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COVID-19 Booster: Johnson & Johnson Alurar Aiki Yanzu WHO ta goyi baya

Written by edita

Johnson & Johnson a yau sun sanar da shawarar wucin gadi ta kungiyar kwararrun masu ba da shawara kan rigakafi (SAGE) ga Hukumar Lafiya ta Duniya (WHO) da ke tallafawa yin amfani da allurar Johnson & Johnson COVID-19 a matsayin harbin da aka yi wa mutane masu shekaru 18 da haihuwa. a sama.

Hukumar ta WHO ta ba da shawarar cewa ya kamata a yi allurar rigakafin watanni biyu zuwa shida bayan rigakafin farko. SAGE tana ba WHO shawara game da manufofin rigakafin rigakafi da rigakafi na duniya, kuma shawarwarinsa suna ba da jagora kan amfani da allurar rigakafin da ake bayarwa ta hanyar COVAX Facility, tsarin raba kasada na duniya don haษ—ar siye da rarraba daidaitattun alluran rigakafin COVID-19 ga duk ฦ™asashe masu shiga.          

SAGE shawarar cewa Johnson & Johnson COVID-19 maganin za a iya amfani homologue (wannan maganin) makon, ta amfani da Company ta maganin duka biyu farko alurar riga kafi da kuma kara amfani harbi. A WHO goyon bayan wani m tsarin kula da heterologous (Mix-da-wasan) makon, ta amfani da Johnson & Johnson COVID-19 maganin a matsayin mai kara amfani ga m mutane shekaru 18 shekaru da mazan da suka karbi wani izini COVID-19 maganin farko regimen.

"Yau shawarwarin daga Strategic Shawarwari Group of Masana a kan rigakafin ga World Health Organization ne m affirmation cewa Johnson & Johnson COVID-19 maganin zai iya taimaka wajen rage nauyin da cutar AIDS," ya ce Mathai Mammen, MD, Ph.D., Shugaban Duniya, Janssen Research & Development, Johnson & Johnson. "Alurar rigakafin mu na COVID-19 na ci gaba da taka muhimmiyar rawa a yakin duniya na kawo karshen wannan annoba, kuma muna maraba da wannan shawarar yayin da muke aiki tare da al'ummomin duniya don kare mutane da yawa daga COVID-19."

Shawarar SAGE na wucin gadi ya dogara ne akan inganci, aminci da bayanan rigakafi daga gwaje-gwajen asibiti na Kamfanin da kuma binciken Sisonke Phase 3b na Hukumar Kula da Kayayyakin Lafiya ta Afirka ta Kudu a Afirka ta Kudu. Lokacin da aka yi amfani da shi azaman ฦ™arami, biyo bayan allurar farko tare da rigakafin Johnson & Johnson COVID-19, yana ba da ฦ™arin kariya daga kamuwa da cuta mai saurin kamuwa da cuta, kuma gabaษ—aya an jure shi sosai.

A farkon wannan shekarar SAGE ta ba da shawarar yin amfani da allurar rigakafin Johnson & Johnson COVID-19 guda ษ—aya bisa ga shaida daga binciken Kamfanin na Mataki na 3 ENSEMBLE, wanda ya nuna inganci ga cututtuka masu tsanani, kuma ya nuna ฦ™aฦ™ฦ™arfan kariya daga asibiti da ke da alaฦ™a da COVID-19. farawa kwanaki 28 bayan alurar riga kafi. Waษ—annan bayanan sun yi daidai da babban binciken shaida na duniya da aka gudanar a Amurka, wanda ya nuna ingantaccen ingantaccen rigakafin rigakafin cututtukan da ke da alaฦ™a da COVID-19 da asibitoci, ba tare da wata shaida ta raguwar tasiri a tsawon lokacin binciken na watanni shida - gami da lokacin da Delta Bambance-bambancen ya zama rinjaye a Amurka (ba a samun bayanan jeri don bincike).

Johnson & Johnson tana ba da alฦ™awarin samar da allurai har miliyan 900 na rigakafin COVID-19 ga Tarayyar Afirka (ta hanyar African Vaccine Acquisition Trust) da COVAX, a hade, har zuwa 2022.

