Clinical and pharmacological group: & nbsp

Antiviral drugs (excluding HIV)

Included in the formulation
  • Minacer®
    pills inwards 
    Apothec Inc.     Canada
  • Fawirox
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  • Famacivir
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    EvoFarm Ltd.     Russia
  • Famvir®
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    Novartis Pharma AG     Switzerland
  • Famciclovir-Teva
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  • АТХ:

    J.05.A.09   Famciclovir

    Pharmacodynamics:Transforms in the body in penciclovir, enters the virus-infected cells, where under the action of viral thymidine kinase is converted to monophosphate, which, with the participation of cellular enzymes, turns into triphosphate. Penciclovir triphosphate is found in virus-infected cells for more than 12 hours, suppressing the synthesis of viral DNA in them, violating the replication of viruses Herpes simplex (types 1 and 2), Varicella zoster, Epstein-Barr and cytomegalovirus.

    Pharmacokinetics:After oral administration, fasted to 77% is absorbed in the gastrointestinal tract. The maximum concentration in the blood plasma is reached after 45 minutes. The connection with plasma proteins is 20%.

    Metabolism in the liver. Do not cumulate.

    The elimination half-life is 2 hours. Elimination by the kidneys in the form of penciclovir.

    Indications:It is used to treat infections caused by Varicella zoster (herpes zoster), including herpes zoster with complications from the side of the eye. Used for infections caused by Herpes simplex (type I and II): primary infection, recurrent chronic infection.

    I.A50-A64.A60   Anogenital herpetic viral infection [herpes simplex]

    I.B00-B09.B00   Infections caused by the herpes simplex virus [herpes simplex]

    I.B00-B09.B02   Shingles [herpes zoster]

    Contraindications:Individual intolerance.

    Carefully:Pregnancy and lactation, kidney failure, hypersensitivity, children under 18 years.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. It is used with caution during pregnancy and lactation in cases where the intended benefit exceeds the risk to the fetus and newborn.

    Dosing and Administration:

    Inside, 250 mg 3 times a day or 500 mg 2 times a day. For patients with weakened immunity and HIV infection, the dose increases to 500 mg 3 times a day.

    The highest daily dose: 1.5 g.

    The highest single dose: 500 mg.

    Side effects:Central and peripheral nervous system: headache, rarely dizziness, hallucinations, confusion.

    Hemopoietic system: thrombocytopenia, granulocytopenia.

    Digestive system: nausea, vomiting.

    Dermatological reactions: a rash.

    Allergic reactions.

    Overdose:

    Headache, convulsions, drowsiness, coma, acute renal failure.

    Treatment is symptomatic, hemodialysis is effective.

    Interaction:Probenecid and other drugs that affect the function of the kidneys can change the level of penciclovir in the blood plasma.

    Special instructions:In the presence of clinical manifestations of genital herpes it is recommended that the drug be taken together by sexual partners who should avoid sexual contact.

    Instructions
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