The first key deception occurred during Gardasil trials. Instead of using a saline solution as the placebo, Merck used the vaccine’s carrier agent minus only the HPV virus components. In addition to sodium chloride and water, the placebo contained aluminum, polysorbate 80 and sodium borate.
Although polysorbate 80 is used as a food additive to increase the water solubility of oils, injection is quite different. According to the Polysorbate 80 Material Safety Data Sheet, it may be both carcinogenic and mutagenic. When injected into prepubescent rats, polysorbate 80 caused abnormal growth of reproductive organs and made the rats sterile. When used intravenously with vitamins it has caused anaphylactic shock.
Sodium borate is widely known as a roach pesticide. The U.S. National Library of Medicine and the National Institutes of Health declared sodium borate to be a dangerous poison. Due to deaths from its use for disinfecting wounds and cleaning nurseries, its medical use had been discontinued – until Gardasil came along. Side effects include: vomiting, diarrhea, skin rash, blisters, collapse, coma, convulsions, drowsiness, fever, lack of desire to do anything, low blood pressure, decreased urine output, sloughing of the skin and twitching of facial muscles, arms, hands, legs, and feet.
An analysis of the actual Gardasil trial data reveals that a shocking 73.3 percent of the participants who received Gardasil acquired a new medical condition ranging from flu-like symptoms to paralysis. Almost 60% had systemic reactions. Though the “placebo” recipients had similar results, obviously no mere saline solution would have produced even a fraction of such reactions. The results would likely have been even higher if the study had lasted longer than 15 days.
Other factors which help skew the picture of Gardasil dangers include:
*The rate of deaths and adverse reactions are reported as a percentage of doses distributed, not doses actually administered.
*Gardasil is given in a series of three injections. Thus the number of adverse reactions per number of patients is triple the adverse events per injection.
*Many parents are not aware of the definition of adverse event or that they can file their own VAERS report.
Already reported deaths and reactions may also be being hidden or altered. When SANEVAX looked at the latest reported VAERS totals, they discovered that five previous death cases were now inexplicably missing.