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Lagevrio
molnupiravir
Adult Dosing .
Dosage forms: CAP: 200 mg
Investigational New Drug (IND)
- [FDA emergency use authorization (EUA)]
- Info: for mild-moderate COVID-19 in pts at high risk for severe dz incl. hospitalization or death, if alternative agents not accessible or clinically appropriate; not FDA approved; avail. from Merck & Co, Inc. or authorized distributors as directed by US government; for clinical trial eligibility and enrollment info, check www.clinicaltrials.gov
- [mandatory reporting]
- Info: serious medication errors and adverse events must be reported to FDA MedWatch (www.fda.gov/medwatch/report.htm or 1-800-FDA-1088) and Merck & Co, Inc. (dpoc.usa@msd.com)
COVID-19, mild-moderate
- [800 mg PO q12h x5 days]
- Start: ASAP w/in 5 days of sx onset; Info: for pts at high risk for severe dz incl. hospitalization or death, if alternative agents not accessible or clinically appropriate
renal dosing
- [no adjustment]
- renal impairment: no adjustment
- HD/PD: no adjustment; no supplement
hepatic dosing
- [no adjustment]
Peds Dosing .
Peds dosing is currently unavailable or not applicable for this drug.