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Primary objective: This is a descriptive study and the primary objective is to determine the incidence of injection site and systemic adverse events after Triaxis administration as a 5th dose of tetanus, diphtheria and acellular pertussis vaccine in 4-6 year old children
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Exclusion criteria
Have been previously vaccinated with a 5th dose of tetanus, diphtheria and pertussis.
Presence of a contra-indication or cautions to vaccination in accordance with the Spanish version of the EU SmPC:
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Data sourced from clinicaltrials.gov
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