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Adefovir dipivoxil excretion

Oral bioavailability of adefovir dipivoxil is about 59% and is unaffected by meals it is rapidly and completely hydrolyzed to the parent compound by intestinal and blood esterases. Protein binding is low (< 5%). The intracellular half-life of the diphosphate is prolonged, ranging from 5 to 18 hours in various cells this makes once-daily dosing feasible. Adefovir is excreted by a combination of glomerular filtration and active tubular secretion and reguires dose adjustment for renal dysfunction however, it may be administered to patients with decompensated liver disease. [Pg.1085]

CICLOSPORIN ADEFOVIR DIPIVOXIL Possible t efficacy and side-effects Competition for renal excretion Monitor renal function weekly... [Pg.364]

ADEFOVIR DIPIVOXIL 1. ANTIBIOTICS -aminoglycosides, vancomycin 2. ANTICANCER AND IMMUNOMODULATING DRUGS - cidosporin, tacrolimus 3. ANTIFUNGALS-amphotericin, 4. ANTIPROTOZOALS-pentamidine 5. ANTIVIRALS - cidofovir, foscarnet sodium, tenofovir Possible t efficacy and side-effects Competition for renal excretion Monitor renal function weekly... [Pg.630]

Adefovir is renally excreted. After oral administration of adefovir dipivoxil, -30-45% of the dose is recovered unchanged in urine within 24 hours the elimination is 5-7.5 hours. Dose reductions are indicated for Cl values <50 mUmin. Adefovir is removed by hemodialysis. [Pg.830]

Adefovir is poorly absorbed orally, but the bioavailability of adefovir dipivoxil reaches approximately 59%. The drug is absorbed to an equal extent with or without the presence of food. Adefovir is excreted renally unchanged. [Pg.1885]


See also in sourсe #XX -- [ Pg.830 ]




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Adefovir dipivoxil

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