Ivomec Classic Injection C+S 500Ml

ed dosage of 1 ml per 50 kg bodyweight, the product controls re-infection with the following nematodes: Barbers pole worm (Haemonchus placei), Small intestinal worm (Cooperia spp.) and Hairworm (Trichostrongylus axei) for 14 days, Brown stomach worm (Ostertagia ostertagi) and Nodular worm (Oesophagostomum radiatum) for 21 days, and Lungworm (Dictyocaulus viviparus) for 28 days after treatment. 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. Sheep Gastrointestinal Roundworms (Adult, L4 and Inhibited L4) Ostertagia circumcincta Haemonchus contortus Gastrointestinal Roundworms (Adult and L4) Ostertagia trifurcata Trichostrongylus colubriformis Cooperia curticei Oesophagostomum columbianum Nematodirus filicollis Chabertia ovina Gastrointestinal Roundworms (Adult) Trichostrongylus axei T. vitrinus Oesophagostomum venulosum Trichuris ovis Lungworms (Adult and L4) Dictyocaulus filaria Lungworms (Adult) Protostrongylus rufescens Nasal Bots Oestrus ovis Mange Mites Psoroptes ovis Benzimidazole-resistant strains of Haemonchus contortus and Ostertagia circumcincta are also controlled. Contra-indications Do not inject intravenously or intramuscularly. The product is specifically for use in the target species. Do not use in other species as severe adverse reactions, including fatalities in dogs, may occur. Special warnings for each target species 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 bodyweight, 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. Resistance to macrocyclic lactones (which includes ivermectin) has been reported in Teladorsagia spp. in sheep and in Cooperia spp. in cattle within the EU. Therefore, the use of this 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. Special precautions for use in animals When treating groups of animals use only an automatic dosing device. Syringes must be filled from the vial through a dry sterile draw-off needle that has been placed in the vial stopper. Vial stoppers must not be broached more than 20 times. Sheep scab (Psoroptes ovis) is an extremely contagious external parasite of sheep. To ensure complete control great care must be taken to avoid re–infestation, as mites may be viable for up to 15 days off the sheep. It is important that all sheep which have been in contact with infected sheep are treated. Contact between treated, infected and untreated flocks must be avoided until at least seven days after treatment. In sheep, treatment of psoroptic mange (sheep scab) with one injection is not recommended because, although clinical improvement may be seen, elimination of all mites may not occur. This product does not contain any antimicrobial preservative. Swab septum before removing each dose. Use a sterile needle and syringe. Special precautions to be taken by the person administering the product to animals Do not smoke, drink or eat while handling the product. Wash hands after use. Take care to avoid self injection: the product may cause local irritation and/or pain at the site of injection. In case of accidental self-injection, seek medical advice and show the label or package leaflet to the physician. Adverse reactions Cattle Mild, transient discomfort has occasionally been observed in cattle following subcutaneous administration. A low incidence of soft tissue swelling at the injection site has been observed. Sheep Discomfort, sometimes intense but usually transient, has been observed in some sheep following subcutaneous administration. In both species these reactions disappear without treatment. Use during pregnancy, lactation or lay IVOMEC Classic Injection for Cattle and Sheep can be administered to cows and ewes at any stage of pregnancy or lactation provided that the milk is not intended for human consumption. It can be used in breeding ewes, rams, bulls and cows without affecting fertility. IVOMEC Classic Injection can be given to all ages of animals including young calves and lambs. Interactions IVOMEC Classic Injection for Cattle and Sheep has been used concurrently without adverse effects with foot and mouth disease vaccine or clostridial vaccine, given at separate injection sites. Adequate vaccination of sheep against clostridial infections is strongly recommended.