FIELD: medicine, infectious diseases. SUBSTANCE: method involves oral administration of lamivudine in the dose 100-150 mg for 12 months additionally to the conventional therapy to patients with light or middle- -severe forms of acute viral hepatitis B. Invention prevents the process synchronization and promotes to reduction of adverse symptoms in treatment of patients with light and middle- severe forms of acute viral hepatitis B. Invention can be used for treatment of acute viral hepatitis B. EFFECT: enhanced effectiveness of treatment.
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