Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine
32 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.
32
Total Reports
23
Deaths Reported
7190.0%
Death Rate
Active Ingredients
Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza3-Respiratory Syncytial Virus Vaccine
Administration Routes
UnknownSubcutaneousParenteral
Species Affected
Cattle 32
Most Affected Breeds
Cattle (unknown) 19
Crossbred Bovine/Cattle 8
Aberdeen Angus 2
Cattle (other) 1
Mixed (Cattle) 1
Red Angus 1
Most Reported Reactions
Death 21
Eye disorder NOS (for photophobia see 'neurological') 8
Skin abscess 8
Claw / hoof / nail disorder NOS 8
Lameness 8
Pneumonia 8
Musculoskeletal disorder NOS 6
Laceration 6
Lack of efficacy (bacteria) - NOS 5
Respiratory signs 5
Ocular discharge 5
Respiratory tract disorder NOS 5
Outcome Breakdown
Died
23 (46.9%)
Outcome Unknown
22 (44.9%)
Recovered/Normal
2 (4.1%)
Euthanized
1 (2.0%)
Ongoing
1 (2.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.