Viracin 200 mg contains a synthetic nucleoside analogue with broad antiviral activity. Although its exact mechanism of action is not fully understood, it is known to interfere with viral nucleic acid synthesis by acting at multiple intracellular sites, including cellular enzymes. The antiviral activity is attributed to its mono- and triphosphate metabolites, which inhibit viral replication. Besides hepatitis C virus, it has demonstrated inhibitory activity against respiratory syncytial virus, influenza virus, and herpes simplex virus.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Viracin 200 mg is indicated for:
Treatment of chronic hepatitis C virus infection in combination with interferon alpha or peg-interferon
Adult patients with compensated liver disease
Adult patients coinfected with HIV and HCV
Viracin 200 mg should never be used as monotherapy.
The recommended duration of therapy depends on prior treatment history, viral genotype, and body weight.
Previously untreated patients: 24 to 48 weeks
Virologic response should be assessed at 24 weeks. Discontinuation should be considered if HCV RNA remains detectable.
Relapse after interferon therapy: 24 weeks
Combination with Interferon Alpha
Genotype 1 & 4:
<75 kg: 1000 mg/day
75 kg: 1200 mg/day
Duration: 48 weeks
Genotype 2 & 3:
Duration: 24 weeks
Combination with Peg-Interferon
Genotype 1 & 4:
<75 kg: 1000 mg/day
75 kg: 1200 mg/day
Duration: 48 weeks
Genotype 2 & 3:
800 mg/day for 24 weeks
Viracin 200 mg may be taken with or without food but should be administered consistently. Adequate hydration is advised to reduce the risk of adverse effects.
Concomitant use with azathioprine may cause severe pancytopenia and increased myelotoxicity
Use with didanosine is contraindicated due to reports of fatal hepatic failure and other serious toxicities
Dose adjustments or discontinuation may be required if combined with nucleoside reverse transcriptase inhibitors or interferon in case of worsening toxicities
Pregnancy and women of childbearing potential
Male patients whose female partners are pregnant
Patients with hemoglobinopathies such as thalassemia major or sickle-cell anemia
Concomitant use with didanosine
Common adverse reactions include:
Psychiatric and central nervous system disorders
Severe ocular complications
Dental and periodontal disorders
Growth inhibition in children and adolescents
Pediatric adverse reactions are generally similar to those seen in adults.
Viracin 200 mg is classified as Pregnancy Category X due to its high risk of embryocidal and teratogenic effects. Strict contraception measures are required during therapy and for several months after treatment. Breastfeeding should be discontinued or therapy stopped, depending on clinical necessity.
High risk of birth defects and fetal death
Mandatory pregnancy testing and dual contraception
Dose adjustment required in renal impairment
Use with caution in elderly patients due to reduced renal function
Store in a cool, dry place, protected from light. Keep out of reach of children.
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