Equipment
210 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.
210
Total Reports
1
Deaths Reported
50.0%
Death Rate
Active Ingredients
Equipment
Administration Routes
UnknownOral
Species Affected
Unknown 209
Cattle 1
Most Affected Breeds
Unknown 209
Cattle (other) 1
Most Reported Reactions
Dispenser, Abnormal 83
Product Defect, General 82
Administration device NOS, malfunction 40
Product problem 31
Administration device NOS, leaking 24
Administration device NOS, abnormal 19
Caps, Abnormal 14
Administration device NOS, missing component 8
Administration device NOS, breakage 8
Containers, Leaking 7
Difficulty of Use 5
Closure, Abnormal 3
Outcome Breakdown
Ongoing
1 (50.0%)
Died
1 (50.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.