Haemophilus Somnus, 10555;Haemophilus Somnus, 8025

14 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.

Total Reports

Deaths Reported

9290.0%

Death Rate

Active Ingredients

Haemophilus Somnus, 10555;Haemophilus Somnus, 8025

Administration Routes

Subcutaneous

Species Affected

Cattle 14

Most Affected Breeds

Mixed (Cattle) 10

Aberdeen Angus 3

Simmental 1

Most Reported Reactions

Death 13

Lack of efficacy - NOS 8

INEFFECTIVE, ANTIBIOTIC 2

Staggering 1

CULTURE/TITER DATA ABNORMAL 1

Lack of efficacy (virus) - NOS 1

Bronchopneumonia 1

Lack of efficacy (bacteria) - NOS 1

Weight loss 1

Malaise 1

Downer animal 1

Loose stool 1

Outcome Breakdown

Died

13 (56.5%)

Outcome Unknown

10 (43.5%)

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