Recommended Dosing of Paxlovid for COVID-19
The standard recommended dose of Paxlovid for COVID-19 is 300 mg nirmatrelvir (two 150 mg tablets) with 100 mg ritonavir (one 100 mg tablet), with all three tablets taken together twice daily for 5 days. 1
Dosing Guidelines
Standard Dosing
- Nirmatrelvir 300 mg (two 150 mg tablets) plus ritonavir 100 mg (one 100 mg tablet)
- Administered orally twice daily for 5 days
- Can be taken with or without food
- Should be administered at approximately the same time each day
- Treatment should be initiated as soon as possible after diagnosis and within 5 days of symptom onset 2, 1
Dose Adjustments for Renal Impairment
Moderate renal impairment (eGFR ≥30 to <60 mL/min):
Severe renal impairment (eGFR <30 mL/min) including those requiring hemodialysis:
Hepatic Impairment
- No dose adjustment is needed for mild to moderate hepatic impairment
- Paxlovid is not recommended in patients with severe hepatic impairment (Child-Pugh Class C) 1
Clinical Efficacy
Paxlovid has demonstrated significant efficacy in reducing the risk of COVID-19 progression to severe disease:
- 89% reduction in risk of hospitalization or death when initiated within 3 days of symptom onset 4
- Significant reduction in viral load by day 5 of treatment 4
- Shorter nucleic acid shedding time (3.26 ± 1.80 vs 7.75 ± 3.68 days) compared to standard treatment 5
Important Considerations
Drug Interactions
- Ritonavir is a strong CYP3A inhibitor that can significantly affect the metabolism of many medications
- Prior to prescribing Paxlovid, review all medications taken by the patient to assess potential drug-drug interactions
- Some medications may require dose adjustment, interruption, or additional monitoring during Paxlovid treatment 1
- The Liverpool COVID-19 drug interaction tool is recommended as a resource for checking drug interactions 2
Common Adverse Effects
- Dysgeusia (altered taste) - 5.6% of patients
- Diarrhea - 3.1% of patients
- Most adverse events are mild in severity 4
Contraindications
- History of clinically significant hypersensitivity to nirmatrelvir or ritonavir
- Co-administration with drugs highly dependent on CYP3A for clearance
- Co-administration with potent CYP3A inducers 1
Special Populations
Pregnancy
- Paxlovid represents an option for pregnant people with COVID-19 to reduce the risk of disease progression
- Limited data on adverse reactions in pregnant or breastfeeding individuals 2
Timing of Treatment
Treatment should be initiated as early as possible in the course of the disease and within 5 days of symptom onset for optimal efficacy 2, 1, 4
Remember that Paxlovid is indicated for the treatment of mild-to-moderate COVID-19 in adults who are at high risk for progression to severe COVID-19, including hospitalization or death. It is not approved for pre-exposure or post-exposure prophylaxis.