Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2009-8-19
pubmed:abstractText
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.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1538-3598
pubmed:author
pubmed:issnType
Electronic
pubmed:day
19
pubmed:volume
302
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
750-7
pubmed:dateRevised
2009-12-31
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Postlicensure safety surveillance for quadrivalent human papillomavirus recombinant vaccine.
pubmed:affiliation
Centers for Disease Control and Prevention, 1600 Clifton Rd NE, Mailstop D-26, Atlanta, GA 30333, USA. bfs9@cdc.gov
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.