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Ribavirin (1-ß-D-ribofuranosyl-1,2,4-triazole). Broad spectrum antiviral
nucleoside.
Pharmacokinetics
- Administration
- oral
- inhalation
- intravenous
- topical
- Inside cells metabolized from nucleoside to ribavirin monophosphate and
then diphosphate and triphosphate
Mode of action
Hypotheses include:
- ribovarin monophosphate inhibits inosine monophosphate dehydrogenase which
results in decreased synthesis of guanosine triphosphate (GTP). GTP is
required for translation, DNA and RNA virus transcription and RNA virus
replication
- inhibition of capping of viral transcripts
- direct inhibition of viral RNA polymerase by ribavirin triphosphate
- modulation of immune response resulting in a reduction of immune-mediated
tissue damage
- ribavirin triphosphate is utilized by viral RNA-dependent RNA polymerase
and causes lethal mutagenesis of the viral genome
Clinical uses
- hepatitis C virus infection (with interferon-alpha)
- severe respiratory syncytial vius infection
- Lassa fever
- some herpes virus infections
- used experimentally to treat:
Adverse effects
- teratogenesis
- interferes with sperm development
- haemolysis
- inhaled form:
- may precipitate in ventilator and interfere with its function
- COPD and asthma for deterioration of respiratory function
- fatigue, headache, insomnia
- nausea, anorexia
Drug interactions
Interacts with other antiretroviral agents including adefovir, didanosine,
lamivudine, stavudine, zalcitabine and zidovudine
Further reading
Cameron CE, Castro C. The mechanism of action of ribavirin:
lethal mutagenesis of RNA virus genomes mediated by the viral RNA-dependent RNA
polymerase. Current Opinion in Infectious Diseases, 2001; 14:757-64
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