WEBVTT

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Tare da coronavirus, an gabatar da
sabuwar fasahar rigakafi, wato fasahar mRNA.

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Yana da muhimmanci a fahimci cewa waɗannan ci gaban
mRNA ba alluran rigakafi ne a ma'anar gargajiya ba.

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Ba a yi wa mutane allurar ƙwayar cuta da aka raunana kuma ba ta
da haɗari wadda ake tsammanin za ta kunna tsarin garkuwar jiki

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ba, sai dai ana yi musu allurar lambar
kwayoyin halitta wadda ke tilasta wa ƙwayoyin jikin

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majinyaci su samar da sababbin nau'ikan furotin.

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Wannan shi ya sa a ke kiran allurar rigakafin mRNA da
allurar kwayoyin halitta ta mRNA ko maganin kwayoyin halitta.

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An lullube mRNA da ake gargaɗa ta sirinji
cikin ƙaramin ƙwallon mai mai layuka biyu .

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Waɗannan ƙananan ƙwayoyin mai, ko LNPs a taƙaice,
suna ba wa mRNA damar shiga cikin ƙwayar halitta.

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Moderna da BioNTech kamfanonin magunguna ne guda biyu
da ake cinikin hannun jarinsu a kasuwar hannun jari.

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Sun samu ribar biliyoyi a lokacin annobar coronavirus.

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Ko da yake ne kawai ƙarƙashin izinin gaggawa,
an yi allurar sinadaran mRNA ga mutane da yawa

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a ƙasashe da dama tun daga kusan Disamba 2020.

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Masana'antar magunguna ta ruɗar jama'a ta ikirarin cewa wannan
allurar kwayoyin halitta don rigakafin cutar

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coronavirus na SARS-CoV-2 tana da aminci,
tana da tasiri, kuma ba ta haifar da illa ba.

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An yi wa muryoyin suka da gargaɗi ƙazamar suna, an toshe su, an
yi musu tsanani, kuma aka halaka su ta fuskar tattalin arziki.

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A wani bambanci mai tsanani, Dr Sabine Stebel ta nuna a cikin
wasiƙar labarai ta "DrBine's" a cikin labarin "Ba za a iya

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yaudara kasuwar hannun jari ba (ba kamar marasa lafiya da
gwamnatoci ba)" na 4 ga Mayu 2025 abin da BioNTech da

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Moderna suka bayyana wa kasuwar hannun jari a rahotanninsu.

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BioNTech da Moderna su ne masu kera alluran
rigakafin coronavirus na mRNA, wato Comirnaty® da Spikevax®.

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A shekarar 2018, Moderna ta rubuta abin da
ke gaba a cikin rahoton kasuwar hannun jari ga

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masu hannun jari a matsayin masu zuba jari:

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"Yawancin kayayyakin bincikenmu ana tsara su kuma ana ba su
a cikin LNP , kodayake mun ƙara inganta LNP ɗinmu, babu

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tabbacin cewa LNP ɗinmu ba za su haifar da mummunan tasiri ba."

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Martanin garkuwar jiki, martanin allurar
magani, martanin kariya ta kariya, martanin antijini.

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An riga an lura da yawancin irin
waɗannan tasirin gefe a cikin LNPs na baya.

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Idan an lura da manyan mummunan lamurra ko wasu sauran illolin
gefe a kowane ɗayan gwaje-gwajenmu na asibiti da

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ke gudana ko na gaba, za mu iya samun wahala
wajen jawo mahalarta don gwaje-gwajenmu na asibiti.

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ko kuma za a tilasta mana mu dakatar da
binciken ko kokarinmu na ci gaba gaba ɗaya.

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Ko da tasirin gefe ba su hana maganin samun ko ci gaba da riƙe
izinin kasuwanci ba, mummunan rabo tsakanin

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amfani da haɗari na iya shafar yadda kasuwa
za ta karɓi samfurin da aka amince da shi.

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Kowane daga cikin waɗannan ci gaban na iya
haifar da mummunan tasiri mai mahimmanci ga

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kasuwancinmu, yanayin kuɗinmu da kuma damar ci gabanmu.

