Revelations of poor practices at a contract research company helping to carry out Pfizer’s pivotal covid-19 vaccine trial raise questions about data integrity and regulatory oversight. Paul D Thacker reports
In autumn 2020 Pfizer’s chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. “As I’ve said before, we are operating at the speed of science,” Bourla wrote, explaining to the public when they could expect a Pfizer vaccine to be authorised in the United States.1
But, for researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.
Poor laboratory management
On its website Ventavia calls itself the largest privately owned clinical research company in Texas and lists many awards it has won for its contract work.2 But Jackson has told The BMJ that, during the two weeks she was employed at Ventavia in September 2020, she repeatedly informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues. Jackson was a trained clinical trial auditor who previously held a director of operations position and came to Ventavia with more than 15 years’ experience in clinical research coordination and management. Exasperated that Ventavia was not dealing with the problems, Jackson documented several matters late one night, taking photos on her mobile phone. One photo, provided to The BMJ, showed needles discarded in a plastic biohazard bag instead of a sharps container box. Another showed vaccine packaging materials with trial participants’ identification numbers written on them left out in the open, potentially unblinding participants. Ventavia executives later questioned Jackson for taking the photos.
Early and inadvertent unblinding may have occurred on a far wider scale. According to the trial’s design, unblinded staff were responsible for preparing and administering the study drug (Pfizer’s vaccine or a placebo). This was to be done to preserve the blinding of trial participants and all other site staff, including the principal investigator. However, at Ventavia, Jackson told The BMJ that drug assignment confirmation printouts were being left in participants’ charts, accessible to blinded personnel. As a corrective action taken in September, two months into trial recruitment and with around 1000 participants already enrolled, quality assurance checklists were updated with instructions for staff to remove drug assignments from charts.
In a recording of a meeting in late September2020 between Jackson and two directors a Ventavia executive can be heard explaining that the company wasn’t able to quantify the types and number of errors they were finding when examining the trial paperwork for quality control. “In my mind, it’s something new every day,” a Ventavia executive says. “We know that it’s significant.”
Ventavia was not keeping up with data entry queries, shows an email sent by ICON, the contract research organisation with which Pfizer partnered on the trial. ICON reminded Ventavia in a September 2020 email: “The expectation for this study is that all queries are addressed within 24hrs.” ICON then highlighted over 100 outstanding queries older than three days in yellow. Examples included two individuals for which “Subject has reported with Severe symptoms/reactions … Per protocol, subjects experiencing Grade 3 local reactions should be contacted. Please confirm if an UNPLANNED CONTACT was made and update the corresponding form as appropriate.” According to the trial protocol a telephone contact should have occurred “to ascertain further details and determine whether a site visit is clinically indicated.”
Worries over FDA inspection
Documents show that problems had been going on for weeks. In a list of “action items” circulated among Ventavia leaders in early August 2020, shortly after the trial began and before Jackson’s hiring, a Ventavia executive identified three site staff members with whom to “Go over e-diary issue/falsifying data, etc.” One of them was “verbally counseled for changing data and not noting late entry,” a note indicates.
Robert Barnes of https://vivabarneslaw.locals.com/ to break down the biggest vaccine whistleblower news in history as the FDA is exposed falsifying data in COVID jab trials.
Leading medical journal The BMJ has published an incendiary report exposing faked data, blind trial failures, poorly trained vaccinators, and a slow follow-up on adverse reactions in the phase-three trial of Pfizer’s Covid jab.
Central to the exposé is Brook Jackson, who, for two weeks, served as regional director at Ventavia Research Group, the company contracted to assist with the pivotal trial. She provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails supporting her concerns.
Jackson reveals that Ventavia staff who conducted quality-control checks were overwhelmed by the volume of problems they were identifying. She repeatedly informed her superiors of poor laboratory management, and patient safety and data integrity issues.
In a cited internal document from August 2020, shortly after the Pfizer trial began, a Ventavia executive identified three site staff members with whom to “go over e-diary issue/falsifying data, etc.” One employee was said to have been subsequently “verbally counseled for changing data” and “not noting late entry.”
