Valacyclovir

Treatment for Varicella And Herpes Zoster

Typical Dosage: 1000mg three times daily for 7 days

Effectiveness
88%
Safety Score
68%
Clinical Trials
13
Participants
20K

Comparative Safety Scale(Higher is safer)

Cyanide☠️
Meth💀
Cigarettes🚬
Chemo☢️
Alcohol🍺
Morphine💊
Antibiotics💉
Tylenol💊
Exercise🏃
Water💧
68
DangerousModerateSafe
Treatment Details
Dosage Range
1000mg three times daily for 7 days
Time to Effect
24-48 hours
Treatment Duration
7 days
Evidence Quality
HIGH
Number Needed to Treat (NNT)
12(Treat 12 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
1000(Treat 1000 patients to see 1 additional serious adverse event)
Confidence Score
90%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$40
Monitoring:$100
Side Effect Mgmt:$10
Total Annual:$150
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
GOOD
QALYs Gained
0.04
Outcome-Based Costs
Cost per Responder
$200
Cost per Remission
$167
Comparison vs Acyclovir
Cost Difference
+$10/year
More expensive
QALY Difference
+0.01 QALYs
Better outcomes
Dominance
No dominance
Valacyclovir Outcomes

for Varicella And Herpes Zoster

Efficacy Outcomes
Overall Effectiveness
+88%
Response Rate
+75%
Remission Rate
+90%
Common Side Effects
Nausea
+15%
Headache
+15%
Abdominal pain
+6%
Diarrhea
+5%

WARNING: LIMITED TRIALS AVAILABLE

You can search for trials, but you probably can't join any because the 1% Treaty hasn't passed yet. Most trials are severely limited by lack of funding and bureaucratic barriers. Help change this!

Active Clinical Trials
No active trials currently recruiting for this treatment

No active trials found in ClinicalTrials.gov

Completed Clinical Trials
8 completed trials for Valacyclovir in Varicella And Herpes Zoster

A Phase 2b Trial of EPB-348 for the Treatment of Herpes Zoster

NCT00831103COMPLETEDPHASE2
View Study
373 participants
INTERVENTIONAL
Houston, United States
Started: Nov 1, 2007

A Study Exploring Efficacy of Peginterferon in Patients With Herpes Zoster

NCT05492591COMPLETEDPHASE2
View Study
50 participants
INTERVENTIONAL
Nanjing, China
Started: Oct 11, 2022

Bioequivalency Study of Valacyclovir Hydrochloride 1000 mg Under Fed Conditions

NCT01132716COMPLETEDNA
View Study
48 participants
INTERVENTIONAL
Fargo, United States
Started: Sep 1, 2006

Bioequivalency Study of Valacyclovir Hydrochloride 1000 mg Under Fasting Conditions

NCT01132729COMPLETEDNA
View Study
48 participants
INTERVENTIONAL
Fargo, United States
Started: Sep 1, 2006

Palatability Testing of a New Paediatric Formulation of Valacyclovir

NCT01682109COMPLETEDPHASE4
View Study
41 participants
INTERVENTIONAL
Nijmegen, Netherlands
Started: Sep 1, 2012

Bioequivalence Study in Healthy Volunteers of a New Paediatric Formulation of Valacyclovir

NCT01689285COMPLETEDPHASE1
View Study
16 participants
INTERVENTIONAL
Nijmegen, Netherlands
Started: Dec 1, 2013

Reduction of Postherpetic Neuralgia in Herpes Zoster

NCT01250561COMPLETEDNA
View Study
133 participants
INTERVENTIONAL
Houston, United States
Started: Feb 1, 2002

A Safety And Tolerability Study Of Valaciclovir Oral Suspension In Infants And Children

NCT00297206COMPLETEDPHASE1
View Study
36 participants
INTERVENTIONAL
Birmingham, United States +12 more
Started: Jan 25, 2003