Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Bruising: reports listing this term

1,539reports listing the term, 1990–20260.1% of all reports
128reports, 12 months to March 2026125 in the 12 months before
74.6%classed serious, as reportedall reports: 38.6%
87.3%of these reports concern dogscat 7.7%

"Bruising" is a coded term listed in 1,539 adverse event reports received by FDA, 0.1% of the database. Terms come from VeDDRA, the veterinary dictionary that FDA and drug companies use to code what a reporter describes.

128 reports listed it in the 12 months to March 2026, close to the 125 of 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 carprofen, maropitant and 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.

87.3% of the reports concern dogs, 7.7% of the reports concern cats and 3.3% of the reports concern exposed people. Of reports listing this term that state seriousness, 74.6% were classed as serious; 25.5% 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
Carprofen2570.5%
Maropitant1671%
Moxidectin1140.2%
Tigilanol tiglate1035.2%
Cefovecin sodium990.7%
Prednisone901%
Meloxicam880.5%
Gabapentin810.8%
Diphenhydramine751.5%
Milbemycin Oxime + Spinosad740.1%
Oclacitinib680.2%
Bedinvetmab670.4%
Buprenorphine670.9%
Butorphanol Tartrate660.9%
Isoflurane561.1%
Famotidine551.8%
Dexamethasone521.8%
Propofol511.1%
Fluralaner500.1%
Deracoxib490.4%
Enrofloxacin480.6%
Dexmedetomidine hydrochloride460.8%
Polysulfated Glycosaminoglycan430.7%
Doxycycline411%
Ketamine Hydrochloride400.6%

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
Carprofen2570.5%
Maropitant1671%
Moxidectin1270.1%
Milbemycin Oxime1070%
Tigilanol tiglate1035.2%
Cefovecin sodium990.7%
Prednisone901%
Spinosad900%
Meloxicam880.5%
Gabapentin810.8%
Diphenhydramine751.5%
Pyrantel Pamoate720%
Butorphanol Tartrate690.9%
Oclacitinib680.2%
Bedinvetmab670.4%
Buprenorphine670.9%
Ivermectin600%
Dexamethasone571.1%
Isoflurane571.1%
Famotidine551.8%
Fluralaner510.1%
Propofol511.1%
Enrofloxacin500.6%
Deracoxib490.4%
Clavulanate Potassium470.6%

Species split

Dog87.3%1,344
Cat7.7%119
Human exposure3.3%51
Horse0.5%8
Cattle0.4%6
Rabbit0.3%5

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

01325Apr 2021: 7May 2021: 4Jun 2021: 5Jul 2021: 12Aug 2021: 12Sep 2021: 9Oct 2021: 7Nov 2021: 4Dec 2021: 7Jan 2022: 72022Feb 2022: 12Mar 2022: 6Apr 2022: 10May 2022: 11Jun 2022: 4Jul 2022: 3Aug 2022: 4Sep 2022: 8Oct 2022: 10Nov 2022: 5Dec 2022: 2Jan 2023: 162023Feb 2023: 10Mar 2023: 2Apr 2023: 10May 2023: 8Jun 2023: 13Jul 2023: 11Aug 2023: 8Sep 2023: 5Oct 2023: 9Nov 2023: 5Dec 2023: 8Jan 2024: 152024Feb 2024: 12Mar 2024: 12Apr 2024: 8May 2024: 7Jun 2024: 14Jul 2024: 14Aug 2024: 7Sep 2024: 12Oct 2024: 20Nov 2024: 7Dec 2024: 14Jan 2025: 112025Feb 2025: 5Mar 2025: 6Apr 2025: 25May 2025: 13Jun 2025: 11Jul 2025: 7Aug 2025: 9Sep 2025: 5Oct 2025: 12Nov 2025: 13Dec 2025: 6Jan 2026: 112026Feb 2026: 11Mar 2026: 5

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.

0711421990: 119901993: 11995: 21996: 219961997: 81998: 141999: 1219992000: 122001: 72002: 720022003: 202004: 242005: 2520052006: 162007: 382008: 2820082009: 312010: 272011: 2720112012: 622013: 792014: 8220142015: 912016: 852017: 8720172018: 722019: 572020: 5620202021: 872022: 822023: 10520232024: 1422025: 1232026: 272026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal12.1%186
Recovered with Sequela1.2%18
Ongoing30.9%475
Died14.9%229
Euthanized10.6%163
Outcome Unknown16.5%254

Age of the animal

Under 1 year6.4%98
1 to 3 years14.8%228
4 to 7 years28%431
8 to 11 years28.1%432
12 years and over18.1%279
Age not given4.6%71
MeasureReports listing this termAll reports
Reports1,5391,357,245
Classed serious, of reports stating it74.6%38.6%
Death or euthanasia recorded, per 1,000 reports254.763.8

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 "Bruising"

What does "Bruising" 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 bruising?

1,539 reports through March 2026 (0.1% of all reports), 128 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: carprofen (257), maropitant (167), moxidectin (114), tigilanol tiglate (103) and cefovecin sodium (99). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (87.3%), cat (7.7%), human exposure (3.3%) and horse (0.5%).

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.