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CHICKENPOX and VARICELLA VACCINE
Chickenpox is an acute, generalized, viral disease of sudden onset with slight fever, mild
constitutional symptoms and skin eruptions. Rarely fatal, a primary viral pneumonia is the
commonest cause of death in adults; septic complications and encephalitis are the common
cause of death in children. Neonates who develop varicella between day 5 and 10 or those
whose mothers contact the disease prior to or within 5 days after delivery are at
increased risk of developing severe generalized chickenpox with a 30% mortality rate.
Herpes zoster is a local manifestation of recurrent, recrudescent or reactivation
infection with the same virus.
Vaccination is now available for the varicella virus. Varivax is a live, attenuated
vaccine approved by the FDA for vaccination against chickenpox. The vaccine safely and
effectively reduces the incidence and severity of natural varicella. It has been useful
following known exposure, and has some efficacy in adults.
An unanswered question is whether the vaccine virus becomes latent, resulting in later
development of herpes zoster (shingles).
 | Candidates for vaccination: |
Children 12 months or older who have not had chickenpox
Persons at risk for developing chickenpox due to recent exposure may benefit from
vaccination to prevent or reduce symptoms of the disease
Persons at risk working in a school, pre-school or health care environment which may
put susceptible children, pregnant women or immunocompromized patients at risk
Women anticipating future pregnancy
 | Precautions: |
Hypersensitive to any of the components, including previous anaphylactic reactions to
neomycin
Febrile illness
Pregnancy and those women planning to become pregnant within the next three months
Nursing women
Blood dyscrasias or other malignant neoplasms
Persons on immunosuppressive therapy
Persons with primary or acquired immunodeficiency
 | Reactions: |
Pain at injection site
Redness and swelling at injection site
Chickenpox-like rash, generalized or localized near the injection
site, pruritis
Hematoma, induration or stiffness
Fever
 | Administration and Dosage: |
The dosage for adults receiving the vaccine is 2 injections in the upper arm given 4 to
8 weeks apart.
Varicella and MMR have been successfully given at the same time at different injection
sites or combined. Vaccination should be deferred for at least 5 months following blood or
plasma transfusions, or administration of IG or VZIG. After vaccination any IG should not
be given for 2 months unless its usefulness outweighs the benefits.
 | Duration of Immunity: |
In healthy adolescents and adults antibody levels were present at least 1 year in 97.2%
of individuals who received 2 injections 4 to 8 weeks apart. The duration of protection is
unknown at present and the need for booster doses is not defined.
 | Post vaccination instructions: |
Avoid pregnancy for at least 3 months
Avoid salicylates for 6 weeks after vaccination as Reye's syndrome has been reported
following salicylate use during natural varicella infections.
Individuals vaccinated with varicella may potentially be capable of transmitting the
vaccine to close contacts. Therefore, vaccine recipients should avoid close association
with susceptible high risk individuals (newborns, pregnant women, immunocompromized
persons).
Review possible reactions
Report any adverse effects to their health care provider.
Resources:
Control of Communicable Diseases in California
Drug Facts and Comparisons
Modern Medicine, Volume 63, May 1995
Kern County Health Department
CSUB STUDENT HEALTH
SERVICES (661) 654-2394
Updated
2/06 ck

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