Abrysvo
Jeneng umum: Respiratory Syncytial Virus Vaccine
Bentuk dosis: bubuk kanggo rekonstitusi
Kelas obat:
Vaksin virus
Panganggone Abrysvo
Abrysvo minangka vaksin RSV sing digunakake kanggo ngimunake wanita ngandhut lan wong diwasa sing umure 60 taun utawa luwih. Abrysvo nglindhungi saka penyakit saluran pernapasan ngisor (LRTD) sing disebabake dening virus respiratory syncytial (RSV) kanggo wong diwasa sing diobati, lan kanthi vaksinasi wanita ngandhut, nglindhungi bayi saka LRTD wiwit lair nganti umur 6 sasi. Abrysvo dianggo kanthi ngembangake kekebalan marang rong protein RSV (antigen) RSVpreF A lan RSVpreF B, supaya yen sampeyan kena RSV, sistem kekebalan bayi utawa wong diwasa bakal bisa ngenali lan ngrusak.
RSV yaiku virus sing umum lan nular sing bisa nyebabake rawat inap lan pati ing pasien sing duwe risiko dhuwur kanggo penyakit sing abot, kalebu bayi lan wong tuwa sing duwe kondisi medis kayata diabetes lan penyakit jantung lan paru-paru kronis.
Abrysvo dadi disetujoni FDA kanggo wong diwasa umur 60 taun lan luwih ing 31 Mei 2023. Abrysvo dadi vaksin RSV pisanan sing disetujoni FDA kanggo wanita ngandhut ing 21 Agustus 2023. Bisa digunakake antarane 32 nganti 36 minggu umur meteng . Iki disetujoni kanggo wanita ngandhut sawise asil positif saka uji klinis Fase 3 (NCT04424316) MATISSE (Studi Imunisasi MAT kanggo Keamanan lan Khasiat).
Abrysvo efek sisih
Abrysvo umume ditoleransi kanthi becik, lan efek samping sing paling umum kalebu lemes, sirah, nyeri situs injeksi, lan nyeri otot. Iki umume mung sedhela.
Sadurunge njupuk Abrysvo
Aja menehi vaksin marang sapa wae sing duwe riwayat reaksi alergi sing abot (kayata anafilaksis) marang Abrysvo utawa komponen apa wae.
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Carane nggunakake Abrysvo
Abrysvo diwenehake kanthi injeksi intramuskular, biasane menyang otot deltoid ing lengen ndhuwur.
Dosis 0,5mL.
Pènget
Reaksi anafilaksis sing bisa ditindakake
Atur ing fasilitas sing bisa nyedhiyakake perawatan medis lan pengawasan sing cocog kanggo ngatur reaksi anafilaksis sing bisa ditindakake sawise administrasi.
Kanggo wong sing ngandhut
Kanggo ngindhari risiko potensial lair prematur, vaksinasi kudu diwènèhaké nalika umur gestasi 32 nganti 36 minggu.
Ing uji klinis ing ngendi Abrysvo ana. dibandhingake karo plasebo, bayi sing lair saka wong sing ngandhut ngalami bobot lair kurang (5,1% Abrysvo dibandhingake karo 4,4% plasebo) lan jaundice (7,2% Abrysvo dibandhingake karo 6,7% plasebo)
Syncope (pingsan)
Semaput bisa kedadeyan sawise administrasi vaksin. Tata cara kudu ditindakake supaya ora cilaka amarga semaput.
Immunosupresi
Wong sing immunocompromised, kalebu sing nampa terapi imunosupresif, bisa uga kurang respon imun marang vaksin.
Watesan
Vaksinasi bisa uga ora nglindhungi kabeh panampa vaksin.
Bocah
Abrysvo ora disetujoni kanggo bocah.
FAQ populer
Arexvy lan Abrysvo minangka vaksin respiratory syncytial virus (RSV) sing disetujoni kanggo digunakake ing wong diwasa sing umure luwih saka 60 taun kanggo nyuda resiko nandhang penyakit saluran pernapasan ngisor (LRTD). Abrysvo uga disetujoni kanggo digunakake ing wanita ngandhut antarane 32 kanggo 36 minggu meteng, kanggo nglindhungi bayi saka LRTD wiwit lair nganti umur 6 sasi. Arexvy digawe dening GSK lan disetujoni tanggal 3 Mei 2023; vaksin RSV pisanan sing disetujoni kanggo wong diwasa lawas. Abrysvo digawe dening Pfizer lan disetujoni tanggal 31 Mei 2023; vaksin RSV kapindho sing disetujoni kanggo wong tuwa. Terus maca
Arexvy lan Abrysvo minangka vaksin respiratory syncytial virus (RSV) sing disetujoni kanggo digunakake ing wong diwasa sing umure luwih saka 60 taun kanggo nyuda resiko nandhang penyakit saluran pernapasan ngisor (LRTD). Abrysvo uga disetujoni kanggo digunakake ing wanita ngandhut antarane 32 kanggo 36 minggu meteng, kanggo nglindhungi bayi saka LRTD wiwit lair nganti umur 6 sasi. Arexvy digawe dening GSK lan disetujoni tanggal 3 Mei 2023; vaksin RSV pisanan sing disetujoni kanggo wong diwasa lawas. Abrysvo digawe dening Pfizer lan disetujoni tanggal 31 Mei 2023; vaksin RSV kapindho sing disetujoni kanggo wong diwasa lawas. Terus maca
Disclaimer
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