By Dylan Housman
The Food and Drug Administration (FDA) approved Pfizer’s antiviral COVID-19 pill Wednesday, granting access to another highly effective therapeutic against the virus.
The drug, Paxlovid, can be prescribed to those aged 12 and up with mild or worse COVID-19 cases and is designed to reduce the risk of severe disease and hospitalization. Early supply of the drug will be limited, but eventually it is expected to provide major relief to hospitals strained by COVID-19 patients.
BREAKING: Pfizer's Covid-19 pill wins FDA emergency-use authorization for people at high risk of severe complications, becoming the first at-home drug to fight the virus https://t.co/80tolbsxCp pic.twitter.com/iM6qiv354S
— Bloomberg (@business) December 22, 2021
Pfizer CEO Albert Bourla said Wednesday the company will begin delivery of the pills immediately. Clinical trials of the drug found it to be 89% effective at stopping high-risk patients from developing serious disease or dying, the company said. The full course of treatment involves taking three pills twice daily for five days after infection. (RELATED: Despite Evidence, Walensky Refuses To Call Omicron ‘Mild’ In Interview With Fox’s Bret Baier)
The treatment must begin within five days of first symptoms in order to be effective, the FDA said. Bourla said there will be 180,000 courses of treatment available by the end of this year and up to 80 million available next year. The Biden administration has already made plans to purchase 10 million courses of the treatment.
