» 산업 뉴스 » The U.S. 미국 의약품청(Drug Administration), 최초의 경구용 코로나19 항바이러스제 긴급 사용 승인

미국. 미국 의약품청(Drug Administration), 최초의 경구용 코로나19 항바이러스제 긴급 사용 승인

2021-12-23

신화통신, 워싱턴, 12월 22 (탄징징 기자) 22 번째, 미국. 식품의 약국 12 경증에서 중등도의 Covid-19 질병이있는 노인, 심각한 질병의 위험이 높은 사람들뿐만 아니라.

The US Drug Administration said in a statement that the oral COVID-19 antiviral medicine by Pfizer is called Paxlovid and consists of two antiviral drugs. Patients must take it as soon as possible after the diagnosis of the new crown, and start taking it within 5 days after the appearance of the new crown symptoms, and the continuous use time cannot exceed 5 날.

The statement said that after evaluating all available scientific evidence, the US Drug Administration believes that Paxlovid may be effective in the treatment of patients with mild to moderate COVID-19, and its known and potential benefits exceed its known and potential risks. Common side effects of this drug may include impaired taste, 설사, 고혈압, and muscle aches.

Cavazzoni, director of the Center for Drug Evaluation and Research of the US Drug Administration, said that with the emergence of new mutant strains, the prevention and control of the COVID-19 epidemic has entered a critical stage, and the emergency authorization to use this oral drug provides a new tool to combat the COVID-19.

 

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