Paxlovid (Nirmatrelvir/Ritonavir)

Antiviralprescriptionoral · inferred

Fixed-dose oral antiviral for acute SARS-CoV-2 infection in patients at high risk for progression to severe COVID-19. Each 'dose' consists of two 150 mg nirmatrelvir tablets plus one 100 mg ritonavir tablet, taken twice daily for 5 days. Nirmatrelvir is the active SARS-CoV-2 Mpro (3CL protease) inhibitor; ritonavir is a pharmacokinetic booster (potent CYP3A4 inhibitor) used to maintain therapeutic nirmatrelvir exposures. Nirmatrelvir plasma half-life ~7h (boosted). CRITICAL DRUG INTERACTIONS: ritonavir's CYP3A4 inhibition causes severe interactions with dozens of common medications (statins, amiodarone, calcineurin inhibitors, rivaroxaban/apixaban, fentanyl, many antipsychotics, sildenafil, ergots, colchicine, etc.). Review all concomitant medications BEFORE prescribing, contraindicated or requires dose hold/adjustment for many. Renal dose adjustment required for eGFR 30-60 mL/min; avoid if eGFR <30.

Projected serum levels — 1 dose (≈ 400 mg), twice daily

Paxlovid (Nirmatrelvir/Ritonavir)
Paxlovid (Nirmatrelvir/Ritonavir) modeled serum levels, 1 dose (≈ 400 mg) twice daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 50 100 150 200 Day 0 Day 4 Day 7 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1
Paxlovid (Nirmatrelvir/Ritonavir) modeled serum levels with a loading dose of 1.3 dose, then 1 dose (≈ 400 mg) twice daily The first dose is larger so levels approach steady state faster. 0 50 100 150 200 Day 0 Day 4 Day 7 Day 11 Day 15 Time on a regular schedule

Maintenance schedule: 1 dose (≈ 400 mg) twice daily (oral).

Loading schedule: 1.3 dose on day 1, then 1 dose (≈ 400 mg) twice daily — reaching therapeutic levels sooner.

Modeled steady state after ~1 days: peak ≈ 183 mg, trough ≈ 50.9 mg body load. Population-based estimate over 15 days for a reference dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Antiviral
Route modeled
Oral
Model confidence
inferred
Half-life
4.9 h
Common dose
1 dose (≈ 400 mg)
Suggested maximum
2 dose/day
Reference dose range
0.50–2 dose (single dose)
Suggested cadence
twice daily

Documented interactions

  • contraindicated
    Alfuzosin (Uroxatral) + Paxlovid (Nirmatrelvir/Ritonavir) CYP inhibition

    Paxlovid (Nirmatrelvir/Ritonavir) mechanism_based of CYP3A4 predicted to change Alfuzosin (Uroxatral) AUC by ~10.00x

  • contraindicated
    Alprazolam (Xanax) + Paxlovid (Nirmatrelvir/Ritonavir) CYP inhibition

    Paxlovid (Nirmatrelvir/Ritonavir) mechanism_based of CYP3A4 predicted to change Alprazolam (Xanax) AUC by ~10.00x

  • contraindicated
    Amlodipine (Norvasc) + Paxlovid (Nirmatrelvir/Ritonavir) CYP inhibition

    Paxlovid (Nirmatrelvir/Ritonavir) mechanism_based of CYP3A4 predicted to change Amlodipine (Norvasc) AUC by ~10.00x

  • contraindicated
    Anastrozole (Arimidex) + Paxlovid (Nirmatrelvir/Ritonavir) CYP inhibition

    Paxlovid (Nirmatrelvir/Ritonavir) mechanism_based of CYP3A4 predicted to change Anastrozole (Arimidex) AUC by ~5.14x

  • contraindicated
    Astaxanthin + Paxlovid (Nirmatrelvir/Ritonavir) CYP inhibition

    Paxlovid (Nirmatrelvir/Ritonavir) mechanism_based of CYP3A4 predicted to change Astaxanthin AUC by ~10.00x

  • contraindicated
    Atogepant (Qulipta) + Paxlovid (Nirmatrelvir/Ritonavir) CYP inhibition

    Paxlovid (Nirmatrelvir/Ritonavir) mechanism_based of CYP3A4 predicted to change Atogepant (Qulipta) AUC by ~10.00x

Serum checks 207 modeled interaction pairings for paxlovid (nirmatrelvir/ritonavir) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.

Research behind this entry

  1. Oral nirmatrelvir for high-risk, nonhospitalized adults with Covid-19 (EPIC-HR) Hammond J et al. · New England Journal of Medicine, 2022 DOI

    Pivotal phase 2/3 trial demonstrating 89% relative risk reduction in COVID-19 hospitalization/death with nirmatrelvir/ritonavir vs placebo when started within 5 days of symptom onset in high-risk unvaccinated adults.

  2. Innovative randomized phase 1 study and dosing regimen selection to accelerate and inform pivotal COVID-19 trial of nirmatrelvir Singh RSP et al. · Clinical and Translational Science, 2022 DOI

    Phase 1 PK study establishing nirmatrelvir 300 mg + ritonavir 100 mg q12h dosing; ritonavir-boosted nirmatrelvir achieves target trough exposures ~6x EC90 for SARS-CoV-2 Mpro inhibition.

2 published studies referenced in the app, each with a plain-language summary.