For the treatment of cerebrocortial necrosis in cattle and sheep. For the treatment of Vitamin B deficiencies in horses, cattle and sheep. For the treatment of bracken poisoning in horses.
Administer by subcutaneous, deep intramuscular or slow intravenous injection. The dose should be repeated daily as required. Normal aseptic precautions should be observed.
|Horses, cattle:||20–30 ml|
|Calves and foals:||5–10 ml|
If dose volume exceeds 20ml, it should be divided and injected into two sites.
Anaphylactoid reactions, particularly in the horse, may occur following intravenous administration. When this route is used Duphafral Extravite should be given slowly, and may be diluted with sterile saline or dextrose saline solution. This may be achieved by drawing the sterile diluting solution into a syringe followed by the required volume of Duphafral Extravite. This diluted product must be administered immediately after preparation and must not be stored. There may be slight irritation at the site of injection when the product is given by the subcutaneous or intramuscular routes. This should resolve naturally within a short period of time.
Cattle, horses, sheep (meat): Zero days. Cattle, sheep (milk): Zero hours.
Care should be taken to avoid accidental self-injection. Wash hands after use.
Do not store above 25°C. Protect from light. Keep container in outer carton. Following withdrawal of the first dose, use the product within 28 days. Discard unused material. Dispose of used containers in the farm refuse. Used containers should not be recycled. When the container is broached (opened) for the first time, using the in-use shelf-life which is specified on this data sheet, the date on which any product remaining in the container should be discarded should be worked out. This discard date should be written in the space provided on the label. Keep out of the reach and sight of children. For animal treatment only.
Duphafral Extravite can be safely administered to pregnant and lactating animals.
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