Jackson reported her concerns to the US Food and Drug Administration (FDA), but was fired later the same day on the basis that she was “not a good fit.”
In a recording of a late September meeting provided by Jackson, in which she met with two Ventavia directors, the unwelcome prospect of an FDA inspection had been openly discussed. “We’re going to get some kind of letter of information at least, when the FDA gets here … I know it,” one said to Jackson.
Another former Ventavia employee has confirmed that the company had been expecting a federal audit of its Pfizer vaccine trial, though this did not materialize. A 2007 US Department of Health report found that, between 2000 and 2005, the FDA inspected just 1% of clinical trial sites, while, in 2020, just 50 on-site visits were conducted.
In the aforementioned recording, an executive can also be heard explaining that, when examining paperwork for trial quality control, the company wasn’t able to quantify the types and number of errors that were being identified. “In my mind, it’s something new every day,” the senior staffer says. “We know that it’s significant.”
An email sent in September to Ventavia by Icon, the research organization with which Pfizer partnered on the trial, shows Icon was dissatisfied with Ventavia’s inability to keep up with data entry queries. Icon reminded Ventavia that “the expectation for this study is that all queries are addressed within 24 hours,” noting that more than 100 queries had remained outstanding for more than three days.
Among those queries were two cases in which test subjects had “reported with severe symptoms/reactions.” According to protocol, subjects experiencing grade-three local reactions – “severe” redness, swelling, or pain at the injection site – should have been contacted. Icon asked for confirmation as to whether contact had indeed been made, so as “to ascertain further details and determine whether a site visit is clinically indicated,” and that the subjects’ forms be updated accordingly.
The BMJ – Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial
Concerns raised
In her 25 September email to the FDA Jackson wrote that Ventavia had enrolled more than 1000 participants at three sites. The full trial (registered under NCT04368728) enrolled around 44 000 participants across 153 sites that included numerous commercial companies and academic centres. She then listed a dozen concerns she had witnessed, including:
Participants placed in a hallway after injection and not being monitored by clinical staff
Lack of timely follow-up of patients who experienced adverse events
Protocol deviations not being reported
Vaccines not being stored at proper temperatures
Mislabelled laboratory specimens, and
Targeting of Ventavia staff for reporting these types of problems.
Within hours Jackson received an email from the FDA thanking her for her concerns and notifying her that the FDA could not comment on any investigation that might result. A few days later Jackson received a call from an FDA inspector to discuss her report but was told that no further information could be provided. She heard nothing further in relation to her report.
In Pfizer’s briefing document submitted to an FDA advisory committee meeting held on 10 December 2020 to discuss Pfizer’s application for emergency use authorisation of its covid-19 vaccine, the company made no mention of problems at the Ventavia site. The next day the FDA issued the authorisation of the vaccine.8
In August this year, after the full approval of Pfizer’s vaccine, the FDA published a summary of its inspections of the company’s pivotal trial. Nine of the trial’s 153 sites were inspected. Ventavia’s sites were not listed among the nine, and no inspections of sites where adults were recruited took place in the eight months after the December 2020 emergency authorisation. The FDA’s inspection officer noted: “The data integrity and verification portion of the BIMO [bioresearch monitoring] inspections were limited because the study was ongoing, and the data required for verification and comparison were not yet available to the IND [investigational new drug].”
Other employees’ accounts
In recent months Jackson has reconnected with several former Ventavia employees who all left or were fired from the company. One of them was one of the officials who had taken part in the late September meeting. In a text message sent in June the former official apologised, saying that “everything that you complained about was spot on.”
Two former Ventavia employees spoke to The BMJ anonymously for fear of reprisal and loss of job prospects in the tightly knit research community. Both confirmed broad aspects of Jackson’s complaint. One said that she had worked on over four dozen clinical trials in her career, including many large trials, but had never experienced such a “helter skelter” work environment as with Ventavia on Pfizer’s trial.
