Wannan lamari ne madaidaiciya, buɗe da rufewa. Aƙalla yana kama da ɗaya a gare ni.
Bisa lafazin labarai, a ranar 5 ga Mayu, 2022, rigakafin J&J adenovirus Covid "An iyakance ga mutane 18 ko sama da haka waɗanda ba za su iya ɗaukar ɗayan sauran alluran rigakafin da ake da su ba don dalilai na likita, ko kuma waɗanda kawai ba za su yarda a yi musu allurar da ɗaya daga cikin allurar RNA da Moderna da Pfizer da abokin aikinta BioNTech suka yi.. "
Dalili?
Peter Marks, shugaban hukumar ta FDA, ya shaidawa STAT cewa hukumar ta cimma matsayar ta bayan wani nazari da aka yi a baya-bayan nan game da rigakafin ya nuna cewa wani mutum a kasar ya mutu bayan karbarsa - na tara irin wannan mutuwa - a farkon kwata na shekara.
[FUSKA FUSKA]
"Idan muka ga mace-mace kuma akwai wani madadin maganin da ba a haɗa shi da mace-mace amma yana da alaƙa da inganci iri ɗaya… mun ji lokaci ya yi a wannan lokacin da za mu yi bayani kan takardar gaskiyar [samfurin] cewa wannan ba rigakafin farko ba ne," in ji Marks.
Tare da mutuwa ɗaya ga kowane allurai miliyan 2 da aka ba a cikin wannan ƙasa, FDA ta yanke shawarar cewa haɗarin yawancin mutane ba sa buƙatar ɗauka, in ji Marks.
Mutuwar tara.
Idan aka kwatanta da "wani madadin maganin da ba shi da alaƙa da mace-mace" - sanarwa da aka yi a ranar 5 ga Mayu, 2022.
Bari mu kalli daya irin wannan “madadin rigakafin:”
A takarda mai kwanan wata 28 GA FABRAIRU, 2021 (kusan kusan shekara guda KAFIN bayanan Peter Marks), kwanan nan mai karatu na Brownstone ya kawo hankalina, yana gabatar da bincike na "rahotanni mara kyau bayan izini" akan rigakafin BioNTech/Pfizer Covid, kamar yadda FDA ta nema don Pfizer/BioNTech's License Licenses License (BLA).
Wannan rahoto, mai alamar "SIRRIN" amma akwai jama'a akan phpt.org, an kwanan watan ne kawai watanni 3 bayan "iznin farko na wucin gadi don samar da gaggawa a kan 01 Disamba 2020," wanda shine lokacin da Birtaniya ta ba da izinin amfani da gaggawa ga samfurin.
A cikin rahoton, mun ga cewa akwai 1,223 mutuwar daga cikin jimillar shari'o'i 42,086 da aka tantance a cikin rahoton. NOTE: jimlar adadin ba shine adadin mutanen da suka karɓi maganin ba. Hakanan ba adadin mutanen da ke cikin gwaji na asibiti ba. Yana da adadin "la'o'i" da Pfizer ya bincikar "a madadin BioNTech" (a gefe: dangantakar Pfizer-BioNTech ta cancanci bincike mai yawa fiye da yadda aka karɓa) bayan da samfurin ya kasance a duniya har tsawon watanni uku.
Sama da mutane 1,000 sun mutu a cikin watanni uku na farko na gwamnati. An sake gyara ainihin adadin allurai da aka aika lokacin da aka buga rahoton. Ba a bayar da rahoton lambar da aka gudanar ba har zuwa wannan ranar.
Tattaunawar Pfizer
Bayanan ba su bayyana wata damuwa ta aminci ko haɗari da ke buƙatar canjin lakabi da goyan bayan fa'ida mai fa'ida mai fa'ida ta rigakafin BNT162b2.
NOTE: Ina tsammanin mabuɗin kalmar nan, don dalilai na shari'a, ita ce "labari." Dole ne sun riga sun san game da duk abubuwan da suka faru a cikin wannan rahoto, gami da mutuwa, kafin samfurin ya ba da izini da rarrabawa, don haka a zahiri wannan rahoton baya haɗa da wani abu "labari," ko sabo.
Pfizer's “Summary AND COCLUSION”
Bitar bayanan da ke akwai don wannan tarin ƙwarewar PM yana tabbatar da fa'ida mai kyau: ma'aunin haɗari don BNT162b2.
NOTE: Babu tattaunawa kan kowane fa'ida a cikin rahoton.
Burina
An iyakance rabon harbin J&J kuma an canza alamar bayan TARA hade da mutuwa. "Madogaran" da ake zaton "ba su da alaƙa da mutuwa." Amma rahoton bayan watanni 3 kacal na izinin farko na ɗayan manyan hanyoyin biyu ya nuna SAMA DA DUBU DAYA sun mutu.
Tabbas yana kama da allurar BioNTech/Pfizer, saboda wani dalili da ba a bayyana ba, an sami gata a kan samfurin J&J ta masu tsarawa, wanda har ma fiye da mutuwar 1,000 a cikin watanni uku ba a la'akari da "damuwa na aminci na labari ko haɗari na buƙatar canje-canjen lakabi." Ba a ma maganar janye samfurin daga kasuwa ba.
Hasashe na
Na yi imani da BioNTech da Moderna Covid mRNA rigakafin an ƙaddara a matsayin kawai samfuran rigakafin Covid waɗanda ba wai kawai lafiyar jama'a da hukumomin da kansu za su tallata su ba, har ma samfuran kawai da za su ci gaba da kasancewa a kasuwa ba tare da la'akari da duk wani mummunan lamari da aka ruwaito, gami da dubban mutuwar.
Dalilin wannan, ina tsammanin (bai isa hujja ba tukuna don tabbatar da wannan tabbataccen da'awar), shine cewa waɗannan samfuran biyu an tsara su ta hanyar hanyar sadarwa ta biowarfare / biodefense ta duniya wacce ke gudanar da cutar ta Covid da martani. Cibiyar sadarwa ta biowarfare ta kasance cikin jahannama kan nuna "aminci da inganci" na dandamalin mRNA mai daraja wanda babu abin da zai iya tsayawa kan hanyar waɗannan samfuran - musamman ba rahotannin ƙarancin ingancinsu da bayanin martaba mai ban tsoro ba.
Kara karantawa game da wanda ke da alhakin mayar da martanin cutar.
Kara karantawa game da samfuran rigakafin mRNA da masana'antar biodefense.
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Debbie Lerman, 2023 Brownstone Fellow, yana da digiri a Turanci daga Harvard. Ita marubuciyar kimiyya ce mai ritaya kuma ƙwararren mai fasaha a Philadelphia, PA.
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