Chanelle Rumenil Oral Suspension For Cattle

Product Description

Uses:

• Oral Use. Shake the product well before use. To ensure administration of a correct dose, body weight should be determined as accurately as possible; accuracy of the dosing device should be checked. If animals are to be treated collectively rather than individually, they should be grouped according to their bodyweight and dosed accordingly, in order to avoid under- or overdosing. Dose according to bodyweight at the rate of 10 mg oxyclozanide per kg bodyweight (cattle)
• Cattle : 3 ml per 10 kg bodyweight
• For example: 
  Bodyweight Dose: ,50 kg 15 ml, 100 kg 30 ml, 150 kg 45 ml, 200 kg 60 ml, 250 kg 75 ml, 300 kg 90 ml, 350 kg and over 105 ml.

Contraindications: 

• Do not use in cases of hypersensitivity to the active substance or to any of the excipients.
• Care should be taken to avoid the following practices because they increase the risk of development of resistance and could ultimately result in ineffective therapy:
• Too frequent and repeated use of anthelmintics from the same class, over an extended period of time
• Underdosing, which may be due to underestimation of body weight, misadministration of the product, or lack of calibration of the dosing device (if any).
• Suspected clinical cases of resistance to anthelmintics should be further investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test). Where the results of the test(s) strongly suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class and having a different mode of action should be used.
• At normal dose levels, oxyclozanide is not active against immature flukes present in liver tissue.
• To date no resistance to oxyclozanide has been reported. Use of the product should be based on local (regional, farm) epidemiological information about susceptibility of nematodes and recommendations on how to limit further selection for resistance to anthelmintics.
• When a dosing gun is used to administer the product, care must be taken to avoid damage to the pharyngeal region.
• Adverse effects are occasionally enhanced in animals suffering from severe liver damage and/or dehydration at the time of dosing.
• Due regard must always be given to the physical condition of animals undergoing treatment, particularly those in advanced pregnancy and/or under stress from adverse weather conditions, poor nutrition, penning, handling etc.
• These effects are occasionally enhanced in animals suffering from severe liver damage and/or dehydration at the time of dosing.
• Oxyclozanide is toxic to dung fauna and aquatic organisms. The risk to aquatic ecosystems and dung fauna can be reduced by avoiding too frequent and repeated use of oxyclozanide in cattle. The risk to aquatic ecosystems will be further reduced by keeping treated cattle away from water bodies for 5 days after treatment.
• Faeces containing oxyclozanide excreted onto pasture by treated animals may reduce the abundance of dung feeding organisms which may impact on dung degradation.
• Oxyclozanide is toxic to aquatic organisms. Oxyclozanide is persistent in soils.
• Can be used during pregnancy or lactation. See special precautions for use in animals.
• Target animals treated with oxyclozanide at the recommended therapeutic doses in several phases of reproduction showed no evidence of foetotoxicity, teratogenicity or effects on fertility.
• In the absence of compatibility studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
• Withdrawal Period:  Meat and offal: 13 days. Milk: 108 hours (4.5 days).

Legal Category: POM-VPS.

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