Bovine Parainfluenza 3 Virus, Modified Live Virus + Bovine Respiratory Syncytial Virus, Modified Live Virus + Bovine Rhinotracheitis Virus, Modified Live Virus + Bovine Virus Diarrhea Type 1, Modified Live Virus + Bovine Virus Diarrhea Type 2, Modified Live Virus
87 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.
87
Total Reports
78
Deaths Reported
8970.0%
Death Rate
Active Ingredients
Bovine Parainfluenza 3 Virus, Modified Live VirusBovine Respiratory Syncytial Virus, Modified Live VirusBovine Rhinotracheitis Virus, Modified Live VirusBovine Virus Diarrhea Type 1, Modified Live VirusBovine Virus Diarrhea Type 2, Modified Live Virus
Administration Routes
UnknownSubcutaneousIntramuscular
Species Affected
Cattle 87
Most Affected Breeds
Cattle (other) 55
Aberdeen Angus 15
Crossbred Bovine/Cattle 7
Cattle (unknown) 6
Holstein-Friesian also known as Holstein 4
Most Reported Reactions
Death 76
Lack of efficacy - NOS 35
Lack of efficacy (bacteria) - NOS 16
Lack of efficacy (virus) - NOS 8
Anaphylaxis 7
Foaming at the mouth 5
Necropsy performed 5
Respiratory signs 4
INEFFECTIVE, ANTIBIOTIC 4
Lack of efficacy (bacteria NOS) 4
Other abnormal test result NOS 3
CULTURE/TITER DATA ABNORMAL 3
Outcome Breakdown
Died
78 (52.0%)
Outcome Unknown
29 (19.3%)
Recovered/Normal
22 (14.7%)
Ongoing
14 (9.3%)
Recovered with Sequela
4 (2.7%)
Euthanized
3 (2.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.