“I’ve never had to do what they were asking me to do, ever,” she told The BMJ. “It just seemed like something a little different from normal—the things that were allowed and expected.”
She added that during her time at Ventavia the company expected a federal audit but that this never came.
After Jackson left the company problems persisted at Ventavia, this employee said. In several cases Ventavia lacked enough employees to swab all trial participants who reported covid-like symptoms, to test for infection. Laboratory confirmed symptomatic covid-19 was the trial’s primary endpoint, the employee noted. (An FDA review memorandum released in August this year states that across the full trial swabs were not taken from 477 people with suspected cases of symptomatic covid-19.)
“I don’t think it was good clean data,” the employee said of the data Ventavia generated for the Pfizer trial. “It’s a crazy mess.”
A second employee also described an environment at Ventavia unlike any she had experienced in her 20 years doing research. She told The BMJ that, shortly after Ventavia fired Jackson, Pfizer was notified of problems at Ventavia with the vaccine trial and that an audit took place.
Since Jackson reported problems with Ventavia to the FDA in September 2020, Pfizer has hired Ventavia as a research subcontractor on four other vaccine clinical trials (covid-19 vaccine in children and young adults, pregnant women, and a booster dose, as well an RSV vaccine trial; NCT04816643, NCT04754594, NCT04955626, NCT05035212). The advisory committee for the Centers for Disease Control and Prevention is set to discuss the covid-19 paediatric vaccine trial on 2 November.
Background Reports of waning vaccine-induced immunity against COVID-19 have begun to surface. With that, the comparable long-term protection conferred by previous infection with SARS-CoV-2 remains unclear.
Methods We conducted a retrospective observational study comparing three groups: (1)SARS-CoV-2-naïve individuals who received a two-dose regimen of the BioNTech/Pfizer mRNA BNT162b2 vaccine, (2)previously infected individuals who have not been vaccinated, and (3)previously infected and single dose vaccinated individuals. Three multivariate logistic regression models were applied. In all models we evaluated four outcomes: SARS-CoV-2 infection, symptomatic disease, COVID-19-related hospitalization and death. The follow-up period of June 1 to August 14, 2021, when the Delta variant was dominant in Israel.
Results SARS-CoV-2-naïve vaccinees had a 13.06-fold (95% CI, 8.08 to 21.11) increased risk for breakthrough infection with the Delta variant compared to those previously infected, when the first event (infection or vaccination) occurred during January and February of 2021. The increased risk was significant (P<0.001) for symptomatic disease as well. When allowing the infection to occur at any time before vaccination (from March 2020 to February 2021), evidence of waning natural immunity was demonstrated, though SARS-CoV-2 naïve vaccinees had a 5.96-fold (95% CI, 4.85 to 7.33) increased risk for breakthrough infection and a 7.13-fold (95% CI, 5.51 to 9.21) increased risk for symptomatic disease. SARS-CoV-2-naïve vaccinees were also at a greater risk for COVID-19-related-hospitalizations compared to those that were previously infected.
Conclusions This study demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalization caused by the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity. Individuals who were both previously infected with SARS-CoV-2 and given a single dose of the vaccine gained additional protection against the Delta variant.
Makaylah ~ Another beautiful little child whose happy childhood has been stolen from her by toxic injections. https://www.gofundme.com/makaykay
“She is now 5 years old. Her video will take you on a journey with her from about the age of 2 to her current medical condition. As you will see in her video, she is a playful, happy, child.
She had the energy and the ability to run, jump and play with cousins, friends and family.
On October 21, 2015 she received her required vaccinations to start school.
(I have shown her vaccination record within the video)
After receiving those vaccines, she told her mom, “she just didn’t feel very well”.
Soon, she began to trip and fall constantly. When playing with her siblings, she began to sit and rest during most of her play time due to loss of energy.
She would use the walls or furniture for support to balance or walk and you could see her body having tremors. After taking her to many doctors and even after many tests, we are often told, “we don’t know.” We were also told she would need special help.
