I-Technivie - I-Hepatitis C Iinkcukacha zoLwelo

I-Technivie (i-ombitasvir + paritaprevir + ritonavir) isalathisi esilungeleleneyo isilwanyana esisetyenziswe kunyango lwe- HTV (HCV) engapheliyo. Amathente amathathu aquka i-Technivie nayo ihlanganiswa kwiipilisi ezimbini ze-HCV, i- Viekira Pak .

I-Technivie yavunywa ngoJulayi 24, 2015 ngu-US Food and Drug Administration (FDA) ukusetyenziswa kubantu abadala kweminyaka eyi-18 okanye ngaphezulu nge-HCV ye-genotype 4 (GT4) ngaphandle kwe- cirrhosis .

I-Technivie ngowona wokuqala, uwonke-ngomlomo, unyango lwe-HCV olungenasiphelo kwi-HCV kwizigulane ze-GT4 ezingapheliyo zokusuleleka kwe-HCV, abantu ngokuqhelekileyo babonwa nzima ukunyanga.

I-Technivie yabikwa ukuba inezinga lokunyanga le-100% langaphambili elingakhange lithathwe ("i-naïve yonyango") izigulane kwisilingo seSigaba IIb esenziwa ngo-Agasti 12, 2012 ukuya kuNovemba 19, 2013.

Isistim

Iipilisi ezimbini (12.5mg ombitasvir, i-75mg paritaprevir, i-50mg ritonavir) ithathwa imihla ngemihla ngesidlo ngaphandle kwesidingo sokudla okunamafutha amaninzi okanye i-caloric. Amacwecwe e-Technivie anesipinki, i-oblong kunye nefilimu eboshwe, kunye ne "AV1" emacaleni kwelinye icala.

Ukucetyiswa kweengcebiso

I-Technivie imiselwe kwiikhosi eziyi-12 kunye ne-ribavirin (isilwanyana esisetyenziselwa ukuvimbela ukuveliswa kwe-RNA). I-dose ephakanyisiweyo ye-ribavirin isekelwe kwisisindo, ngolu hlobo:

Ikhosi ye-Technivie yeeveki ezili-12 iyakucatshangelwa yonyango i-naïve isigulane engakwazi ukunyamezela i-ribavirin.

Iziphumo eziPhakathi

Iziphumo eziqhelekileyo ezimalunga nokusetyenziswa kwe-Technivie (ezenzeka ubuncinane kwi-7% yezigulane) zi:

IMilly Contraindicated

La machiza alandelayo akufanele athathwe xa usebenzisa i-Technivie:

Ukungqinelana nokuqwalasela

I-Technivie ayikhuthazwa izigulane ezineempembelelo eziphambili ze-hepatic (i-Child-Pugh score B) kwaye iyaphikiswa kwizigulane ezinobungozi obunzima (i-Child-Pugh score C).

I-Technivie inqatshelwe ukusetyenziswa kwezigulane ezine-hypersensitivity eyaziwayo kwi- ritonavir (oko kukuthi, ngubani oye wabona uStevens-Johnson Syndrome okanye i-epidermal necrolysis enetyhefu).

Nangona i-Technivie iyodwa ingavunyelwanga ukuba isebenzise ekukhulelweni, ukuhlanganiswa kwe-Technivie kunye ne-ribavirin kwaye akufanele isetyenziswe kubafazi abakhulelweyo okanye amadoda anamaqabane abo abafazi abakhulelweyo. Ngokuphathelele ukuncelisa, akukho ziphumo zentengiso engavumelekanga yokuphuhlisa umntwana kwisifundo sezilwanyana; Ukucebisana kweengcali kucetyiswa ukuba kuxubushe iingeniso ezintle kunye nemiphumo emibi yokuncelisa xa i-Technivie.

Umthombo:

US Administration and Drug Administration (FDA). "I-FDA iyayivumela i-Technivie ukuba yonyango lwe-hepatitis C engapheliyo 4." Silver Spring, eMaryn; ukukhutshwa kwenkcazelo ekhutshwe ngoJulayi 24, 2015.

Hézode, C; Asselah, T .; Reddy, R .; okqhubekayo. "I-Ombitasvir kunye neparitaprevir kunye ne-ritonavir kunye okanye ngaphandle kwe-ribavirin kwizigulane ezinezigulane zonyango kunye ne-genotype 4 yokusuleleka kwintsholongwane ye-hepatitis C engapheliyo (PEARL-I). Lancet. NgoJuni 20, 2015; 384 (9986): 2502-2509.