Bovine Virus*5/Past M+Mh Lv/Lb

243 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.

243

Total Reports

211

Deaths Reported

8680.0%

Death Rate

Active Ingredients

Bovine Virus*5/Past M+Mh Lv/Lb

Administration Routes

SubcutaneousUnknownSubmucosal

Species Affected

Cattle 243

Most Affected Breeds

Cattle (other) 118

Crossbred Bovine/Cattle 44

Aberdeen Angus 38

Red Angus 13

Holstein-Friesian also known as Holstein 8

Mixed (Cattle) 6

Cattle (unspecified) 4

Charolais 4

Simmental 2

Hereford cattle 2

Most Reported Reactions

Death 190

Lack of efficacy - NOS 125

Lack of efficacy (bacteria) - NOS 38

Respiratory signs 20

Found dead 13

NT - Abnormal necropsy finding NOS 11

Lack of efficacy (endoparasite NOS) 9

CULTURE/TITER DATA ABNORMAL 8

Anaphylaxis 8

Lack of efficacy (mycoplasma) - NOS 8

Necropsy performed 8

INEFFECTIVE, ANTIBIOTIC 6

Outcome Breakdown

Died

209 (42.8%)

Ongoing

133 (27.3%)

Recovered/Normal

93 (19.1%)

Outcome Unknown

44 (9.0%)

Euthanized

7 (1.4%)

Recovered with Sequela

2 (0.4%)

Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.