Mycoplasma Bovis

16 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

9380.0%

Death Rate

Active Ingredients

Mycoplasma Bovis

Administration Routes

SubcutaneousUnknown

Species Affected

Cattle 16

Most Affected Breeds

Cattle (other) 5

Mixed (Cattle) 5

Holstein-Friesian also known as Holstein 3

Cattle (unknown) 1

Jersey 1

Salers 1

Most Reported Reactions

Death 13

Lack of efficacy - NOS 9

Lack of efficacy (virus) - coronavirus - NOS 3

Necropsy performed 3

Lack of efficacy (mycoplasma) - NOS 3

Lack of efficacy (virus) - bovine viral diarrhoea virus 2

Lack of efficacy (bacteria) - Histophilus somni 2

Lack of efficacy (bacteria) - Mannheimia haemolytica 2

Lack of efficacy (bacteria) - Pasteurella multocida 2

Found dead 1

Bloated 1

INEFFECTIVE, ANTIBIOTIC 1

Outcome Breakdown

Died

14 (45.2%)

Outcome Unknown

7 (22.6%)

Ongoing

5 (16.1%)

Euthanized

3 (9.7%)

Recovered/Normal

2 (6.5%)

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