Abstract
GARDASIL has been shown to reduce the incidence of pre-cancerous cervical, vulvar, and vaginal lesions, and external genital warts causally related to HPV6/11/16/18. Because of its expected public health benefit on reduction of cervical cancer and other HPV-related diseases, this vaccine has been rapidly implemented in the routine vaccination programs of several countries. It is therefore essential to assess its impact and safety through post-licensure surveillance programs. Here, we present a summary of 16 post-licensure safety and impact studies across 20 countries. These studies address general safety, including autoimmune disorders, long-term effectiveness, and type replacement. A summary of the surveillance efforts of the Unites States Centers for Disease Control and Prevention can be found in the accompanying article by Markowitz et al.
Originalsprog | Engelsk |
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Tidsskrift | Vaccine |
Vol/bind | 28 |
Udgave nummer | 30 |
Sider (fra-til) | 4719-30 |
Antal sider | 12 |
ISSN | 0264-410X |
DOI | |
Status | Udgivet - 5 jul. 2010 |