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ZOSTAVAX

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Generic Name for ZOSTAVAX

Varicella zoster vaccine, live, attenuated; minimum of 19,400 PFU/0.65mL dose; pwd for SC inj after reconstitution; contains porcine gelatin, neomycin and bovine serum (trace); preservative-free.

Legal Classification:

Rx

Manufacturer of ZOSTAVAX

Merck & Co., Inc.

Indications for ZOSTAVAX

Prevention of herpes zoster (shingles) in adults ≥50 years of age.

Adult dose for ZOSTAVAX

<50yrs: not recommended. ≥50yrs: one 0.65mL dose by SC inj once in upper arm. Administer immediately upon reconstitution.

Children's dosing for ZOSTAVAX

Not recommended.

Contraindications for ZOSTAVAX

Immunodeficiency (eg, HIV, leukemia, lymphoma, bone marrow or lymphatic cancer, immunosuppressive therapy). Pregnancy (during and 3 months after vaccination).

Warnings/Precautions for ZOSTAVAX

Not for treating zoster or postherpetic neuralgia. Not for preventing primary varicella infection. Defer in untreated tuberculosis. Consider deferral in acute illness. Have epinephrine inj (1:1000) available. May not protect 100% of recipients. Virus transmission may occur between recipients and susceptible contacts. Nursing mothers.

Interactions for ZOSTAVAX

See Contraindications. Immunosuppressants may cause disseminated disease.

Adverse Reactions for ZOSTAVAX

Inj site reactions (eg, erythema, pain, swelling, pruritus), headache, cardiovascular diseases (eg, CHF, pulmonary edema).

Notes for ZOSTAVAX

To register pregnant patients exposed to Zostavax: (800) 986-8999. To report adverse events to VAERS: (800) 822-7967.

How is ZOSTAVAX supplied?

Single-dose vials—1, 10 (w. diluent)

Related Disease:

Immunization
Shingles~vaccines

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