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Valtrex: profile and news
Antiviral Drugs Help Relieve Enduring Shingles Pain May 9, 2006 Antiviral Drugs may Help Treat Shingles May 10, 2006 Antiviral Drugs May Cut Shingles Pain May 8, 2006 I have herpes, is my sex life ruined? May 2, 2006 Profits up 27% in first quarter at GSK Apr 27, 2006 Blisters may be shingles Apr 18, 2006 Tristan Taormino's Reality Porn! May 3, 2006 Combo treatments eliminate prostate cancer May 2, 2006 GSK posts Q1 profits well ahead of forecasts - UPDATE Apr 27, 2006 GlaxoSmithKline Q1 Profit Rise 25% Apr 27, 2006 The Ramble: Vick "Settles" With Herpes Case, Bush Is Burning ... Apr 25, 2006 Sex in the Classic City For Her Apr 21, 2006 Student Health garners criticism from women Apr 20, 2006 Other information Indication For the treatment and management of herpes zoster (shingles), genital herpes, and chickenpox Pharmacology Acyclovir is a synthetic deoxyguanosine analog and it is the prototype antiviral agent that is activated by viral thymidine kinase. The selective activity of acyclovir is due to its affinity for the thymidine kinase enzyme encoded by HSV and VZV. Mechanism Of Action Viral (HSV-1, HSV-2 and VZV) thymidine kinase converts acyclovir to the acyclovir monophosphate, which is then converted to the diphosphate by cellular guanylate kinase, and finally to the triphosphate by phosphoglycerate kinase, phosphoenolpyruvate carboxykinase, and pyruvate kinase. Acyclovir triphosphate competitively inhibits viral DNA polymerase and competes with the natural deoxyguanosine triphosphate, for incorporation into viral DNA. Once incorporated, acyclovir triphosphate inhibits DNA synthesis by acting as a chain terminator. Drug Category Antivirals; Nucleosides and Nucleotides (08:18.32); ATC:J05AB Brand Names/Synonyms AC2; Aciclovier; Aciclovir; Acycloguanosine; Acyclovir; Acyclovir Sodium; Alti-Acyclovir; Avirax; BW-248U; Valtrex; Vipral; Virorax; Wellcome-248u; Zovirax; Zovirax Wellstat Pac; Zovirax Zostab Pac Dosage Forms Intravenous Infusion; Capsules; Tablets; Suspension; Topical Cream; Topical Ointment Absorption Oral _ Bioavailability 10 to 20% Interactions Co-administration of probenecid with acyclovir has been shown to increase the mean half-life and the area under the concentration-time curve. Urinary excretion and renal clearance were correspondingly reduced. The clinical effects of this combination have not been studied. Chemical IUPAC Name 2-amino-9-(2-hydroxyethoxymethyl)-3H-purin-6-one Chemical Formula C8H11N5O3 Half Life 2.5-3.3 hours Drug Type Approved Drug # Accession No APRD00567 CAS Registry Number 59277-89-3 |
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