Ibr/Brsv/P13/Bvd T1, T2(Us) Lv
96 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.
96
Total Reports
85
Deaths Reported
8850.0%
Death Rate
Active Ingredients
Ibr/Brsv/P13/Bvd T1, T2(Us) Lv
Administration Routes
SubcutaneousUnknownOral
Species Affected
Cattle 96
Most Affected Breeds
Cattle (other) 44
Crossbred Bovine/Cattle 14
Aberdeen Angus 14
Mixed (Cattle) 7
Holstein-Friesian also known as Holstein 6
Cattle (unspecified) 5
Brahman 1
Red Angus 1
Charolais 1
Wagyu 1
Most Reported Reactions
Death 79
Lack of efficacy - NOS 53
Lack of efficacy (bacteria) - NOS 16
Respiratory signs 6
NT - Abnormal necropsy finding NOS 6
Death by euthanasia 5
Lameness 5
Necropsy performed 5
Lethargy (see also Central nervous system depression in 'Neurological') 4
Pneumonia 4
Lateral recumbency 4
INEFFECTIVE, WEIGHT INC 4
Outcome Breakdown
Died
82 (41.0%)
Ongoing
50 (25.0%)
Recovered/Normal
42 (21.0%)
Outcome Unknown
20 (10.0%)
Euthanized
6 (3.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.