Remdesivir Dosing for COVID-19
For hospitalized adults and pediatric patients ≥40 kg, administer remdesivir 200 mg IV loading dose on day 1, followed by 100 mg IV daily, with treatment duration of 5 days for those not requiring mechanical ventilation/ECMO, 10 days for those requiring mechanical ventilation/ECMO, and 3 days for non-hospitalized high-risk patients. 1, 2
Adult and Pediatric Patients ≥40 kg Dosing
Loading and Maintenance Doses:
Treatment Duration by Clinical Setting:
Hospitalized Patients NOT on Mechanical Ventilation/ECMO
- Standard duration: 5 days (total of 5 doses) 1, 2
- If clinical worsening occurs during the 5-day course requiring supplemental oxygen (but not mechanical ventilation), extending treatment beyond 5 days should be based on clinical judgment 1
- May extend up to 10 days total if patient does not demonstrate clinical improvement 2
Hospitalized Patients on Mechanical Ventilation/ECMO
- Duration: 10 days 1, 2
- If a patient progresses to requiring mechanical ventilation or ECMO during the initial 5-day course, extend treatment to 10 days 1
Non-Hospitalized High-Risk Patients
- Duration: 3 days 1, 2
- Must initiate within 7 days of symptom onset 1, 2
- Indicated for patients with mild-to-moderate COVID-19 and at least one risk factor for progression to severe disease (immunosuppression, malignancy, hematological malignancies) 1
Pediatric Dosing (<40 kg)
For pediatric patients weighing 1.5 kg to <40 kg: 2
Term neonates <28 days old and ≥1.5 kg:
- Loading dose: 2.5 mg/kg IV on day 1
- Maintenance: 1.25 mg/kg IV once daily from day 2 2
Patients ≥28 days old weighing 1.5 kg to <3 kg:
- Loading dose: 2.5 mg/kg IV on day 1
- Maintenance: 1.25 mg/kg IV once daily from day 2 2
Patients ≥28 days old weighing 3 kg to <40 kg:
- Loading dose: 5 mg/kg IV on day 1
- Maintenance: 2.5 mg/kg IV once daily from day 2 2
Critical Timing Considerations
Initiate treatment as soon as possible after diagnosis of symptomatic COVID-19 1, 2
- Greatest mortality benefit occurs in patients requiring low-flow oxygen at baseline, with mortality reduction risk ratios of 0.21-0.24 1
- Early initiation within 1-4 days from symptom onset is more effective than days 5-7 for preventing oxygen desaturation 3
Absolute Contraindications
Do not use remdesivir in patients with: 1
- eGFR <30 mL/min/1.73 m² 1, 2
- ALT ≥5 times the upper limit of normal 1
- History of clinically significant hypersensitivity to remdesivir 1
When NOT to Initiate Remdesivir
Do not start remdesivir in patients already on mechanical ventilation or ECMO at baseline, as evidence shows potential for increased mortality in this population 1
Required Monitoring
Before starting treatment: 1, 2
During treatment: 1
- Discontinue if ALT increases to >10 times the upper limit of normal 1
- Discontinue if ALT elevation is accompanied by signs or symptoms of liver inflammation 1
Renal Impairment Adjustments
No dosage adjustment required for any degree of renal impairment, including patients on dialysis 2
- Remdesivir may be administered without regard to timing of dialysis 2
- However, do not initiate if eGFR <30 mL/min/1.73 m² 1
Administration Requirements
- Route: Intravenous infusion only 2
- Setting: Must be administered where healthcare providers have immediate access to medications for treating severe infusion/hypersensitivity reactions and ability to activate emergency medical system 2
- Preparation: Must be diluted prior to IV infusion; two formulations exist (lyophilized powder and solution) with different preparation requirements 2