# E-DRUG: Acyclovir or valazyclovir?

**URL:** <https://talk.edrugplus.org/t/e-drug-acyclovir-or-valazyclovir/3813>\
**Category:** e-drug\
**Created:** [November 12, 1998, 5:58am UTC](https://talk.edrugplus.org/t/e-drug-acyclovir-or-valazyclovir/3813 "1998-11-12T05:58:10Z")\
**Posts on this page:** 1\
**Page:** 1

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**Author:** ![joel.lexchin](https://avatars.discourse-cdn.com/v4/letter/j/e9c0ed/32.png) [@joel.lexchin](https://talk.edrugplus.org/u/joel.lexchin)\
**Post date:** [November 12, 1998, 5:58am UTC](https://talk.edrugplus.org/t/e-drug-acyclovir-or-valazyclovir/3813/1 "1998-11-12T05:58:10Z")

</div>

E-DRUG: Acyclovir or valazyclovir? (4)  
--------------------------------------

Here is a reprint of an article on this topic that appeared in the  
Therapeutic Letter which is a product of the Therapeutic Initiative in  
British Columbia. Basically, there is no evidence that any one of the  
three drugs (acyclovir, famciclovir or valacyclovir) is superior.  
------------------------

Famciclovir (Famvirr) and Valacyclovir (Valtrexr)

Both are new antiherpesviral prodrugs (in the same class as acyclovir).

Indication: Acute herpes zoster in the immunocompetent host. (Their role in  
genital herpes will be discussed in a future Therapeutics Letter).

Mechanism of Action: Reduce viral replication by inhibiting viral DNA  
polymerase.

Pharmacokinetics: Valacyclovir is a prodrug of, and metabolized to  
acyclovir; the oral bioavailability of acyclovir from valacyclovir is 54%  
as compared to 15-30% for acyclovir. Famciclovir is a prodrug for the  
active metabolite penciclovir; the mean oral bioavailability of penciclovir  
from famciclovir is 77%. Penciclovir plus acyclovir are primarily  
eliminated unchanged by the kidneys and have mean half-lives of 2.5 hours.

Evidence of efficacy: If given within 72 hours of the first herpes zoster  
lesion, famciclovir(1) and valacyclovir(2) (like acyclovir(3)) provide  
modest decreases in the time to full crusting (e.g. median 5.5 days for  
famciclovir, 7 days for placebo(1)), healing and cessation of pain . The  
benefit is greatest in patients with the most severe infections (many  
lesions and severe pain)(1),(3),(4). At present the evidence is  
inconclusive as to whether any antiviral or other therapy has an effect on  
the overall clinical impact of post-herpetic neuralgia.(4) The new prodrugs  
have not been studied in children or immunocompromised hosts.

Major adverse effects: These drugs, like acyclovir, produce a low incidence  
(similar to placebo) of minor adverse effects, including diarrhea, nausea  
and headache.

Dose and Cost: Acute herpes zoster: famciclovir, 500 mg TID for 7 days  
($155.61), valacyclovir, 1 g TID for 7 days ($126.84), acyclovir, 800 mg 5  
times daily for 7 days ($138.60). Longer durations of therapy are not more  
effective; shorter courses have not been tested.

Conclusions: Anti-viral drugs have a modest beneficial effect if given  
early (rash \<72 hr) to immunocompetent patients (\>50 yr) with moderate to  
severe rash or pain associated with acute herpes zoster (shingles).

References:

1.Tyring S, Barbarash RA, Nahlik JE, et al. Famciclovir for the treatment  
of acute herpes zoster: effects on acute disease and postherpetic  
neuralgia. A randomized, double-blind, placebo-controlled trial.  
Collaborative  
Famciclovir Herpes Zoster Study Group. Annals of Internal Medicine. 1995  
July 15; 123(2):89-96.

2.Beutner KR, Friedman DJ,Forszpaniak C, et al. Valaciclovir compared with  
acyclovir for improved therapy for herpes zoster in immunocompetent adults.  
Antimicrob Agents Chemother. 1996;39:1546-53.

3.Whitley RJ, Weiss H, Gnann JW, et al. Acyclovir with and without  
prednisone for the treatment of Herpes Zoster. A placebo-controlled trial.  
Ann Intern Med. 1996; 125:376-383.

4.Kost RG, Straus SE. Postherpetic neuralgia - pathogenesis, treatment, and  
prevention. NEJM. 1996 July 4; 335:32-42.  
-----------------------  
Joel Lexchin

Joel Lexchin MD  
121 Walmer Rd.  
Toronto, Ontario  
CANADA M5R 2X8  
Phone: (416)-964-7186  
Fax: (416)-923-9515  
e mail: joel.lexchin@utoronto.ca

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