he Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Tuesday, Oct. 26, approved the emergency use of Pfizer’s Wuhan coronavirus (COVID-19) vaccine for children aged five to 11. But during the eight-hour discussion, one doctor made a shocking admission: There was no way to guarantee how safe a vaccine is unless you start giving it to people.
Are vaccines really safe?
Six hours into the conference, Dr. Eric Rubin, editor-in-chief of the New England Journal of Medicine, commented on how widespread the rollout of the coronavirus vaccine should be.
Rubin admitted that despite Big Pharma’s insistence that coronavirus vaccines are safe and that they are key to ending the pandemic, it’s impossible to find out how safe the vaccines are unless they’re administered first. He added that this is usually the case for vaccines and their many side effects and rare complications.
Vaccines and Related Biological Products Advisory Committee – 10/26/2021
Join the U.S. Food and Drug Administration for an upcoming meeting of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) to discuss newly available data for the currently available COVID-19 vaccines. The committee will meet to discuss a request to amend Pfizer-BioNTech’s Emergency Use Authorization (EUA) for administration of their COVID-19 mRNA vaccine to children 5 through 11 years of age.
The Food And Drug Administration (FDA) approved an emergency use authorization for the Pfizer-BioNTech vaccine for children as young as 5 years old despite the fact that its Pfizer-connected advisory committee knew about numerous adverse events that were reported in Pfizer’s clinical trials for children, including adverse events that were determined to be “related” to the clinical vaccine trial.
The Briefing Packet for the FDA advisory committee meeting shows that the FDA advisers used clinical studies sponsored by BioNTech and conducted by or supported by Pfizer to approve the vaccine for young children.
ON PAGE 39 the FDA document states (emphasis added):
“Lymphadenopathy is considered an adverse reaction to vaccine and is noted as such in the EUA Fact Sheet. Among approximately 2250 children 5 to <12 years of age randomized 2:1 to receive BNT162b2 or placebo, as of the data cutoff date (06 September 2021), 13 participants (0.9%) in the BNT162b2 group and 1 participant (0.1%) in the placebo group had events of lymphadenopathy.” Lymphadenopathy is a lymph nodes disease. On page 40 the document states that “Lymphadenopathy has been identified as related to BNT162b2 in individuals ≥12 years of age and it is also observed in the pediatric 5 to <12 years of age group.” The document states that “One participant in the BNT162b2 group had a related AE of mild arthralgia (right elbow joint pain), with an onset the same day as Dose 2 (administered in the left deltoid muscle), that was reported as resolved the next day.” The document states that “One participant in the BNT162b2 group had a related AE of moderate paresthesia (bilateral lower extremity tingling) with onset at 1 day post-Dose 2 and reported as recovered/resolved 3 days after onset.” The document states that “In the BNT162b2 group, a psychiatric disorder event of tic was reported in 1 participant: One participant in the BNT162b2 group had an AE of Grade 3 tic with onset at 7 days post Dose 2 and reported as recovering/resolving at the time of the data cutoff. The AE was considered by the investigator as related to study intervention.” The document later notes that “There were 6 participants (0.4%) in the BNT162b2 group and 3 participants (0.4%) in the placebo group had events of lymphadenopathy.”
On PAGE 42 the document states that a trial participant dropped out of the trial due to an Adverse Event, stating “One participant (0.1%) in the BNT162b2 group discontinued from the vaccination period due to an AE (details in Section 3.7.2) and two participants (0.1%) in the BNT162b2 group and 1 participant (0.1%) in the placebo group withdrew from the study before the 1-month post Dose 2 visit. Neither of these withdrawals was reported as due to an AE.”
One participant had blood that passed through his/her anus, which is known as hematochezia, characterized by bloody stool. The document states that “One participant in the BNT162b2 group had a non-serious related AE reported by the investigator as moderate hematochezia 4 days after Dose 2. The participant had heme occult positive stool; was seen in the emergency department, and had no further tests done; and went home and the event resolved the same day without sequelae. This participant had a medical history of asthma and nondrug allergy and had no other reported AEs.”
