MULTICLOS

CattleSheepGoats

Product Class

Product Details - MULTICLOS



Reg. No. G3392  Act 36/1947
Namibia Reg. No. N-SR 1159

INDICATIONS

Multiclos is a vaccine for the active immunisation of healthy cattle and sheep against blackleg, malignant oedema (gas gangrene), bacillary haemoglobinuria, black disease (infectious necrotic hepatitis), diarrhoea, haemorragic enterotoxaemia and pulpy kidney disease.

COMPOSITION
Multiclos is a water based injectable, including an alum precipitate, containing toxoids obtained from cultures in liquid media of suitable strains of Clostridium septicum, Clostridium novyi type B (also known as Clostridium oedematiens type B), Clostridium sordellii and Clostridium Perfringens type C and D (also known as Clostridium welchii type C and D), as well as anacultures of Clostridium chauvoei and Clostridium haemolyticum (also known as Clostridium novyi type D), inactivated and concentrated in such manner that immunogenic activity is retained.

Although Clostridium perfringens type B is not a component of the vaccine, immunity may be provided against the beta and epsilon toxins produced by Clostridium perfringens type B as a result of the combination of type C (beta toxin) and type D (epsilon toxin) fractions.

WARNINGS

  • ANIMALS SHOULD NOT BE SLAUGHTERED FOR HUMAN CONSUMPTION WITHIN 3 WEEKS OF VACCINATION.
  • Vaccinate only healthy cattle and sheep.
  • As with all vaccines, occasional hypersensitivity reactions may occur.  In such cases, appropriate treatment such as adrenaline and/or antihistamines should be administered without delay.
  • As usual with all vaccines, absolute immunity cannot be guaranteed in all animals.  Therefore, it is advisable to consult a veterinarian regarding additional control measures, instead of relying on the vaccine alone.
  • Usually no marked reaction follows vaccination although a transient swelling may appear at the site of inoculation, and some animals may show a moderate rise of temperature for one or two days.
  • Partly used containers containing left-over vaccine, should be disposed of at the end of each day’s operation since under field conditions it may be difficult to avoid accidental contamination of the vaccine.
  • Keep out of reach of children and uninformed persons.
  • Although this vaccine has been extensively tested under a large variety of conditions failure thereof may ensue as a result of a wide range of reasons.  If this is suspected seek veterinary advice and notify the registration holder.

PRECAUTIONS

  • Only sterile needles and properly sterilized vaccinator should be used.  In order to maintain proper hygiene, it is advisable to change to clean sterile needles as frequently as possible.
  • In case of long fleece, it is necessary to make sure that the needle has penetrated the skin before injecting the product.
  • Do not mix the vaccine with other veterinary medicinal products.

DIRECTIONS FOR USE – USE ONLY AS DIRECTED

  • SHAKE WELL BEFORE USE.
  • Inoculate by subcutaneous injection.

DOSAGE AND ADMINISTRATION

  • For animals that have never been immunised before, two doses should be given separated by an interval of 3 to 4 weeks.
  • Animals should be revaccinated annually prior to periods of extreme risk or parturition.
  • For Clostridium haemolyticum and Clostridium novyi, a booster inoculation should be administered every 5 to 6 months.
  • Animals vaccinated before 3 months of age should be revaccinated at weaning or 4 to 6 months of age.
  • Immunity is established within 3 to 4 weeks after inoculation, and should last for ± 1 year, except for Clostridium haemolyticum and Clostridium novyi – as indicated above.

DOSAGE
Cattle  : 5 mℓ subcutaneously
Sheep : 3 mℓ subcutaneously

STORAGE

  • Store between 2ºC and 8ºC.
  • Protect from light.
  • DO NOT FREEZE.

PRESENTATION
100ml and 250 ml containers.

REGISTRATION HOLDER
Intervet S.A. (Pty) Ltd
Co. Reg. No. 1991/006580/07