She cannot attend school alone. Her balance and stamina are not improving. Her motor functions, speech and food nutrients processing are in rapid decline.
On her last doctor visit in September 2016, they spoke of possibly incorporating a feeding tube.
Even after receiving the diagnosis of some form of “Ataxia”, some doctors still do not agree and believe the cause may be a toxin. Myself and the family believe it was caused by a toxin.
Corresponding with the multiple toxins she received in the form of vaccines on October 21, 2015.
I am Robert, her grandfather. I have seen her struggle with needing to use a walker and a wheel chair or just wondering why her body now reacts like it does.
She does not understand any of this because it was not long ago that she could run, play and just be a child. She often wakes up with seizures and trembling.
Her latest challenge is feeding herself. Please help us help Makayla in this medical mystery.
We appreciate your contributions, donations and prayers for Makayla.
May God Bless You Always for Sharing.” gofund.me/makaykay
See this video also: https://www.facebook.com/RevolutionForChoice/posts/181799735560954 #RevolutionForChoice #VAXXED #InformedConsent #WeAreVAXXED #VAXXEDNation
Andy Wakefield peeps talk #vaxxed #Praybig
At the time of this report in 2009, there had been 27 confirmed deaths in America due to Gardasil injections in the 3 short years after the vaccine was introduced in 2006, along with over 10,000 reports of vaccine-injury and disability. As of April 2017, there have been 318 documented deaths and more than 50,000 reports of serious injury. Keep in mind, only a small percentage of vaccine related deaths and injuries are properly reported, as many health care workers have come forward revealing that they were prevented from properly filing the VAERS documentation when they attempted to do so. With this insidious censorship of the crucial information that ALL parents have the right to know before they subject their children to these medical experiments, the worldwide death and injury toll on our population is incalculable.
>>> Education is empowerment – 9 part replay, happening now: tinyurl.com/9Episodes
Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
Follow us: facebook.com/RevolutionForChoice
Read all vaccine inserts: tinyurl.com/ReadTheVaccineInsert #RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #Gardasil #Cervarix #VaccineDeath
These ARE NOT isolated incidences❗ These ARE NOT coincidences❗
Educate yourselves on VACCINE TRUTH right here: tinyurl.com/9Episodes
Little Benjamin’s Story… http://www.littlebentrust.com/
Ten days after his son received his measles, mumps, and rubella (MMR) and Chickenpox vaccines his father and mother noted changes in Lil Ben’s behavior. His appetite was off, he was sleeping more, and he no longer played appropriately with his toys. On Nov. 27, 2004 while Father was changing his son’s diaper, he noticed that the baby’s eyes did not look right. Ben was lifeless when his father lifted him.
Zeller called Emergency Rescue and his neighbor, a registered nurse, who came to the Zeller’s home and revived Lil Ben. An Emergency Medical Service (EMS) team arrived and took Ben to a nearby hospital. In these first frantic moments that foreshadowed Ben’s painful future, Zeller had a realization: the MMR vaccine that Ben had received 10 days prior was the cause of his seizure.
The Zellers were sent home from the hospital on the night of Ben’s first seizure with Motrin. They were told Ben’s fever and seizures were adverse effects of his vaccination. But the trips to the emergency room continued throughout that week. Zeller brought his son to the hospital several times as a result of recurring 5-30 seizures per day.
In December, Ben was admitted to a hospital in Miami, where he would stay for 11 days. “They did an MRI,” says Zeller, “and they found that his brain was degenerating. The seizures became worse. He would have 10, 20, and then 30 in one day, all within one month.” The Zellers were told repeatedly that Ben was suffering from a genetic disorder, but all genetic testing came back with inconclusive results.
The Vaccine Court Case
Israeli Zeller Family decided to sue the United States Federal Government, United States Department of Justice and United States Human Health Services in Washington D.C. in Vaccine Court and U.S. Federal Claims Court ruled in favor of compensation for the Zeller family in July 2008. The Zeller family was one of the largest settlements in Vaccine court’s history.
