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  • Liều dùng thuốc Molnupiravir 400mg - Vinmec
    1 Thuốc Molnupiravir 400mg là gì? Thuốc Molnupiravir 400mg là sản phẩm được bác sĩ chỉ định để điều trị bệnh nhân COVID-19 mức độ từ nhẹ đến trung bình ở người trưởng thành Chỉ định sử dụng thuốc Molnupiravir 400mg được đặt ra khi bệnh nhân có xét nghiệm dương tính với SARS-CoV-2 và kèm theo ít nhất 1
  • Molnupiravir for Treatment of COVID-19 in Solid Organ Transplant . . .
    Molnupiravir acts as a substrate for SARS-CoV-2 RNA polymerase and impairs SARS-CoV-2 replication and infection 4 It retains antiviral activity against all known variants of SARS-CoV-2 3 In a recent clinical trial, patients treated with molnupiravir resulted in faster time to recovery and reduced viral detection and load 5
  • Intended - U. S. Food and Drug Administration
    Molnupiravir may only be used for the treatment of mild-to-moderate COVID-19 in adults with positive results of direct SARS-CoV-2 viral testing, and who are at high-risk for progression to severe
  • Comparison of effectiveness and safety of molnupiravir versus . . .
    Molnupiravir is an oral antiviral medication approved by the US Food and Drug Administration (FDA) for treating high-risk patients with mild to moderate COVID-19, aiming to prevent progression to severe disease 9 The recommended dosage is a 800 mg oral intake twice daily for 5 days, available as 200-mg capsules 10 Studies have demonstrated
  • Molnupiravir: Mechanism of action, clinical, and translational science . . .
    Molnupiravir is an oral prodrug of the broadly active, antiviral ribonucleoside analog N-hydroxycytidine (NHC) The primary circulating metabolite NHC is taken up into cells and phosphorylated to NHC-triphosphate (NHC-TP) NHC-TP serves as a competitive substrate for viral RNA-dependent RNA polymera …
  • Molnupiravir Dosage Guide + Max Dose, Adjustments - Drugs. com
    Usual Adult Dose for COVID-19 For investigational use only 800 mg orally every 12 hours for 5 days Comments: The US FDA issued an Emergency Use Authorization (EUA) to allow the emergency use of the unapproved drug molnupiravir for the treatment of patients with mild to moderate COVID-19 who are at high risk for progression to severe COVID-19, including hospitalization or death and for whom
  • Real-world effectiveness of early molnupiravir or nirmatrelvir . . .
    Background: Data on the effectiveness of oral antivirals in patients with mild-to-moderate COVID-19 are urgently needed This retrospective cohort study aimed to evaluate the clinical and virological outcomes associated with molnupiravir or nirmatrelvir-ritonavir use in hospitalised patients with mild-to-moderate COVID-19 during a pandemic wave dominated by the omicron BA 2 subvariant
  • Viral target- and metabolism-based rationale for combined use of . . .
    Molnupiravir, nirmatrelvir and remdesivir are newly authorized COVID-19 medicines that have demonstrated high efficacy with reasonable safety profiles They differ in the mechanism of action, presenting a strong foundation for combined use Indeed, some in vitro and animal studies have shown promise of their combined use for enhanced activities


















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