Dog /
FDA CVM · 2025 release 17 reports on file

Boerboel - FDA Adverse Event Profile

Adverse-event records for Boerboel (Dog) from the FDA Center for Veterinary Medicine.

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Annual adverse-event report trend Yearly FDA CVM adverse-event report counts for this breed. 3 2.25 1.5 0.75 0 2018 2019 2020 2021 2022 2023 2024 2025 Reports filed Death-coded reports
Annual report volume for Boerboel drawn from FDA CVM filings.

Data updated June 2026

The record at a glance

Boerboel's FDA record: #389 most-reported dog breed, 17 total reports, 5.9% death-coded (1 reports).

#389
most-reported dog breed
5.9%
death-coded report share
6
Vomiting - top reaction
3.6 yr
average age at report

Higher volume usually means a more popular breed, not a riskier one, compare against how common the breed is.

Total Reports

17

FDA CVM filings

Deaths Reported

1

of 17 reports

Death Rate

5.9%

death-coded share

Avg Age at Report

3.6 yr

55.8 kg avg weight

Death-Coded Outcome Share

Boerboel death-coded reports 5.9%
Cross-breed median

5.9% of 17 boerboel reports involved a death outcome.

How to read this number

Read alongside breed popularity, veterinary access, and owner awareness, these shape how many events ever reach the FDA. The comparison line marks the cross-breed median death-coded share (about 4.8%) among breeds with 50 or more reports; values above it suggest higher reporting bias toward severe outcomes, not necessarily higher true mortality.

Average weight at time of report: 55.8 kg (123.0 lbs)

Top Reported Reactions

Vomiting 6
Lack of efficacy (endoparasite) - heartworm 3
Lack of efficacy (ectoparasite) - flea 2
Lethargy (see also Central nervous system depression in 'Neurological') 2
Loose stool 1

Most Referenced Drugs

Milbemycin Oxime + Spinosad 6
Ivermectin + Pyrantel As Pamoate Salt 5
Grapiprant 2
Fluralaner Chew Tablets 2
Fluralaner 13.64% 12-Week Chew 2

Outcome Breakdown

Recovered/Normal
6 (35.3%)
Ongoing
5 (29.4%)
Outcome Unknown
5 (29.4%)
Died
1 (5.9%)

Gender Distribution

Male 10 (58.8%)
Female 7 (41.2%)

Reports by Year

Year Reports Trend
2013 1
2017 1
2018 2
2019 1
2020 2
2021 2
2022 2
2023 1
2024 2
2025 3

Boerboel Pet Health Insights

Boerboel accounts for 17 FDA adverse event reports, ranking #389 by volume among dog breeds, with 1 reports (5.9%) coded as a death outcome. Mean age at report: 3.6 years, average weight 55.8 kg (123.0 lbs).

Top reported signs: Vomiting (6), Lack of efficacy (endoparasite) - heartworm (3), Lack of efficacy (ectoparasite) - flea (2). Most-referenced drug: Milbemycin Oxime + Spinosad (6 reports), followed by Ivermectin + Pyrantel As Pamoate Salt (5) and Grapiprant (2).

Outcome coding on 17 status-recorded reports is dominated by Recovered/Normal (35.3%). Annual submissions ranged 2,013-2,025 across 10 years on file.

Dog Breeds With a Similar Report Volume

Frequently Asked Questions

How many FDA adverse event reports involve Boerboel?
There are 17 adverse event reports involving Boerboel in the FDA database, with 1 reports involving death (5.9% death rate). Boerboel ranks #389 by report volume.
What are the most common adverse reactions reported for Boerboel?
The most commonly reported adverse reactions for Boerboel are Vomiting (6 reports), Lack of efficacy (endoparasite) - heartworm (3 reports), Lack of efficacy (ectoparasite) - flea (2 reports), Lethargy (see also Central nervous system depression in 'Neurological') (2 reports), Loose stool (1 reports).
What drugs are most frequently associated with Boerboel adverse events?
The drugs most frequently referenced in Boerboel adverse event reports are Milbemycin Oxime + Spinosad (6 reports), Ivermectin + Pyrantel As Pamoate Salt (5 reports), Grapiprant (2 reports), Fluralaner Chew Tablets (2 reports), Fluralaner 13.64% 12-Week Chew (2 reports).
What is the average age of Boerboel in adverse event reports?
The average age of Boerboel at the time of adverse event reports is 3.6 years, with an average weight of 55.8 kg (123.0 lbs).
Does a high number of adverse event reports mean Boerboel is unhealthy?
No. FDA adverse event reports are voluntarily submitted and do not prove causation. Popular breeds with more veterinary visits tend to have more reports. The data reflects reporting patterns, not actual incidence rates. Always consult a veterinarian for health decisions.
Where does this Boerboel safety data come from?
All data comes from the FDA Center for Veterinary Medicine's adverse event reporting system. Pet owners, veterinarians, and manufacturers voluntarily submit reports about adverse events potentially linked to animal drugs and other products.

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. Breed figures are computed directly from FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.