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The rate of absorption conversion and elimination of albendazole sulfoxide appeared to be prolonged with mean t max and serum elimination half-life values of 10 hours and 31.

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Paasitic sistanc talbndazol is causd by changs in aminacids that sult in changs in th ?- tubulin potin. This causs ducd binding th dug t?-tubulin.

Polongd us: Albndazol is not gnally usd ov polongd piods tim. I pscibd in this way, qunt whit cll counts and liv unction tsts should b don.

Lvations in liv unction tsts, and vsibl ductions in total whit cll counts and pancytopnia hav bn potd. Mild gastointstinal distubancs, hadachs, dizzinss, alopcia (limitd tthinning th hai) hav alsbn potd.

Albndazol is apidly convtd in th liv tth pimay mtabolit, albndazol suloxid, which is uth mtabolizd talbndazol sulon and oth pimay oxidativ mtabolits that hav bn idntiid in human uin. ollowing oal administation, albndazol has not bn dtctd in human uin. Uinay xction albndazol suloxid is a minlimination pathway with lss than 1% th dos covd in th uin. Biliay limination psumably accounts a potion th limination as vidncd by biliay concntations albndazol suloxid simila tthos achivd in plasma.

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though the present results showed only 44 of drug release from the guar gum matrix tablets of albendazole, it is possible that the formulation may release majority of the drug in the physiological environment of human colon.