Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran
نویسندگان
چکیده
منابع مشابه
Adverse reactions following immunization with MMR vaccine in children at selected provinces of Iran.
BACKGROUND Several adverse events following immunization (AEFI) have been attributed to immunization with live attenuated measles, mumps, and rubella (MMR) vaccines. The MMR vaccine was introduced into the routine infant immunization schedule in 2003, followed by a second dose of vaccine at school-entry for children 4 to 6 years of age. The objective of this study was to characterize adverse re...
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INTRODUCTION Post-licensure vaccine safety studies are essential to identify uncommon events that may be difficult to assess during pre-licensure studies. The aim of our study was to evaluate the safety of serogroup C meningococcal conjugate (MCC) vaccine in Tuscany from 2005 to 2012. METHODS All adverse events (AEs) to MCC vaccine notified from 2005 to 2012 were obtained from the regional he...
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Rotavirus is the most common cause of diarrhea leading to hospitalization in young children. Rotavirus vaccines are available in Canada but have not been introduced in all provinces. In a controlled trial, 2 study sites (Prince Edward Island and the Capital District Health Authority (District 9, Nova Scotia) introduced universal rotavirus vaccine programs for infants at 2 and 4 months of age be...
متن کاملAdverse Events Following Immunization (AEFI) in Children under 7- year of Age during 2014 in Hamedan Province, Iran
Background: The surveillance of adverse events following immunization (AEFI) is essential to improve high standard of vaccine safety, and maintain public trust in immunization programs. This study aimed to determine the AEFI and their related factors in children. Materials and Methods: This cross-sectional study including all children under 7- year of age, in Hamadan Province, the West of Iran,...
متن کاملAdverse events reported following live, cold-adapted, intranasal influenza vaccine.
CONTEXT In June 2003, the US Food and Drug Administration licensed a trivalent live, attenuated influenza vaccine (LAIV-T) for intranasal administration to healthy persons 5 to 49 years of age. Although prelicensure testing involved 20 228 vaccinees, clinical trials were not of sufficient size to detect rare adverse events reliably. OBJECTIVE To identify adverse events reported following LAIV...
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ژورنال
عنوان ژورنال: BMC Immunology
سال: 2017
ISSN: 1471-2172
DOI: 10.1186/s12865-017-0226-8