Active substanceInterferon alfa-2bInterferon alfa-2b
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  • Dosage form: & nbsprectal suppositories
    Composition:

    1 suppository WIFERON® 150000 ME contains active substance: interferon alfa-2b human recombinant 150,000 ME, auxiliary substances: alpha-tocopherol acetate 0.055 g, ascorbic acid 0.0054 g, sodium ascorbate 0.0108 g, disodium edetate dihydrate 0.0001 g, polysorbate-80 0.0001 g, cocoa butter and confectionery fat up to 1 g.

    1 suppository WIFERON® 500,000 ME contains active substance: interferon alfa-2b human recombinant 500,000 ME, auxiliary substances: alpha-tocopherol acetate 0.055 g, ascorbic acid 0.0081 g, sodium ascorbate 0.0162 g, disodium edetate dihydrate 0.0001 g, polysorbate-80 0.0001 g, cocoa butter and confectionery fat up to 1 g.

    1 suppository WIFERON® 1000000 ME contains active substance: interferon alfa-2b human recombinant 1000000 ME, auxiliary substances: alpha-tocopherol acetate 0.055 g, ascorbic acid 0.0081 g, sodium ascorbate 0.0162 g, disodium edetate dihydrate 0.0001 g, polysorbate-80 0.0001 g, cocoa butter and confectionery fat up to 1 g.

    1 suppository WIFERON® 3000000 ME contains active substance: interferon alfa-2b human recombinant 3,000,000 ME, auxiliary substances: alpha-tocopherol acetate 0.055 g, ascorbic acid 0.0081 g, sodium ascorbate 0.0162 g, disodium edetate dihydrate 0.0001 g, polysorbate-80 0.0001 g, cocoa butter and confectionery fat up to 1 g.

    Description:

    The suppository is bullet-shaped, white with a yellowish tinge, of a uniform consistency.Color heterogeneity in the form of marble is allowed. On the longitudinal section there is a funnel-shaped depression. The diameter of the suppository is not more than 10 mm.

    Pharmacotherapeutic group:Immunomodulatory and antiviral agents
    ATX: & nbsp

    L.03.A.B.05   Interferon alfa-2b

    Pharmacodynamics:
    Interferon alfa-2b human recombinant possesses antiviral, immunomodulating, antiproliferative properties, suppresses the replication of RNA and DNA-containing viruses. Immunomodulatory properties of interferon alfa-2b, such as an increase in the phagocytic activity of macrophages, an increase in the specific cytotoxicity of lymphocytes to target cells cause its mediated antibacterial activity.
    In the presence of ascorbic acid and alpha-tocopherol acetate, the specific antiviral activity of interferon alfa-2b increases, its immunomodulating effect increases, which allows increasing the efficiency of the organism's own immune response to pathogenic microorganisms. When using the drug, the level of secretory immunoglobulins class A increases, the level of immunoglobulin E normalizes, and the endogenous system of interferon alfa-2b is restored. Ascorbic acid and alpha-tocopherol acetate, being highly active antioxidants, have anti-inflammatory, membrane-stabilizing, and regenerative properties. It was found that when using the preparation VIFERON® there are no side effects arising from the parenteral administration of interferon alfa-2b preparations, antibodies that neutralize the antiviral activity of interferon alfa-2b are not formed. The use of the preparation VIFERON® as part of complex therapy allows to reduce therapeutic doses of antibacterial and hormonal drugs, as well as to reduce the toxic effects of this therapy.
    Cocoa butter contains phospholipids, which allow not to use synthetic toxic emulsifiers in production, and the presence of polyunsaturated fatty acids facilitates the introduction and dissolution of the drug.
    Indications:
    acute respiratory viral infections, including influenza, including those complicated by bacterial infection, pneumonia (bacterial, viral, chlamydial) in children and adults as part of complex therapy;
    infectious and inflammatory diseases of newborn children, including premature: meningitis (bacterial, viral), sepsis,intrauterine infection (chlamydia, herpes, cytomegalovirus infection, enterovirus infection, candidiasis, including visceral, mycoplasmosis) as part of complex therapy;
    chronic viral hepatitis B, C, D in children and adults as part of complex therapy, including in combination with the use of plasmapheresis and hemosorption in chronic viral hepatitis of severe activity complicated by cirrhosis;
    Infectious and inflammatory diseases of the urogenital tract (chlamydia, cytomegalovirus infection, ureaplasmosis, trichomoniasis, gardnerellez, papillomavirus infection, bacterial vaginosis, recurrent vaginal candidiasis, mycoplasmosis) in adults as part of complex therapy;
    primary or recurrent herpetic infection of the skin and mucous membranes, a localized form, a mild and moderately severe course, including the urogenital form in adults.
    Contraindications:Hypersensitivity to any of the components of the drug.
    Pregnancy and lactation:
    The drug is approved for use from 14 weeks of pregnancy. Has no restrictions to use during breastfeeding.
    Dosing and Administration:
    The drug is used rectally.1 suppository contains, as active substance, human recombinant interferon alpha-2b at indicated dosages (150,000 IU, 500,000 IU, 1,000,000 IU, 3,000,000 IU).
    In the complex therapy of various infectious and inflammatory diseases in newborn children, including premature infants: newborns, including preterm infants with a gestational age of more than 34 weeks, appoint VIFERON® 150000 ME daily for 1 suppository 2 times a day after 12 hours. The course of treatment is 5 days.

