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Contra-indications, warnings, etc
Known hypersensitivity to the active ingredient.
Special warnings
Cattle suffering from severe lung damage due to heavy lungworm infestation may continue to cough for some weeks after infection.
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 and extended period of time.
∙ Underdosing, which may be due to undersestimation 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 results strongly suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class having a different mode of action should be used.
Resistance to benzimidazoles (which includes albendazole) has been reported in Teladorsagia Haemonchus, Cooper and Trichostrongylus species in small ruminants in a number of countries, including the EU. Resistance to albendazole has been reported in Cooperia and Teladorsagia species in cattle in developed countries such as New Zealand. 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
Not to be diluted or mixed with other products.
Avoid the introduction of contamination during use.
Care must be taken not to damage the pharyngeal region during dosing, particularly in sheep.
Intensive use or misuse of anthelmintics can give rise to resistance. To reduce the risk, dosing programmes should be discussed with a veterinary surgeon.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Wash hands after use.
Avoid direct contact with the product.
Wear suitable protective clothing including impermeable rubber gloves.
In the event of accidental eye exposure, flush eye thoroughly with running water. If irritation persists, seek medical attention.
In the event of accidental skin exposure, wash the effected area with soap and water. If irritation persists, seek medical attention.
Adverse reactions (frequency and seriousness)
None known
Use during pregnancy, lactation or lay
Do not dose ewes at the 'fluke and worm' dose rate, (7.5 mg/kg), during tupping or for 1 month after removing the rams. Can be safely used during lactation.
Use of the product in breeding bulls or pregnant cattle is not expected to interfere with their reproductive performance.
Interaction with other medicinal products and other forms of interaction
None known.
Overdose (symptoms, emergency procedures, antidotes), if necessary
No treatment specified.
Withdrawal period(s)
Cattle:
Meat & Offal: 14 days
Milk: 60 hours
Sheep:
Meat & Offal: 5 days
Not to be used in sheep producing milk for human consumption.