Scott provides updates on efforts to get FDA approval for fluvoxamine as a COVID-19 treatment and reports on the early approval of Paxlovid. Longer summary

This post is an addendum to a previous article about Luvox and COVID-19 treatment. It updates readers on recent developments in the effort to get FDA approval for fluvoxamine (Luvox) as a COVID-19 treatment. Scott reports that Dr. Ed Mills and colleagues have found a way to submit an Emergency Use Authorization (EUA) application to the FDA for fluvoxamine, despite the initial hurdle of not having a sponsoring drug company. The post also mentions the FDA's approval of Paxlovid, another COVID-19 drug, which happened earlier than expected according to prediction markets. Shorter summary

Scott Alexander critiques the FDA's slow approval process for Paxlovid, a promising COVID-19 treatment, despite its proven effectiveness. Longer summary

Scott Alexander discusses the FDA's delay in approving Paxlovid, a highly effective COVID-19 treatment. He criticizes the FDA for taking an estimated six weeks to approve the drug despite stopping trials early due to its effectiveness. The post explores the inconsistency in the FDA's approach, questions potential reasons for the delay, and emphasizes the urgency of approval given the ongoing COVID-19 deaths. Scott also addresses potential criticisms by comparing the situation to ivermectin and acknowledging the risk of unforeseen issues with Paxlovid. Shorter summary

Scott summarizes and responds to comments on his previous article about FDA approval of Paxlovid, acknowledging some valid points while maintaining his criticism of the approval process. Longer summary

This post summarizes comments on Scott's previous article about FDA approval of Paxlovid. It covers manufacturing challenges, FDA approval processes, production capacity, ongoing studies, and ethical considerations. Scott acknowledges some valid points raised by commenters about reasons for FDA delays, but maintains his criticism of the approval process, suggesting a need for different levels of approval and questioning the current drug approval system. Shorter summary