Total Reports
62
FDA CVM filings
Goat /
2026 FDA CVM data 62 reports on file official source
Boer — FDA Adverse Event Profile
Adverse-event records and label data for Boer (Goat), sourced from the FDA Center for Veterinary Medicine. Refreshed as new reports are filed. Cite PlainBreed when reusing this analysis.
Boer (Goat) has 62 FDA adverse event reports on record, with 38 deaths reported (6130.0% death rate) — ranking #261 by report volume. The most frequently reported reaction is Death (30 cases). The top associated drug is Monensin Sodium. Average age at report: 1.5 years.
Deaths Reported
38
of 62 reports
Death Rate
6130.0%
death-coded share
Avg Age at Report
1.5 yr
41.2 kg avg weight
Death-Coded Outcome Share
Boer death-coded reports 100.0%
Database median
6130.0% of 62 reports involved a death outcome. Read alongside breed popularity, veterinary access, and owner awareness — these shape how many events ever reach the FDA. The 12% comparison line is the rough cross-breed median in the FDA CVM database; values above suggest higher reporting bias toward severe outcomes, not necessarily higher true mortality.
Average weight at time of report: 41.2 kg (90.8 lbs)
Top Reported Reactions
Death 30
Recumbency 6
Weight loss 5
Lack of efficacy - NOS 4
Abortion 4
Agalactia 4
INEFFECTIVE, WORMS NOS 3
Ataxia 3
Anorexia 3
Liver failure 3
Diarrhoea 3
Drug administration error 3
Overdose 3
Lethargy (see also Central nervous system depression in 'Neurological') 3
Necropsy performed 3
Most Referenced Drugs
Monensin Sodium 16
Fenbendazol Suspension 7
Progesterone 7
Albendazole 5
Doramectin 3
Monensin 3
Tilmicosin Phosphate 2
Pyrantel Tartrate 2
Ceftiofur Crystalline Free Acid 2
Tulathromycin 2
Vit E/ Selenite Inj Solution 2
Ivermectin 2
Fluralaner 13.64% 12-Week Chew 2
Chlorhexidine 1
Moxidectin, Praziquantel 1
Outcome Breakdown
Died
37 (51.4%)
Outcome Unknown
26 (36.1%)
Recovered/Normal
6 (8.3%)
Ongoing
2 (2.8%)
Euthanized
1 (1.4%)
Gender Distribution
Mixed 22 (35.5%)
Female 20 (32.3%)
Unknown 10 (16.1%)
Male 10 (16.1%)
Reports by Year
| Year | Reports | Trend |
|---|---|---|
| 2010 | 8 | |
| 2011 | 3 | |
| 2012 | 4 | |
| 2013 | 2 | |
| 2014 | 2 | |
| 2015 | 6 | |
| 2016 | 2 | |
| 2017 | 6 | |
| 2018 | 3 | |
| 2019 | 5 | |
| 2020 | 8 | |
| 2021 | 4 | |
| 2022 | 5 | |
| 2023 | 4 | |
Boer Pet Health Insights
Across the FDA Center for Veterinary Medicine adverse event database, Boer accounts for 62 submitted reports and currently ranks #261 by report volume within the goat population. Of those reports, 38 involved a death outcome — a 6130.0% case-fatality figure calculated directly from the underlying FDA records rather than from external mortality studies. The mean age at time of reporting is 1.5 years, with an average recorded body weight of 41.2 kg (90.8 lbs). These figures reflect the voluntary reporting pool only and should be read alongside breed popularity, veterinary access, and owner awareness — all of which shape how many events ever reach the FDA.
The most frequently reported clinical signs for Boer are Death (30 reports), Recumbency (6 reports), Weight loss (5 reports), together capturing a substantial share of the top-reaction traffic seen in this breed's record. On the product side, Monensin Sodium appears in 16 reports and is the single most-referenced drug, followed by Fenbendazol Suspension (7) and Progesterone (7). Counts like these surface which therapeutic classes dominate the reporting stream — useful context when comparing reactions across breeds of the same goat species.
Outcome coding on the 72 reports with a recorded status is dominated by Died (51.4% of coded outcomes). Annual submission volume ranges from 2,010 to 2,023 reports across the 14 years on file, indicating the reporting trend is shaped as much by awareness cycles as by underlying clinical events. Because FDA adverse event reports describe correlation rather than causation, these numbers are most useful as a signal of where to ask further questions with a veterinarian — not as a standalone risk score for any individual goat.
Understanding Boer Adverse Event Data
Boer has 62 adverse event reports on file. Lower report volumes may reflect a less common breed, lower reporting rates, or genuinely fewer adverse events.
The 6130.0% death rate is above average, though this statistic should be interpreted cautiously. Death reports may be overrepresented because serious outcomes are more likely to be reported than mild reactions.
The most frequently referenced drug in adverse reports is Monensin Sodium, appearing in 16 reports. This may indicate widespread use of the medication rather than a specific safety concern for Boer.
Other Goat Breeds
Frequently Asked Questions
How many FDA adverse event reports involve Boer? ▼
There are 62 adverse event reports involving Boer in the FDA database, with 38 reports involving death (6130.0% death rate). Boer ranks #261 by report volume.
What are the most common adverse reactions reported for Boer? ▼
The most commonly reported adverse reactions for Boer are Death (30 reports), Recumbency (6 reports), Weight loss (5 reports), Lack of efficacy - NOS (4 reports), Abortion (4 reports).
What drugs are most frequently associated with Boer adverse events? ▼
The drugs most frequently referenced in Boer adverse event reports are Monensin Sodium (16 reports), Fenbendazol Suspension (7 reports), Progesterone (7 reports), Albendazole (5 reports), Doramectin (3 reports).
What is the average age of Boer in adverse event reports? ▼
The average age of Boer at the time of adverse event reports is 1.5 years, with an average weight of 41.2 kg (90.8 lbs).
Does a high number of adverse event reports mean Boer 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 Boer 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.
Guides & Resources
Understanding Adverse Events
What FDA reports are and how they are collected
Breed-Specific Risks
Why some breeds appear in more adverse event reports
Pet Medication Safety
Evaluating medication risks using FDA data
Most Reported Medications
Drugs that appear most in adverse event reports
How FDA CVM Tracks Events
The reporting process and database limitations
Related Data Sources
Data Sources & Methodology
Adverse event data sourced from the FDA Center for Veterinary Medicine via the openFDA Animal & Veterinary Adverse Events API. Reports are voluntarily submitted by pet owners, veterinarians, and product manufacturers.
Boer ranks #261 by total report volume. Death rate (6130.0%) reflects the proportion of reports involving death and should not be interpreted as a breed-specific mortality rate. Reporting biases, breed popularity, and veterinary access all influence report counts.
Read our methodology — how this data is sourced, computed, and verified.
Related
Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial