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Adverse events following pandemic influenza A (H1N1) 2009 monovalent and seasonal influenza vaccinations during the 2009-2010 season in the active component U.S. military and civilians aged 17-44years reported to the Vaccine Adverse Event Reporting System.
タグ:
VAERS
2016/7/28
Post-Marketing Surveillance of Human Rabies Diploid Cell Vaccine (Imovax) in the Vaccine Adverse Event Reporting System (VAERS) in the United States, 1990 E015.
タグ:
FAERS
VAERS
2016/7/15
Quadrivalent human papillomavirus vaccine and autoimmune adverse events: a case-control assessment of the vaccine adverse event reporting system (VAERS) database.
タグ:
VAERS
2016/7/14
Surveillance systems and methods for monitoring the post-marketing safety of influenza vaccines at the Centers for Disease Control and Prevention.
タグ:
VAERS
2016/6/9
A new algorithmic approach for the extraction of temporal associations from clinical narratives with an application to medical product safety surveillance reports.
タグ:
VAERS
2016/6/22
Can the vaccine adverse event reporting system be used to increase vaccine acceptance and trust?
タグ:
VAERS
2016/4/7
Post-licensure safety surveillance of 23-valent pneumococcal polysaccharide vaccine in the Vaccine Adverse Event Reporting System (VAERS), 1990-2013.
タグ:
VAERS
2016/4/19
Post-licensure surveillance of quadrivalent inactivated influenza (IIV4) vaccine in the United States, Vaccine Adverse Event Reporting System (VAERS), July 1, 2013-May 31, 2015.
タグ:
FAERS
VAERS
2016/3/27
Enhanced surveillance of tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccines in pregnancy in the Vaccine Adverse Event Reporting System (VAERS), 2011-2015.
タグ:
VAERS
2016/3/26
A Two-Phase Case-Control Study of Autism Risk Among Children Born From the Late 1990s Through the Early 2000s in the United States.
タグ:
VAERS
2016/12/30
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