Alurar rigakafin Johnson & Johnson COVID-19 ya dace da daidaitaccen ajiyar allurar rigakafi da tashoshi na rarraba tare da sauฦ™in isarwa zuwa yankuna masu nisa. An kiyasta cewa maganin zai tsaya tsayin daka har tsawon shekaru biyu a -4ยฐF (-20ยฐC), kuma mafi girman watanni shida a yanayin sanyi na yau da kullun na 36ยฐ zuwa 46ยฐF (2ยฐ zuwa 8ยฐC). Ba za a sake daskarar da maganin COVID-19 ba idan an rarraba shi a yanayin zafi na 36ยฐF zuwa 46ยฐF (2ยฐ-8ยฐC).

Alurar rigakafin Johnson & Johnson COVID-19, wanda kuma ake kira da Janssen COVID-19 Vaccine, ya sami Izinin Amfani da Gaggawa na farko (EUA) a Amurka a ranar 27 ga Fabrairu, 2021, da EUA a matsayin harbi mai ฦ™arfi a ranar 20 ga Oktoba. Har ila yau, ya karษ“i Izinin Kasuwancin Yanayi ta Hukumar Tarayyar Turai a ranar 11 ga Maris. Hukumar ta WHO ta ba da Lissafin Amfani da Gaggawa a ranar 12 ga Maris, kuma Kamfanin ya sami shawarwarin wucin gadi kan rigakafin farko ta SAGE a ranar 17 ga Maris. A ranar 24 ga Nuwamba, Lafiyar Kanada ta amince da kamfanin guda ษ—aya- allurar rigakafin COVID-19. An ba da ฦ™arin izini da izini da yawa a cikin ฦ™asashe na duniya, gami da ฦ™asashe 50 na Afirka, tare da ฦ™arin gabatar da ka'idoji.

Johnson & Johnson na ci gaba da gabatar da bayanan da suka dace ga sauran masu mulki, WHO da Kungiyoyin Ba da Shawarwari na Fasaha na Allurar rigakafi (NITAGs) a duk duniya don sanar da yanke shawara kan dabarun sarrafa rigakafin gida, kamar yadda ake bukata.

Tare da haษ—in gwiwar ฦ™ungiyoyin ilimi a Afirka ta Kudu da ma duniya baki ษ—aya, Kamfanin yana kuma kimanta tasirin rigakafin COVID-19 a cikin bambance-bambancen, yanzu gami da sabon nau'in Omicron mai saurin yaduwa. Bugu da kari, Kamfanin yana bin takamaiman rigakafin Omicron kuma zai ci gaba da shi yadda ake buฦ™ata.

Don ฦ™arin bayani kan hanyoyin da Kamfanin ke bi don taimakawa yaฦ™i da cutar, ziyarci: www.jnj.com/covid-19.

Amfani da Izini

An ba da izinin allurar Janssen COVID-19 don amfani a ฦ™arฦ™ashin Izinin Amfani da Gaggawa (EUA) don yin rigakafi mai aiki don hana Cutar Coronavirus 2019 (COVID-19) wanda ke haifar da mummunar cutar numfashi ta coronavirus 2 (SARS-CoV-2).

โ€ข Tsarin allurar riga-kafi na Janssen COVID-19 Alurar riga-kafi ษ—aya ce (0.5 ml) da ake gudanarwa ga mutane masu shekaru 18 da haihuwa.

โ€ข Janssen COVID-19 guda ษ—aya na ฦ™arar maganin rigakafi (0.5 ml) ana iya ba da shi aฦ™alla watanni 2 bayan rigakafin farko ga mutane masu shekaru 18 da haihuwa.

โ€ข Za a iya ba da kashi ษ—aya na rigakafin Janssen COVID-19 (0.5 ml) ga mutane masu shekaru 18 da haihuwa a matsayin ฦ™aramar haษ“akawa daban-daban bayan kammala rigakafin farko tare da wani izini ko yarda da maganin COVID-19. Matsakaicin adadin alluran ฦ™ararrawa na heterologous daidai yake da wanda aka ba da izini don ฦ™ara adadin maganin da aka yi amfani da shi don rigakafin farko.