Ultimately the court highlighted the fact that Ben had been progressing and was neurologically stable until he received the MMR vaccine. (Judge) Special Master Richard Abell noted that if regression had been occurring prior to the vaccination, there would be mention of it in the thorough documentation that was presented to the court. “The first note of regression noted in the medical records appears to be from December of 2004,” read the entitlement ruling, “following the vaccination, the initial seizure ten days subsequent, and the bout of successive seizures in early December. The medical progress notes from 17 December 2004 include a description of Benjamin’s ‘developmental regression and seizures.’”The court also found that neurodegeneration was not taking place prior to the vaccination, as Wiznitzer postulated. . “If not but for the administration of the vaccines, Ben would not have suffered brain damage and seizures” #RevolutionForChoice #VAXXED #InformedConsent
Cannabis could make life easier for children with autism
…7 top activist in the fight for YOUR RIGHT to decide what drugs go into you and your children’s bodies...DON’T tell me you are drug FREE when you are shooting up on vaccines with all their constituents including carcinogens, allergens, neurotoxins, not to mention the pus grown on dead animal parts and aborted human fetuses…and you only eat organic but your vaccines are loaded with glyphosate ie round up…and you are for animal rights as they slaughter animals and pro-life as the use cell lines from aborted fetuses…just read the package insert BRO! Sherri Tenpenny HighWire with Del Bigtree Del Bigtree Suzanne Humphries NVIC Advocacy Barbara Loe Fisher We Are Vaxxed Vaxxed – A Revolution For Choice Vaxxed: From Cover-Up to Catastrophe Robert F. Kennedy, Jr World Mercury Project Patrick Gentempo VaccinesRevealed Dr. Tenpenny on Vaccines and Current Events David Wolfe Norman Colby Michael B. Dibley Jack Wolfson Jodi Hauver Dr Wakefield’s work must continue
NIÑAS DEL CARMEN DE BOLÍVAR, del corregimiento Caracoli COLOMBIA, con TRASTORNO POST VACUNAL que vienen descritos o advertidos en las fichas técnicas. Presentan SÍNCOPE CON MOVIMIENTOS TÓNICOS CLÓNICOS. . . En esta población se requiere de médicos voluntarios #NEURÓLOGOS #CARDIÓLOGOS Las niñas de esta población se encuentran en total abandono por parte del Sistema de Salud.
La narración de la persona que grabó este vídeo muestra la angustia que se vive en esta población, es la voz del rector de la escuela donde las niñas asisten.
Esperamos que los ojos del mundo volteen a ver esta tragedia y los gobernantes que toman la decisión de seguir con la aplicación de esta vacuna ya sea #Gardasil o #cervarix dejen de minimizar los riesgos. ¿Cómo es posible que esto siga sucediendo? . No comprendo cómo el interés del gobierno y sector salud sea proteger la reputación de la vacuna de VPH y claramente no es la protección de las niñas menores que han resultado dañadas, se está vulnerando su derecho a tener vida sana, plena a su edad. DÓNDE QUEDA LOS DERECHOS HUMANOS INTERNACIONALES, UNICEF, VOLTEEN Y MIREN LA REALIDAD DE MÁS DE 40 MIL VÍCTIMAS A NIVEL MUNDIAL. NO ES CASUALIDAD TODAS ERAN NIÑAS SANAS AHORA LAS NIÑAS TIENEN UNA VIDA CON DISCAPACIDAD Y DIFICULTAD PARA PODER LLEVAR SUS DÍAS COTIDIANOS DESPUÉS DE LA VACUNA. #VPH #MEXICO #NO #MAS #VACUNA #PARA #PAPILOMA #HUMANO. 3RA SEMANA DE VACUNACIÓN DEL 6 AL 10 DE OCTUBRE EN TODO EL PAÍS. MIREN LO QUE ESTÁ PASANDO EN COLOMBIA Y EN MUCHOS PAÍSES INCLUIDO MÉXICO Y SI FUERA SU HIJA….??? NO MÁS RULETA RUSA. Las imágenes son reales y hablan por sí solas. #NO # 🚫💉 PAPILOMA HUMANO
