Clos P*2/Cl Oth*5/H.Somnus Kb
13 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.
13
Total Reports
11
Deaths Reported
8460.0%
Death Rate
Active Ingredients
Clos P*2/Cl Oth*5/H.Somnus Kb
Administration Routes
SubcutaneousUnknown
Species Affected
Cattle 13
Most Affected Breeds
Cattle (other) 5
Aberdeen Angus 4
Hereford cattle 2
Cattle (unspecified) 2
Most Reported Reactions
Death 8
Lack of efficacy - NOS 5
Lack of efficacy (bacteria) - NOS 3
NT - Abnormal necropsy finding NOS 2
Increased mortality rate 1
General illness 1
Weight loss 1
Abnormal necropsy finding 1
NT - fibrinous (broncho) pneumonia/fibrinous pleuropneumonia 1
Lameness 1
Skin swelling 1
Death by euthanasia 1
Outcome Breakdown
Died
10 (38.5%)
Recovered/Normal
8 (30.8%)
Ongoing
5 (19.2%)
Euthanized
2 (7.7%)
Outcome Unknown
1 (3.8%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.