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An Overview of Quadrivalent Human Papillomavirus Vaccine Safety: 2006 to 2015.

Identifieur interne : 003182 ( Main/Exploration ); précédent : 003181; suivant : 003183

An Overview of Quadrivalent Human Papillomavirus Vaccine Safety: 2006 to 2015.

Auteurs : Michelle Vichnin [France] ; Paolo Bonanni ; Nicola P. Klein ; Suzanne M. Garland ; Stan L. Block ; Susanne K. Kjaer ; Heather L. Sings ; Gonzalo Perez ; Richard M. Haupt ; Alfred J. Saah ; Fabio Lievano ; Christine Velicer ; Rosybel Drury ; Barbara J. Kuter

Source :

RBID : pubmed:26107345

Descripteurs français

English descriptors

Abstract

A quadrivalent human papillomavirus (HPV4) type 6/11/16/18 vaccine (GARDASIL/SILGARD®) has been licensed in many countries around the world for the prevention of cervical, vulvar, vaginal, and anal cancers and precancers, as well as external genital warts causally related to HPV types 6/11/16/18. Across 7 phase 3 clinical trials involving more than 29,000 males and females ages 9-45 years, vaccination was generally well tolerated. Because of its expected public health benefit in reducing cervical cancer and other HPV-related diseases, the vaccine has been implemented in the national vaccination programs of several countries, with over 178 million doses distributed worldwide.

DOI: 10.1097/INF.0000000000000793
PubMed: 26107345


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Vichnin, Michelle" sort="Vichnin, Michelle" uniqKey="Vichnin M" first="Michelle" last="Vichnin">Michelle Vichnin</name>
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<nlm:affiliation>From the *Merck & Co., Inc., Kenilworth, New Jersey; †University of Florence, Florence, Italy; ‡Kaiser Permanente Vaccine Study Center, Oakland, California; §The Royal Women's' Hospital, Murdoch Childrens Research Institute, University of Melbourne, Parkville, Victoria, Australia; ¶Kentucky Pediatric Research, Inc., Bardstown, Kentucky; ‖Danish Cancer Society Research Center, Copenhagen, Denmark; **Department of Gynaecology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark; ††Universidad del Rosario, Bogota, Colombia; and ‡‡Sanofi Pasteur MSD, Lyon, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>From the *Merck & Co., Inc., Kenilworth, New Jersey; †University of Florence, Florence, Italy; ‡Kaiser Permanente Vaccine Study Center, Oakland, California; §The Royal Women's' Hospital, Murdoch Childrens Research Institute, University of Melbourne, Parkville, Victoria, Australia; ¶Kentucky Pediatric Research, Inc., Bardstown, Kentucky; ‖Danish Cancer Society Research Center, Copenhagen, Denmark; **Department of Gynaecology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark; ††Universidad del Rosario, Bogota, Colombia; and ‡‡Sanofi Pasteur MSD, Lyon</wicri:regionArea>
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<name sortKey="Velicer, Christine" sort="Velicer, Christine" uniqKey="Velicer C" first="Christine" last="Velicer">Christine Velicer</name>
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<nlm:affiliation>From the *Merck & Co., Inc., Kenilworth, New Jersey; †University of Florence, Florence, Italy; ‡Kaiser Permanente Vaccine Study Center, Oakland, California; §The Royal Women's' Hospital, Murdoch Childrens Research Institute, University of Melbourne, Parkville, Victoria, Australia; ¶Kentucky Pediatric Research, Inc., Bardstown, Kentucky; ‖Danish Cancer Society Research Center, Copenhagen, Denmark; **Department of Gynaecology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark; ††Universidad del Rosario, Bogota, Colombia; and ‡‡Sanofi Pasteur MSD, Lyon, France.</nlm:affiliation>
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<term>Drug-Related Side Effects and Adverse Reactions (epidemiology)</term>
<term>Drug-Related Side Effects and Adverse Reactions (pathology)</term>
<term>Female</term>
<term>Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18 (administration & dosage)</term>
<term>Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18 (adverse effects)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Papillomavirus Infections (prevention & control)</term>
<term>Pregnancy</term>
<term>Product Surveillance, Postmarketing</term>
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<term>Effets secondaires indésirables des médicaments (anatomopathologie)</term>
<term>Effets secondaires indésirables des médicaments (épidémiologie)</term>
<term>Enfant</term>
<term>Femelle</term>
<term>Grossesse</term>
<term>Humains</term>
<term>Infections à papillomavirus ()</term>
<term>Jeune adulte</term>
<term>Mâle</term>
<term>Surveillance post-commercialisation des produits de santé</term>
<term>Vaccin recombinant quadrivalent contre les papillomavirus humains de type 6, 11, 16 et 18 (administration et posologie)</term>
<term>Vaccin recombinant quadrivalent contre les papillomavirus humains de type 6, 11, 16 et 18 (effets indésirables)</term>
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<term>Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18</term>
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<term>Vaccin recombinant quadrivalent contre les papillomavirus humains de type 6, 11, 16 et 18</term>
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<div type="abstract" xml:lang="en">A quadrivalent human papillomavirus (HPV4) type 6/11/16/18 vaccine (GARDASIL/SILGARD®) has been licensed in many countries around the world for the prevention of cervical, vulvar, vaginal, and anal cancers and precancers, as well as external genital warts causally related to HPV types 6/11/16/18. Across 7 phase 3 clinical trials involving more than 29,000 males and females ages 9-45 years, vaccination was generally well tolerated. Because of its expected public health benefit in reducing cervical cancer and other HPV-related diseases, the vaccine has been implemented in the national vaccination programs of several countries, with over 178 million doses distributed worldwide.</div>
</front>
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<name sortKey="Block, Stan L" sort="Block, Stan L" uniqKey="Block S" first="Stan L" last="Block">Stan L. Block</name>
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