CHILDREN OF THE CARMEN OF BOLIVAR, of the Caracoli district COLOMBIA, with POST VACCINE DISORDER that come from the warnings in the technical data sheets. They present SYNCOPE WITH CLONIC TONIC MOVEMENTS. . . This population requires volunteer doctors # NEUROLOGISTS # CARDIOLOGISTS Girls in this population are in total abandonment by the Health System. The narrative of the person who recorded this video shows the anguish that is lived in this population, is the Voice of the rector of the school where the girls attend. We hope that the eyes of the world returned to see this tragedy and the rulers who make the decision to continue with the device of this vaccine #Gardasil or #cervarix stopped minimizing the risks . How is it possible to keep happening? . I do not understand how the interest of the government and the health sector protect the the reputation of the HPV and clearly not in protecting young girls who have been harmed, is violating their right to have a healthy, full life At this age. WHEREIN INTERNATIONAL HUMAN RIGHTS, UNICEF, TURN AND SEE THE REALITY OF MORE THAN 40 THOUSAND VICTIMS AT WORLDWIDE. IT IS NOT CASUALITY ALL WERE HEALTHY GIRLS NOW THE GIRLS HAVE A LIVING WITH DISABILITY AND DIFFICULTY TO BE ABLE TO TAKE THEIR DAILY DAYS AFTER THE VACCINE. #VPH # MEXICO #NO #MAS #VACUNA #PARA #PAPILOMA #HUMAN. 3TH WEEK OF VACCINATION FROM 6TH TO 10TH OF OCTOBER IN THE WHOLE COUNTRY. SEE WHAT IS HAPPENING IN COLOMBIA AND IN MANY COUNTRIES INCLUDING MEXICO AND IF YOU WERE YOUR DAUGHTER …. ??? NO MORE RUSSIAN ROULETTE. The images are real and speak for themselves. #NO # 🚫💉 HUMAN PAPILOMA
Girls of the Carmen de bolívar, of the corregimiento Colombia, with post-vaccination disorder that are described or warned in the technical sheets. Syncope with movements. . In this population it is necessary to volunteer doctors #neurologists #cardiologists the girls of this population are in total neglect by the health system.
The narration of the person who recorded this video shows the anguish that lives in this population, is the voice of the school rector where the girls attend.
We hope that the eyes of the world will turn to see this tragedy and the rulers who make the decision to continue with the application of this vaccine be #gardasil or #cervarix stop minimizing the risks. How is it possible for this to continue? . I do not understand how the interest of the government and health sector is to protect the reputation of the HPV vaccine and clearly not the protection of minor girls who have been damaged, the right to healthy life is being violated. Where International Human Rights, UNICEF, turn and look at the reality of more than 40 thousand victims worldwide. It’s no coincidence they were all healthy girls now girls have a life with disabilities and difficulty in getting their daily days after the vaccine. #Hpv #Mexico #no #more #vaccine #for #papilloma #human. 3rd week of vaccination from 6 to 10 October throughout the country. Look what’s going on in Colombia and in many countries including Mexico and if it were your daughter….??? no more Russian roulette. The Images Are real and speak for themselves. #No # 🚫💉 human papilloma
CHILDREN OF THE CARMEN OF BOLIVAR, of the Caracoli district COLOMBIA, with POST VACCINE DISORDER that come from the warnings in the technical data sheets. They present SYNCOPE WITH CLONIC TONIC MOVEMENTS. . . This population requires volunteer doctors # NEUROLOGISTS # CARDIOLOGISTS Girls in this population are in total abandonment by the Health System. The narrative of the person who recorded this video shows the anguish that is lived in this population, is the Voice of the rector of the school where the girls attend. We hope that the eyes of the world returned to see this tragedy and the rulers who make the decision to continue with the device of this vaccine #Gardasil or #cervarix stopped minimizing the risks . How is it possible to keep happening? . I do not understand how the interest of the government and the health sector protect the the reputation of the HPV and clearly not in protecting young girls who have been harmed, is violating their right to have a healthy, full life At this age. WHEREIN INTERNATIONAL HUMAN RIGHTS, UNICEF, TURN AND SEE THE REALITY OF MORE THAN 40 THOUSAND VICTIMS AT WORLDWIDE. IT IS NOT CASUALITY ALL WERE HEALTHY GIRLS NOW THE GIRLS HAVE A LIVING WITH DISABILITY AND DIFFICULTY TO BE ABLE TO TAKE THEIR DAILY DAYS AFTER THE VACCINE. #VPH # MEXICO #NO #MAS #VACUNA #PARA #PAPILOMA #HUMAN. 