Bravoxin 10 100ml

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Vaccines

Bravoxin 10 100ml Cheap Veterinary Drugs Online

Vaccines

25.14 excluding VAT

Clostridium perfringens type A, C.perfringens type B, C.perfringens type C, C.perfringens type D, Clostridium chauvoei, Clostridium novyi type B, Clostridium septicum, Clostridium sordellii and Clostridium haemolyticum and against tetanus caused by Clostridium tetani.

Dose

Sheep from 2 weeks of age

Dose 1 ml

Cattle from 2 weeks of age

Dose 2 ml

Primary vaccination: Two doses should be administered, 46 weeks apart.

Booster vaccination: A single dose should be administered at 6 to 12 month intervals.

Administration

By subcutaneous injection at a suitable site. The recommended site is the loose skin on the side of the neck. The bottle should be well shaken before any vaccine is withdrawn. Syringes and needles should be sterile before use and the injection should be made through an area of clean, dry skin taking precautions against contamination.

Use in pregnancy: To provide passive protection of the offspring, via the colostrum, a single booster dose should be administered between 8 and 2 weeks before parturition, provided that animals have received a full primary vaccination course before pregnancy.
Contraindications, warnings, etc

75 100% of animals vaccinated with Covexin 10 may experience reactions to vaccination. These reactions are usually localised swelling or induration at the injection site but may also include mild hyperthermia, abscess or other reaction in the underlying tissues at the injection site.

Swelling at the injection site occurs in the majority of animals. This may reach up to a mean value of 6 cm in sheep and 15 cm diameter in cattle occasionally reactions of up to 25 cm diameter may be seen in cattle. Most local reactions resolve in 36 weeks in sheep and less than 10 weeks in cattle, but may persist longer in a minority of animals. An abscess may develop in some animals. Vaccination may give rise to reactions in the underlying tissues at the injection site.

Skin discolouration at the injection site (which returns to normal as the local reaction resolved) may occur. Localised pain at the injection site for 12 days post vaccination may occur.

The local reactions do not affect the general health, demeanour, feeding or weight gain of the animals.

No information is available on the safety and efficacy of the concurrent use of this vaccine with any other. It is therefore recommended that no other vaccines should be administered within 14 days before or after vaccination with this product.

In the event of an anaphylactic reaction appropriate treatment such as adrenaline should be administered without delay. Do not vaccinate sick or immunodeficient animals.

In the case of accidental selfinjection, encourage bleeding and wash the area immediately with water. If a local reaction develops, seek medical advice showing the package insert or the label to the physician.

Withdrawal periods

Zero days.


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Gwyn Longfield Jones MRCVS reg no M100414X is responsible for the supply of VMP.