What's the dose of medication for Hepatitis C treatment?

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Last updated: September 25, 2025View editorial policy

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Hepatitis C Treatment Dosing Guidelines

The appropriate dose for Hepatitis C treatment depends on the specific medication regimen selected, with several FDA-approved options available in fixed-dose combinations that are taken once daily. 1

Available Medications and Dosing

Direct-Acting Antivirals (DAAs) - First-Line Options

Medication Dose Administration
Sofosbuvir 400 mg One tablet once daily (morning) [1]
Sofosbuvir/ledipasvir 400 mg/90 mg One tablet once daily (morning) [1]
Paritaprevir/ombitasvir/ritonavir 75 mg/12.5 mg/50 mg Two tablets once daily (morning) [1]
Dasabuvir 250 mg One tablet twice daily (morning and evening) [1]
Simeprevir 150 mg One capsule once daily (morning) [1]
Daclatasvir 30 or 60 mg One tablet once daily (morning) [1]
Glecaprevir/pibrentasvir Fixed-dose Preferred for severe renal impairment [1]
Grazoprevir/elbasvir Fixed-dose For genotype 1b with severe renal impairment [1]

Older Regimens (Less Commonly Used)

  • PegIFN-α2a: 180 μg subcutaneous injection once weekly 1
  • PegIFN-α2b: 1.5 μg/kg subcutaneous injection once weekly 1
  • Ribavirin: Weight-based dosing
    • <75 kg: 1000 mg daily (2 capsules morning, 3 evening)
    • ≥75 kg: 1200 mg daily (3 capsules morning, 3 evening) 1

Treatment Selection Algorithm

  1. Determine HCV genotype and subtype - This is essential for selecting the appropriate regimen
  2. Assess liver fibrosis/cirrhosis status - Patients with decompensated cirrhosis need specific regimens
  3. Evaluate renal function - eGFR impacts medication choice
  4. Check for drug interactions - Especially important with HIV medications, immunosuppressants
  5. Consider prior treatment history - Treatment-experienced patients may need longer duration

Special Population Considerations

Renal Impairment

  • Mild to moderate impairment (eGFR >30 ml/min/1.73 m²): No dose adjustment needed for most DAAs 1
  • Severe impairment (eGFR <30 ml/min/1.73 m²):
    • Preferred: Glecaprevir/pibrentasvir or grazoprevir/elbasvir (for genotype 1b) 1
    • Sofosbuvir should be used with caution due to increased exposure of metabolite GS-331007 1

Decompensated Cirrhosis

  • With mild-moderate renal impairment: Sofosbuvir/velpatasvir with ribavirin for 12 weeks 1
  • With severe renal impairment: Sofosbuvir/velpatasvir without ribavirin for 24 weeks 1

HIV Coinfection

  • Same regimens as HCV monoinfection but must consider drug interactions 1
  • Ledipasvir/sofosbuvir may increase tenofovir levels, requiring careful monitoring 1

Common Pitfalls and Caveats

  1. Drug interactions: Many HCV medications interact with common drugs. For example:

    • P-gp inducers (rifampin, carbamazepine, St. John's wort) significantly decrease sofosbuvir plasma concentrations 2
    • Ritonavir in HCV regimens can boost HIV protease inhibitors 1
  2. Renal function monitoring: Required for sofosbuvir-based regimens in patients with impaired renal function

  3. Ribavirin contraindications:

    • Pregnancy (Category X) - strict birth control required during and 6 months after treatment
    • Hemoglobin <10 g/dL
    • Severe renal impairment without close monitoring
  4. Treatment prioritization: While all patients with HCV should be considered for treatment, priority should be given to those with:

    • Significant fibrosis or cirrhosis (METAVIR F3-F4)
    • Decompensated cirrhosis
    • HIV or HBV coinfection
    • Pre/post-liver transplant
    • Significant extrahepatic manifestations 1

By following these evidence-based dosing guidelines and considering patient-specific factors, treatment of hepatitis C can achieve sustained virologic response rates exceeding 90% with modern DAA regimens.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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.

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