stage IV kidney cancer, hairy-cell leukemia, malignant skin lymphadenosis, Kaposi's sarcoma, basal cell and squamous cell carcinoma of the skin, keratoacanthoma, chronic myelogenous leukemia, histiocytosis-X, subleukemic myelosis, essential thrombocytopenia;
disseminated sclerosis.
In combined therapy of children:
acute lymphoblastic leucosis in remission period;
respiratory laryngeal papillomatosis.
Form of release, composition and packaging
Lyophilizate for preparation of solution for injections and local application 500,000 IU, 1,000,000 IU, 3,000,000 IU, 5,000,000 IU of active ingredient per 1 vial. 1, 5,10 or 20 vials of the drug with application instructions are put into cardboard package or 1, 5,10 or 20 vials of the drug in contour cellular package or in cassette contour package with application instructions are put into cardboard package.
Indications for use
In combined therapy of adults:
for acute viral hepatitis В
moderate and severe forms in the beginning of icteritous period up to the 5th day of icterus (later administration of the drug is less effective; it is not effective for developing hepatic coma and cholestatic course of disease);
for acute prolonged hepatitis B, chronic active hepatitis В and D without signs of cirrhosis and when signs of hepatic cirrhosis appear;
for chronic viral hepatitis C;
for viral (influenza-like, adenoviral, enteroviral, herpetic, parotitic), viral and bacterial and mycoplasmal encephalomeningitis. Drug administration is the most efficient in the first 4 days of the disease;
for viral conjunctivitis, keratoconjunctivitis, keratitis, keratouveitis;
for stage IV kidney cancer, hairy-cell leukemia, malignant skin lymphadenosis (mycosis fungoidea, polymorphic reticulosis), Kaposi's sarcoma, basal cell and squamous cell carcinoma of the skin, keratoacanthoma, chronic myelogenous leukemia, histiocytosis-X, subleukemic myelosis, essential thrombocytopenia;
for disseminated sclerosis.
In combined therapy of children:
for acute lymphoblastic leucosis in remission period after completion of inductive chemotherapy (in 4-5 months of remission);
for respiratory laryngeal papillomatosis, starting from the day following papilloma removal.
Мы используем файлы cookie для улучшения пользовательского опыта. Продолжая сессию на нашем сайте, вы соглашаетесь с политиками по обработке персональных данных.
Узнайте больше о том как работают файлы cookie.