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Buy Amiksin (Tiloron) online. Free worldwide shipping.

Brand: Pharmstandard-Tomskkhimfarm

Drug form: Сoated tablets

Manufacturers: Russia

Active substance: Tiloron

Group: Antiviral agents of different groups

Expiration date: 3 years

 

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Amiksin (Tiloron) 125мг №6; №10

$57.00Price
  • Indications for use of Amiksin (Tiloron) are:

    In adults, treatment and prevention of influenza, other acute respiratory viral infections, treatment of viral hepatitis A, B and C, treatment of herpes and cytomegalovirus infections; as part of the complex therapy of infectious-allergic and viral encephalomyelitis (multiple sclerosis, leukoencephalitis, uveoencephalitis, etc.), as part of the complex therapy of urogenital and respiratory chlamydia, in the complex therapy of pulmonary tuberculosis. For children over 7 years old - for the treatment of influenza and other acute respiratory viral infections.

    Pharmachologic effect:

    Low molecular weight synthetic interferon inducer that stimulates the formation of alpha, beta and gamma interferons in the body. The main producers of interferon in response to the administration of tilorone are intestinal epithelial cells, hepatocytes, T-lymphocytes, neutrophils and granulocytes. After oral administration, the maximum production of interferon is determined in the sequence intestine - liver - blood after 4-24 hours. The drug has an immunomodulatory and antiviral effect. In human leukocytes, it induces the synthesis of interferon. Stimulates bone marrow stem cells, depending on the dose, increases antibody production, reduces the degree of immunosuppression, restores the ratio of T-suppressors and T-helpers. Effective against various viral infections, including influenza viruses, other acute respiratory viral infections, hepatitis viruses and herpes viruses. The mechanism of antiviral action is associated with inhibition of translation of virus-specific proteins in infected cells, as a result of which the reproduction of viruses is suppressed. After oral administration, it is rapidly absorbed from the gastrointestinal tract. Bioavailability - 60%. About 80% of the drug binds to plasma proteins. The drug is excreted practically unchanged through the intestines (70%) and through the kidneys (9%). The half-life is 48 hours. The drug does not undergo biotransformation and does not accumulate in the body.

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