Aivlosin 625 mg/g Granules for Use in Drinking Water for Pigs
Active ingredient: Tylvalosin
Form
Powder
Species
Manufacturer
Eco Animal Health Ltd
VMD MA No.
13277/5004
What it's used for
Treatment and metaphylaxis of porcine proliferative enteropathy (ileitis) caused by . Treatment and metaphylaxis of swine enzootic pneumonia caused by susc...
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Prescription required
Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.
Aivlosin 625 mg/g Granules for Use in Drinking Water for Pigs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
caused by .
Treatment and metaphylaxis of swine enzootic pneumonia caused by
susceptible strains of Mycoplasma.
The presence of the disease in the group must be established before
metaphylaxis.
None known.
Issued: December 2024
AN: 02144/2023
Reporting adverse events is important. It allows continuous safety monitoring of
a veterinary medicinal product. Reports should be sent, preferably via a
veterinarian, to either the marketing authorisation holder or its local
representative or the national competent authority via the national reporting
system. See also section 16 of the package leaflet for contact details.
a suitable injectable veterinary medicinal product prescribed by a veterinarian.
At the recommended dose, lung lesions and clinical signs are reduced but
infection with Mycoplasma hyopneumoniae is not eliminated.
Issued: December 2024
AN: 02144/2023
Special precautions for use in animals
Official, national and regional antimicrobial policies should be taken into account
when the product is used.
Good management and hygiene practices should be followed to reduce the risk
of re-infection.
It is sound clinical practice to base treatment on susceptibility testing of the
bacteria isolated from the animal. If this is not possible, therapy should be
based on local (regional, farm level) epidemiological information about
susceptibility of target bacteria.
Use of the veterinary medicinal product deviating from the instructions in the
SPC may increase the risk of development and selection of resistant bacteria
and decrease the effectiveness of treatment with other macrolides due to the
potential for cross-resistance.
An antibacterial with a lower risk of antimicrobial resistance selection, if
available for the same indication, should be used for first line treatment where
susceptibility testing suggests the likely efficacy of this approach.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Tylvalosin has been shown to cause hypersensitivity (allergic) reactions in
laboratory animals; therefore, people with known hypersensitivity to tylvalosin
should avoid contact with this 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 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
product. Wash contaminated skin.
In case of accidental ingestion, seek medical advice immediately and show the
package leaflet or the label to the physician.
Special precautions for the protection of the environment:
Not applicable.
Other precautions:
Not applicable.
required.
Issued: December 2024
AN: 02144/2023
The 40 g sachet is sufficient to treat a total of 5,000 kg of pigs (e.g. 250 pigs
with the heaviest pig weighing 20 kg) for one day.
The 160 g sachet is sufficient to treat a total of 20,000 kg of pigs (e.g. 400 pigs
with the heaviest pig weighing 50 kg) for one day.
The 400 g sachet is sufficient to treat a total of 50,000 kg of pigs (e.g. 1000 pigs
with the heaviest pig weighing 50 kg) for one day.
Swine enzootic pneumonia caused by susceptible strains of Mycoplasma
hyopneumoniae
The dose is 10 mg tylvalosin per kg bodyweight per day in drinking water for 5
consecutive days.
Calculate the total amount of product required with the following formula:
Total weight of product in grams = total bodyweight of the heaviest pig to be
treated in kg x number of pigs to be treated x 10 / 625.
Select the correct number of sachets according to the amount of product
required.
The 40 g sachet is sufficient to treat a total of 2,500 kg of pigs (e.g. 125 pigs
with the heaviest pig weighing 20 kg) for one day.
The 160 g sachet is sufficient to treat a total of 10,000 kg of pigs (e.g. 200 pigs
with the heaviest pig weighing 50 kg) for one day.
The 400 g sachet is sufficient to treat a total of 25,000 kg of pigs (e.g. 500 pigs
with the heaviest pig weighing 50 kg) for one day.
Mixing instructions:
In order to achieve a correct dose, accurate and properly calibrated equipment
should be used for weighing out the required amount of product.
The veterinary medicinal 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 1,500 ml, 160 g of product per 6,000 ml or 400 g of product per
15,000 ml water and it is necessary to mix the solution for 10 minutes. After this
time, any remaining cloudiness will not affect the efficacy of the veterinary
medicinal product.
Issued: December 2024
AN: 02144/2023
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.
After end of the medication period, the water supply system should be cleaned
appropriately to avoid intake of subtherapeutic amounts of the active substance.
As an adjunct to medication, good management and hygiene practices should
be introduced in order to reduce the risk of infection and to control the build-up
of resistance.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
No signs of intolerance have been observed in pigs at up to 100 mg tylvalosin
per kg bodyweight per day for 5 days.
4.11 Withdrawal period(s)
Meat and offal: 2 days.
5.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Other Products Containing Tylvalosin
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
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