Moraxella Bovis Bacterin

21 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

2860.0%

Death Rate

Active Ingredients

Moraxella Bovis Bacterin

Administration Routes

UnknownSubcutaneousParenteral

Species Affected

Cattle 21

Most Affected Breeds

Cattle (other) 13

Cattle (unknown) 2

Aberdeen Angus 2

Crossbred Bovine/Cattle 1

Brangus 1

Holstein-Friesian also known as Holstein 1

Mixed (Cattle) 1

Most Reported Reactions

Lack of efficacy - NOS 7

Death 3

Partial lack of efficacy 2

Nasal discharge 2

Sudden death 2

Pneumonia 2

Pink eye 2

Rectal prolapse 2

INEFFECTIVE, PARASITE(S) NOS 1

Keratoconjunctivitis 1

Oral bleeding 1

Respiratory signs 1

Outcome Breakdown

Recovered/Normal

8 (33.3%)

Died

6 (25.0%)

Outcome Unknown

5 (20.8%)

Ongoing

5 (20.8%)

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