Health workers in Syria rush to vaccinate 320,000 children amid sudden polio outbreak
One of the cases is in Raqqa – Isis’s de facto capital
Health officials in Syria are scrambling to urgently vaccinate 320,000 children in some of the country’s most difficult to access areas, following an outbreak of polio that has left at least 22 children paralysed. Health workers will likely have to coordinate with Isis and other extremist groups to carry out the work.
It was recently revealed that 17 children had been affected by an outbreak of vaccine-derived polio.
One of the cases was in Raqqa, the de facto Syrian capital of Isis, while the remainder were in the Mayadeen district of eastern Syria.
SIDS Listed As Adverse Reaction on DTaP Vaccine Insert plus others
What is Sudden Infant Death Syndrome (SIDS)?
Sudden Infant Death Syndrome (SIDS) is when a child suddenly stops breathing and dies. It normally happens during sleep. According to the Centers For Disease Control, SIDS is rare, only occurring in less than 3,000 babies per year, and only 1,500 in 2013.
The problem with the above chart and statistics is that these numbers are not even remotely accurate. Again, we are first looking at this from a conscious parents’ perspective. We do not take “It just happens” as an acceptable answer and we do not take “Unknown Cause” as an acceptable answer. After the “Back To Sleep” Campaign launched in 1994, SIDS cases seemed to plummet. But what isn’t publicized is that after that campaign launched, causes of death titles were also changing from “SIDS” to “Unknown Causes” and a plethora of other titles. The percentages of “Unknown Causes” or other muddled titles went up, and the SIDS rates went down.
According to The CJ Foundation For Sids, fewer and fewer medical examiners and coroners are using SIDS (Sudden Infant Death Syndrome) as a cause of death. While the definition of SIDS is: “sudden death of an infant under one year of age which remains unexplained after a thorough case investigation, including performance of a complete autopsy, examination of the death scene and review of the clinical history,” the word “syndrome” incorrectly implies a diagnoses or illness, when it is in fact a diagnosis of exclusion. There are no clinically significant findings that indicate cause of death.
Five years ago, your baby’s cause of death probably would have been ruled SIDS. The fact that there is no national standard for terminology for these types of infant deaths AND that medical examiners/ coroners are increasingly reluctant to use SIDS as a cause of death has led to parental and bureaucratic confusion. The CDC’s National Center for Health Statistics lists ALL of the following as definitions of SIDS for coding purposes:
Sudden Death in Infancy or SDII
Sudden Infant Death or SID
Sudden Unexplained Death or SUD
Sudden Unexplained (unexpected) Death in Infancy or SUDI
Sudden Unexplained Infant Death or SUID
Sudden plus (Unexpected) or (Unattended) or (Unexplained)
Death plus (Cause Unknown) or (in Infancy) or (Syndrome)
Infant Death plus (Syndrome)
Presumed SIDS, Probably SIDS, Consistent with SIDS
The 1918 Influenza Epidemic was a Vaccine-caused Disease
Posted on July 11, 2009 by Barbara Peterson
I. Honorof, E. McBean (Vaccination The Silent Killer p28)
Source: Dr. Rebecca Carley
Very few people realize that the worst epidemic ever to hit America, the Spanish Influenza of 1918 was the after effect of the massive nation-wide vaccine campaign. The doctors told the people that the disease was caused by germs. Viruses were not known at that time or they would have been blamed. Germs, bacteria and viruses, along with bacilli and a few other invisible organisms are the scapegoats, which the doctors like to blame for the things they do not understand. If the doctor makes a wrong diagnosis and treatment, and kills the patient, he can always blame it on the germs, and say the patient didn’t get an early diagnosis and come to him in time.
If we check back in history to that 1918 flu period, we will see that it suddenly struck just after the end of World War I when our soldiers were returning home from overseas. That was the first war in which all the known vaccines were forced on all the servicemen. This mish-mash of poison drugs and putrid protein of which the vaccines were composed, caused such widespread disease and death among the soldiers that it was the common talk of the day, that more of our men were being killed by medical shots than by enemy shots from guns. Thousands were invalided home or to military hospitals, as hopeless wrecks, before they ever saw a day of battle. The death and disease rate among the vaccinated soldiers was four times higher than among the unvaccinated civilians. But this did not stop the vaccine promoters. Vaccine has always been big business, and so it was continued doggedly.
It was a shorter war than the vaccine-makers had planned on, only about a year for us, so the vaccine promoters had a lot of unused, spoiling vaccines left over which they wanted to sell at a good profit. So they did what they usually do, they called a meeting behind closed doors, and plotted the whole sordid program, a nationwide (worldwide) vaccination drive using all their vaccines, and telling the people that the soldiers were coming home with many dread diseases contracted in foreign countries and that it was the patriotic duty of every man, woman and child to get “protected” by rushing down to the vaccination centers and having all the shots.
Healthy 12-year-old girl dies shortly after receiving HPV vaccine
Friday, September 26, 2014 by: Ethan A. Huff
(NaturalNews) Another young girl has died from Gardasil, the infamous HPV vaccine manufactured by Merck & Co., and the medical establishment claims that it was a fluke. Twelve-year-old Meredith Prohaska from Waukesha, Wisconsin, died just a few hours after getting her Gardasil shot, and her parents are sure that the vaccine was the cause of death.
According to FOX6Now.com, Meredith was an otherwise healthy, fun-loving girl prior to her death. She did have a sore throat the day that she died, which is why her parents took her to the doctor in the first place. But it was a minor ailment that, in light of the events of that fateful day, couldn’t possibly have killed her that quickly or coincidentally.
Reports indicate that Meredith’s parents took her to the doctor during the morning hours of August 7. Around 10:30 am, she received her first HPV vaccine, which about 30 minutes later appeared to lull her into a deep sleep. Meredith’s mother Rebecca recalls having had to repeatedly wake her up so she could make it through the day.
Later that afternoon at around 3:30 pm, Rebecca left the house for about 30 minutes to get some food. When she returned, she found her daughter lying on the floor unconscious, upon which she initiated CPR — Rebecca served as an EMT (emergency medical technician) for the National Guard for 14 years, so she knew what she was doing.
When the CPR failed, Rebecca immediately called 911, and Meredith was rushed to the hospital. But it was too late — the girl was pronounced dead upon arrival, without explanation.
There is NO Science that shows Vaccines Cause Autism, EXCEPT in ALL THESE Government Published Studies which show Vaccines Cause Autism
Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010. http://www.ncbi.nlm.nih.gov/pubmed/22531966
Comparing vaccination rates in 34 developed nations revealed a significant correlation between infant mortality rates and the number of vaccine doses infants receive. The U.S. requires the most vaccines and has the highest infant mortality
Research shows the more vaccines an infant receives simultaneously, the greater their risk of being hospitalized or dying compared to those receiving fewer vaccines
The earlier in infancy a child is vaccinated, the greater their risk of being hospitalized or dying compared to children receiving the same vaccines at a later time
Routine childhood vaccination is an important public health tool to reduce the morbidity and mortality associated with infectious diseases, but the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.
4,250% Increase in Fetal Deaths Reported to VAERS After Flu Shot Given to Pregnant Women
July 4, 2017
By Christina England
Documentation received from the National Coalition of Organized Women (NCOW) states that between 2009 and 2010 the mercury-laden combined flu vaccinations have increased Vaccine Adverse Events Reporting Systems (VAERS) fetal death reports by 4,250 percent in pregnant women. Eileen Dannemann, NCOW’s director, made abundantly clear that despite these figures being known to the Centers for Disease Control (CDC), the multiple-strain, inactivated flu vaccine containing mercury (Thimerosal) has once again been recommended to pregnant women as a safe vaccination this season.
Outraged by the CDC’s total disregard for human life, Ms. Dannemann accused the CDC of ‘willful misconduct,’ saying that they are responsible for causing the deaths of thousands of unborn babies. She stated that the CDC deliberately misled the nation’s obstetricians and gynecologists and colluded with the American Journal of Obstetrics and Gynecology (AJOG) to mislead the public by advertising the flu vaccine as a safe vaccine for pregnant women when they knew fully well that it was causing a massive spike in fetal deaths.
In a letter to Dr. Joseph Mercola, Ms. Dannemann wrote:
“Not only did the CDC fail to disclose the spiraling spike in fetal death reports in real time during the 2009 pandemic season as to cut the fetal losses, but also we have documented by transcript Dr. Marie McCormick, chairperson of the Vaccine Safety Risk Assessment Working Group (VSRAWG) on September 3, 2010, denying any adverse events in the pregnant population during the 2009 Pandemic season.” 
HIDING LIFE-OR-DEATH EVIDENCE
Because the H1N1 pandemic vaccine had never been tested on the pregnant population, and to lessen the intensity of fears of the unknown risks, Dr. Marie McCormick of the CDC was employed to keep track of all adverse events during the 2009 pandemic season, including those adverse events in the pregnant population. Dr. McCormick was responsible for sending monthly reports to the Secretary of the Health and Human Services (HHS), citing any suspicious adverse events.
According to Ms. Dannemann, NCOW has been unable to obtain access to these monthly reports. After sending a Freedom of Information Act request to the CDC, she was told that she may have to wait 36 months to access what should be published public reports.
The Mercola letter continues:
“The Advisory Committee on Childhood Vaccines (ACCV) and CDC were confronted with the VAERS data from NCOW on September 3, 2010, in Washington, D.C., and then again by conference call on September 10, and then again in Atlanta, Georgia, on October 28, 2010. On both September 3 and September 10, Dr. Marie McCormick clearly denied that there were any adverse events for pregnant women from the 2009 flu vaccine.”
HHS National vaccine advisory committee – Government admits vaccine fails #VaXism NEWS #MMR
For many parents, the commercial was offensive, for others, they considered it laughable. Some people in the comments even went so far as to say they contracted HPV even after taking the vaccine. In what is either bravery on the part of Merck, or a general lack of Internet awareness, the comments remain turned on which has led to Internet savages taking it to them as recent as this month.
For many, the ad is an oversimplification of an issue they consider to be much broader in scope. The HPV vaccine has been scrutinized for alleged side-effects in teens. Merck has, in essence, ignored all accusations with this advertisement which portrays parents as being perpetrators of cervical cancer. The comments show that parents are revolting in a public setting, which isn’t always the normal when it comes to vaccine controversies.
Former Merck Scientists Sue Merck Alleging MMR Vaccine Efficacy Fraud
Stephen A. Krahling and Joan A. Wlochowski, former Merck virologists blew the whistle by filing a qui tam action lawsuit — U.S. v Merck & Co. — in August 2010. The scientists allege that the efficacy tests for the measles, mumps, rubella vaccine (MMR) were faked. The document was unsealed in June, 2012.
This is a major federal case alleging fraud in vaccine testing; it encapsulates how medical research can be manipulated to achieve desired results, and why it may be wise to question the integrity and the validity of “science-based medicine.”
The suit charges that Merck knew its measles, mumps, rubella (MMR) vaccine was less effective than the purported 95% level, and it alleges that senior management was aware and also oversaw testing that concealed the actual effectiveness. According to the lawsuit, Merck began a sham testing program in the late 1990’s to hide the declining efficacy of the vaccine. The objective of the fraudulent trials was to “report efficacy of 95% or higher regardless of the vaccine’s true efficacy.”
According to Krahling and Wlochowski’s complaint, they were threatened with jail were they to alert the FDA to the fraud being committed.
In January 31, 2016, the court ordered that discovery, the process of gathering evidence, must be completed by 1 March 2017, over a year from now. The court also ordered that expert discovery needs to be completed by 31 October 2017.
Other motions must be filed by 20 December 2017. A motion for class action certification must be filed by 1 March 2018; and Merck must file its opposition to class certification by 5 April 2018.
The plaintiffs charge that Merck defrauded the U.S. for more than a decade by faking a vaccine efficacy rate of 95% even though the real rate was significantly lower.
“As the single largest purchaser of childhood vaccines (accounting for more than 50 percent of all vaccine purchasers), the United States is by far the largest financial victim of Merck’s fraud. But the ultimate victims here are the millions of children who every year are being injected with a mumps vaccine that is not providing them with an adequate level of protection against mumps. And while this is a disease the CDC targeted ts the single largest purchaser of childhood vaccines (accounting for more than 50 percent of all vaccine purchasers), the United States is byo eradicate by now, the failure in Merck’s vaccine has allowed this disease to linger with significant outbreaks continuing to occur,” the suit alleges. (Forbes June 6, 2012)
According to the suit, the objective of the fraudulent trials was to “report efficacy of 95% or higher regardless of the vaccine’s true efficacy.”
One Big Reason to Consider NOT getting the HPV Vaccine
Dr. Suzanne Humphries is a conventionally educated medical doctor who was a participant in the conventional hospital system from 1989 until 2011. Like a growing number of people in the medical community, Dr. Humphries began to question vaccines after continually hearing stories of patients who experienced severe adverse reactions after vaccination. Dr. Humphries has been a stalwart worldwide crusader for true health knowledge, lecturer and author since she walked away from her six-figure career in 2011.
Recently Dr. Humphries appeared alongside HighWire host Del Bigtree to spotlight bombshell information regarding the human papilloma virus (HPV) vaccine. The untested medical assumptions, research fraud, and dangers of the HPV vaccine are lengthy. Severe injuries and death among teenage girls and boys from the shot are mounting globally as regulatory and health agencies hide within the safe shadows of their long-debunked ‘safe and effective’ buzzwords refusing to acknowledge the failed HPV vaccine paradigm.
Perhaps one of the most concerning, and still not properly addressed, issues about the HPV vaccine is the use of Merck’s patented amorphous aluminum hydroxyphosphate sulfate (AAHS) adjuvant within the shot. Merck’s proprietary compound is used in the HPV vaccine because of its high potential to cause inflammation and antibody formation. However the structure of the AAHS is such that it traps and irreversibly binds the HPV viral DNA to its structure. The AAHS, with its HPV viral DNA along for the ride, is then able to slip into human cells at which point the foreign material lights up a bonfire of inflammation within the body. For reason’s unknown, Merck’s new  Gardasil 9 has more than double the amount of AAHS contained in the vaccine compared to its previous Gardasil product. The Food and Drug Administration has ignored direct requests to investigate and comment on the DNA fragments being attached to the aluminum adjuvant.
“I predict that 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 manufacturers.” Dr. Bernard Dalbergue 2014, former Merck physician
Polio: Vaccinated British man shed virus for 30 years
28 August 2015
A British man who was vaccinated against polio has been producing the virus for nearly 30 years.
He had an immune disorder that mean the weakened polio virus used to vaccinate him in childhood survived in his body.
Over time it has mutated into a form of the virus that can cause paralysis and he had no idea the jab had not worked.
Polio is only endemic in Pakistan, Afghanistan and Nigeria although Nigeria has now gone more than a year without a case.
The discovery was made by a team from the National Institute for Biological Standards and Control in Potters Bar, Hertfordshire.
They now warn that similar cases could trigger new outbreaks and hamper efforts to eradicate the disease.
They wrote in the journal PLOS Pathogens: “While maintaining high immunisation coverage will likely confer protection against paralytic disease caused by these viruses, significant changes in immunisation strategies might be required to effectively stop their occurrence and potential widespread transmission.”
The man had a full course of polio vaccinations, including three doses of weakened live virus at five, seven and 12 months old, followed by a booster when he was about seven.
He was later diagnosed with a condition that suppresses the immune system, affecting its ability to kill viruses in the gut.
Big Pharma’s Dirty Little Secret: Vaccine-Induced Autoimmune Injury
Posted on: Tuesday, May 17th 2016 at 6:45 am
Written By: Celeste McGovern
This article is copyrighted by GreenMedInfo LLC, 2016
Scientists reveal how a hyperactivated immune system can unleash disease
Bobby Hunter was 10 years old when his mother noticed her usually energetic boy was struggling to stay awake and he looked exhausted all the time. Then he began collapsing. Eventually Bobby was diagnosed with narcolepsy, a lifelong incurable condition where victims suddenly drop into deep dream sleep, sometimes a dozen times a day or more. It can be accompanied by bizarre and terrifying symptoms: waking hallucinations of demons, insomnia, sleep paralysis and a sudden loss of muscle control or cataplexy often triggered by strong emotions. Bobby now has to be accompanied everywhere he goes in case he falls unconscious; he’ll never bathe or drive or cross a street alone. But his case is particularly cruel. Now, he is a child who is afraid to smile or laugh because it might trigger an attack.
