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Who qualifies for Paxlovid?

Paxlovid(Nirmatrelvir/ritonavir) is recommended for adults and pediatric patients 12 years and older weighing at least 40 kg (88 lb) with positive SARS-CoV-2 test results who are at high risk for progression to severe COVID-19.

What are the benefits of taking lagevrio?

LAGEVRIO is an antiviral drug that works against the virus that causes COVID-19. You are being given LAGEVRIO for the treatment of coronavirus disease 2019 (COVID-19). LAGEVRIO may help you to feel better and stay out of hospital.

What is an EUA fact sheet?

The Fact Sheet is similar in purpose and content to vaccine information statements (VISs) for licensed vaccines but differs in that the EUA Fact Sheet is specific to each authorized COVID-19 vaccine, is developed by the manufacturer of the vaccine, and is authorized by the FDA.

What exactly does lagevrio do?

Lagevrio is an oral antiviral used to help fight the coronavirus infection by stopping the coronavirus from replicating in the body.

Who Cannot take Paxlovid?

Paxlovid is not recommended for patients with severe kidney problems, and a different dose is needed for patients with moderate kidney problems. Patients should talk with their health care provider if they have a history of kidney problems.

What are the severe side effects of lagevrio?

A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.

How long does it take for molnupiravir to start working?

Its important that you start taking molnupiravir within 5 days of getting COVID-19 symptoms. Molnupiravir starts working very soon after taking it.

When is lagevrio recommended?

LAGEVRIO (molnupiravir) is an investigational medicine used to treat mild-to-moderate COVID-19 in adults: who are at risk for progression to severe COVID-19 including hospitalization or death, and for whom other COVID-19 treatment options approved or authorized by the FDA are not accessible or clinically appropriate.

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