EN
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Pigs: for the treatment of anaerobic dysentery, enzootic swine pneumonia, infections caused by mycoplasmas, secondary infections caused by germs sensitive to tiamulin hydrogen fumarate.
Broilers: for the treatment of chronic respiratory disease, mycoplasmosis and infectious arthritis caused by germs sensitive to tiamulin hydrogen fumarate.
Tiamulin hydrogen fumarate 800 mg/g
Do not use in herbivores.
Do not use in cases of known hypersensitivity to the active substances or any of the excipients.
In rare cases, hypersensitivity to tiamulin can appear, usually manifested by cutaneous erythema. If you notice any serious reactions or other effects not mentioned in this leaflet, please inform your veterinarian.
For oral administration only after incorporation in feed. TIAGEN 80% is administered for 3 to 7 consecutive days, in different doses, depending on the species, age, body weight, clinical condition and health. To ensure a correct dosage body weight should be determined as accurately as possible to avoid underdosing.
For the mass treatment the animals should be grouped according to body weight and should be properly dosed to avoid under- or overdose.
In order to ensure a good homogenization of the product, it must first be mixed with an appropriate amount of feed, obtaining a pre-mixture, before being incorporated into the final feed.
Pigs: 8-10 mg active substance/kg body weight/day, equivalent to 10-12,5 mg Tiagen 80%/kg body weight /day.
Broilers: 15-20 mg active substance/kg body weight/ day, equivalent to 19-25 mg Tiagen 80%/kg body weight/day.
During the treatment, the animals should only eat medicated feed.
Feed consumption should be monitored to ensure proper dosing. If the consumption of feed does not correspond to the quantities for which the recommended concentrations have been calculated, the concentration of TIAGEN 80% must be adjusted so that the animals assimilate the recommended dose, otherwise another medication must be considered.
Meat and offal:
Pigs: 6 days
Broilers: 4 days
Not authorised for use in birds producing eggs for human consumption.
Keep out of the sight and reach of children. Do not store above 25 °C. Store in the original package. Store in a dry place. Protect from direct sunlight.
Do not use this veterinary medicinal product after the expiry date which is stated on the label.
Shelf-life of the veterinary medicinal product as packaged for sale: 2 years.
Shelf-life after first opening the immediate packaging: 28 days.
Shelf life after incorporation into meal or pelleted feed: 28 days.
Special warnings for each target species
The uptake of medication by animals can be altered as a consequence of illness. For animals with a reduced feed intake, treat parenterally using an appropriate injectable product.
Special precautions for use in animals
The use of the product will be performed based on susceptibility tests of isolated bacteria. If this is not possible, therapy should be based on local epidemiological information (at regional, farm level) about the susceptibility of the target bacteria. The use of the product outside the instructions in the SPC may increase the prevalence of resistance to tiamulin and may decrease the efficacy of pleuromutilin antimicrobial group due to cross-resistance.
Special precautions to be taken by the person administering the medicinal product to animals
People with known hypersensitivity to any of the components of the product should avoid contact with it.
The product may cause irritation of the respiratory tract and eyes in case of inhalation or contact. If irritation persists, consult a physician and show the package leaflet or the label of the product.
Appropriate protective measures must be taken when incorporating the product into the feed. Wear either a disposable half-mask respirator conforming to European standard EN 149 or a non-disposable respirator to European Standard EN 140 with a filter to EN 143, chemically resistant gloves, protective coveralls and goggles while incorporating the premix into feed. In case of accidental eye contact, rinse thoroughly with clean tap water.
Do not smoke, eat or drink while handling this product. Wash hands after use.
Use during pregnancy, lactation or lay
Studies on laboratory animals have not shown embryotoxic or teratogenic potential.
The safety of the product has not been established during pregnancy and lactation.
The use of the product during pregnancy and lactation is established after the evaluation of the risk-benefit balance by the veterinarian.
Not authorised for use in birds producing eggs for human consumption.
Interaction with other medicinal products and other forms of interaction
Do not use in combination with monensin, narasin and salinomycin.
Overdose (symptoms, emergency procedures, antidotes), if necessary
Do not exceed the recommended dose.
In case of overdose, salivation or vomiting may occur.
Major incompatibilities
In the absence of compatibility studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
Polyethylene terephthalate laminated foil bag/aluminum/low density polyethylene x 50 g, 100 g, 1 kg, 5kg.
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