    Preterm infants with gestational age less than 34 weeks are prescribed VIFERON® 150000 ME daily for 1 suppository 3 times a day after 8 hours. The course of treatment is 5 days.

    The recommended number of courses for various infectious and inflammatory diseases in children, including newborns and prematurity: ARVI, including influenza, including those complicated by bacterial infection - 1-2 courses; pneumonia (bacterial, viral, chlamydial) 1-2 courses, sepsis 2-3 courses, meningitis 1-2 courses, herpetic infection 2 courses, enterovirus infection 1-2 courses, cytomegalovirus infection -2-3 courses, mycoplasmosis , candidiasis, including visceral, - 2-3 courses. The break between the courses is 5 days.According to clinical indications, therapy can be continued.

    In the complex therapy of chronic viral hepatitis B, C, D in children and adults: children with chronic viral hepatitis drug prescribed in the following dose levels: up to 6 months 300000-500000 ME per day; from 6 to 12 months - 500,000 IU per day. At the age from 1 year to 7 years - 3 million ME at 1 m2 body surface area per day. At the age of over 7 years - 5000000 ME per 1 m2 body surface area per day. Calculation of the dose of the drug for each particular patient is made by multiplying the recommended dose for the given age by the body surface area, calculated from the nomogram to calculate the surface area of ​​the body in terms of height and weight according to Garford, Terry and Rourke, divided into 2 injections, rounded to the dosage of the corresponding suppository. The drug is used 2 times a day at 12 h the first 10 days daily, then three times a week every other day for 6-12 months. The duration of treatment is determined by clinical efficacy and laboratory parameters.

    Children with chronic viral hepatitis of marked activity and cirrhosis prior to plasmapheresis and / or hemosorption show the use of the drug for 14 days daily for 1 suppository 2 times a day after 12 hours (children under 7 years old VIFERON® 150000 ME, children over 7 years - VIFERON® 500,000 ME).

    Adults with chronic viral hepatitis are prescribed VIFERON® 3,000,000 IU at 1 suppository 2 times a day after 12 hours for 10 days daily, then three times a week every other day for 6-12 months. The duration of treatment is determined by clinical efficacy and laboratory performance.

    In complex therapy in adults, including pregnant women, with urogenital infection (chlamydia, cytomegalovirus infection, ureaplasmosis, trichomoniasis, gardnerellez, papillomavirus infection, bacterial vaginosis, recurrent vaginal candidiasis, mycoplasmosis), with primary or recurrent herpetic infection of the skin and mucous membranes ( a localized form, an easy, moderate course, including the urogenital form).

    Adults, with the above infections, except herpetic, appoint VIFERON® 500000 ME per 1 suppository 2 times a day after 12 hours. Course 5-10 days. According to clinical indications, therapy can be continued with interruptions between courses of 5 days.

    When herpetic infection is prescribed VIFERON® 1000000 ME per 1 suppository 2 times a day after 12 hours. The course of treatment is 10 days or more with a recurrent infection.It is recommended to start treatment immediately with the appearance of the first signs of skin and mucous membrane damage (itching, burning, redness). In the treatment of recurrent herpes it is desirable to begin treatment in the prodromal period or at the very beginning of the manifestation of signs of relapse.

    In pregnant women with urogenital infection, including herpetic infection, in the second trimester of pregnancy (starting from week 14) - VIFERON® 500000 ME per 1 suppository after 12 hours (2 times per day) for 10 days, then 1 suppository after 12 hours (2 times a day) twice a week - 10 days. After 4 weeks, preventive courses of the preparation VIFERON® 150000 ME per 1 suppository every 12 hours - for 5 days, the preventive course is repeated every 4 weeks. If necessary, it is possible to conduct a treatment course before childbirth.
    In the complex therapy of acute respiratory viral infections, including influenza, including those complicated by bacterial infection in adults. Apply VIFERON® 500000 ME to 1 suppository 2 times a day after 12 hours daily. The course of treatment is 5-10 days.

    Side effects:In rare cases, it is possible to develop allergic reactions (skin rashes, itching).These phenomena are reversible and disappear after 72 hours after discontinuation of the drug.
    Overdose:Not installed.
    Interaction:VIFERON®, suppositories rectal, compatible and well combined with all drugs used in the treatment of the above diseases (antibiotics, chemotherapy, glucocorticosteroids).
    Effect on the ability to drive transp. cf. and fur:Not installed.
    Form release / dosage:Suppositories rectal 150000 ME, 500000 ME, 1000000 ME, 3,000,000 ME.
    Packaging:For 10 suppositories in a PVC / PVC loop type container Rotoplast. 1 pack with instructions for use in a pack of cardboard.
    Storage conditions:At a temperature of 2 to 8 ° C, in a dark place. Keep out of the reach of children.
    Shelf life:2 years.
    Do not use the drug after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:P N000017 / 01
    Date of registration:06.10.2010
    Expiration Date:Unlimited
    The owner of the registration certificate:FERON, LLC FERON, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp28.02.2017
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