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Peramivir: A Novel Intravenous Neuraminidase Inhibitor for Treatment of Acute Influenza Infections

机译:Peramivir:新型的静脉内神经氨酸酶抑制剂治疗急性流感感染。

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摘要

Peramivir is a novel cyclopentane neuraminidase inhibitor of influenza virus. It was approved by the Food and Drug Administration in December 2014 for treatment of acute uncomplicated influenza in patients 18 years and older. For several months prior to approval, the drug was made clinically available under Emergency Use authorization during the 2009 H1N1 influenza pandemic. Peramivir is highly effective against human influenza A and B isolates as well as emerging influenza virus strains with pandemic potential. Clinical trials demonstrated that the drug is well-tolerated in adult and pediatric populations. Adverse events are generally mild to moderate and similar in frequency to patients receiving placebo. Common side effects include gastrointestinal disorders and decreased neutrophil counts but are self-limiting. Peramivir is administered as a single-dose via the intravenous route providing a valuable therapeutic alternative for critically ill patients or those unable to tolerate other administration routes. Successful clinical trials and post-marketing data in pediatric populations in Japan support the safety and efficacy of peramivir in this population where administration of other antivirals might not be feasible.
机译:Peramivir是一种新型的流感病毒环戊烷神经氨酸酶抑制剂。该药已于2014年12月获得美国食品药品监督管理局(FDA)的批准,可用于治疗18岁及以上的急性单纯性流感。在批准前的几个月中,该药物在2009年H1N1流感大流行期间已根据紧急使用授权在临床上可用。帕拉米韦对人类甲型和乙型流感分离株以及具有大流行潜力的新兴流感病毒株非常有效。临床试验表明,该药物在成人和儿童人群中耐受性良好。不良事件一般为轻度至中度,发生频率与接受安慰剂的患者相似。常见的副作用包括胃肠道疾病和嗜中性白血球数量减少,但这是自限性的。帕拉米韦通过静脉途径单剂量给药,为重症患者或无法耐受其他给药途径的患者提供了有价值的治疗选择。在日本的儿科人群中,成功的临床试验和上市后数据支持了帕拉米韦在该人群中的安全性和有效性,在这种人群中,其他抗病毒药物的管理可能不可行。

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