FDA CVM · 2025 release 34 reports on file

Wolf Hybrid - FDA Adverse Event Profile

Adverse-event records for Wolf Hybrid (Other Canids) 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. 7 5.25 3.5 1.75 0 2014 2015 2017 2018 2019 2020 2024 2025 Reports filed Death-coded reports
Annual report volume for Wolf Hybrid drawn from FDA CVM filings.

Data updated June 2026

The record at a glance

Wolf Hybrid's FDA record: #304 most-reported other canids breed, 34 total reports, 2.9% death-coded (1 reports).

#304
most-reported other canids breed
2.9%
death-coded report share
10
Vomiting - top reaction
5.0 yr
average age at report

Read report counts next to breed popularity: a bigger number often just means more owners and more vet visits.

Total Reports

34

FDA CVM filings

Deaths Reported

1

of 34 reports

Death Rate

2.9%

death-coded share

Avg Age at Report

5.0 yr

36.9 kg avg weight

Death-Coded Outcome Share

Wolf Hybrid death-coded reports 2.9%
Cross-breed median

2.9% of 34 wolf hybrid 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: 36.9 kg (81.4 lbs)

Top Reported Reactions

Vomiting 10
Lethargy (see also Central nervous system depression in 'Neurological') 4
Lack of efficacy (endoparasite) - heartworm 4
UNPALATABLE 3
Laboured breathing 3

Most Referenced Drugs

Spinosad 6
Milbemycin Oxime + Spinosad 5
Ivermectin + Pyrantel As Pamoate Salt 5
Ivermectin/Pyrantel Pamoate Chewable 272Mcg/652Mg 3
Afoxolaner 3

Outcome Breakdown

Recovered/Normal
14 (41.2%)
Outcome Unknown
12 (35.3%)
Ongoing
5 (14.7%)
Recovered with Sequela
2 (5.9%)
Euthanized
1 (2.9%)

Gender Distribution

Male 23 (67.6%)
Female 11 (32.4%)

Reports by Year

Year Reports Trend
2011 2
2012 2
2013 4
2014 3
2015 7
2017 2
2018 3
2019 3
2020 1
2024 4
2025 3

Wolf Hybrid Pet Health Insights

Wolf Hybrid accounts for 34 FDA adverse event reports, ranking #304 by volume among other canids breeds, with 1 reports (2.9%) coded as a death outcome. Mean age at report: 5.0 years, average weight 36.9 kg (81.4 lbs).

Top reported signs: Vomiting (10), Lethargy (see also Central nervous system depression in 'Neurological') (4), Lack of efficacy (endoparasite) - heartworm (4). Most-referenced drug: Spinosad (6 reports), followed by Milbemycin Oxime + Spinosad (5) and Ivermectin + Pyrantel As Pamoate Salt (5).

Outcome coding on 34 status-recorded reports is dominated by Recovered/Normal (41.2%). Annual submissions ranged 2,011-2,025 across 11 years on file.

Frequently Asked Questions

How many FDA adverse event reports involve Wolf Hybrid?
There are 34 adverse event reports involving Wolf Hybrid in the FDA database, with 1 reports involving death (2.9% death rate). Wolf Hybrid ranks #304 by report volume.
What are the most common adverse reactions reported for Wolf Hybrid?
The most commonly reported adverse reactions for Wolf Hybrid are Vomiting (10 reports), Lethargy (see also Central nervous system depression in 'Neurological') (4 reports), Lack of efficacy (endoparasite) - heartworm (4 reports), UNPALATABLE (3 reports), Laboured breathing (3 reports).
What drugs are most frequently associated with Wolf Hybrid adverse events?
The drugs most frequently referenced in Wolf Hybrid adverse event reports are Spinosad (6 reports), Milbemycin Oxime + Spinosad (5 reports), Ivermectin + Pyrantel As Pamoate Salt (5 reports), Ivermectin/Pyrantel Pamoate Chewable 272Mcg/652Mg (3 reports), Afoxolaner (3 reports).
What is the average age of Wolf Hybrid in adverse event reports?
The average age of Wolf Hybrid at the time of adverse event reports is 5.0 years, with an average weight of 36.9 kg (81.4 lbs).
Does a high number of adverse event reports mean Wolf Hybrid 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 Wolf Hybrid 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.