We hear a lot about vaccine studies not using the right placebos or any placebo at all.
The critical difference between using an inert and non-inert substance as a control can be clearly seen from the trials relied upon to license Gardasil in 2006.
The manufacturer’s package insert for Gardasil states that it was licensed based on a clinical trial in which:
- 10,706 women received Gardasil;
- (ii) 9,092 women received 225 mcg or 450 mcg of Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) – the so-called “AAHS Control” (aluminum adjuvant, such as AAHS, is a known cytotoxic and neurotoxic substance used to induce autoimmunity in lab animals, and which numerous peer-reviewed publications implicate in various autoimmune conditions58); and
- (iii) 320 women received a “Saline Placebo.”
During the six-month study follow-up, 2.3% of the women receiving Gardasil (the “test group”) and 2.3% of the women receiving the AAHS Control or Saline Placebo (the “combined control group”) reported developing a systemic autoimmune disorder.
Since the rate of systemic autoimmune disorders in the “test group” and the “combined control group” were similar, the vaccine was deemed safe and licensed by Health and Human Services (HHS).
What the manufacturer’s package insert for Gardasil given to the public failed to disclose is that the Saline Placebo group had zero cases of systemic autoimmune disorder (when 7 cases – 2.3% of 320 subjects – would be expected if autoimmune disorders were equally distributed among the Saline Placebo and AAHS Control recipients).
You can look yourself at this link:
This fact was obfuscated by combining the small Saline Placebo group with the large AAHS Control group into a single control group and reporting their combined systemic autoimmune disorder rate, even though all the cases of autoimmunity came from the AAHS control group as you can see:
The fact that the Saline Placebo group had no cases of systemic autoimmune disorder is what would be expected.
It is not normal for 2.3% of previously healthy girls and women to develop a systemic autoimmune disorder within six months of the commencement of a clinical trial unless there was some environmental exposure that caused the harm, such as an injection of Gardasil or AAHS. This finding is nonetheless ignored because, to license this vaccine, HHS permitted AAHS to serve as the control, which is completely ridiculous. They knew aluminum was a problem, so they compared aluminum vs. aluminum in order to mask or hide any potential side effects.
It was also unethical to inject almost 10,000 girls and women with a known neurotoxin like AAHS, which has no therapeutic benefit.
The transparent purpose of this unethical study design was to create a “control group” that would yield a similar adverse event rate to the “test group” receiving Gardasil.
In this manner, the trial masked a serious safety issue with Gardasil that should have prevented its licensure.
Furthermore, there was no excuse for not requiring a placebo control (saline injection) in clinical trials for Gardasil because, at that time, no other vaccine was yet licensed for the four HPV strains Gardasil was intended to prevent.
The Gardasil licensing process was purely criminal.
Gardasil is most likely the worst vaccine ever produced!
It has never been tested properly and some countries like Japan removed it from their vaccination schedule.
On top of that, the HPV virus has never been shown to cause cervical cancer. Actually, the evidence we have so far supports that this virus is not implicated at all. I will come back to this point in a few minutes
But first, the most commonly reported side effects with Gardasil are pain, swelling, and redness at the injection site, nausea, headache, fever, fatigue, and muscle or joint pain.
The CDC is working with researchers to follow up on two neurological deaths after HPV vaccination, and the CDC and FDA are both undertaking studies on the link between the HPV vaccine and fainting and blood clots
Dr. Bernard Dalbergue stated:
“Gardasil will become the greatest medical scandal of all
times because at some point in time, the evidence will add up to prove
that this vaccine, technical and scientific feat that it may be, has absolutely
no effect on cervical cancer and that all the very many adverse effects which
destroy lives and even kill, serve no other purpose than to generate profit for
The Vaccine Adverse Events Reporting System shows the following adverse reactions to Gardasil (as of April 2019):
Did Not Recover 11,507
Abnormal Pap Smear 648
Cervical Dysplasia 304
Cervical Cancer 135
Admitted to Emergency Room 15,278
Extended Hospital Stay 429
Serious Adverse Events 8,343
Total Adverse Events 57,287
The VAERS is a voluntary reporting system with about 1% of
issues being reported. In other words, these numbers could be much worse!