The aim of this study is to generate local data on the safety of Menactra® in individuals 2 to 55 years of age in the Russian Federation. Primary Objective: * To describe the safety profile after 1 dose of Menactra® administered in individuals 2-55 years of age under standard health care practices.
Participants will be enrolled after receipt of one dose of Menactra® during a routine health care visit. They will be monitored for safety throughout the study.
Study Type
OBSERVATIONAL
Enrollment
100
No vaccine will be provided as part of this study
No vaccine will be provided as part of this study
No vaccine will be provided as part of this study
Unnamed facility
Moscow, Russia
Number of participants reporting solicited injection site and systemic reactions after a single dose of Menactra® vaccine
Solicited injection site: Pain, Erythema and Swelling, Solicited systemic: Fever (Temperature), Headache, Malaise and Myalgia
Time frame: Day 0 to Day 7 post-vaccination
Number of participants reporting unsolicited adverse events and serious adverse events after a single dose of Menactra® vaccine
Time frame: Day 0 to Day 28 post-vaccination
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