lukasb comments on Submit comments on Paxlovid to the FDA (deadline Nov 29th).

[lukasb]

This seems like a good idea.

I submitted the following comment:

I urge the FDA to schedule its review of Paxlovid and to make the timeline 3 weeks or less, as it did with the COVID vaccine.

1000 people are dying of COVID in the US every day. With an efficacy of 89%, Paxlovid could prevent many of these deaths. The earlier Paxlovid is approved, the more lives will be saved.

Thank you for your consideration.

I wasn’t sure what topic to put it under so I chose “Drug Industry—C0022.”

[DirectedEvolution]

Thank you for taking action!