M-M-R® II

05/22/2024
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Product Information

  • Name: M-M-R® II
  • Type: Measles, mumps, and rubella virus vaccine, live, attenuated, Merck Std.
  • 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.
  • Rare: Anaphylaxis, thrombocytopenia, febrile convulsions, encephalitis, Guillain-Barré syndrome, arthritis.

Drug Interactions

  • Immune globulins can interfere with the immune response; defer vaccination for at least 3 months after administration of immune globulin.

Dosage and Administration

  • Dose: 0.5 mL subcutaneous injection.
  • Primary Vaccination: Two doses, first at 12-15 months and second at 4-6 years.
  • Revaccination: Required for infants vaccinated before 12 months and for specific high-risk groups.
  • Concurrent Administration: Can be given with other vaccines, but at different sites and using separate syringes.

Storage and Stability

  • Store refrigerated at 2°C to 8°C. Protect from light. Use reconstituted vaccine within 8 hours if stored at 2°C to 8°C.

Clinical Trials and Efficacy

  • Efficacy: High seroconversion rates with strong immune responses against measles, mumps, and rubella.
  • Safety: Generally well-tolerated with mild to moderate adverse reactions; severe reactions are rare.
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Written By Paul Kim

Medical Director - APN, NSWOC, RNP

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