Bobby’s mother Amanda is adamant he first became ill after he received the nasal flu vaccine at his school. But could such a small thing cause such a devastating disorder?
Narcolepsy Nightmare Explained
This month at the 10th Autoimmunity Congress in Leipzig, Germany a leading pharmaceutical researcher presented his international team’s findings suggesting that vaccination could indeed have the “unexpected” effect of inducing crippling narcolepsy, an autoimmune disease.
Sohail Ahmed, lead author of a ground breaking paper published last summer in Science Translational Medicine explained how the now-retracted Pandemrix vaccine was implicated in a narcolepsy epidemic of more than 1,300 children in several European countries and spates of cases linked to other vaccines for the 2009 swine flu pandemic that never materialized.
It turns out, part of the influenza nucleoprotein in the swine flu vaccine looked (molecularly) just like a receptor for a neurotransmitter in the brain called orexin that regulates the sleep/wake cycle, explained, Ahmed former global head of clinical sciences at Novartis and later GlaxoSmithKline who is currently with Roche Pharmaceuticals.
When the vaccine was injected with an adjuvant to ramp up the immune response, the immune system went into overdrive. Something — maybe chemical ingredients in the vaccine, maybe inflammation – breached the blood brain barrier and the immune system targeting the vaccine virus also locked in on the receptors in the brain sleep centre. Narcoleptic patients’ own immune system then destroyed a hub of 70,000 or so orexin-producing cells in their brains before their hosts started knocking out. The autoimmune reaction can’t be turned off because the immune system is programmed to relentlessly attack anything it perceives as a foreign invader. It’s a case of mistaken identity and in immunology it’s called a “cross-reaction.”
But could other vaccines still in circulation that contain the H1N1 virus trigger narcolepsy too? Could the same mechanism cause kids like Bobby Hunter to get narcolepsy from the nasal flu vaccine?
Both Ahmed and immunologist Maria Teresa Arango at Leipzig confirmed that it could indeed. Bobby probably carries the HLA-DQB1*0602 genetic marker that leaves him at a higher risk of getting narcolepsy. But so does 20% of the US population. For pharmaceutical industry dependents like Ahmed, so long as cases like Bobby’s are not epidemic as they were with Pandemrix, they are collateral damage the pharmaceutical industry is willing continue to keep flu vaccines rolling.
But what if other vaccine proteins are acting in more unexpected ways, contributing to other autoimmune diseases?
Arango said such cross-reactivity could be the underlying mechanism for widely varied and unexpected documented vaccine adverse autoimmune events affecting other parts of the brain or body. She pointed to the work of Dr. Darja Kanduc.
Massive Peptide Sharing, Massive Autoimmunity?
Adults, Not Children, Get Most Vaccine Injury Compensation Awards
The estimated 1,000 claims that the VICP anticipates being filed in 2016 are projected to cost $224 million. Although the VICP was originally created by Congress to shield drug companies producing government licensed, recommended and mandated vaccines for children, today it is not children but adults injured by influenza vaccine who are receiving most of the compensation.
Some Vaccine Injured Adults Can Sue Vaccine Manufacturers
In effect, unlike the legal requirement under the 1986 law that shields vaccine manufacturers from civil liability for government recommended vaccines for children that are also used by adults, vaccine injuries sustained by adults from Vaccine injury compensationvaccines used exclusively by adults (like shingles and PNEUMOVAX 23 vaccines) can pursue civil lawsuits against vaccine manufacturers and negligent physicians in order to obtain vaccine injury compensation.
HPV Vaccine Uptake Remains Low
Though this vaccine has been marketed as an anti-cancer vaccine, the CDC’s HPV Fact Sheet 16 states that “there is no way to know which people who have HPV will develop cancer or other health problems.” Given these facts, it is difficult to understand how any reduction in HPV related cancers can be measured and/or attributed to the vaccine, regardless of the number of doses.