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Varicella-Zoster Vaccine Live

Published: July 26, 2026Updated: August 24, 2026

The Varicella-Zoster Virus Vaccine Live (Oka-Merck) Strain is a live attenuated vaccine designed to prevent chickenpox (varicella) caused by the varicella-zoster virus. It contains the Oka-Merck strain of the virus, which has been modified to stimulate immunity while minimizing the risk of wild-type disease. The vaccine is primarily used in children as a routine immunization and may also be given to susceptible adults.

Quick summary

Live attenuated vaccine for prevention of chickenpox using the Oka-Merck virus strain.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy

Key facts at a glance

ATC
J07BK01
RxNorm
1292422
Generic
Varicella-Zoster Virus Vaccine Live (Oka-Merck) Strain
Class
atc-j07
Brands
Varivax, ProQuad
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Vaccine; not applicable - toxic dose thresholds differ from small molecule drugs. Overdose may refer to administration errors rather than pharmacological toxicity.
Chronic overdose: N/A - vaccine is administered as single or limited doses per immunization schedule
Immediate actions
Contact healthcare provider or poison control for vaccine-specific exposure incidents
Antidote
N/A - no specific antidote exists for live vaccines; manage symptomatically(N/A)
Poison Control: 1-800-222-1222

Special Populations

6 groups
✗

pregnancy

all trimesters
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

Live attenuated varicella vaccine should be avoided during pregnancy. Women should be advised to avoid pregnancy for at least 3 months after vaccination.

Monitor

regular prenatal monitoring if accidentally exposed

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

Generally considered compatible with breastfeeding. The live attenuated virus is not excreted in significant amounts in breast milk.

Monitor

infant monitoring for signs of varicella infection

Use with caution and monitor for adverse effects.

✓

pediatric_age

12 months to 12 years
safe
FDA Category
N
Dose Adjustment

standard pediatric dosing

Key Recommendations

Administer 0.5 mL subcutaneously at 12-15 months of age with a booster dose at 4-6 years. For catch-up vaccination, two doses at least 3 months apart are recommended.

Monitor

standard post-vaccination observation for 15-20 minutes

⚠

geriatric

60 years and older
caution
FDA Category
N
Dose Adjustment

not indicated for primary varicella prevention

Key Recommendations

The original varicella vaccine (Varivax) is not routinely indicated for adults over 60 for shingles prevention. For shingles prevention, use zoster vaccine (Zostavax or Shingrix) instead.

Monitor

standard post-vaccination monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

no standard dosage adjustment

Key Recommendations

Use with caution in patients with severe renal impairment, especially if immunocompromised. Live vaccines are generally contraindicated in patients on immunosuppressive therapy for renal disease.

Monitor

monitor for vaccine-related rash and signs of infection

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

no standard dosage adjustment

Key Recommendations

Use with caution in patients with moderate to severe hepatic impairment, particularly those with ascites or immunocompromise. Live vaccines generally contraindicated in advanced liver disease.

Monitor

monitor for vaccine-related complications and liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA Approval Year

Value:1995

Varivax (varicella vaccine) FDA approval year

drug_classCDC
2023

Vaccine Type

Value:Live attenuated virus vaccine

Classification of the Oka-Merck strain vaccine type

usageFDA
2023

Primary Indication

Value:Prevention of varicella (chickenpox)

Main therapeutic use of Varivax and ProQuad vaccines

efficacyCDC
2023

Vaccine Efficacy (2 doses)

Value:98-99%

Clinical efficacy of two-dose varicella vaccination regimen

Prevention of chickenpox (varicella) in children, adolescents, and adults who have not had varicella disease or been previously vaccinated. May also be considered for post-exposure prophylaxis in susceptible individuals.

The live attenuated Oka-Merck strain of varicella-zoster virus replicates in the body and stimulates the immune system to produce antibodies against the virus, providing active immunity against future varicella infection.

This is a live vaccine and is contraindicated in immunocompromised patients, pregnant women, and those with severe allergic reactions to any vaccine component. Should not be given with other live vaccines unless specified. Local injection site reactions and fever may occur after vaccination.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 24, 2026. · Read our editorial policy