Acyclovir

Treatment for Shingles

Typical Dosage: 800 mg five times daily for 7-10 days

Effectiveness
85%
Safety Score
75%
Clinical Trials
31
Participants
50K

Comparative Safety Scale(Higher is safer)

Cyanide☠️
Meth💀
Cigarettes🚬
Chemo☢️
Alcohol🍺
Morphine💊
Antibiotics💉
Tylenol💊
Exercise🏃
Water💧
75
DangerousModerateSafe
Treatment Details
Dosage Range
800 mg five times daily for 7-10 days
Time to Effect
1-3 days for symptom improvement
Treatment Duration
7-10 days
Evidence Quality
HIGH
Number Needed to Treat (NNT)
11(Treat 11 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
100(Treat 100 patients to see 1 additional serious adverse event)
Confidence Score
95%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$15
Monitoring:$50
Side Effect Mgmt:$10
Total Annual:$75
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
EXCELLENT
ICER
$15,000/QALY
QALYs Gained
0.06
Outcome-Based Costs
Cost per Responder
$93.75
Cost per Remission
$107.14
Comparison vs Valacyclovir
Cost Difference
$-15/year
Less expensive
QALY Difference
-0.01 QALYs
Worse outcomes
Dominance
No dominance
Prescription Access Economics
Annual Societal Loss per Patient
$-312.5
Cost of prescription-only barriers (visits, time, admin, price premium)
Physician Visit Cost
$120/year
Time Cost
$40/year
Travel + wait time
Insurance Admin Cost
$20/year
Prior auth, claims
Rx Price
$15/year
Potential OTC Price
$7.5/year
Estimated if OTC available
Early Treatment Benefit
+0.02 QALYs
From faster OTC access
Risk Assessment
Misuse Risk
LOW
Missed Diagnosis Risk
MODERATE
Acyclovir Outcomes

for Shingles

Efficacy Outcomes
Overall Effectiveness
+85%
Response Rate
+80%
Remission Rate
+70%
Common Side Effects
Nausea
+12%
Headache
+12%
Vomiting
+8%
Diarrhea
+8%

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
2 active trials recruiting for Acyclovir in Shingles

Ultrasound Guided Serratus Anterior Versus Erector Spinae Block in Pain Alleviation in Acute Herpes Zoster

NCT06476080NOT YET RECRUITINGNA
View Study
120 participants
INTERVENTIONAL
Started: Jul 5, 2024

Pharmacokinetics of Intravenous Acyclovir in Oncologic Paediatric Patients

NCT05198570RECRUITING
View Study
200 participants
OBSERVATIONAL
Trieste, Italy
Started: Sep 15, 2021
Completed Clinical Trials
14 completed trials for Acyclovir in Shingles

Efficacy of Oral Famciclovir Versus Aciclovir Treatment in Patients With Herpes Zoster

NCT01327144COMPLETEDPHASE3
View Study
177 participants
INTERVENTIONAL
Porto Alegre, Brazil +4 more
Started: Jun 1, 2012

Efficacy and Safety of Foscarnet Sodium and Sodium Chloride Injection in Patients With Herpes Zoster

NCT02151240COMPLETEDPHASE4
View Study
94 participants
INTERVENTIONAL
Beijing, China
Started: May 1, 2014

Long-Term Oral Acyclovir Usage to Prevent Herpes Zoster Virus Infection After Bone Marrow Transplant

NCT00209352COMPLETEDPHASE3
View Study
120 participants
INTERVENTIONAL
Seattle, United States
Started: Jun 1, 1985

A Comparison of 882C87 Versus Acyclovir in the Treatment of Herpes Zoster in Patients With Weakened Immune Systems

NCT00002315COMPLETEDPHASE3
View Study
400 participants
INTERVENTIONAL
Birmingham, United States +24 more

Comparison of Brovavir Versus Acyclovir in the Treatment of Herpes in HIV-Infected Patients

NCT00000953COMPLETEDPHASE2
View Study
180 participants
INTERVENTIONAL
Birmingham, United States +43 more

A Study of FV-100 Versus Valacyclovir in Patients With Herpes Zoster

NCT00900783COMPLETEDPHASE2
View Study
350 participants
INTERVENTIONAL
Started: May 1, 2009

A Study Exploring Efficacy of Peginterferon in Patients With Herpes Zoster

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

Zoster Eye Disease Study

NCT03134196COMPLETEDPHASE4
View Study
527 participants
INTERVENTIONAL
Birmingham, United States +77 more
Started: Aug 23, 2017

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

Valacyclovir in Immunocompromised Children

NCT00059592COMPLETEDPHASE1
View Study
37 participants
INTERVENTIONAL
Philadelphia, United States +1 more
Started: Apr 7, 1998

Dose-finding Study of ASP2151 in Subjects With Herpes Zoster

NCT00487682COMPLETEDPHASE2
View Study
403 participants
INTERVENTIONAL
Chūbu, Japan +4 more
Started: Nov 13, 2007

Phase III Study of ASP2151 in Herpes Zoster Patients

NCT01959841COMPLETEDPHASE3
View Study
751 participants
INTERVENTIONAL
Sapporo, Japan +2 more
Started: Aug 1, 2013

Bioequivalency Study of Valacyclovir Hydrochloride 1000 mg Under Fasting Conditions

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

Bioequivalency Study of Valacyclovir Hydrochloride 1000 mg Under Fed Conditions

NCT01132716COMPLETEDNA
View Study
48 participants
INTERVENTIONAL
Fargo, United States
Started: Sep 1, 2006
Showing 20 of 31 total trials