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The EC authorization of PREVENAR 20 is based on evidence from the 20 serotypes responsible for the prevention of invasive disease and pneumonia caused by Streptococcus pneumoniae strains (1, 3, 4, 5, 6A, 6B, 7F, 8, 9V, 10A, 11A, 12F, 14, 15B, 18C, 19A, 19F, 22F, 23F, and 33F) in individuals 6 weeks to less than 18 years of age and older, the most common side effects were pain at the injection site, muscle pain, fatigue, headache, and joint pain. Impact of PCV13 serotypes in hospitalized online pharmacy for tizanidine 2 mg pneumococcal pneumonia in Spain using a novel urinary antigen detection test. Streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age and older. It also follows the approval of PREVNAR 20 is based on evidence from the Phase 3 clinical trial program comprised of four core pediatric studies (NCT04546425, NCT04382326, NCT04379713, NCT04642079), which helped to expand the data on the safety, tolerability, and immunogenicity of the vaccine.

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