CLOSTRIVAX

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COMPOSITION

Each vaccine contains: inactivated culture of Clostridium chauvoei not less than 30 OU, inactivated culture of Clostridium novyi B not less than 7.5 OU, inactivated culture of Clostridium novyi D not less than 7.5 OU, toxoid of Clostridium novyi B to induce a serological response not less than 3.5 IU per ml of serum, toxoid of Clostridium novyi D to induce a serological response not less than 10 IU per ml of serum, ß toxoid of Clostridium perfringens to induce a serological response not less than 10 IU per ml of serum, toxoid of Clostridium perfringens to induce a serological response not less than 5 IU per ml of serum, toxoid Clostridium septicum to induce a serological response not less than 2.5 IU per ml of serum, toxoid of Clostridium tetani to induce a serological response not less than 2.5 IU per ml of serum.

PHARMACEUTICAL FORM

Injectable suspension.

TARGET SPECIES

Cattle and sheep.

INDICATIONS

Prevention of diseases caused by Clostridium perfringens B, C and D, Clostridium novyi B and D, Clostridium chauvoei, Clostridium septicum and Clostridium tetani in cattle and sheep, including: enterotoxaemia, lamb dysentery, necrotic enteritis, pulpy kidney disease, infectious necrotic hepatitis, bacillary haemoglobinuria, red water disease, malignant edema, blackleg and tetanus.

DOSAGE
In cattle inject one dose subcutaneously, according to the following scheme: 2 inoculations with an interval of 4 weeks.
Boosters every 6 months.
In sheep inject one dose subcutaneously, according to the following scheme:
Basic vaccination programme: 2 inoculations with an interval of 4 weeks.
Adult ewes: booster 2-4 weeks before each lambing.
Lambs of vaccinated ewes: basic vaccination programme starting at 8-10 weeks of life.
Lambs of unvaccinated ewes: basic vaccination programme at 2-3 weeks of life.

Produced by: FATRO S.p.A. , Italy
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