“…In addition, disease due to certain serotypes, such as 3 and 19A, continues to persist, owing to either a lack of inclusion in the PCV being used [10-valent PCV (PCV10)] or low vaccine effectiveness ]. 13,[33][34][35][36][37] V114 (VAXNEUVANCE, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ) is a 15-valent PCV containing all 13 serotypes in PCV13 (Prevnar 13, Wyeth LLC, marketed by Pfizer, New York, NY) plus serotypes 22F and 33F, 2 epidemiologically important serotypes associated with a high degree of invasiveness and antimicrobial resistance. 35,[38][39][40][41][42][43][44] V114 is approved for use and recommended as part of the standard of care in individuals ≥6 weeks of age in the United States, the United Kingdom, European Union and Canada, 39,[45][46][47] and is currently being evaluated for pediatric use by other regulatory authorities.…”