Mannheimia Haemolytica Toxoid

25 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

9200.0%

Death Rate

Active Ingredients

Mannheimia Haemolytica Toxoid

Administration Routes

UnknownSubcutaneousParenteralIntramuscular

Species Affected

Cattle 25

Most Affected Breeds

Cattle (other) 14

Cattle (unknown) 5

Crossbred Bovine/Cattle 3

Unknown 1

Charolais 1

Aberdeen Angus 1

Most Reported Reactions

Death 20

Lack of efficacy - NOS 8

Respiratory signs 3

Lack of efficacy (virus) - NOS 3

Foaming at the mouth 2

Death by euthanasia 2

INEFFECTIVE, ANTIBIOTIC 2

Anaphylaxis 2

Lack of efficacy (bacteria) - NOS 2

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

Injection site oedema 1

Stiff gait 1

Outcome Breakdown

Died

22 (59.5%)

Outcome Unknown

8 (21.6%)

Recovered/Normal

3 (8.1%)

Euthanized

2 (5.4%)

Ongoing

2 (5.4%)

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