What is the recommended dose of Remdesivir (Veklury) for COVID-19 treatment?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 29, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

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:

  • Day 1: 200 mg IV loading dose 1, 2
  • Day 2 onwards: 100 mg IV once daily 1, 2

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

  • Assess hepatic function (ALT/AST) 1, 2
  • Assess renal function (eGFR) 1, 2
  • Check prothrombin time 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

Common Adverse Events

  • Metabolic: hyperglycemia 1
  • Hepatic: increased ALT/AST 1
  • Renal events 1
  • Nausea (9-10% vs 3% standard care) 4
  • Hypokalemia (6% vs 2% standard care) 4
  • Headache (5% vs 3% standard care) 4

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.