FIELD: medicine. SUBSTANCE: composition is produced as globules with controlled release of drugs having nucleus with regular seed or seed with homogeneously distributed glycocorticosteroid described in the invention application. Regular seed nucleus has budesonide or its 22R-isomer layer. The drugs show significant advantages when compared to other glycocorticosteroids of systemic activity and other drugs earlier applied for treating Kron disease. EFFECT: no systemic adverse side effects; high speed in passing metabolism pathway; high reliability when applied as supporting therapy in acute phase of disease. 25 cl, 8 tbl
Title | Year | Author | Number |
---|---|---|---|
16α,17a-ACETAL-SUBSTITUTED ANDROSTANE-17b-CARBOXYLIC ACID ESTERS OR THEIR STEREOISOMERS | 1991 |
|
RU2081879C1 |
22R- OR 22S-EPIMERS OF COMPOUNDS, METHOD OF PREPARATION THEREOF, PHARMACEUTICAL COMPOSITION, AND METHOD OF TREATING ALLERGIC AND INFLAMMATORY DISEASES | 1992 |
|
RU2111212C1 |
STEROID ESTERS OR THEIR STEREOISOMERS, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION | 1992 |
|
RU2112775C1 |
METHOD SYNTHESIS OF (22R,S)-α-BUTYLIDENEDIHYDROXY-a-DIHYDROXYPREGNA-1,4-DIENE- -3,20-DIONE | 1990 |
|
RU2048472C1 |
0 |
|
SU1779257A3 | |
METHOD OF OBTAINING 16,17-ACETAL-SUBSTITUTED PREGNANE-21 ACID AS THEIR STEREOISOMERS | 0 |
|
SU1839673A3 |
METHOD OF OBTAINING DERIVATIVES OF 4-PREGNENE OR MIX OF THEIR STEREOISOMERS OR THEIR 22-EPIMERS | 0 |
|
SU1156600A3 |
DIDEOXYDIDEHYDROCARBOCYCLIC NUCLEOSIDES, PHARMACEUTICAL COMPOSITION | 1989 |
|
RU2114846C1 |
METHOD FOR CONDITIONING SUBSTANCES | 1994 |
|
RU2148992C1 |
APPLICATION OF H, K-ATPase INHIBITOR FOR TREATING NASAL POLYPS | 1997 |
|
RU2197966C2 |
Authors
Dates
1999-08-10—Published
1990-11-15—Filed