Amagosa ezempilo e-Mississippi abongoza abahlali ukuba bangathathi iziyobisi ezisetyenziselwa iinkomo kunye namahashe endaweni yokufumana iyeza lokugonya le-COVID-19.
Utyando kulawulo lwetyhefu lutsala umnxeba kwilizwe elinenqanaba lesibini elisezantsi lokugonyelwa i-coronavirus libangele iSebe lezeMpilo laseMississippi ukuba likhuphe isilumkiso ngolwesiHlanu malunga nokungeniswa kwechiza.ivermectin.
Ekuqaleni, isebe lathi ubuncinane iipesenti ezingama-70 zeefowuni zakutshanje kumaziko olawulo lwetyhefu zinxulumene nokuthatha ichiza elisetyenziselwa ukunyanga iintsholongwane zeenkomo kunye namahashe. Iziko lolawulo lilonke, kwaye ama-70 ekhulwini aloo minxeba ayenxulumene nabantu abathatha ubisi olungumgubo.
Ngokwesilumkiso esibhalwe nguGqr. Paul Byers, ugqirha wezifo zesifo sikarhulumente, ukusela ichiza kunokubangela irhashalala, isicaphucaphu, ukugabha, iintlungu zesisu, iingxaki zemithambo-luvo kunye ne-hepatitis enzima enokufuna ukulaliswa esibhedlele.
NgokukaMississippi Free Press, uByers uthe iipesenti ezingama-85 zabantu abafowunele emvaivermectinUkusetyenziswa kwakuneempawu ezithambileyo, kodwa ubuncinane omnye walaliswa esibhedlele ngetyhefu ye-ivermectin.
Ivermectinngamanye amaxesha imiselwe abantu ukuba banyange iintwala zentloko okanye iimeko zolusu, kodwa yenziwe ngendlela eyahlukileyo kubantu nakwizilwanyana.
"Iziyobisi zezilwanyana zigxile kakhulu kwizilwanyana ezikhulu kwaye zinokuba yingozi kakhulu ebantwini," utshilo u-Byers kwisilumkiso.
Ngenxa yokuba iinkomo kunye namahashe ziyakwazi ukulinganisa ngokulula ngaphezu kweekhilogram ze-1,000 kwaye ngamanye amaxesha ngaphezu kweetoni, isixa se-ivermectin esisetyenziswe kwimfuyo asifanelekanga kubantu abalinganisa iqhekeza.
I-FDA iphinde yabandakanyeka, ibhala kwi-tweet kule mpelaveki, “Awulilo ihashe.Awuyonkomo.Ngokunyanisekileyo, nina bafana.Yeka."
I-tweet iqulethe ikhonkco kulwazi malunga nokusetyenziswa okuvunyiweyo kwe-ivermectin kwaye kutheni ingasetyenziselwa uthintelo okanye unyango lwe-COVID-19. I-FDA iphinde yalumkisa ngomahluko kwi-ivermectin eyenzelwe izilwanyana kunye nabantu, iphawula ukuba izithako ezingasebenziyo ekwenziweni kwezilwanyana zinokubangela. iingxaki ebantwini.
"Izithako ezininzi ezingasebenziyo ezifunyenwe kwiimveliso zezilwanyana azikavavanywa ukuba zisetyenziswe ebantwini," utshilo i-arhente.“Okanye zibakho ngezixa ezikhulu kakhulu kunezo zisetyenziswa ngabantu.Kwezinye iimeko, asizazi ezi zithako zingasebenziyo.Indlela izithako ziya kuyichaphazela ngayo indlela ivermectin efunxwa ngayo emzimbeni. "
I-Ivermectin ayivunywanga yi-FDA ukunqanda okanye ukunyanga i-COVID-19, kodwa ezi zitofu zibonakaliswe ziwunciphisa kakhulu umngcipheko wokugula kakhulu okanye ukufa.NgoMvulo, isitofu sokugonya se-Pfizer se-COVID-19 ibe yeyokuqala ukufumana imvume epheleleyo ye-FDA.
Ngelixa esi kunye nezinye izitofu zokugonya zihlangabezana ne-FDA engqongqo, indlela yesayensi yogunyaziso losetyenziso olungxamisekileyo, njengogonyo lokuqala lwe-COVID-19 olwamkelwe yi-FDA, uluntu lunokuba nentembelo enkulu yokuba olu gonyo luyahlangabezana nokhuseleko, ukusebenza ngokufanelekileyo kwaye Lenziwe kumgangatho ophezulu we-FDA. ineemfuno ezisemgangathweni kwiimveliso ezivunyiweyo, "uBambelela uMkomishinala we-FDA uJanet Woodcock kwingxelo.
Izitofu zokugonya zikaModerna kunye noJohnson & Johnson zisafumaneka phantsi kogunyaziso losetyenziso olungxamisekileyo.I-FDA iphinda iphonononge isicelo sikaModerna sokwamkelwa ngokupheleleyo, kunye nesigqibo esilindelwe kungekudala.
Amagosa ezempilo karhulumente anethemba lokuba ukuvunywa ngokupheleleyo kuya konyusa ukuzithemba kubantu abathe bathandabuza ukufumana isitofu sokugonya, into eyavunywa nguWoodcock ngoMvulo.
Ngelixa izigidi zabantu ziye zagonyelwa ngokukhuselekileyo i-COVID-19, siyaqonda ukuba, kwabanye, imvume ye-FDA yogonyo ngoku inokufaka ukuzithemba ngakumbi ekugonyweni,” utshilo uWoodcock.
Kumnxeba weZoom kwiveki ephelileyo, igosa lezempilo laseMississippi uGqr. Thomas Dobbs ukhuthaze abantu ukuba basebenze nogqirha wabo wobuqu ukuze bagonywe kwaye bafunde iinyani malunga ne-ivermectin.
“Ngamayeza.Awuyifumani ichemotherapy kwivenkile yokutya,” utshilo uDobbs.” Ndiyathetha ukuba, awufuni ukusebenzisa iyeza lesilwanyana sakho ukunyanga inyumoniya yakho.Kuyingozi ukuthatha idosi engalunganga yeyeza, ngakumbi amahashe okanye iinkomo.Ngoko ke siyayiqonda imeko esihlala kuyo. Kodwa, okubaluleke kakhulu ukuba abantu banezidingo zonyango ngokuya kugqirha okanye kumboneleli wakho.”
Ulwazi olungeyonyani olujikeleze i-ivermectin luyafana neentsuku zokuqala zobhubhane, xa abaninzi babekholelwa, ngaphandle kobungqina, ukuba ukuthatha i-hydroxychloroquine kunokunceda ukuthintela i-COVID-19.
"Kukho ulwazi oluninzi olungelulo malunga, kwaye mhlawumbi uvile ukuba kulungile ukuthatha idosi ephezulu ye-ivermectin.Ayilunganga loo nto,” ngokutsho kwe-FDA post.
Ukwanda kokusetyenziswa kwe-ivermectin kuza ngexesha apho ukwahluka kwe-delta kuye kwakhokelela ekuqhutyweni kweemeko kwilizwe lonke, kuquka ne-Mississippi, apho kuphela i-36.8% yabemi igonywe ngokupheleleyo.Ilizwe kuphela elinezinga eliphantsi lokugonywa laliyi-Alabama engummelwane. , apho i-36.3% yabemi yagonywa ngokupheleleyo.
NgeCawa, urhulumente uxele ngaphezulu kwe-7,200 yamatyala amatsha kunye ne-56 entsha yokusweleka.
Ixesha lokuposa: Jun-06-2022