Moraxella Bovis Bacterin (Solidtech)

13 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

2310.0%

Death Rate

Active Ingredients

Moraxella Bovis Bacterin (Solidtech)

Administration Routes

SubcutaneousUnknown

Species Affected

Cattle 13

Most Affected Breeds

Cattle (other) 6

Aberdeen Angus 2

Mixed (Cattle) 2

Hereford cattle 1

Holstein-Friesian also known as Holstein 1

Red Angus 1

Most Reported Reactions

Lack of efficacy (bacteria) - NOS 7

Lack of efficacy - NOS 4

Death 2

Keratoconjunctivitis 2

Cloudy eye (for Miosis, Mydriasis, Anisocoria, Nystagmus - see 'Neurological') 2

Impaired vision 2

CULTURE/TITER DATA ABNORMAL 1

Abnormal necropsy finding 1

Pulmonary disorder NOS 1

Incorrect route of drug administration 1

Abortion 1

Stillbirth 1

Outcome Breakdown

Outcome Unknown

11 (64.7%)

Died

3 (17.6%)

Recovered/Normal

2 (11.8%)

Ongoing

1 (5.9%)

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