" 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 bad taste?

281 reports through March 2026 (0% of all reports), 17 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: fluralaner (29), selamectin (29), imidacloprid + moxidectin (26), tilmicosin (23) and milbemycin oxime + spinosad (19). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

human exposure (99.6%).

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 30 Sep 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.