Zoetis Cydectin 10% Solution Injection For Cattle

Product Description

Uses:

• A clear yellow, slightly viscous, sterile solution containing 100mg/ml moxidectin as the active ingredient.
• In cattle weighing from 100 to 500 kg body weight, treatment and prevention of mixed infestations by the following gastro-intestinal nematodes, respiratory nematodes and certain arthropod parasites:
• Adult and immature gastro-intestinal nematodes: Haemonchus placei, Haemonchus contortus, Ostertagia ostertagi (including inhibited larvae), Trichostrongylus axei, Trichostrongylus colubriformis, Nematodirus helvetianus (adults only), Nematodirus spathiger, Cooperia surnabada, Cooperia oncophora, Cooperia pectinata, Cooperia punctata, Oesophagostomum radiatum, Bunostomum phlebotomum (adults only), Chabertia ovina (adults only), Trichuris spp. (adults only)
• Adult and immature respiratory tract nematode: Dictyocaulus viviparus
• Warble grubs (migrating larvae): Hypoderma bovis, Hypoderma lineatum
• Lice: Linognathus vituli, Haematopinus eurysternus, Solenopotes capillatus, Bovicola bovis (aid in control)
• Mange mites: Sarcoptes scabiei, Psoroptes ovis, Chorioptes bovis (aid in control)
• The drug has a persistent action and protects cattle for certain duration against infection or re-infection with the following parasites for the period indicated: Dictyocaulus vivparus (120 days), Ostertagia ostertagi (120 days), Haemonchus placei (90 days), Oesophagostomum radiatum (150 days), Trichostrongylus axei (90 days), Linognathus vituli (133 days). 
• The veterinary medicinal product is effective against Hypoderma larvae at the time of treatment but its persistent activity against Hypoderma has not been evaluated.
• If the veterinary medicinal product is given before the end of the fly season complimentary treatment with a product effective against Hypoderma may be required. 

Dosage: 

• Do not use in animals less than 100 kg bodyweight or greater than 500 kg.
• Do not inject the veterinary medicinal product by intravascular route. Intravascular injection may result in ataxia, paralysis, convulsions, collapse and death. 
• Unnecessary use of antiparasitics or use deviating from the instructions given in the SPC may increase the resistance selection pressure and lead to reduced efficacy. The decision to use the product should be based on confirmation of the parasitic species and burden, or of the risk of infestation based on its epidemiological features, for each individual herd.
• 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. Repeated use for an extended period, particularly when using the same class of substances, increases the risk of resistance development. Within a herd, maintenance of susceptible refugia is essential to reduce that risk. Systematically applied interval-based treatment and treatment of a whole herd should be avoided. Instead, if feasible, only selected individual animals or subgroups should be treated (targeted selective treatment). This should be combined with appropriate husbandry and pasture management measures. Guidance for each specific herd should be sought from the responsible veterinarian.
• Under-dosing which may due to underestimation of body weight, misadministration of the veterinary medicinal 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 moxidectin has been reported in Cooperia spp. and Ostertagia spp. in cattle.
• Psoroptes ovis is an extremely contagious external parasite of sheep and cattle. To ensure complete control, great care must be taken to avoid reinfestation, as mites may be viable for up to 15 days off the animal. It is important that all animals which have been in contact with infected ones are treated with an appropriate product. Contact between treated, infected and untreated herds must be avoided until at least seven days after treatment.
• Resistance to moxidectin has been reported in Psoroptes ovis scab mites in sheep and in cattle. Cases of side-resistance with other macrocyclic lactones (ivermectin and doramectin) have been reported as well. The use of this product should take into account local information about susceptibility of the target parasites, where available.
• Can be used during pregnancy.
• Withdrawal Period: Meat and offal: 108 days.
• Milk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals which are intended to produce milk for human consumption within 80 days of expected parturition.
• The withdrawal period is based solely on a single injection at the ear site of injection.

Legal Category: POM-VPS.

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