Eflornithine
Jeneng merek: Vaniqa
Kelas obat:
Agen Antineoplastik , Agen Antineoplastik
Panganggone Eflornithine
Amarga obat iki ora kasedhiya ing pasar AS, materi ing bagean iki ora dianyari maneh dening AHFS DI. Yen obat iki digunakake ing negara liyane saka AS, penting yen label pabrikan dikonsultasi kanggo informasi sing luwih anyar kasedhiya.
Ngurangi rambut rai sing ora dikarepake
Ngurangi rambut sing ora dikarepake ing wanita.
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Carane nggunakake Eflornithine
Umum
Amarga obat iki ora kasedhiya ing pasar AS, materi ing bagean iki ora dianyari maneh dening AHFS DI. Yen obat iki digunakake ing negara liyane saka AS, penting yen label pabrikan dikonsultasi kanggo informasi sing luwih anyar sing kasedhiya.
Administrasi
Administrasi Topikal
Aplikasi ing kulit minangka krim 13,9%.
Gunakake mung ing wilayah sing kena pengaruh ing pasuryan lan wilayah sing ana ing jejere dagu; ora dimaksudaké kanggo oral, ophthalmic, utawa intravaginal.
Gunakake film tipis lan gosok kanthi sak tenane.
Aja wisuh area sing diobati paling ora 4 jam sawise aplikasi.
Terusake teknik mbusak rambut (umpamane, plucking, tweezing, motong, cukur), yen perlu, sajrone perawatan. Aja nggunakake krim paling sethithik 5 menit sawise ngilangi rambut.
Bisa nggunakake produk kosmetik lan tabir surya sawise krim wis garing.
Dosis
Kasedhiya minangka eflornithine hidroklorida; dosis sing dituduhake ing syarat-syarat uyah.
Dewasa
Ngurangi Topikal Rambut Rai sing Ora DikarepakeAplikasiake film tipis kaping pindho saben dina paling sethithik 8 jam (utawa kaya sing diarahake dening dokter).
Yen iritasi utawa intoleransi kulit berkembang, kurangi frekuensi aplikasi dadi sapisan saben dina. Yen iritasi terus, mungkasi terapi.
Pènget
Kontraindikasi
Pènget/PanandhapPènget
Amarga obat iki ora kasedhiya ing pasar AS, materi ing bagean iki ora dianyari maneh dening AHFS DI. Yen obat iki digunakake ing negara liyane saka AS, penting yen label pabrikan dikonsultasi kanggo informasi sing luwih anyar kasedhiya.
Reaksi Sensitivitas
Reaksi HipersensitivitasBanjur terapi yen ana reaksi hipersensitivitas.
Pancegahan Umum
Efek DermatologiKamungkinan stinging utawa kobong transien yen ditrapake ing kulit abraded utawa pecah.
Iritasi kulit bisa kedadeyan ing pasien sing rentan utawa sing nggunakake dosis sing luwih dhuwur tinimbang sing disaranake.
Populasi Spesifik
KandhutanKategori C.
LaktasiOra dingerteni manawa eflornithine disebarake menyang susu. Ati-ati yen digunakake ing wanita sing nyusoni.
Panggunaan PediatrikKeamanan lan khasiat ora ditetepake ing bocah-bocah <12 taun.
Panggunaan GeriatrikOra ana bedane sing signifikan babagan safety kanggo wong diwasa sing luwih enom.
p>Efek Umum sing Sabar
Kulit kobong, stinging, lan/utawa tingling; eritema; rame.
Apa obatan liyane bakal mengaruhi Eflornithine
Amarga obat iki ora kasedhiya ing pasar AS, materi ing bagean iki ora dianyari maneh dening AHFS DI. Yen obat iki digunakake ing negara liyane saka AS, penting yen label pabrikan dikonsultasi kanggo informasi sing luwih anyar kasedhiya.
Ora dingerteni manawa eflornithine topikal berinteraksi karo obat topikal liyane.
Disclaimer
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