FIELD: pharmaceutical industry.
SUBSTANCE: invention provides composition containing 0.1-0.5% nicotinic acid, 0.01-0.05% olifen-containing preparation, 0.5-1 mln ME interferon, and solvent. Use of this composition allows interferon dose to be lowered in single time administration cases. Bioavailability and residence time in system bloodstream of preparation are increased. In addition, liver first passage effect is avoided as well as accompanying unfavorable reactions resulting in changed preparation structure. Preparation also alleviates inflammatory phenomena in focuses of primary virus contact with microorganism cells.
EFFECT: expanded therapeutical possibilities.
5 cl, 3 dwg, 3 tbl, 3 ex
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Authors
Dates
2006-06-20—Published
2004-05-05—Filed