Post-Marketing Safety Study of Menactra® in Healthy Children, Adolescents, and Adults in the Philippines

Inclusion Criteria: * Aged 2 to 11 years of age on the day of inclusion (Group 1) * Aged 12 to 17 years of age on the day of inclusion (Group 2) * Aged 18 to 55 years of age on the day of inclusion (Group 3) * Provision of informed consent form signed by the parent(s) or legal representative (Group 1) * Provision of assent form signed by the subject and informed consent form signed by the parent (s) or legal representative (Group 2) * Provision of informed consent form signed by the subject (Group 3) * If the subject (Group 3) or the subject's parents or legally accepted representative (Group 1 and 2) are illiterate, an independent witness is required to sign the consent form * Subject and parent/legally acceptable representative (if applicable) able to attend all scheduled visits and comply with all trial procedures * For a woman of child-bearing potential, sexually active, use of a medically acceptable and effective method of contraception for at least 4 weeks prior to vaccination, until at least 4 weeks after vaccination (not applicable for females not of child-bearing potential or not sexually active). Exclusion Criteria: * For a woman of child-bearing potential sexually active, known or suspected pregnancy or positive serum/urine pregnancy test (not applicable for females not of child-bearing potential or not sexually active) * Breast-feeding woman * Participation in another clinical trial investigating a vaccine, drug, medical device, or a medical procedure in the 4 weeks preceding the trial vaccination * Planned participation in another clinical trial during the present trial period * Known or suspected congenital or acquired immunodeficiency, immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within the preceding 6 months or long-term systemic corticosteroid therapy * Known systemic hypersensitivity to any of the vaccine components or history of a life-threatening reaction to the trial vaccine or to a vaccine containing any of the same substances * Chronic illness at a stage that could interfere with trial conduct or completion, in the opinion of the Investigator * Receipt of any vaccine in the 4 weeks preceding the trial vaccination * Planned receipt of any vaccine during the present trial period * Known personal or maternal Human Immunodeficiency virus (HIV), Hepatitis B antigen or Hepatitis C seropositivity as reported by the subject/parent/guardian and/or based on medical history * History of seizures * Thrombocytopenia, bleeding disorder or anticoagulants in the 3 weeks preceding inclusion contraindicating intramuscular injection * Personal of family history of Guillain-Barré Syndrome.