MUHIMMAN BAYANI AKAN KIYAYYA

ME YA KAMATA KA AMBACI GA MAI BARKA DA ALLURAR KUWA KAFIN KA SAMU ALLURAR COVID-19 JANSSEN?

Faษ—a wa mai bada alurar riga kafi game da duk yanayin lafiyar ku, gami da idan kun:

โ€ข suna da duk wani rashin lafiyan halayen

โ€ข zazzabi

โ€ข suna da matsalar zubar jini ko kuma suna kan mai rage jini

โ€ข suna da rigakafi ko kuma suna kan maganin da ke shafar tsarin garkuwar jikin ku

โ€ข suna da ciki ko shirin yin ciki

โ€ข suna shayarwa

โ€ข sun sami wani maganin COVID-19

โ€ข sun taษ“a suma tare da allura

WAYE YA KAMATA YA SAMU JANSSEN COVID-19 VACCINE?

Bai kamata ku sami Janssen COVID-19 Vaccine ba idan kun:

โ€ข ya yi mummunan rashin lafiyan bayan allurar baya ta wannan allurar

โ€ข ya kamu da rashin lafiya mai tsanani ga kowane sinadari na wannan maganin.

TA YAYA AKE BA JANSSEN COVID-19 VACCINE?

Za a ba ku Allurar Janssen COVID-19 a matsayin allura a cikin tsoka.

Allurar Farko: Ana gudanar da allurar Janssen COVID-19 azaman kashi ษ—aya.

Adadin ฦ˜arfafawa:

Za'a iya yin allurar rigakafi guda ษ—aya na Janssen COVID-19 aฦ™alla watanni biyu bayan rigakafin farko tare da Janssen COVID-19 Vaccine.

โ€ข Za a iya ba da kashi ษ—aya na rigakafin Janssen COVID-19 ga mutane masu shekaru 18 da haihuwa waษ—anda suka gama rigakafin farko tare da wani izini daban ko yarda da maganin COVID-19. Da fatan za a bincika tare da mai ba da lafiyar ku game da lokacin da adadin ฦ™arar ฦ™arar.

MENENE HADARIN ALJANIN COVID-19 JANSSEN?

Illolin da aka ruwaito tare da Janssen COVID-19 Vaccine sun haษ—a da:

โ€ข Hanyoyin shafin allura: zafi, jajayen fata, da kumburi.

โ€ข Illolin gaba ษ—aya: ciwon kai, jin kasala sosai, ciwon tsoka, tashin zuciya, zazzabi.

โ€ข Kumburi na lymph nodes.

โ€ข Jinin jini.

โ€ข Jin daษ—i da ba a saba gani ba a cikin fata (kamar tingling ko jiษ“in jijiya) (paresthesia), raguwar ji ko ฦ™ima, musamman a cikin fata (hypoesthesia).

โ€ข Ringi mai dagewa a cikin kunnuwa (tinnitus).

โ€ข Zawo, amai.

Matsanancin Maganin Allergic

Akwai dama mai nisa cewa rigakafin Janssen COVID-19 na iya haifar da mummunan rashin lafiyan. Muguwar rashin lafiyan yakan faru a cikin 'yan mintoci kaษ—an zuwa awa ษ—aya bayan samun allurar Janssen COVID-19. Don haka, mai ba da rigakafin ku na iya tambayar ku da ku zauna a wurin da kuka karษ“i maganin ku don saka idanu bayan rigakafin. Alamomin rashin lafiyar mai tsanani na iya haษ—awa da:

โ€ข Wahalar numfashi

โ€ข Fuskar fuskarka da makogwaro

โ€ข bugun zuciya mai sauri

โ€ข Mummunan kurji a jikinka

โ€ข Dizziness da rauni

Jini na jini tare da ฦ™ananan matakan platelets

Ruwan jini da ya shafi tasoshin jini a cikin kwakwalwa, huhu, ciki, da ฦ™afafu tare da ฦ™ananan matakan platelet (ฦ™wayoyin jinin da ke taimaka wa jikin ku daina zubar jini), sun faru a wasu mutanen da suka karษ“i Allurar Janssen COVID-19. A cikin mutanen da suka haษ“aka waษ—annan ษ—igon jini da ฦ™ananan matakan platelet, alamun sun fara kusan mako ษ—aya zuwa biyu bayan alurar riga kafi. Bayar da rahoton waษ—annan dunฦ™ulewar jini da ฦ™ananan matakan platelet ya kasance mafi girma a cikin mata masu shekaru 18 zuwa 49. Damar samun wannan ta faru tana da nisa. Ya kamata ku nemi kulawar likita nan da nan idan kuna da ษ—ayan alamun da ke biye bayan samun Janssen COVID-19 Vaccine:

