Breaking: FDA Emergency Use Decision

Breaking News

(ReclaimingAmerica.net) – BREAKING NOW: Just moments ago, the United States Food and Drug Administration (FDA) announced that it had issued an emergency use authorization for a new pill – Pfizer’s Paxlovid – for the treatment of COVID-19.

As reported by the Washington Post:

“Federal regulators Wednesday authorized the first easy-to-take pill to treat covid-19, a five-day regimen developed by Pfizer that will help refill the nation’s medicine cabinet even as the omicron variant has thwarted most other options…

“Patrizia Cavazzoni, director of the FDA’s Center for Drug Evaluation and Research, said in a statement that the pill was ‘a major step forward.’

“‘This authorization provides a new tool to combat COVID-19 at a crucial time in the pandemic as new variants emerge and promises to make antiviral treatment more accessible to patients who are at high risk for progression to severe COVID-19,” Cavazzoni said.” [emphasis added]

Reports indicate that each pill pack will contain 30 tablets that the patient will consume over a five-day period. The government believes the challenge now is to produce enough of the new pills to meet a demand that they think will exhaust the supply in short order.

What do you think? What is your opinion? Email [email protected] and share your thoughts and opinion about the United States Food and Drug Administration issuing an emergency use authorization for Pfizer’s Paxlovid for the treatment of COVID-19. Thank you, and have a good day.

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