Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Quiet: reports listing this term

770reports listing the term, 2015–20260.1% of all reports
172reports, 12 months to March 2026153 in the 12 months before
62.5%classed serious, as reportedall reports: 38.6%
71.3%of these reports concern dogscat 25.6%

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

172 reports listed it in the 12 months to March 2026, up 12% from 153 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, fluralaner and pyrantel pamoate + sarolaner. 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.

71.3% of the reports concern dogs, 25.6% of the reports concern cats and 2.9% of the reports concern horses. Of reports listing this term that state seriousness, 62.5% were classed as serious; 15.8% 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
Maropitant980.6%
Fluralaner790.1%
Pyrantel Pamoate + Sarolaner540.1%
Buprenorphine530.7%
Gabapentin500.5%
Carprofen460.1%
Bedinvetmab420.2%
Sarolaner410.2%
Ivermectin + Pyrantel Pamoate350%
Moxidectin350.1%
Isoflurane320.6%
Afoxolaner290%
Oclacitinib290.1%
Prednisone290.3%
Diphenhydramine260.5%
Lotilaner250.2%
Milbemycin Oxime + Praziquantel250.1%
Cefovecin sodium240.2%
Butorphanol Tartrate230.3%
Doxycycline220.5%
Meloxicam220.1%
Melarsomine Dihydrochloride210.1%
Ondansetron212.6%
Capromorelin200.7%
Trilostane200.2%

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
Pyrantel Pamoate1230%
Sarolaner1100.1%
Maropitant980.6%
Fluralaner900.1%
Moxidectin700.1%
Praziquantel570.1%
Buprenorphine530.7%
Milbemycin Oxime530%
Gabapentin500.5%
Carprofen460.1%
Ivermectin450%
Bedinvetmab420.2%
Afoxolaner390.1%
Isoflurane320.6%
Oclacitinib290.1%
Prednisone290.3%
Lotilaner280.2%
Diphenhydramine260.5%
Butorphanol Tartrate240.3%
Cefovecin sodium240.2%
Selamectin240%
Doxycycline220.5%
Meloxicam220.1%
Melarsomine Dihydrochloride210.1%
Ondansetron212.6%

Species split

Dog71.3%549
Cat25.6%197
Horse2.9%22
Parrot0.1%1
Pig0.1%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

01122Apr 2021: 7May 2021: 15Jun 2021: 5Jul 2021: 6Aug 2021: 2Sep 2021: 7Oct 2021: 6Nov 2021: 9Dec 2021: 2Jan 2022: 32022Feb 2022: 7Mar 2022: 2Apr 2022: 6May 2022: 9Jun 2022: 7Jul 2022: 10Aug 2022: 4Sep 2022: 7Oct 2022: 10Nov 2022: 3Dec 2022: 4Jan 2023: 102023Feb 2023: 3Mar 2023: 8Apr 2023: 6May 2023: 12Jun 2023: 8Jul 2023: 15Aug 2023: 7Sep 2023: 8Oct 2023: 11Nov 2023: 7Dec 2023: 10Jan 2024: 122024Feb 2024: 9Mar 2024: 12Apr 2024: 6May 2024: 11Jun 2024: 12Jul 2024: 14Aug 2024: 14Sep 2024: 11Oct 2024: 14Nov 2024: 12Dec 2024: 20Jan 2025: 92025Feb 2025: 15Mar 2025: 15Apr 2025: 22May 2025: 16Jun 2025: 15Jul 2025: 11Aug 2025: 16Sep 2025: 21Oct 2025: 15Nov 2025: 12Dec 2025: 8Jan 2026: 82026Feb 2026: 17Mar 2026: 11

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.

0881752015: 220152017: 120172018: 3620182019: 5120192020: 6720202021: 7820212022: 7220222023: 10520232024: 14720242025: 17520252026: 362026

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal24.8%191
Recovered with Sequela0.8%6
Ongoing40.6%313
Died6.1%47
Euthanized9.7%75
Outcome Unknown18.3%141

Age of the animal

Under 1 year13.6%105
1 to 3 years21%162
4 to 7 years23.8%183
8 to 11 years21.7%167
12 years and over17.9%138
Age not given1.9%15
MeasureReports listing this termAll reports
Reports7701,357,245
Classed serious, of reports stating it62.5%38.6%
Death or euthanasia recorded, per 1,000 reports158.463.8

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 "Quiet"

What does "Quiet" 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 quiet?

770 reports through March 2026 (0.1% of all reports), 172 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: maropitant (98), fluralaner (79), pyrantel pamoate + sarolaner (54), buprenorphine (53) and gabapentin (50). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (71.3%), cat (25.6%), horse (2.9%) and parrot (0.1%).

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.