Dr. Scott Gottlieb FDA Food gardasil Headline HPV vaccine Medicine Watch

Public Petitions FDA to Investigate Gardasil Vaccine Fraud



by SaneVax, Inc.

The next open letter to FDA Commissioner, Dr. Scott Gottlieb, calling for quick investigations into many sides of the medical trials for Gardasil sponsored by Merck was emailed immediately.

In case you help this request, please depart a word within the remark part right here that features your identify, title, and group. Assist the FDA perceive how deeply involved you’re concerning the sanity of HPV vaccination packages.


Dr. Scott Gottlieb
Meals and Drug Administration Commissioner
10903 New Hampshire Avenue
Silver Spring, MD 20993-0002

November 9, 2018

Pricey Dr. Gottlieb:



Gardasil Vaccine Medical Trial Investigation

This open letter, written on behalf of medical shoppers all over the world, is an pressing request for you to examine potential malfeasance perpetrated by Merck throughout their medical trials of Gardasil, the human papillomavirus vaccine that the FDA accepted in June 2006. A brand new guide, The HPV Vaccine on Trial: In search of Justice for a Era Betrayed, by Holland, Rosenberg, and Iorio, outlines at the very least 4 areas requiring the FDA’s pressing consideration. (A replica has been despatched to you underneath separate cowl.)

Protocol V501-018

Protocol V501-018 was the one managed trial within the goal age group of 9-15-year-olds. This Protocol is the idea for the one long-term security and effectiveness analysis on this inhabitants. Pediatric Infectious Illness Journal and Pediatrics have revealed outcomes suggesting that the vaccine is protected and efficient after ten years of use. Nevertheless, the FDA’s June 2006 Medical Evaluate Desk 210 (Appendix I) exhibits that the vaccine formulation in Protocol 018 contained solely half the quantity of Merck’s adjuvant amorphous aluminum hydroxyphosphate sulfate (AAHS) in contrast to marketed Gardasil. This failure to examine the marketed vaccine, containing 225 mcgs of AAHS, towards the service answer management, suggests the intent to mislead. It additionally suggests reckless overexposure of youngsters worldwide who acquired the marketed vaccine to double the AAHS quantity in Protocol 018, serving to to clarify the excessive degree of reported accidents and deaths worldwide. An rising scientific consensus finds that aluminum-containing vaccine adjuvants, together with AAHS, doubtless trigger a myriad of great well being issues. (Appendix II).

New Medical Circumstances

About half of all medical trial individuals for Gardasil and Gardasil 9 reported “new medical conditions” throughout or instantly after receiving the vaccine collection. (Appendix III). “New medical condition” just isn’t an outlined time period in Merck’s research protocol.  How is the FDA sure that “new medical conditions” that emerged after vaccination will not be merely antagonistic reactions in disguise? What documentation did trial investigators present to the FDA for “new medical conditions” as in contrast to “adverse reactions” or “adverse events”? How did the FDA consider these circumstances in half of all beforehand wholesome trial members?

Protocol 015 Deprivation of Knowledgeable Consent

Documentation in HPV Vaccine on Trial exhibits that medical trial topics in Denmark acquired false details about Gardasil security and the placebo used. The authors present proof from two medical trial topics, who reported that they didn’t give knowledgeable consent due to the false info they acquired concerning the placebo and vaccine security profile. The deprivation of knowledgeable consent to these and probably different topics calls into query the ethics and legality of the medical trials.

Use of an Undisclosed and Unapproved Adjuvant

The FDA has beforehand acknowledged that Gardasil accommodates HPV DNA fragments, regardless of earlier denials. Dr. Sin Cling Lee, who first detected the DNA fragments in each tissue samples and Gardasil vials, has theorized that these fragments are TLR9 agonists appearing as an adjuvant, additional boosting the vaccine’s immunogenicity. This extra undisclosed and unapproved adjuvant, together with the AAHS adjuvant, makes the vaccine probably extra poisonous and harmful. Merck filed a TLR9 agonist vaccine adjuvant patent and joined with different corporations to broaden this adjuvant’s business use. Dr. Lee has testified to the Nationwide Vaccine Damage Compensation Program on accidents arising from this undisclosed adjuvant. What’s the FDA’s information of this know-how and its use within the Gardasil vaccine?

Every of the problems famous above – Protocol 018, “New Medical Conditions,” Protocol 015 Deprivation of Knowledgeable Consent, and Use of an Undisclosed and Unapproved Adjuvant – name into query the security, ethics, effectiveness, and legality of Gardasil and Gardasil 9.  We’re gravely involved that the FDA failed to evaluation the Gardasil medical trials with enough rigor.

We hope to hear from you within the close to future relating to a reopened, thorough investigation of the Gardasil medical trials. Medical shoppers worldwide will anxiously await your response.

Sincerely yours,

Norma Erickson,

President, SaneVax, Inc.

View attachments to this letter right here.

Learn this letter in Spanish right here.

Learn the complete article at SaneVax.org.

Touch upon this text at VaccineImpact.com.


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Dr. Andrew Moulden: Each Vaccine Produces Hurt


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Canadian doctor Dr. Andrew Moulden offered clear scientific proof to show that each dose of vaccine given to a toddler or an grownup produces hurt. The reality that he uncovered was rejected by the traditional medical system and the pharmaceutical business. However, his warning and his message to America stays as a strong legacy of the person who stood up towards massive pharma and their program to vaccinate each individual on the Earth.

Dr. Moulden died unexpectedly in November of 2013 at age 49.

Due to the robust opposition from massive pharma regarding Dr. Moulden’s analysis, we turned involved that the identify of this sensible researcher and his life’s work had almost been deleted from the web. His status was being disparaged, and his message of warning and hope was being distorted and buried and not using a tombstone. This ebook summarizes his educating and is a must-read for everybody who needs to study the “other-side” of the vaccine debate that the mainstream media routinely censors.

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E-book – The Vaccine Courtroom, by Wayne Rohde – 240 pages

“The Dark Truth of America’s Vaccine Injury Compensation Program”

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Massive Pharma and authorities well being authorities try to cross legal guidelines mandating vaccines for all youngsters, and even adults.

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Revealed on November 11, 2018

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