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Ribavirin

Antiviral · Antiviral for Chronic Hepatitis C and Lassa Fever

Also known as REBETRON

AntiviralAntiviral for Chronic Hepatitis C and Lassa Fever
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
5 major
SEVERE in our sources
PREGNANCY
(see Useful
FDA category + note
Top interactionssee all 6
  • AzathioprineSevereDatabaseDDInter
  • BexaroteneSevereDatabaseDDInter
  • DidanosineSevereDatabaseDDInter
  • Interferon Α2bSevereDatabaseKimi deep-research + Cla

Mechanism

Ribavirin inhibits a wide range of DNA and RNA viruses.

Indications

Chronic hepatitis C (in combination with peginterferon alfa)Chronic hepatitis C (in combination with interferon alfa)Chronic hepatitis C (in combination with sofosbuvir)Chronic hepatitis C (in triple therapy with peginterferon alfa and one protease inhibitor or sofosbuvir)Chronic hepatitis C genotype 1 or 4 with advanced liver disease or other negative prognostic factors (e.g., prior treatment experience) when used in combination with daclatasvir and sofosbuvirChronic hepatitis C genotype 3 in treatment-experienced patients, with or without compensated cirrhosis (in combination with daclatasvir and sofosbuvir)Chronic hepatitis C genotype 4 (in combination with daclatasvir and peginterferon alfa)Chronic hepatitis C genotype 1 with or without compensated cirrhosis (in combination with ombitasvir, paritaprevir, ritonavir, and possibly dasabuvir)Chronic hepatitis C genotype 4 with or without compensated cirrhosis (in combination with ombitasvir, paritaprevir, and ritonavir)Chronic hepatitis C genotypes 1, 2, 3, 4, 5, or 6 in patients with compensated liver disease (in combination with sofosbuvir, with or without peginterferon alfa)Chronic hepatitis C in patients with compensated liver function not previously treated with IFN-α-2b or who have relapsed after IFN-α-2b therapy (in combination with IFN-α-2b)Lassa fever (unlicensed indication)Chronic HCV infection in combination with DAAs (e.g., with sofosbuvir and ledipasvir or velpatasvir in decompensated cirrhosis; with grazoprevir/elbasvir in genotype 1a HCV with preexisting NS5A RASs)Respiratory syncytial virus (aerosolized form)Hemorrhagic fever (intravenous form)Severe influenza (intravenous form)chronic hepatitis C (first line, combined with peginterferon)respiratory syncytial virus bronchiolitis in infants and children (nebulized)severe influenza A/B and measles in immunosuppressed patients (not first line)herpes virus infections (not first line)acute hepatitis (not first line)Severe encephalitis due to California encephalitis (La Crosse) virus (isolated cases reported)Severe adenovirus or rotavirus encephalitis (in rare patients, typically infants or young children)Encephalitis due to LCMV or other arenavirusessevere RSV-induced lower respiratory tract infection (in children, aerosol formula)adenovirus infections (intravenous)hantavirus infections (intravenous)measles virus infections (intravenous)PIV infections (intravenous)influenza virus infections (intravenous)Lassa FeverHemorrhagic Fever with Renal Syndrome (HFRS)Hantavirus Pulmonary Syndrome (HPS) (efficacy not shown in trial)

Dosing

Adult
is given by mouth for the treatment of chronic hepatitis C infection, in double therapy with peginterferon alfa, interferon alfa, or sofosbuvir, or in triple therapy with peginterferon alfa and one protease inhibitor or sofosbuvir. Ribavirin is also effective in Lassa fever [unlicensed indication].…
Pediatric
400 to 1200 mg daily depending on body weight, administered in two divided doses, for children 5 years or older
Renal adjustment
Reduced for renal impairment (eGFR ≤50 mL/min/1.73 m2)

Pharmacokinetics

Half-life
7–10 days (plasma and intracellular derivatives)
Bioavailability
Approximately 50% (oral); increased by food
Protein binding
Widely distributed into tissues
Metabolism
Hepatic metabolism (deribosylation and hydrolysis to a triazole carboxamide)
Excretion
35 ± 8%

Contraindications

  • Men and women attempting conception (and for 6 months following treatment cessation)

Side effects

Common
Conjunctival irritation (aerosolized)RashTransient wheezing (aerosolized)Rigors (bolus intravenous infusion)Dose-related reversible hemolytic anemiaFatigueCoughPruritusReversible anemia
Serious
  • Reversible deterioration in pulmonary function (aerosolized)
  • Teratogenic
  • Embryotoxic
  • Oncogenic
  • Possibly gonadotoxic
  • anaemia
  • bone marrow depression
  • haemolysis
  • CNS symptoms
  • g.i. symptoms
  • irritation of mucosae (aerosol)
  • bronchospasm (aerosol)
  • Hemolysis (with resulting anemia)
  • Dependent hemolytic anemia
  • Bone marrow suppression

Pregnancy & lactation

Pregnancy

(see Useful

Drug interactions

Azathioprine
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Bexarotene
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Didanosine
Severe
Database

Not specified, but combination should not be used.

Should not be used together. Avoid combination.

Source: DDInter

Interferon Α2b
Severe
Database

Synergistic + additive teratogenicity

Strict contraception; haematology monitoring

Source: Kimi deep-research + Cla

Mercaptopurine
Severe
Database

Clinical effect not specified

Source: DDInter

Pegylated Interferon Alfa
Moderate
Textbook

Increased hematological toxicity.

Monitor hematological parameters.

Source: G&G 14e · p1231

6 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Other Antiviral drugs

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Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, BNF·Verified: 2026-05-13 · House clinical team