Home
SANEVAX ASKS SECRETARY OF HEALTH RESCIND APPROVAL OF GARDASIL Print E-mail

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 than in the unvaccinated women. The increased rate of infections caused by carcinogenic HPV types other than those targeted by Gardasil® in vaccinated women is 4 to 10 times higher than the reduction in HPV 16/18 infections.[1]

These statistics are not exactly encouraging when it comes to demonstrating efficacy for Gardasil®. In fact, quite the opposite – these figures seem to indicate that women who receive Gardasil® may indeed increase their risk of developing cervical cancer from high-risk HPV types that are not targeted by the vaccine.

Medical consumers cannot afford to take the chance of increasing their risk of contracting a disease that has been virtually eradicated by good gynecological care in the United States (cervical cancer) by taking a series of HPV vaccines and hoping they will find out decades later the vaccine worked. It is certainly not a risk children should have to take.

Armed with the knowledge that any drug approved under the FDA’s accelerated approval process using a surrogate endpoint, such as Gardasil®, requires post-marketing studies “to verify and describe the drugs clinical benefit and to resolve remaining uncertainty as to the relation of the surrogate endpoint upon which approval was based to clinical benefit…[2],” the SaneVax Team felt compelled to appeal to the person in charge of FDA/CDC oversight, Kathleen Sebelius, Secretary of Health and Human Services.

On 31 January 2012, SaneVax Inc. sent an open letter to Ms Sebelius[3] asking her to rescind approval for Gardasil® based on the lack of efficacy demonstrated in the ATHENA study referenced above.

If the Department of Health and Human Services is truly interested in public health and safety, they will do the right thing and rescind Gardasil® approval until the manufacturer can provide scientifically sound data proving this new drug is actually effective.

In the meantime, medical consumers around the globe have a choice. Is poke and hope good enough for you and your children? Or, are you going to demand scientific proof of efficacy before submitting to HPV vaccination?



[1] http://www.ncbi.nlm.nih.gov/pubmed/21944226 (see table 3, The ATHENA human papillomavirus study: design, methods, and baseline results.)

[2] http://www.fda.gov/ohrms/dockets/ac/03/

briefing/3936B1_01_B-Attachment%201.pdf (57 FR 58942)

[3] Copy of letter to Kathleen Sebelius,

Secretary of Health and Human Services

 
GARDASIL - BIG PHARMA KILLING US SOFTLY Print E-mail

By | January 25th, 2012

With complete disregard for the welfare and safety of the people who take their products, the pharmaceutical industry has made a habit of putting profits above all else. Despite a track record of bringing us drugs that kill and maim, such as Vioxx, AZT, Fen Phen, and Thalidomide, there is never an apology, never a commitment to improve, never even an acknowledgement that they have done anything wrong. Now, as if we have learned nothing from history, the drama is unfolding yet again, this time with Gardasil.

Gardasil, the human papillomavirus vaccine produced by Merck, was brought to market in 2006 with great fanfare, widely proclaimed as the first ever anti-cancer vaccine. Merck created a market for Gardasil out of thin air with deceptive and dishonest advertising,[1] and thereby planted fear in the mind of consumers: fear of an enormous, yet unknown health crisis, an invisible time bomb waiting to explode and harm women everywhere. When criticized for their aggressive marketing, Merck countered that they were performing a public service by raising awareness about the human papillomavirus and weren’t selling anything.[2] Really?

This lie became public as Merck was caught lobbying the 50 states for mandatory Gardasil vaccination before it had even secured FDA approval![3] The fact is that there was never a need for Gardasil in the first place: regular Pap testing had already lowered the incidence of cervical cancer by 80% in the US to a few thousand cases a year and the vast majority of all HPV infections resolve of their own accord.[4]

But by lining the coffers of such groups as Women in Government (WIG), and, of course, the American Legislative Exchange Council (ALEC), Merck was able to influence legislation such that almost immediately after the vaccine was approved, it was part of the vaccine schedule recommended for all girls.[5] If it hadn’t been for Governor Rick Perry’s blunder of trying to mandate Gardasil for school attendance in Texas in the face of huge conflict of interest and a $50 million contribution to his presidential campaign, Gardasil might have gone even further.[6]

There is something deeply wrong with a giant pharmaceutical company spending hundreds of millions of dollars to manipulate women and influence legislation in order to generate a revenue stream of billions of dollars a year for themselves at the expense of a gullible public. Because what is wrong with Gardasil isn’t just that it is unnecessary. Gardasil is possibly the most dangerous vaccine on the market with the potential to injure, maim, or even kill the children who receive it.

