Beasley, Allen, Crow, Methvin, Portis & Miles, P.C.

Despite outcry from parents of girls who have received the HPV vaccine Gardasil, and criticism about the vaccine’s effectiveness from one of its own creators, this month the American Academy of Pediatrics endorsed its use for boys. This follows a similar recommendation from the Centers for Disease Control and Prevention (CDC). Critics of the vaccine, which has been linked to thousands of complaints of serious adverse side effects, are left to wonder why their voices are not being heard.

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As expected, a U.S. Centers for Disease Control and Prevention (CDC) advisory committee this week recommended expanding the use of the Gardasil vaccine, manufactured by Merck, to include boys and young men. The vaccine, which targets the human papillomavirus (HPV), previously has been recommended for girls, as a way to prevent cervical cancer caused by certain types of HPV. Gardsil use had already been approved by the FDA to treat boys in October 2009, although it was not yet given “recommended” status. The CDC reports that approximately 32 million doses of the vaccine have been distributed in the United States since the vaccine was initially approved in 2006.

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In this week’s GOP Presidential debate, candidate Michele Bachmann criticized Texas Governor and presidential candidate Rick Perry for his attempt to mandate the use of Gardasil in his state. Gardasil, manufactured by Merck, is promoted as a preventive treatment against human papillomavirus (HPV), a sexually transmitted virus linked to the development of cervical cancer. Following a public outcry in the state of Texas, the mandate was overturned. Bachmann objected to the mandate for political reasons, but also expressed concerns that any parent might feel about being required to give their child a relatively new vaccine, about possible adverse side effects.

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There is much debate about the vaccine Gardasil, which was introduced in 2006 for girls, and marketed as a weapon against cervical cancer. The vaccine actually targets human papillomavirus (HPV), a sexually transmitted virus that is linked to the development of cervical cancer. While originally targeted only at girls and young women, the FDA recently expanded approval of the drug for use in boys and young men, to prevent the spread of HPV.

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S.A.N.E. Vax, Inc., a non-profit organization established to promote safe, affordable, necessary, effective vaccines and vaccination practices, has announced a combined effort of concerned citizens worldwide to insist on government compliance with regulations and guidelines in the implementation and monitoring of vaccines. In particular, the outreach effort is focusing on Gardasil, manfuactured by Merck and marketed as a preventive for cervical cancer by targeting the human papillomavirus (HPV). According to a recent news release, SaneVax is encouraging an open letter writing campaign addressing the issue of vaccine safety.

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Gardasil, a vaccine manufactured by Merck and promoted as a prevention for cervical cancer, was approved by the FDA in 2006. Later the same month, the vaccine was added to a list of recommended vaccines for girls ages 11-12 years. This, despite the fact that the first phase 3 trials of the vaccine were not yet complete. It would be almost a year later – May 2007 – before these studies were complete. Why the big rush?

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Teenager Kirsten Jamison made a short film in 2009, dedicated to her friend Gabby Swank, who she said was seriously injured after receiving a series of Gardasil vaccines. The vaccine has been promoted since 2006 for girls and young women, as a preventive treatment against cervical cancer. The vaccine protects against four kinds of human papillomavirus (HPV), which is a sexually transmitted virus that can lead to cervical cancer.

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Recently, WTVR CBS-6 News in Richmond, Virginia, brought viewers a troubling report of serious adverse events and 16 deaths linked to the Gardasil vaccine. The vaccine, which is intended to prevent four types of human papillomavirus (HPV) that cause cervical cancer, is required for girls in Virginia prior to entering the sixth grade unless their parents object. The story, which is based on a new FDA adverse event report obtained by the government watchdog group Judicial Watch, sparked debate in the area and is generating interest nationwide.

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SM Mohammed Idris, president of the Consumers Association of Penang, recently wrote an opinion piece for the Malaysia Kini website, asking that the government reconsider its decision to vaccinate all 13-year-old girls in the country with Gardasil or Cervarix. According to the column, the country’s Ministry of Health (MOH) will spend RM 150 million annually for the vaccinations, which will affect about 300,000 girls. Idris warns the vaccine is “unnecessary, unscientific and unsafe.”

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S.A.N.E. VAX, Inc., is newly established non-profit organization dedicated to promoting  safe, affordable, necessary and effective vaccines and vaccination practices through education and information. Its mission is two-fold: to provide information individuals need to make informed decisions prior to vaccination, and to help people locate appropriate medical and legal assistance if they or a loved one suffers from a serious adverse event after a vaccination. The organization is beginning its work with a critical evaluation of the drug Gardasil.

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