Form: Single-dose vials, lyophilized powder for injection (0.5 mL/dose after reconstitution)
Manufacturer: Merck Canada Inc.
Indications and Clinical Use
Indication: Simultaneous vaccination against measles, mumps, and rubella in persons 12 months of age or older.
Special Populations:
Infants less than 12 months may fail to respond to the measles component.
Infants vaccinated before 12 months should be revaccinated with two additional doses after reaching 12 months of age.
Vaccination is recommended for susceptible individuals in high-risk groups such as students at post-secondary institutions, health care workers, and military personnel.
Prior to international travel, susceptible individuals should receive M-M-R® II.
Contraindications
Hypersensitivity to any component, including gelatin and neomycin.
Pregnant women should not receive the vaccine, and pregnancy should be avoided for one month following vaccination.
Individuals with severe febrile respiratory illness or other active febrile infection.
Patients receiving immunosuppressive therapy or with primary/acquired immunodeficiency states.
Individuals with active untreated tuberculosis.
Warnings and Precautions
General: Do not give intravascularly; only subcutaneous administration.
Severe Allergic Reactions: Anaphylaxis can occur; epinephrine should be available.
Monitoring: Monitor individuals with a history of convulsions or cerebral injury.
Immune Compromised Individuals: Vaccination may be less effective; monitor for vaccine-preventable diseases.
Transmission: Theoretical risk of transmission of rubella virus; no confirmed evidence for measles or mumps.
Adverse Reactions
Common: Injection site pain, fever, rash, headache, dizziness, irritability.