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preparati aqveiTebs Sardgamomyofi gzebis gluvi muskulaturis tonuss,<br />

detruzoris kumSvadobis aqtivobas, aseve amcirebs nerwyvdenas.<br />

Terapiulze maRali dozebis miRebisas iwvevs Sardis buStis arasrul<br />

daclas da zrdis darCenili Sardis raodenobas.<br />

tolterodinis Terapiuli efeqti miiRweva 4 kviraSi.<br />

tolterodini ar ainhibirebs CYP2D6, 2C19, 3A4 da 1A2.<br />

farmakokinetika<br />

Sewova<br />

preparatis SigniT miRebisas tolterodini swrafad Seiwoveba kuW-nawlavis<br />

traqtidan (knt). SratSi maqsimaluri koncentracia (C max ) miiRweva 1-2 saaTSi.<br />

Terapiuli dozebis intervaliT (1-4 mg) miRebisas arsebobs xazovani<br />

damokidebuleba sisxlis SratSi C max mniSvnelobasa da preparatis dozas<br />

Soris.<br />

tolterodinis sruli bioSeRwevadoba Seadgens 65%-s CYP2D6 ukmarisobis<br />

mqone pirebSi da 17%-s pacientTa umravlesobaSi.<br />

sakvebi ar moqmedebs preparatis bioSeRwevadobaze, magram tolterodinis<br />

koncentracia izrdeba misi sakvebTan miRebisas.<br />

ganawileba<br />

tolterodini da 5-hidroqsimeTiluri metaboliti ukavSirdeba upiratesad<br />

orozomukoids. SeukavSirebeli fraqciebi Seadgens 3,7% da 36%, Sesabamisad.<br />

tolterodinis ganawilebis moculoba Seadgens 113 l.<br />

tolterodinisa da 5-hidroqsimeTiluri metabolitis cilebTan SekavSirebis<br />

gansxvavebis gamo tolterodinis mrudis qveS farTobi ~koncentracia – dros~<br />

(AUC) CYP2D6 ukmarisobis mqone pirebSi axlosaa tolterodinisa da 5-<br />

hidroqsimeTiluri metabolitis AUC sidideebis jamTan pacientTa<br />

umravlesobaSi dozirebis erTnairi reJimis dros. aqedan gamomdinare,<br />

preparatis usafrTxoeba, amtanoba da klinikuri efeqti ar aris damokidebuli<br />

CYP2D6 aqtivobaze.<br />

metabolizmi<br />

tolterodini ZiriTadad metabolizdeba RviZlSi polimorfuli fermenti<br />

CYP2D6 saSualebiT farmakologiurad aqtiuri 5-hidroqsimeTiluri<br />

metabolitis warmoqmniT, romelic Semdeg metabolizdeba 5-karbonis mJava da<br />

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