Ibr / Pi3 (Orig S-P Us) Lv
49 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.
49
Total Reports
45
Deaths Reported
9180.0%
Death Rate
Active Ingredients
Ibr / Pi3 (Orig S-P Us) Lv
Administration Routes
NasalUnknownSubcutaneous
Species Affected
Cattle 49
Most Affected Breeds
Cattle (other) 23
Aberdeen Angus 11
Crossbred Bovine/Cattle 6
Charolais 2
Mixed (Cattle) 2
Red Angus 1
Holstein-Friesian also known as Holstein 1
Hereford cattle 1
Cattle (unknown) 1
Cattle (unspecified) 1
Most Reported Reactions
Death 42
Lack of efficacy - NOS 29
Respiratory signs 7
Lack of efficacy (bacteria) - NOS 7
Lameness 6
Death by euthanasia 5
INEFFECTIVE, ANTIBIOTIC 4
Lack of efficacy (endoparasite NOS) 4
Digestive tract disorder NOS 4
Other abnormal test result NOS 3
INEFFECTIVE, WEIGHT INC 3
Necropsy performed 3
Outcome Breakdown
Died
43 (38.1%)
Ongoing
28 (24.8%)
Recovered/Normal
20 (17.7%)
Outcome Unknown
14 (12.4%)
Euthanized
5 (4.4%)
Recovered with Sequela
3 (2.7%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.