famciclovir (Famvir)
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Introduction
Tradename: Famvir.
Indications
- out-patient Herpes simplex virus (HSV) infection
- treatment of acute Herpes zoster (shingles) or Herpes simplex type-2 (genital Herpes)
- not responsive to acyclovir
Dosage
Herpes Zoster: 500 mg PO every 8 hours for 7 days
Tabs: 500 mg. Dose adjustment for renal failure:
Creatinine clearance | dose |
---|---|
> 60 mL/min | 500 mg every 8 hours |
40-59 mL/min | 500 mg every 12 hours |
10-39 mL/min | 500 mg every 24 hours |
> 10 mL/min | 250 mg every 24 hours |
Pharmacokinetics
- food decreased peak & the time to peak concentrations, but overall absorption is the same
- oral bioavailability is 77% (much better than acyclovir)
- rapidly deacylated & oxidized to penciclovir
- 1/2life of penciclovir is 2-3 hours (10-22 hours ESRD)
- > 90% of penciclovir is eliminated unchanged in the urine
elimination via kidney
Adverse effects
- common (> 10%)
- less common (1-10%)
- other
Drug interactions
- cimetidine
- digoxin increased by 20%
- probenecid increases penciclovir concentration
Mechanism of action
- undergoes rapid bio-transformation to penciclovir
- penciclovir is converted intracellularly by viral thymidine kinase to penciclovir triphosphate
- penciclovir triphosphate inhibits viral DNA synthesis
More general terms
Additional terms
References
- ↑ The Pharmacological Basis of Therapeutics, 9th ed. Gilman et al, eds. Permagon Press/McGraw Hill, 1996
- ↑ Drug Information & Medication Formulary, Veterans Affairs, Central California Health Care System, 1st ed., Ravnan et al eds, 1998
- ↑ Kaiser Permanente Northern California Regional Drug Formulary, 1998
- ↑ Sanford Guide to antimicrobial therapy 2001
- ↑ Mubareka S, Leung V, Aoki FY, Vinh DC. Famciclovir: a focus on efficacy and safety. Expert Opin Drug Saf. 2010 Jul;9(4):643-58 PMID: https://www.ncbi.nlm.nih.gov/pubmed/20429777
- ↑ Deprecated Reference