Betavet
46 adverse event reports submitted to the FDA
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
46
Total Reports
2
Deaths Reported
430.0%
Death Rate
Active Ingredients
Betavet
Administration Routes
UnknownIntra-Articular
Species Affected
Unknown 30
Horse 16
Most Affected Breeds
Unknown 30
Quarter Horse 5
Horse (unknown) 3
Warmblood (unspecified) 3
Thoroughbred 3
Warmblood - Dutch 1
Trakehner 1
Most Reported Reactions
Product Defect, General 22
Lameness 10
Injection site joint reaction 4
Joint effusion 3
Color, Abnormal 2
Joint pain 2
Joint inflammation 2
Fever 2
Laminitis 2
Death by euthanasia 2
Cellulitis 2
INEFFECTIVE, ANTIINFLAMMATORY 1
Outcome Breakdown
Outcome Unknown
7 (43.8%)
Ongoing
4 (25.0%)
Recovered/Normal
3 (18.8%)
Euthanized
2 (12.5%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.