Umuthi wokugoma we-Pfizer's COVID-19 Ungowokuqala Ukuvunyelwa Ngokugcwele yi-FDA

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Ukuphathwa Kwezokudla Nezidakamizwa eU.S. enkulu ingqophamlando ngoMsombuluko ngokunikeza imvume yemithi yokugoma i-Pfizer-BioNTech COVID-19 yabantu abaneminyaka engu-16 noma ngaphezulu.Umuthi wokugomela we-Pfizer-BioNTech onemithamo emibili, othole ukukhanya okuluhlaza ukuze ugunyazwe ukusetshenziswa okuphuthumayo yi-FDA ngoDisemba odlule, manje usuwumuthi wokuqala wokugomela i-coronavirus ukuthola ukugunyazwa okuphelele yinhlangano.

“Yize lokhu kanye neminye imithi yokugoma ihlangabezane nezindinganiso eziqinile, zesayensi ze-FDA zokugunyazwa ukusetshenziswa kwezimo eziphuthumayo, njengomgomo wokuqala ogunyazwe yi-FDA we-COVID-19, umphakathi ungaba nethemba elikhulu lokuthi lo mgomo uhlangabezana nezindinganiso eziphakeme zokuphepha, ukusebenza kahle, kanye nokukhiqiza. ikhwalithi edingwa yi-FDA yomkhiqizo ovunyelwe, "kusho uJanet Woodcock, MD, oyibamba likakhomishani we-FDA, esitatimendeni ngoMsombuluko. "Ngenkathi izigidi zabantu sezivele ziyithole ngokuphepha imijovo ye-COVID-19, siyabona ukuthi kwabanye, ukuvunyelwa kwe-FDA komuthi wokugoma manje kungafaka ukuzethemba okwengeziwe kokugonywa. Ingqophamlando yanamuhla isisondeza eduze ekuguquleni inkambo yalesi sifo i-US" (Okuhlobene: Usebenza Kanjani Umuthi Wokugomela i-COVID-19)

Njengamanje, abantu baseMelika abangaphezu kwezigidi eziyi-170 bagonywe ngokuphelele i-COVID-19, ngokusho kwedatha yakamuva evela kuCenters for Disease Control and Prevention, okulingana namaphesenti angama-51.5 wabantu. Kulabo bantu abayizigidi eziyi-170, abangaphezu kwezigidi ezingama-92 bathole umuthi wokugomela imithamo emibili iPfizer-BioNTech, ngokwe-CDC.

Ngenkathi abantu abangaphezu kwezigidi ezingama-64 e-US begonywe ngokuphelele ngomuthi wokugomela we-Moderna onemithamo emibili, ngokusho kwemininingwane yakamuva ye-CDC, abalawuli basacubungula isicelo senkampani sokuvunywa ngokuphelele komgomo wayo we-COVID-19, I-New York Times kubika uMsombuluko. Ngaphansi kwe-EUA - esebenza futhi kumuthi wokugoma owodwa kaJohnson & Johnson - i-FDA ivumela ukusetshenziswa kwemikhiqizo yezokwelapha engagunyaziwe ngesikhathi sezimo eziphuthumayo zezempilo zomphakathi (njengesifo se-COVID-19) ukwelapha noma ukuvimbela izifo ezisongela impilo.

Njengoba amacala e-COVID-19 eqhubeka nokukhuphuka ezweni lonke ngenxa yokwehluka kwe-Delta okutheleleka kakhulu, ukugunyazwa kwe-FDA komuthi wokugomela i-Pfizer-BioNTech kungase kuholele ezidingweni zokugoma phakathi kwamakolishi, izinhlangano kanye nezibhedlela, ngokusho kombiko. I-New York Times. Amadolobha athile, okuhlanganisa ne-New York, asevele adinga abasebenzi nabaxhasi ukuthi babonise ubufakazi bokugoma ukuze babambe iqhaza emisebenzini eminingana yasendlini, okuhlanganisa ukuzijabulisa nokudla.

Ukuzifihla nokwenza ukuziqhelanisa nomphakathi kubalulekile ekulweni ne-COVID-19, kepha imigomo ihlala iyindlela engcono kakhulu yokuzivikela nabanye. Ngemuva kwezindaba zangoMsombuluko ezibucayi ezivela ku-FDA, mhlawumbe lokhu kuzofaka ukuzethemba komuthi wokugoma kulabo abangase bakuxwaye ukuthola umthamo.

Imininingwane ekule ndaba inembile njengesikhathi sokushicilela. Njengoba izibuyekezo mayelana ne-coronavirus COVID-19 ziqhubeka nokuvela, kungenzeka ukuthi ulwazi oluthile nezincomo kule ndaba kushintshile kusukela ekushicilelweni kokuqala. Sikukhuthaza ukuthi uhlole njalo izinsiza ezifana ne-CDC, i-WHO, kanye nomnyango wezempilo womphakathi wendawo ukuze uthole imininingwane yakamuva nezincomo.

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