Pet Drug Reports

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Breed · Dog

Briard: adverse event reports

FDA breed label "Berger de Brie (Briard) - Briard" · single-breed animals only

104reports, 1996–20250% of dog reports
1reports, 12 months to March 20262 in the 12 months before
40.8%classed serious, as reportedall dogs: 38.3%
19.2%name carprofenall dogs: 4.8%

104 adverse event reports received by FDA describe an animal recorded as Briard (FDA breed label "Berger de Brie (Briard) - Briard"). That is 0% of all reports about dogs. Crossbred animals are not counted here, only reports that give this single breed.

1 reports arrived in the 12 months to March 2026, down 50% from 2 in the 12 months before. A breed's count mostly mirrors how common the breed is; registration and ownership figures by breed are not public data, so no per-animal rate can be given.

By active ingredient, the drugs named most often are carprofen, spinosad and afoxolaner. Carprofen is named in 19.2% of this breed's reports, a larger share than in reports about all dogs (4.8%).

The terms listed most often are vomiting (23.1%), diarrhoea (15.4%) and depression (11.5%). Vomiting appears in 23.1% of reports, about the same share as in all dog reports (19.7%). 40.8% of reports stating seriousness were classed as serious, against 38.3% for dogs overall.

Drugs named most often, by active ingredient

Active ingredients recorded for the drugReportsShare of Briard reportsShare of all dog reports
Carprofen2019.2%4.8%
Spinosad1312.5%5.8%
Afoxolaner98.7%5.7%
Milbemycin Oxime + Spinosad87.7%13.1%
Ivermectin + Pyrantel Pamoate76.7%14.9%
Imidacloprid54.8%0.5%
Lufenuron + Milbemycin Oxime54.8%2.7%
Nitenpyram54.8%1.1%
Fluralaner43.8%6.7%
Milbemycin Oxime43.8%3%
Deracoxib32.9%1.1%
Firocoxib32.9%0.8%
Meloxicam32.9%0.8%
Bedinvetmab21.9%1.9%
Cyclosporine21.9%1.5%
Enrofloxacin21.9%0.4%
Ivermectin21.9%1.3%
Sarolaner21.9%1.7%
Selamectin21.9%3%
Acetylsalicylic Acid11%0%

Ordered by report count. Differences from the species column often come from body size (which drugs a breed is prescribed) and from how common the breed was in the years a drug sold most. FDA states that these data cannot be used to estimate risk or to compare one product with another. Brand and manufacturer names are masked by FDA in these records.

Signs listed in reports

share of Briard reports listing the termall dog reports

  1. Vomiting23.1%24
  2. Diarrhoea[diarrhea]15.4%16
  3. Depression[dull, quiet or withdrawn]11.5%12
  4. Anorexia[not eating]10.6%11
  5. Ataxia[unsteady, uncoordinated movement]7.7%8
  6. Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]5.8%6
  7. Emesis[vomiting]5.8%6
  8. Behavioural disorder NOS[behaviour change, type not specified]4.8%5
  9. Death4.8%5
  10. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]4.8%5
  11. Lethargy[unusually tired or inactive]4.8%5
  12. Death by euthanasia[the animal was euthanized]3.8%4
  13. Elevated serum alkaline phosphatase (SAP)[a liver and bone enzyme above the normal range]3.8%4
  14. Convulsion[seizure]2.9%3
  15. Elevated creatinine[a kidney value above the normal range]2.9%3
  16. Elevated liver enzymes[liver enzymes above the normal range]2.9%3
  17. Fever2.9%3
  18. Haematochezia[fresh blood in the stool]2.9%3
  19. Hypersalivation[drooling]2.9%3
  20. Lack of efficacy - NOS[the product did not have the expected effect]2.9%3
  21. Melaena[dark, tarry stool containing digested blood]2.9%3

Age and weight

Age of the animal

Under 1 year10.6%11
1 to 3 years20.2%21
4 to 7 years14.4%15
8 to 11 years29.8%31
12 years and over22.1%23
Age not given2.9%3

Weight of the animal

Under 5 kg (11 lb)1%1
5 to 9.9 kg (11–22 lb)1.9%2
10 to 24.9 kg (22–55 lb)12.5%13
25 to 44.9 kg (55–99 lb)70.2%73
45 kg and over (99 lb+)10.6%11
Weight not given3.8%4

Coloured bar: Briard reports. Grey bar: all dog reports.

Trend and outcomes

024Apr 2021: 0May 2021: 0Jun 2021: 0Jul 2021: 0Aug 2021: 0Sep 2021: 0Oct 2021: 0Nov 2021: 0Dec 2021: 0Jan 2022: 02022Feb 2022: 1Mar 2022: 0Apr 2022: 0May 2022: 2Jun 2022: 0Jul 2022: 0Aug 2022: 0Sep 2022: 0Oct 2022: 0Nov 2022: 0Dec 2022: 4Jan 2023: 02023Feb 2023: 0Mar 2023: 0Apr 2023: 1May 2023: 0Jun 2023: 0Jul 2023: 0Aug 2023: 0Sep 2023: 0Oct 2023: 0Nov 2023: 0Dec 2023: 0Jan 2024: 02024Feb 2024: 0Mar 2024: 1Apr 2024: 0May 2024: 0Jun 2024: 0Jul 2024: 0Aug 2024: 0Sep 2024: 0Oct 2024: 0Nov 2024: 0Dec 2024: 1Jan 2025: 02025Feb 2025: 0Mar 2025: 1Apr 2025: 0May 2025: 1Jun 2025: 0Jul 2025: 0Aug 2025: 0Sep 2025: 0Oct 2025: 0Nov 2025: 0Dec 2025: 0Jan 2026: 02026Feb 2026: 0Mar 2026: 0

Reports by month FDA received them. The newest months are incomplete because FDA posts reports with a delay of three to six months.

Outcome recorded in the report

Recovered/Normal18.3%19
Recovered with Sequela0%0
Ongoing10.6%11
Died8.7%9
Euthanized0%0
Outcome Unknown17.3%18

Beside all dogs

MeasureBriardAll dogs
Reports104985,675
Latest 12 months153,292
Classed serious, of reports stating it40.8%38.3%
Death or euthanasia recorded, per 1,000 reports86.555

Questions about Briard reports

How many FDA adverse event reports involve Briards?

104 reports through March 2026, 0% of reports about dogs; 1 in the latest 12 months.

Which drugs are named most often in Briard reports?

By active ingredient: carprofen (20), spinosad (13), afoxolaner (9), milbemycin oxime + spinosad (8) and ivermectin + pyrantel pamoate (7). Brands are masked in the public data.

What signs are reported most for this breed?

vomiting (23.1%), diarrhoea (15.4%), depression (11.5%), anorexia (10.6%) and ataxia (7.7%).

Is the Briard more sensitive to certain drugs?

Report counts cannot answer that. They show what was reported, not what a drug did, and they are not adjusted for how many Briard animals exist or were treated. Breed-related drug sensitivities that are established are described on FDA-approved labels; a veterinarian is the person to ask about an individual animal.

Why are crossbreds not included?

FDA records crossbred animals with one or more component breeds. Counting them under each component would double count, so breed pages use single-breed reports only. Crossbreds remain in the species totals.

How do I report a problem?

Call the drug company using the number on the label, or send Form FDA 1932a to FDA. See the guide on how to report.

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. Breed names are FDA's labels rearranged into everyday order ("Berger de Brie (Briard) - Briard" becomes "Briard"). 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.