FIELD: medicine, pharmacy.
SUBSTANCE: invention relates to a composition in the form of preliminary prepared emulsion or microemulsion concentrate designated for oral administration and comprising cyclosporine or macrolide and a carrier and also to soft or solid gelatin capsule containing the indicated composition and to a method for reducing variability of bioavailability levels of cyclosporine or macrolide using the indicated composition. Composition elicits improved indices of bioavailability and reduced variability of bioavailability parameters.
EFFECT: improved and valuable properties of composition.
18 cl, 1 tbl, 1 ex
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