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Too Fast or Not Too Fast: The FDA’s Approval of Merck’s HPV Vaccine Gardasil

November 14, 2012 By Norma Leave a Comment

Tomljenovic L, Shaw CA. Early career postdoctoral fellow in the Neural Dynamics Research Group at the University of British Columbia. Professor in the Department of Ophthalmology and Visual Sciences at the University of British Columbia and holds cross appointments with the Program in Experimental Medicine and the Graduate Program in Neuroscience. Abstract There are not many […]

Filed Under: Gardasil/Silgard Efficacy, Vaccine Related Research Tagged With: FDA approval, Gardasil

GSK’s MenHibrix Approval: What is Wrong with this Picture?

June 17, 2012 By Norma Leave a Comment

[SaneVax:  MenHibrix vaccine, manufactured by GlaxoSmithKline, was just approved for use in the U.S. based on data gathered from the inoculation of 7,521 infants and toddlers in five countries with ‘at least one dose.’ The problem is, this vaccine is given in a four dose regimen. How did the FDA determine that this vaccine was […]

Filed Under: GlaxoSmithKline, HIB, Meningitis Vaccines Tagged With: FDA approval, GSK, Haemophilus b vaccine, meningococcal groups C and Y

SaneVax Writes Open Letter to Kathleen Sebelius, Secretary of Health: Rescind approval of Gardasil® due to lack of efficacy during post-licensure monitoring

February 2, 2012 By Norma 7 Comments

      By Norma Erickson, President. According to a recently published, industry-sponsored study conducted on 12,852 young women, HPV vaccination was found to reduce HPV-16 infections a mere 0.6% in vaccinated women versus unvaccinated women. At the same time, other high-risk (carcinogenic) HPV infections were diagnosed in vaccinated women 2.6% to 6.2% more frequently […]

Filed Under: SANE Vax Press Releases Tagged With: FDA approval, Gardasil, HHS, Kathleen Sebelius, lack of efficacy, rescind approval

FDA approves Roche HPV test to identify cervical cancer risk

April 21, 2011 By Norma Leave a Comment

Submitted by Mechele R. Dillard The U.S. Food and Drug Administration has approved a test identifying women at highest risk for cervical cancer. The U.S. Food and Drug Administration has approved the Roche cobas HPV(Human Papillomavirus) Test, which identifies women at highest risk for cervical cancer. It can potentially help doctors make earlier, more accurate […]

Filed Under: FDA, HPV Science, Women's Health Tagged With: FDA, FDA approval, HPV test, HPV test approved, PCR sequencing

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This Week’s Survivor

Gardasil Changed Our Definition of Normal

Categories

Links

  • Creating an HPV Industry
  • File a VAERS Report
  • Gardasil and Unexplained Deaths
  • HPV Industry Timeline
  • HPV Mechanisms of Action in Women
  • HPV Vaccine Fact Sheet
  • Petition: Rescind HPV Vaccine Approval
  • Presentation to the FDA
  • Supreme Court Arguments

HPV Vaccine VAERS Reports

Description 12/14/2019  TOTAL
Disabled 3,092
Deaths 523
Did Not Recover 13,072
Abnormal Smear 695
Cervical Cancer 186
Infertility 52
Life-threatening 1,001
Emergency Room 15,419
Hospitalized 6,448
Extended Hosp. Stay 304
Serious 9,497
Total Adverse Events 64,270

Access expanded report here.

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