Chanelle Animec Super Injection For Cattle 500ml

Product Description

Uses:

• For the treatment of mixed infestations of adult liver fluke and gastro-intestinal roundworms, lungworms, eye worms, and/or mites and lice of beef and non lactating dairy cattle.
• Animec Super Injection is a broad-spectrum endo- and ecto-parasiticide. One dose is effective against many parasites. It is convenient to use.
• A clear colourless to pale yellow coloured sterile solution containing 10mg/ml ivermectin and 100mg/ml clorsulon.

Dosage:

• Dosage: 1ml per 50 kg bodyweight by subcutaneous injection (based on a recommended dosage level of 200µg of ivermectin and 2mg of clorsulon per kg bodyweight).
• Over 300kg give 1ml per 50kg bodyweight.
• To ensure a correct dosage, bodyweight 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, to avoid under- or over-dosing, they should be grouped according to their bodyweight and dosed accordingly. Inject only by the subcutaneous route.
• Divide doses in excess of 10ml between different injection sites.
• The timing of treatment should be based on epidemiological factors and should be customised for each individual farm. A dosing program should be established by a qualified professional person.
• A sterile 17 gauge ½ inch (15-20 mm) needle is recommended.
• Different injection sites should be used for other parenteral products administered concurrently. When using the 500 ml pack size use only automatic syringe equipment. For the 50 ml pack size, use of a multidose syringe is recommended.
• The product should be administered under the loose skin in front of or behind the shoulder.

Contraindications: 

• Do not use this product intravenously or intramuscularly.
• Animec Super Injection is a low volume product authorised for use in cattle. It must not be used in other species as severe adverse reactions, including fatalities in dogs, may occur, especially Collies, Old English Sheepdogs and related breeds and crosses. Do not use in animals with a known sensitivity to the active ingredient 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.
• This product does not contain any antimicrobial preservative - swab septum before removing each dose.
• To avoid secondary reactions due to the death of Hypoderma larvae in the oesophagus or the spine, it is recommended to administer the product at the end of the period of fly activity and before the larvae reach their resting sites: seek professional advice on the correct timing of treatment.
• Divide doses in excess of 10 ml between different injection sites and use different sites to those used for other parenteral medications.
• Treated cattle should not have direct access to ponds, streams or ditches for 14 days after treatment.
• Can be used in pregnancy and lactation. Can be used in breeding animals.
• In the absence of compatibilities studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
• Withdrawal Period: Meat and offal: 66 days.
• Milk: Do not use in cattle producing milk for human consumption. Do not use in non-lactating dairy cows including pregnant heifers within 60 days of calving.

Legal Category: POM-VPS.

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