The program of coercion to vaccinate every 11 to 26 year-old girl with Gardasil is relentless. This vaccine is given not just in doctor’s offices, where doctors have been known to “fire” non-compliant patients, but in schools and colleges, where the pressure on girls and their parents to conform can be extreme. These institutions all have quotas — sometimes including financial rewards — and they are anxious to prove high rates of compliance.[7]

But there is no informed consent prior to vaccination, so most of these girls and their parents have no idea what they are risking by agreeing to vaccination with Gardasil. While Merck, the FDA, the CDC and the medical establishment all deny that there have been serious, life-altering adverse events associated with Gardasil, the fact is that compared with the mandated vaccines which are given with greater frequency, Gardasil still has the most adverse events reported to the Vaccine Adverse Event Reporting System (VAERS) of any vaccine. And since reporting of adverse events is not mandatory in the US (although outbreaks of so-called vaccine-preventable illness are), it is likely that only 10% even get reported![8]

Read more...
 
GSK lab fined over vaccine tests that killed 14 babies Print E-mail

POSTED 6 January 2012

GlaxoSmithKline Argentina Laboratories company was fined 400,000 pesos ($93,000USD) by Judge Marcelo Aguinsky following a report issued by the National Administration of Medicine, Food and Technology (ANMAT in Spanish) for the killing of 14 babies during illegal lab vaccine trials conducted between 2007 and 2008.

Likewise, two doctors -Héctor Abate, and Miguel Tregnaghi- were fined with 300,000 pesos each for irregularities during the studies.

The charges included experimenting with human beings, falsifying parental authorizations so babies could participate in vaccine-trials conducted by the laboratory from 2007 to 2008.

Since 2007, 15,000 children under the age of one from Mendoza, San Juan and Santiago del Estero have been included in the research protocol, a statement of what the study is trying to achieve. Babies were recruited from poor families that attended to public hospitals.

A total of 7 babies died in Santiago del Estero; 5 in Mendoza; and 2 in San Juan.

Pediatrician Ana Marchese, who reported the case through the Argentine Federation of Health Professionals (FESPROSA in Spanish), and was working at the Eva Perón children's public hospital in Santiago del Estero when the studies wee being conducted, said this morning in conversations with Continental AM radio that “GSK Argentina set an protocol at the hospital, and recruited several doctors working there.”

“These doctors took advantage of many illiterate parents whom take their children for treatment by pressuring and forcing them into signing these 28-page consent forms and getting them involved in the trials.”

“Laboratories can't experiment in Europe or the United States, so they come to do it in third-world countries."

Colombian and Panama were also chosen by GSK as staging grounds for trials of the vaccine against the pneumococcal bacteria.

Likewise, Marchese, explained the modus operandi: “Once a picked patient arrived, it would automatically disappear to be taken somewhere else in order to be treated by those doctors specially recruited by GSK. These kind of practices are not legal and occurred without any type of state control, plus they don’t comply with minimum ethical requirements.”

Marchese also remembered that “laboratory trials on human beings are not legalized in Argentina.”

Furthermore, the pediatrician explained that “it is also known that in various particular cases, the doctors who had conducted the trials did not answer the calls made by the worried parents after witnessing their babies’ reactions to the vaccines.”

According to Marchese, “there already exist very good vaccines for the same diseases, but we all know how laboratories work, they only care for their own business.”

To end, Doctor Marchese aimed to Santiago del Estero Governor, Gerardo Zamora, who “never ever came out to stage to comment on the case, and same happened with national deputies and senators that didn’t even bother into discussing a hot topic that was echoed worldwide. I’m also ashamed of the scientific community that also kept its mouth shut.”

Read more...
 
HPV VACCINE & EVIDENCE BASED MEDICINE-ARE THEY AT ODDS? Print E-mail

Natural News

Wednesday, January 11, 2012
by: Rosemary Mathis, Vice President of Victim Support, SANE VAX, INC.

Written by Norma Erickson & Leslie Carol Botha

On January 12, 2011 the Annals of Medicine published a ground-breaking peer-reviewed paper titled, Human papillomavirus (HPV) vaccine policy and evidence-based medicine: Are they at odds?, 1written by renowned researchers Lucija Tomljenovic, Ph.D., and Christopher Shaw, Ph.D., with the Neural Dynamics research Group, University of British Columbia, in Vancouver. 2.

The article points out to the medical community what most consumers now know about the fraudulent global health agency policies in combination with the pharmaceutical companies lack of science based evidence demonstrating the safety and efficacy of Gardasil and Cervarix before they were unleashed on unsuspecting parents of adolescents.

Clinical Trials on Healthy People vs. Mass Vaccination Campaigns

Tomljenovic and Shaw clearly state the obvious in their abstract by stating that vaccines represent 'a special category of drugs generally given to healthy individuals and therefore a small level of risk for adverse reactions is acceptable.'

