Sometribove
556 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.
556
Total Reports
26
Deaths Reported
470.0%
Death Rate
Active Ingredients
Sometribove
Administration Routes
UnknownParenteralSubcutaneousOralCutaneous
Species Affected
Cattle 422
Unknown 118
Human 16
Most Affected Breeds
Holstein-Friesian also known as Holstein 257
Unknown 134
Cattle (unknown) 68
Jersey 30
Crossbred Bovine/Cattle 27
Mixed (Cattle) 26
Cattle (other) 3
Guernsey 2
Holstein-Friesian - French Black Pied 2
Shorthorn - Milking 2
Most Reported Reactions
INEFFECTIVE, PRODUCTION (MILK) 168
Milk production decrease 76
Product syringe issue 71
Mastitis NOS 59
Product problem 57
Alteration of milk quality 46
Lack of efficacy - NOS 38
Syringe, Abnormal 24
Death 23
Mammary gland disorder NOS 20
Abnormal number of offspring 18
Reduced conception rate 17
Outcome Breakdown
Outcome Unknown
288 (68.9%)
Recovered/Normal
76 (18.2%)
Died
24 (5.7%)
Ongoing
16 (3.8%)
Recovered with Sequela
12 (2.9%)
Euthanized
2 (0.5%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.