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Protease inhibitors Etoposide

Pharmacokinetic studies in dogs demonstrated a 3.5-fold increase in oral bioavailability of phenytoin when administered as the disodium phosphate prodrug versus sodium phenytoin [54]. A few additional examples of investigations with this strategy include the steroids betamethasone [55] and hydrocortisone [56], HIV protease inhibitors [57], and the anticancer drug etoposide [58,59]. Comprehensive reviews of this strategy are also available [52,60,61]. [Pg.121]

Anticancer drugs etoposide, doxorubicin, vincristine Ca + channel blockers dUtiazem, verapamil HIV protease inhibitors indinavir, ritonavir Antibiotics/antifungals erythromycin, ketoconazole Hormones testosterone, progesterone Immunosuppressants cyclosporine, FK506 (tacrolimus)... [Pg.36]

Characteristics Nucleotide analogues Anticancer drugs 6-mercaptopurine Cyclic nucleotides cyclic AMP, cyclic GMP HIV protease inhibitors adefovir Anticancer drugs doxorubicin, etoposide ... [Pg.37]

Use of protease inhibitor-based regimens has been found to be associated with a higher incidence of infections and neutropenia in patients receiving cyciophosphamide, doxorubicin and etoposide (CDE) than use of a NNRTI-based regimen. [Pg.615]


See other pages where Protease inhibitors Etoposide is mentioned: [Pg.491]    [Pg.495]    [Pg.500]    [Pg.306]    [Pg.139]    [Pg.615]    [Pg.616]    [Pg.169]    [Pg.169]    [Pg.5]   
See also in sourсe #XX -- [ Pg.615 ]




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Etoposide

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