โ€ข Numfashin numfashi,

โ€ข Ciwon kirji,

โ€ข kumburin kafa,

โ€ข Ciwon ciki mai ษ—orewa,

โ€ข Ciwon kai mai tsanani ko na ci gaba ko duhun gani.

โ€ข Sauฦ™aฦ™e rauni ko ฦ™ananan ษ—igon jini a ฦ™arฦ™ashin fata bayan wurin allurar.

Waษ—annan ฦ™ila ba su zama duk illolin da ke tattare da rigakafin Janssen COVID-19 ba. Mummunan sakamako da ba zato ba tsammani na iya faruwa. Har yanzu ana nazarin rigakafin Janssen COVID-19 a gwajin asibiti.

Guillain Barrรฉ ciwo

Ciwon Guillain Barrรฉ (cuta ce ta jijiyoyin jiki wanda tsarin garkuwar jiki ke lalata ฦ™wayoyin jijiya, yana haifar da raunin tsoka kuma wani lokacin naฦ™asa) ya faru a wasu mutanen da suka karษ“i Allurar Janssen COVID-19. A yawancin waษ—annan mutanen, alamun sun fara a cikin kwanaki 42 bayan karษ“ar Janssen COVID-19 Vaccine. Damar samun wannan faruwar ta ragu sosai. Yakamata ku nemi kulawar likita nan da nan idan kun sami ษ—ayan alamun da ke biyo bayan karษ“ar Janssen COVID-19 Vaccine:

โ€ข Rauni ko raษ—aษ—i, musamman a ฦ™afafu ko hannaye, wanda ke daษ—a muni da yaduwa zuwa wasu sassan jiki.

โ€ข Wahalar tafiya.

โ€ข Wahala da motsin fuska, gami da magana, taunawa, ko hadiyewa.

โ€ข Gani biyu ko rashin iya motsa idanu.

โ€ข Wahala tare da sarrafa mafitsara ko aikin hanji.

ME YA KAMATA NA YI GAME DA ILLOLIN GABA?

Idan kun fuskanci mummunan rashin lafiyan, kira 9-1-1, ko je asibiti mafi kusa.

Kira mai ba da rigakafin ko mai ba da lafiyar ku idan kuna da wasu illolin da ke damun ku ko kuma ba su tafi ba.

Bayar da illolin allurar rigakafi ga FDA/CDC Tsarin Ba da Rahoto Mara Kyau (VAERS). Lambar kyauta ta VAERS ita ce 1-800-822-7967 ko bayar da rahoto akan layi zuwa https://vaers.hhs.gov/reportevent.html. Da fatan za a haษ—a da "Janssen COVID-19 Vaccine EUA" a cikin layin farko na akwatin #18 na fam ษ—in rahoton. Bugu da kari, zaku iya bayar da rahoton illa ga Janssen Biotech Inc. a 1-800-565-4008.

ZAN IYA SAMUN JANSSEN COVID-19 VACCINE A LOKACI DA SAURAN VACCINES?

Har yanzu ba a miฦ™a bayanai ga FDA kan gudanar da rigakafin Janssen COVID-19 a lokaci guda da sauran alluran rigakafi ba. Idan kuna tunanin karษ“ar Janssen COVID-19 Vaccine tare da wasu alluran rigakafi, tattauna zaษ“in ku tare da mai ba da lafiya.

Shafin Farko

Game da marubucin

edita

Edita a shugaba na eTurboNew ita ce Linda Hohnholz. Ta dogara ne a HQ eTN a Honolulu, Hawaii.

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