Bovine Rhinotraceheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus
15 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.
15
Total Reports
13
Deaths Reported
8670.0%
Death Rate
Active Ingredients
Bovine Rhinotraceheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus
Administration Routes
SubcutaneousUnknown
Species Affected
Cattle 15
Most Affected Breeds
Cattle (other) 9
Aberdeen Angus 2
Holstein-Friesian also known as Holstein 2
Brangus 1
Crossbred Bovine/Cattle 1
Most Reported Reactions
Death 12
Lethargy (see also Central nervous system depression in 'Neurological') 4
Lack of efficacy - NOS 4
Pneumonia 4
NT - Abnormal necropsy finding NOS 3
Fever 3
Lack of efficacy (protozoa) - Coccidia 2
Respiratory signs 2
Abnormal necropsy finding 2
Anorexia 2
CULTURE/TITER DATA ABNORMAL 2
INEFFECTIVE, WORMS NOS 2
Outcome Breakdown
Died
13 (52.0%)
Recovered/Normal
5 (20.0%)
Outcome Unknown
4 (16.0%)
Ongoing
1 (4.0%)
Recovered with Sequela
1 (4.0%)
Euthanized
1 (4.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.