| Literature DB >> 26954689 |
Sven Arne Silfverdal1, Vanessa Coremans2, Nancy François2, Dorota Borys2, Jan Cleerbout2.
Abstract
Safety and reactogenicity data were reviewed following 10 years of experience with the 10-valent pneumococcal non-typeable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) in clinical development and from post-licensure settings. Analyses of pooled clinical trial data and post-marketing reports provided an overview of its safety profile and allowed assessment of rare adverse events that might not have been identified previously. The safety of PHiD-CV was also evaluated in children at higher risk for pneumococcal infection (preterm and HIV-infected or HIV-exposed infants), for different vaccination schedules and co-administered pediatric vaccines, and with a focus on special categories of adverse events (febrile convulsions, apnea, Kawasaki disease and sudden deaths). Following the distribution of over 235 million doses, PHiD-CV has been well tolerated when co-administered with other pediatric vaccines to children aged less than 5 years from diverse ethnic and geographic backgrounds. Detailed examination of various aspects has confirmed its favorable benefit: risk profile.Entities:
Keywords: PHiD-CV; Pneumococcal conjugate vaccine; adverse events; children; clinical trial; infants; pneumococcal disease; post-licensure; reactogenicity; safety
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Year: 2016 PMID: 26954689 DOI: 10.1586/14760584.2016.1164044
Source DB: PubMed Journal: Expert Rev Vaccines ISSN: 1476-0584 Impact factor: 5.217