The purpose of this post-marketing surveillance study is to evaluate the safety of Synflorix™ when administered according to the local Prescribing Information to healthy Filipino infants.
Study Type
OBSERVATIONAL
Enrollment
28
Intramuscular administration of three doses/two doses/one dose of primary vaccination/the booster dose/ catch-up dose(s) of Synflorix according to local prescribing information.
GSK Investigational Site
Quezon City, Philippines
GSK Investigational Site
Santa Mesa, Manila, Philippines
Occurrence of grade 3 unsolicited adverse events.
Time frame: Within 31 days (Day 0 - Day 30) after each vaccination.
Occurrence of unsolicited adverse events.
Time frame: During 31 days (Day 0 - Day 30) follow-up period after each vaccination/vaccine dose.
Occurrence of serious adverse events.
Time frame: From the Dose 1 up to study end.
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