I-Paxlovid

Incazelo emfushane:

Igama le-API Inkomba Umsunguli Idethi yokuphelelwa yisikhathi kwelungelo lobunikazi(e-US)
I-Paxlovid I-COVID-19 I-Pfizer  

 


Imininingwane Yomkhiqizo

Omaka bomkhiqizo

IMINININGWANE YOMKHIQIZO

I-Paxlovid iwumuthi wophenyo osetshenziselwa ukwelapha i-COVID-19 emaphakathi kuya kokumaphakathi kubantu abadala nasezinganeni [ezineminyaka engu-12 ubudala nangaphezulu ezinesisindo esingamakhilogremu angama-88 (40 kg)] ngemiphumela emihle yokuhlolwa kwegciwane okuqondile kwe-SARS-CoV-2, futhi abasengozini enkulu yokudlulela ku-COVID-19 enzima, okuhlanganisa ukulaliswa esibhedlela noma ukufa. I-Paxlovid iyaphenywa ngoba isacwaningwa. Kunolwazi olulinganiselwe mayelana nokuphepha nokusebenza kahle kokusebenzisa i-Paxlovid ukwelapha abantu abane-COVID-19 emaphakathi kuya kokumaphakathi.
I-FDA igunyaze ukusetshenziswa okuphuthumayo kwe-Paxlovid ekwelapheni i-COVID-19 emaphakathi kuya kokumaphakathi kubantu abadala nasezinganeni [ezineminyaka engu-12 ubudala nangaphezulu ezinesisindo esingamakhilogremu angama-88 (40 kg)] ngokuhlolwa ukuthi unalo yini leli gciwane. kubangela i-COVID-19, futhi abasengozini enkulu yokudlulela ku-COVID-19 enzima, okuhlanganisa ukulaliswa esibhedlela noma ukufa, ngaphansi kwe-EUA.

I-Paxlovid akuwona umuthi ogunyazwe yi-FDA e-United States. Khuluma nomhlinzeki wakho wokunakekelwa kwezempilo mayelana nezinketho zakho noma uma unemibuzo. Kuyisinqumo sakho ukuthatha i-Paxlovid.

I-Paxlovid iqukethe imithi emibili: i-nirmatrelvir ne-ritonavir.

I-Nirmatrelvir [PF-07321332] iyi-SARS-CoV-2 main protease (Mpro) inhibitor (eyaziwa nangokuthi i-SARS-CoV2 3CL protease inhibitor) esebenza ngokuvimbela ukuphindaphindeka kwegciwane ezigabeni zokuqala zesifo ukuvimbela ukuqhubekela phambili ku-COVID- 19.

I-Ritonavir isetshenziswa ngokubambisana ne-nirmatrelvir ukusiza ukubambezela i-metabolism yayo ukuze ihlale isebenza emzimbeni isikhathi eside ekugxilweni okuphezulu ukusiza ukulwa naleli gciwane.

ISItifiketi

2018 GMP-2
原料药GMP证书201811 (captopril,thalidomide njll)
I-GMP-of-PMDA-in-Chanyoo-平成28年08月03日 Nantong-Chanyoo-Pharmatech-Co
I-FDA-EIR-Letter-201901

UKUPHATHWA KWEKHWALITHI

Ukuphathwa kwekhwalithi1

Isiphakamiso18Amaphrojekthi Wokuhlola Ukuvumelana Kwekhwalithi asegunyaziwe4, futhi6amaphrojekthi angaphansi kokugunyazwa.

Ukuphathwa kwekhwalithi2

Uhlelo lokuphatha ikhwalithi yamazwe ngamazwe oluthuthukile lwenze isisekelo esiqinile sokuthengisa.

Ukuphathwa kwekhwalithi3

Ukugadwa kwekhwalithi kusebenza kuwo wonke umjikelezo wempilo womkhiqizo ukuze kuqinisekiswe ikhwalithi nomphumela wokwelapha.

Ukuphathwa kwekhwalithi4

Ithimba Lezindaba Zokulawula Ochwepheshe lisekela izimfuno zekhwalithi ngesikhathi sokufaka isicelo nokubhaliswa.

UKUPHATHWA KOMKHIQIZO

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UZAkwethu

Ukubambisana kwamazwe ngamazwe
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