Aivlosin 625 mg/g Granules for Use in Drinking Water for Pheasants
Company name: ECO Animal Health Ltd
Address: 78 Coombe Road
Telephone: 020 8447 8899
Fax: 020 8447 9292
Aivlosin® 625 mg/g Granules for Use in Drinking Water for Pheasants is a white granular powder containing 625 mg/g tylvalosin (as tylvalosin tartrate).
Indicated for treatment of respiratory disease associated with Mycoplasma gallisepticum in pheasants.
For use in drinking water.
The dosage is 25 mg tylvalosin per kg bodyweight per day in drinking water for 3 consecutive days.
Determine the combined bodyweight (in kg) of all the birds to be treated. For example, one sachet of 40g is sufficient to treat a total of 1,000 birds with an average bodyweight of 1kg; one sachet of 400g is sufficient to treat a total of 10,000 birds with an average bodyweight of 1kg.
In order to achieve a correct dose, the preparation of a concentrated (stock) solution might be required (e.g. to treat a total of 500 kg total bird weight, only 50% of the prepared stock solution prepared from the 40 g sachet should be used).
The veterinary medicinal product should be added to a volume of water that the birds will consume in one day. The intake of medicated water depends on the clinical condition of the animals. In order to obtain the correct dosage the concentration of Aivlosin has to be adjusted accordingly.
No other source of drinking water should be available during the medication period.
The product may be mixed directly into the drinking water system or first mixed as a stock solution into a smaller amount of water, which is then added into the drinking water system.
When mixing the product directly into the drinking water system, the contents of the sachet should be sprinkled onto the surface of the water and mixed thoroughly until a clear solution is produced (usually within 3 minutes).
When preparing a stock solution, the maximum concentration should be 40 g of product per 1500 ml and it is necessary to mix the solution for 10 minutes. After this time, any remaining cloudiness will not affect efficacy of the product.
No known incompatibilities.
Withdrawal period: Meat and offal: 2 days.
Treat as soon as possible after clinical signs suggestive of mycoplasmosis are observed.
Treat all the birds in the affected flock.
Do not release pheasants for at least two days after the end of medication.
Not authorised for use in laying birds producing eggs for human consumption.
Use during pregnancy, lactation or lay
The safety of the veterinary medicinal product has not been established during lay.
Tylvalosin has been shown to cause hypersensitivity reactions in laboratory animals; therefore, people with known hypersensitivity to tylvalosin tartrate should avoid contact with the veterinary medicinal product.
When mixing the veterinary medicinal product and handling the medicated water, direct contact, with eyes, skin and mucous membranes should be avoided. Personal protective equipment should consisting of impervious gloves and a half-mask respirator conforming to European Standard EN 149 or a non-disposable respirator conforming to European Standard EN 140, with a filter conforming to European Standard EN 143 should be worn when mixing the veterinary medicinal product. Wash contaminated skin.
In case of accidental ingestion, seek medical advice immediately and show the package leaflet or the label to the physician.
For animal treatment only. Keep out of reach and sight of children. Do not use after the expiry date stated on the packaging.
40g Sachet: Do not store above 30°C.
400g Sachet: Do not store above 25°C
Opened sachets should not be stored.
Shelf-life of the veterinary medicinal product as packaged for sale:
40g Sachet: 3 years
400g Sachet 2 years
Shelf-life of the medicated drinking water: 24 hours
Only a sufficient amount of medicated drinking water should be prepared to cover the daily requirements.
Medicated drinking water should be replaced every 24 hours.
Aluminium foil laminated sachets containing 40g or 400g granules.
Good management and hygiene practices should be introduced in order to reduce the risk of re-infection.
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
For any information about this veterinary medicinal product, please contact the local representative of the marketing authorisation holder.
EU/2/04/044/012 - 40g.
EU/2/04/044/014 - 400g.