Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Dullness: reports listing this term

744reports listing the term, 2005–20260.1% of all reports
62reports, 12 months to March 202679 in the 12 months before
82.4%classed serious, as reportedall reports: 38.6%
80%of these reports concern dogscat 16.3%

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

62 reports listed it in the 12 months to March 2026, down 22% from 79 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 milbemycin oxime + spinosad, maropitant and fluralaner. 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.

80% of the reports concern dogs, 16.3% of the reports concern cats and 2.8% of the reports concern horses. Of reports listing this term that state seriousness, 82.4% were classed as serious; 33.6% 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
Milbemycin Oxime + Spinosad1370.1%
Maropitant770.5%
Fluralaner720.1%
Moxidectin380.1%
Bedinvetmab370.2%
Spinosad350%
Carprofen330.1%
Cefovecin sodium320.2%
Gabapentin290.3%
Ivermectin290.1%
Afoxolaner270%
Prednisone270.3%
Buprenorphine250.3%
Pyrantel Pamoate + Sarolaner250%
Meloxicam210.1%
Famotidine190.6%
Oclacitinib190.1%
Trilostane190.2%
Diphenhydramine180.4%
Insulin180.1%
Butorphanol Tartrate160.2%
Enrofloxacin160.2%
Ivermectin + Pyrantel Pamoate160%
Dexamethasone150.5%
Sarolaner150.1%

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
Spinosad1690.1%
Milbemycin Oxime1670.1%
Maropitant770.5%
Fluralaner750.1%
Pyrantel Pamoate600%
Ivermectin580%
Moxidectin560.1%
Sarolaner460.1%
Bedinvetmab370.2%
Praziquantel370%
Carprofen330.1%
Cefovecin sodium320.2%
Gabapentin290.3%
Afoxolaner270%
Prednisone270.3%
Buprenorphine250.3%
Lufenuron210.1%
Meloxicam210.1%
Dexamethasone190.4%
Famotidine190.6%
Oclacitinib190.1%
Trilostane190.2%
Diphenhydramine180.4%
Insulin180.1%
Selamectin180%

Species split

Dog80%595
Cat16.3%121
Horse2.8%21
Cattle0.4%3
Goat0.1%1
Other Bovine0.1%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 0.1% of all cat reports.

Trend

0612Apr 2021: 4May 2021: 4Jun 2021: 3Jul 2021: 6Aug 2021: 4Sep 2021: 6Oct 2021: 4Nov 2021: 3Dec 2021: 2Jan 2022: 22022Feb 2022: 3Mar 2022: 5Apr 2022: 0May 2022: 2Jun 2022: 3Jul 2022: 4Aug 2022: 6Sep 2022: 3Oct 2022: 4Nov 2022: 0Dec 2022: 2Jan 2023: 32023Feb 2023: 2Mar 2023: 2Apr 2023: 0May 2023: 1Jun 2023: 3Jul 2023: 2Aug 2023: 2Sep 2023: 4Oct 2023: 5Nov 2023: 5Dec 2023: 1Jan 2024: 92024Feb 2024: 1Mar 2024: 3Apr 2024: 5May 2024: 9Jun 2024: 8Jul 2024: 2Aug 2024: 7Sep 2024: 12Oct 2024: 8Nov 2024: 4Dec 2024: 9Jan 2025: 42025Feb 2025: 3Mar 2025: 8Apr 2025: 5May 2025: 7Jun 2025: 9Jul 2025: 4Aug 2025: 4Sep 2025: 5Oct 2025: 6Nov 2025: 4Dec 2025: 7Jan 2026: 12026Feb 2026: 8Mar 2026: 2

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.

039772005: 120052007: 12008: 120082009: 12011: 1420112012: 502013: 7720132014: 482015: 4520152016: 472017: 6020172018: 462019: 4720192020: 382021: 5020212022: 342023: 3020232024: 772025: 6620252026: 11

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal26.2%195
Recovered with Sequela4.4%33
Ongoing23.1%172
Died8.7%65
Euthanized25.3%188
Outcome Unknown13%97

Age of the animal

Under 1 year16%119
1 to 3 years20.7%154
4 to 7 years21.4%159
8 to 11 years22.7%169
12 years and over18.1%135
Age not given1.1%8
MeasureReports listing this termAll reports
Reports7441,357,245
Classed serious, of reports stating it82.4%38.6%
Death or euthanasia recorded, per 1,000 reports33663.8

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 "Dullness"

What does "Dullness" 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 dullness?

744 reports through March 2026 (0.1% of all reports), 62 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: milbemycin oxime + spinosad (137), maropitant (77), fluralaner (72), moxidectin (38) and bedinvetmab (37). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (80%), cat (16.3%), horse (2.8%) and cattle (0.4%).

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.