Open AccessPostlicensure Safety Surveillance for Quadrivalent Human Papillomavirus Recombinant Vaccine
Author(s) -
Barbara A. Slade
Publication year - 2009
Publication title -
jama
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.688
H-Index - 680
eISSN - 1538-3598
pISSN - 0098-7484
DOI - 10.1001/jama.2009.1201
Subject(s) - medicine , adverse effect , adverse event reporting system , vaccination , pediatrics , immunology
In June 2006, the Food and Drug Administration licensed the quadrivalent human papillomavirus (types 6, 11, 16, and 18) recombinant vaccine (qHPV) in the United States for use in females aged 9 to 26 years; the Advisory Committee on Immunization Practices then recommended qHPV for routine vaccination of girls aged 11 to 12 years.
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