Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Mannheimia Haemolytica Toxoid
44 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.
44
Total Reports
37
Deaths Reported
8410.0%
Death Rate
Active Ingredients
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Mannheimia Haemolytica Toxoid
Administration Routes
SubcutaneousSubconjunctivalUnknown
Species Affected
Cattle 44
Most Affected Breeds
Cattle (other) 28
Crossbred Bovine/Cattle 8
Aberdeen Angus 5
Holstein-Friesian also known as Holstein 2
Cattle (unknown) 1
Most Reported Reactions
Death 36
Respiratory signs 13
Lack of efficacy - NOS 13
NT - Abnormal necropsy finding NOS 8
Anorexia 7
Death by euthanasia 7
Pneumonia 6
Lethargy (see also Central nervous system depression in 'Neurological') 6
Fever 6
Other abnormal test result NOS 5
Nasal discharge 4
Lack of efficacy (bacteria) - NOS 4
Outcome Breakdown
Died
36 (48.6%)
Recovered/Normal
19 (25.7%)
Ongoing
8 (10.8%)
Euthanized
6 (8.1%)
Outcome Unknown
4 (5.4%)
Recovered with Sequela
1 (1.4%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.