Trade Names:M-M-R-II- Powder for Injection Mixture of 3 viruses: at least 1,000 measles TCID 50 (tissue culture infectious doses), at least 20,000 mumps TCID 50 and at least 1,000 rubella TCID 50 per 0.5 mL dosePriorix (Canada)
Induces protective antibodies against measles, mumps, and rubella viruses.
Vaccination of individuals known to be susceptible to measles, mumps, or rubella; prevention of occurrence of congenital rubella syndrome (CRS) among offspring of women who contract rubella during pregnancy. Preferred immunizing agent for most children and many adults.
Pregnancy; moderate to severe hypersensitivity reaction to eggs; immunosuppressive therapy; blood dyscrasia, leukemia, lymphoma of any type or other malignant neoplasms affecting the bone marrow or lymphatic systems; primary or acquired immunodeficiency; active untreated tuberculosis; family history of congenital or hereditary immunodeficiency, until immune competence of potential vaccine recipient is demonstrated.Exception
Vaccinate asymptomatic children with HIV infection.
Subcutaneous 0.5 mL. Optimal schedule: Give first dose at 12 to 15 mo; revaccinate routinely at 5 to 6 yr of age or 11 to 12 yr of age.
Store in refrigerator (36° to 46°F). Protect from light. Discard unused reconstituted vaccine if not used within 8 h.
To avoid inactivating vaccine, give MMR 2 to 4 wk before or 3 to 11 mo after AGIV, depending on dose. Susceptible postpartum women who received blood products or Rho(D) immune globulin may receive rubella vaccine prior to discharge, provided that rubella titer is measured 6 to 8 wk after vaccination to ensure seroconversion.Immunosuppressants, interferon, meningococcal vaccine
May inhibit response to MMR vaccine.
May cause delayed hypersensitivity skin tests (eg, tuberculin, histoplasmin) to appear falsely negative. Effect may persist for several weeks after vaccination. Methacoline inhalation challenge may be falsely positive for a few days.
Fever; headache; encephalitis; dizziness; polyneuritis; arthralgia; arthritis (rarely chronic); convulsions or seizures.
Urticaria; rash; erythema multiforme.
Sore throat; optic neuritis.
Nausea; vomiting; diarrhea.
Local pain, induration, erythema or allergic reaction at injection site; mild regional lymphadenopathy; malaise.
Category C (contraindicated).
Excreted in breast milk (vaccine-strain rubella).
Defer immunization during course of any acute febrile illness.
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