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Descriptive, Post-marketing, Passive Surveillance Safety Study of ADACELâ„¢ Vaccine Summary To further characterize the vaccine safety profile and to identify any signals of potentially vaccine-related adverse events (AEs) not detected during pre-licensure studies.
View Full Description Full Description Surveillance using a healthcare organization with large comprehensive medical encounter databases will be used in this study to identify any risks or uncommon events associated with use of the recently licensed Adacel vaccine that may occur in routine clinical usage in a large population. No investigational vaccines will be administered in this study. Participants will be included in the study on the basis of their having received Adacel vaccine as part of routine care.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Receipt of ADACEL vaccine during the study period Exclusion Criteria: None
Check Your Eligibility
Let’s see if you might be eligible for this study.
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There is 1 Location for this study
Oakland California, , United States
Aurora Colorado, , United States
Portland Oregon, , United States
How clear is this clinincal trial information?
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