in PAXLOVID


What it isSARS-CoV-2 main protease inhibitor, given with ritonavir; early COVID-19 in those at risk of progression.
Why this oneSubstantial reduction in hospitalization when started within five days of symptom onset.
What limits itThe ritonavir booster is the problem: it is a strong CYP3A4 inhibitor, so statins, some anticoagulants and many other drugs must be held. Renally adjusted.
Read the full label on DailyMed ↗
| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Mild-to-moderate COVID-19 at high risk of progression to severe disease | adult | 300 mg nirmatrelvir + 100 mg ritonavir BID × 5 days | 300 mg/100 mg BID × 5 days |
Renal Moderate (eGFR 30–<60): 150 mg/100 mg BID; severe (<30, incl. hemodialysis): 300/100 once Day 1 then 150/100 QD Days 2–5; no adjustment if mild
Hepatic Not recommended in severe (Child-Pugh C); no adjustment for mild–moderate
Complete the full 5-day course
Available strengths
Pregnancy Human data insufficient; ritonavir observational data show no increased birth-defect risk
Lactation Present in breast milk in small amounts (<2%); weigh benefits and risks
| Strength | #/mo | generic $/mo | CostPlus | |
|---|---|---|---|---|
| 150 mg | tab | 60 BID | not offered |
Available combined with: nirmatrelvir / ritonavir
⚠ BOXED WARNING
Principal riskThe ritonavir booster’s CYP3A4 interactions
Open Nirmatrelvir in the interactive console ↗
