Valacyclovir: Difference between revisions

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In [[pharmacology]] and [[virology]], '''valacyclovir''' ('''Valtrex''') is "a prodrug of [[acyclovir]]; 53% of oral dose excreted as acyclovir in the  urine; a 200-400% improvement on acyclovir; used in the management of [[Herpes simplex virus|HSV]] and [[Varicella zoster virus|VZV]] infections and the prophylaxis of [[Cytomegalovirus|HCMV]] infections; RN given  refers to the monohydrochloride L-valine isomer."<ref>{{MeSH}}</ref>
In [[pharmacology]] and [[virology]], '''valacyclovir''' ('''Valtrex''') is "a prodrug of [[acyclovir]]; 53% of oral dose excreted as acyclovir in the  urine; a 200-400% improvement on acyclovir; used in the management of [[Herpes simplex virus|HSV]] and [[Varicella zoster virus|VZV]] infections and the prophylaxis of [[Cytomegalovirus|HCMV]] infections; RN given  refers to the monohydrochloride L-valine isomer."<ref>{{MeSH}}</ref>


==History==
==History==  
Valtrex brand of valacyclovir was approved by the [[Food and Drug Administration]] in the [[United States]] with a [http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/NewDrugApplicationNDA/ New Drug Application] (NDA) in 1995.<ref>[http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.SearchAction&SearchType=BasicSearch&Search_Button=Submit&searchTerm=020487 Drugs@FDA]. U S Food and Drug Administration</ref> A generic version was approved with a [http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/AbbreviatedNewDrugApplicationANDAGenerics/ Abbreviated New Drug Application] (ANDA) in 2007.<ref>[http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.SearchAction&SearchType=BasicSearch&Search_Button=Submit&searchTerm=076588 Drugs@FDA]. U S Food and Drug Administration</ref>
Valtrex brand of valacyclovir was approved by the [[Food and Drug Administration]] in the [[United States of America|United States]] with a [http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/NewDrugApplicationNDA/ New Drug Application] (NDA) in 1995.<ref>[http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.SearchAction&SearchType=BasicSearch&Search_Button=Submit&searchTerm=020487 Drugs@FDA]. U S Food and Drug Administration</ref> A generic version with a AB [[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code|Therapeutic Equivalence Code]] was approved with a [http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/AbbreviatedNewDrugApplicationANDAGenerics/ Abbreviated New Drug Application] (ANDA) in 2007.<ref>[http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.SearchAction&SearchType=BasicSearch&Search_Button=Submit&searchTerm=076588 Drugs@FDA]. U S Food and Drug Administration</ref>
 
==Pharmacology==
===Administration===
===Distribution===
===Metabolism===
===Excretion===
===Toxicity===
[[Drug toxicity]] includes


==Usage==
==Usage==
Valacyclovir suppressive therapy can reduce the frequency of recurrence of [[herpes labialis]] from [[herpes simplex virus]]; however, this usage is not approved by the [[United States]] [[Food and Drug  Administration]].<ref name="pmid12661753">{{cite journal| author=Baker D, Eisen D| title=Valacyclovir for prevention of recurrent herpes labialis: 2 double-blind, placebo-controlled studies. | journal=Cutis | year= 2003 | volume= 71 | issue= 3 | pages= 239-42 | pmid=12661753 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12661753 }} </ref><ref name="pmid18541820">{{cite journal| author=Cernik C, Gallina K, Brodell RT| title=The treatment of herpes simplex infections: an evidence-based review. | journal=Arch Intern Med | year= 2008 | volume= 168 | issue= 11 | pages= 1137-44 | pmid=18541820 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18541820 | doi=10.1001/archinte.168.11.1137 }} </ref>
Valacyclovir suppressive therapy can reduce the frequency of recurrence of [[herpes labialis]] from [[herpes simplex virus]]; however, this usage is not approved by the [[United States of America|United States]] [[Food and Drug  Administration]].<ref name="pmid17668537">{{cite journal| author=Gilbert SC| title=Suppressive therapy versus episodic therapy with oral valacyclovir for recurrent herpes labialis: efficacy and tolerability in an open-label, crossover study. | journal=J Drugs Dermatol | year= 2007 | volume= 6 | issue= 4 | pages= 400-5 | pmid=17668537
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17668537 }} </ref><ref name="pmid12661753">{{cite journal| author=Baker D, Eisen D| title=Valacyclovir for prevention of recurrent herpes labialis: 2 double-blind, placebo-controlled studies. | journal=Cutis | year= 2003 | volume= 71 | issue= 3 | pages= 239-42 | pmid=12661753 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12661753 }} </ref><ref name="pmid18541820">{{cite journal| author=Cernik C, Gallina K, Brodell RT| title=The treatment of herpes simplex infections: an evidence-based review. | journal=Arch Intern Med | year= 2008 | volume= 168 | issue= 11 | pages= 1137-44 | pmid=18541820 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18541820 | doi=10.1001/archinte.168.11.1137 }} </ref>


Valacyclovir suppressive therapy can reduce the frequency of recurrence of [[herpes genitalis]] from [[herpes simplex virus]] and this usage is approved by the [[United States]] [[Food and Drug Administration]].<ref  name="pmid18541820">{{cite journal| author=Cernik C, Gallina K,  Brodell RT| title=The treatment of herpes simplex infections: an  evidence-based review. | journal=Arch Intern Med | year= 2008 | volume=  168 | issue= 11 | pages= 1137-44 | pmid=18541820 |  url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18541820  | doi=10.1001/archinte.168.11.1137 }} </ref>
Valacyclovir suppressive therapy can reduce the frequency of recurrence of [[herpes genitalis]] from [[herpes simplex virus]] and this usage is approved by the [[United States of America|United States]] [[Food and Drug Administration]].<ref  name="pmid18541820"/>


==External links==
==External links==
{{CZMed}}
{{CZMed}}
==References==
==References==
<references/>
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Latest revision as of 13:56, 21 October 2024

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In pharmacology and virology, valacyclovir (Valtrex) is "a prodrug of acyclovir; 53% of oral dose excreted as acyclovir in the urine; a 200-400% improvement on acyclovir; used in the management of HSV and VZV infections and the prophylaxis of HCMV infections; RN given refers to the monohydrochloride L-valine isomer."[1]

History

Valtrex brand of valacyclovir was approved by the Food and Drug Administration in the United States with a New Drug Application (NDA) in 1995.[2] A generic version with a AB Therapeutic Equivalence Code was approved with a Abbreviated New Drug Application (ANDA) in 2007.[3]

Usage

Valacyclovir suppressive therapy can reduce the frequency of recurrence of herpes labialis from herpes simplex virus; however, this usage is not approved by the United States Food and Drug Administration.[4][5][6]

Valacyclovir suppressive therapy can reduce the frequency of recurrence of herpes genitalis from herpes simplex virus and this usage is approved by the United States Food and Drug Administration.[6]

External links

The most up-to-date information about Valacyclovir and other drugs can be found at the following sites.


References