Merck's clinical trials were flawed because they used an aluminum adjuvant as a 'placebo' and only used saline as a comparative for minor, non-serious adverse reactions. With serious adverse reactions, they pooled the results from the saline group and the aluminum 'placebo' group. By doing this, they concealed the true rate of serious reactions.

If FDA approved drugs and vaccines were as safe and effective as Pharma would like consumers to believe the risk level should be negligible to none. The FDA removal of drugs after they have been on the market and damaged desperate people looking for cures who then have to file lawsuits to recover damages is simply unacceptable.

Medical Ethics Questioned

The authors also point out the myth of informed consent - basically a waiver signed by medical consumers that they have been 'educated' about the risk vs. benefit ratio of the drug about to be administered. Tomljenovic and Shaw open their paper citing that 'medical ethics demand that vaccination be carried out with the participant's full and informed consent' and not just the handing out of the HPV vaccine Patient Product Insert - prepared by none other than the vaccine's manufacturer.

What the authors do not cover in this paper is what happens to informed consent when governments grant children the right to consent to medical procedures, such as California's recent passage of AB 499 - basically granting parental rights of children ages 12 and older to the state for the treatment of STD's. Is it really because the 'state' knows better - or is it because legislatures have been paid off by the pharmaceutical companies?

The authors go on to state:

"What is more disconcerting than the aggressive marketing strategies employed by the vaccine manufacturers is the practice by which the medical profession has presented partial information to the public, namely, in a way that generates fear, thus promoting vaccine uptake.........It thus appears that to this date, medical and regulatory entities worldwide continue to provide inaccurate information regarding cervical cancer risk and the usefulness of HPV vaccines, thereby making informed consent regarding vaccination impossible to achieve."

Read more...
 
MY UNVACCINATED CHILDREN ARE ALIVE AND MY VACCINATED SON IS DEAD Print E-mail

BY:- Stephanie Messenger

This is my journey….

I can’t say I believed in vaccination. I knew nothing about it, but had it done anyway. It’s what you do, right? You do what doctors and baby health clinics tell you and what your parents and the media advise you to do. Well I did it, without so much as a question or thought into it. Within moments of my son receiving his immunisations he was screaming. This continued for most of the day and when he wasn’t screaming he was crying. This was unusual as he was a very happy, placid baby, who was already rolling over at 8 weeks and gooing and gahing at the first sight of his mother. The doctor told me his reactions were ’normal’ and he’d be OK in a couple of days.

After the first day he had almost recovered with only some irritability and restlessness noticeable. As the weeks passed he continued to reach milestones and all appeared Ok.

At 4 months of age I dutifully took him for his next round of vaccinations. This time he screamed louder and I could not console him at all. I would breastfeed him, only to have him projectile vomit it back up and still the screaming continued. He had never before vomited at all, ever. After he had vomited 2 feeds I called the doctor and told her what was happening and she said to stop breastfeeding and give him juice only. He kept some of it down but still vomited often.

The next day I called the doctor and told her I think the vaccines have done this and she told me ’ no, it’s just a coincidence’ but to bring him back in, which I did. She referred me to a specialist. While waiting for the specialist appointment in a few days, my baby boy started doing strange things. He started arching his back and crying out in pain. He was as stiff as a board. His eyes would roll into the back of his head. He didn’t have a temperature. He had also started shuddering but he wasn’t cold. (I later learnt from the doctor these were convulsions and seizures). The vomiting continued and I was convinced to give up breastfeeding by the clinic sister. He vomited up the formula also. I was getting very scared.

We went to the specialist appointment and he took some blood for tests and then we had to wait. His symptoms continued and after several days word came from the specialist that the tests showed he was allergic to wheat. I stopped giving him the cereal I had started him on weeks before, but none of the symptoms went away. (when I thought about it later, it was actually rice cereal anyway)

I decided to move to a large city to get more help. Once I saw a doctor there he was immediately admitted to hospital for a battery of test – many of which were conducted under anaesthetic, which of course required my signature to say I have been notified that my baby could die while under. I had not been advised of this, but I signed it not knowing all the medical jargon as I needed to get my baby well again and trusted they knew what they were doing.

By this time my dear little son had lost a lot of weight and nothing I was doing (under advice from doctors and baby health clinics) was working.

After months of tests in the hospital (he stayed there) we were summoned in to an office to be told that they ’didn’t know why my baby was deteriorating, but they estimate he will pass away within a couple of months’.

Soon after I took my baby home to die.

Read more...
 


Page 1 of 10

© Copyright Off The Radar | Supplied by SPF Websites