Panacur Worming Bolus For Cattle 12g

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Item: 173763

MPN: 702489

Panacur Bolus is a continuous-release intraruminal device containing fenbendazole; a broad spectrum benzimidazole anthelmintic used against gastrointestinal parasites.

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Product Description
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Product Description

Uses:

The intraruminal device treats and prophylactically controls gastrointestinal nematode infections in cattle caused by Ostertagia spp., Trichostrongylus spp., Haemonchus spp., Cooperia spp. and Oesophagostomum spp. The intraruminal device aids in the control of parasitic bronchitis caused by Dictyocaulus viviparus.
For use in ruminating cattle in their first grazing season weighing between 100 kg and 300 kg on the day of administration. When administered at turnout, the intraruminal device controls parasitic gastroenteritis throughout the grazing season by reducing the build-up of infective larvae on the pasture. Reduced pasture contamination in the autumn lowers the risk of inhibited Ostertagia larvae accumulating in sufficient numbers to cause winter ostertagiasis. When administered later in the season, the intraruminal device is effective in the treatment of established parasitic infections and continues to have a prophylactic effect up to 140 days after administration. This period may be reduced if cattle are moved to heavily infected pasture.

Dosage:

Oral use.
One intraruminal device to be administered orally to each animal before being turned out to grass. Alternatively, animals which have already been turned out can be administered an intraruminal device later in the grazing season.
To ensure a correct dosage, body weight should be determined as accurately as possible.
All animals within a group grazing the same pasture must be treated with the veterinary medicinal product to ensure maximum benefits from the system.
All newcomers to the group must also be administered the veterinary medicinal product before being turned out to grass.
Administration is achieved using the Panacur Bolus Applicator which helps to administer the intraruminal device directly into the top of the oesophagus.
Insert an intraruminal device into the applicator.
Restrain the animal and extend the head forward, keeping the neck straight.
Insert the applicator into the front of the mouth and firmly but gently push it over the back of the tongue. Keeping the neck straight, tilt the head upwards and the animal will begin to swallow the end of the applicator - indicated by easier passage of the applicator down the throat.
The intraruminal device can then be ejected into the oesophagus by squeezing the release trigger on the applicator. Do not use force when administering the intraruminal device.
Observe the animal for a short time to ensure the intraruminal device has been swallowed.
As the metal of the intraruminal device can be detected, the correct position of the intraruminal device can be checked by a suitable metal detector.

Contraindications:

Do not use in pre-ruminating cattle, or cattle less than 3 months of age.
Do not administer to cattle weighing less than 100 kg or cattle over 300 kg.
If an intraruminal device treated animal is sold during the season, the purchaser must be informed of the date on which the intraruminal device was administered.
The intraruminal device can interfere with the detection of foreign bodies (hardware disease) by an electronic metal detector.
Immunity to nematodes depends on adequate exposure to infection. Although not normally the case, circumstances could occur in which anthelmintic control measures might increase the vulnerability of cattle to re-infection. Animals may be at risk towards the end of their first grazing season, particularly if the season is long, or in the following year if they are moved onto heavily contaminated pasture. In such circumstances, further control measures may be necessary.
Where specific preventative control of lungworm is required, it is advised that cattle are given an appropriate lungworm vaccine. As the veterinary medicinal product allows a small percentage of lungworm to reach the lungs when cattle are exposed, it will not interfere with the development of immunity.
Under conditions of heavy larval challenge, clinical signs of lungworm may become evident. Therefore, if clinical signs of lungworm occur in treated cattle they should be dosed immediately with an appropriate anthelmintic. Without additional control measures, such as vaccination, lungworm infestations can sometimes occur during the life of the intraruminal device.
Intensive use or misuse of anthelmintics can give rise to resistance. To reduce this risk dosing programmes should be discussed with veterinary surgeon.
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.
Under dosing, 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.
Resistance to benzimidazoles has been reported in Teladorsagia, Haemonchus, Cooperia and Trichostrongylus species in small ruminants.
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.
The veterinary medicinal product has been used successfully and without undesirable effects in pregnant cows but is not intended for use in this class of animal.
None known. However, the veterinary medicinal product has not been evaluated for compatibility with other medicinal intraruminal devices and therefore use with other medicinal intraruminal devices is not recommended.
Withdrawal Period: Meat and offal: 200 days.
Not authorised for use in cattle producing milk for human consumption or to dairy heifers within 200 days of parturition.

Legal Category POM-VPS.

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Delivery

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Local Delivery

Local FREE deliveries are available to anyone within a 20 mile radius of our Country Stores upon request (FREE for a minimum order of £350 or over), deliveries under £350 will be charged at a standard rate of £35. Deliveries are kerbside only and at the drivers discretion. Any deliveries requiring more than one person or outside of our local delivery area will incur additional fees. Please contact web@moleavon.co.uk with your postcode and order details to place your order and for more information. Alternatively you can order for Click & Collect from any of our stores, or place an order online for delivery of smaller items. Please contact us via web@moleavon.co.uk or 01363 720757 with any questions you may have.