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A ƙarshen shekarar 2021, bayan allurar rigakafin mRNA ta sami
izinin kasuwanci na wucin gadi kuma an riga

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an yi amfani da ita sau miliyoyin, Moderna
cikin mamaki ta maimaita bayanan da ta yi a baya.

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BioNTech ta rubuta abu ɗaya game da allurar
rigakafin mRNA ɗinta Comirnaty® a rahoton

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kasuwar hannun jari a ƙarshen shekarar 2019:

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"Kayan gwajinmu na iya kasa aiki yadda aka nufa, na iya haifar da
illa marasa so, ko kuma na iya nuna wasu halaye daban da za su

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iya jinkirta ko hana amincewarsu, takaita damar kasuwanci na
magani da aka amince da shi, ko haifar da manyan mummunan

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sakamako bayan amincewar kasuwa, idan har aka amince da su."

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Rahoton BioNTech na 2022 ya bayyana: "Samfuran da muke haɓakawa
na iya kasa yin tasiri, ko kuma su yi tasiri ne kaɗan, ko kuma su

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haifar da illa marasa so ko ba a yi niyya ba,
guba ko wasu halaye da za su iya hana amincewar

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kasuwa ko iyakance amfani da su na kasuwanci."

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Bayan shekaru biyu na gudanar da gwaje-gwaje masu yawa a
kan biliyoyin mutane a duk faɗin duniya, ko bai kamata an

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riga an fayyace batun tasiri da aminci ba tun da daɗewa?

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Amma a'a, har zuwa ƙarshen shekarar 2023,
watakila har yanzu ba a warware wannan tambayar ba,

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kamar yadda BioNTech ta rubuta a rahoton shekararta:

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"Wataƙila ba za mu iya nuna isasshen tasiri ko aminci na allurar
rigakafin COVID-19 ɗinmu ba don samun amincewa ta

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dindindin a ƙasashen da aka amince da ita don amfani na
gaggawa ko kuma ta sami izinin sayarwa na sharadi."

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Rahoton shekara-shekara na BioNTech na 2024 ya bayyana: "Mun
karɓi ƙorafe-ƙorafen alhakin samfur kan allurar

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rigakafin COVID-19 ɗinmu kuma muna sa ran karɓar
ƙarin ƙorafe-ƙorafen alhakin samfur a nan gaba."

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Idan ba mu iya kare kanmu yadda ya kamata daga
ikirarin cewa kayayyakinmu da/ko abubuwan da muke gwadawa

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sun yi lahani ba, za mu iya fuskantar manyan alhaki.

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Waɗannan rahotannin kasuwar hannun jari daga Moderna da BioNTech
sun sake tabbatar da yadda aka yaudare mutane ba tare da wata

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tausayi ba, aka ƙaryata su kuma aka sarrafa su da gangan ta
hannun masana'antar magunguna, 'yan siyasa da kafofin watsa

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labarai domin su shiga cikin waɗannan gwaje-gwajen likitanci.

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Ko da yake kamfanonin biyu sun bayyana a
fili cewa alluran rigakafin mRNA na iya

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haifar da manyan illa, an ɓoye wannan ga jama'a.

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Abu ɗaya kawai ne ya kasance a fili
yana da muhimmanci kuma mai yanke hukunci:

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Riba a kowane hali! Ko da menene farashin, har da rayukan mutane!

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Tunda waɗannan amincewa ne na gaggawa ga alluran
rigakafi, ba a buƙatar masu kera su biya kuɗin

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duk wani rauni da ke da alaƙa da alluran rigakafi.

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An haɗa tanade-tanaden alhaki da suka dace a
cikin kwangiloli da masana'antun alluran rigakafi.

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Wannan saboda yanayin doka na amincewar gaggawa ne.

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Kasashen Tarayyar Turai, misali, suna biya
masana'antun alluran rigakafin COVID-19 diyya idan aka

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same su da alhaki saboda illolin da majiyyata suka ji.

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Wato, mutanen da aka yaudare kuma aka
cutar ne za su biya wannan da harajinsu.

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Shin kuna jin takaici, fushi ko wasu motsin rai a
gaban irin wannan yaudara da damfara da aka yi wa mutane?

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Shiga cikin jerin 'yan jarida masu
bincike ka kuma fallasa ƙarya da yaudara.

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