3TH WEEK OF VACCINATION FROM 6TH TO 10TH OF OCTOBER IN THE WHOLE COUNTRY. SEE WHAT IS HAPPENING IN COLOMBIA AND IN MANY COUNTRIES INCLUDING MEXICO AND IF YOU WERE YOUR DAUGHTER …. ??? NO MORE RUSSIAN ROULETTE. The images are real and speak for themselves. #NO # 🚫💉 HUMAN PAPILOMA
Two reasons you should say no to Gardasil.
Dr. Stephanie Seneff shared: The movie Vaxxed has done a great service to inform the public of a potential link between the MMR vaccine and autism. I have been aware of this link for many years, after having studied the FDA’s VAERS database of vaccine events, with a specific focus on potential autism links. MMR is much more frequently associated with mentions of autism than the other vaccines administered at the same age (P=0.007). Furthermore, MMR in the second half of the database (from 2003 to 2016) is associated with many more severe adverse events, including autism, than was the MMR vaccine during the early half, despite the fact that, to my knowledge, the formulation has not changed. MMR contains neither mercury nor aluminum, two ingredients in other vaccines that are highly neurotoxic. However, MMR has significantly more gelatin than the other vaccines, and that is its Achilles’ heel. In this talk, I will explain how glyphosate contamination in the vaccine, most likely from the gelatin, is leading to an autoimmune attack on the myelin sheath, which disrupts long-distance transport among nerve fibers, contributing to autism.
Poznań za sądami! Łańcuch światła po raz trzeci! Nie odpuścimy! Podajcie dalej! Poznań for the courts! A chain of light for the third time! We won’t let it go! Pass it on!
I missed the small symptoms that had been present at the age of 14 whenever HPV vaccination and HPV vaccination were given. Also the inoculation doctor did not notice.
The missing of small symptoms after vaccination changed to a big symptom.
Involuntary movements and muscle spasms occur every morning when they wake up to the daughter who is 20 years old this year. Although it was the main left foot this morning, symptoms may appear in the whole body.
The sequelae diagnosis after HPV vaccination has been done. What is it that you will suffer for a long time with these symptoms? Other weakness, sudden headache, whole body pain and joint pain, nausea, dizziness and numbness come out as symptoms suddenly. Even if you can send your daily life by treatment, the difficult situation for your daughter will not change after six years
Vaccines Don’t Work: Malignant Mumps In MMR Vaccinated Children
Posted on: Monday, November 24th 2014 at 7:15 pm
Written By: Sayer Ji, Founder
This article is copyrighted by GreenMedInfo LLC, 2014
A new study finds highly malignant mumps infections in those successfully vaccinated against the virus…
A provocative new study titled, “Epidemic of complicated mumps in previously vaccinated young adults in the South-West of France,” reveals that the MMR vaccine, despite generating high rates of presumably protective IgG antibodies against mumps, does not always translate into real-world immunity against infection as we have repeatedly been told. To the contrary, the study details cases where, despite the detection of high levels of antibodies against the mumps virus, patients contracted a malignant form of mumps that only rarely follows from natural, community acquired infection.
Vaccine Failure Is Well Established In the Scientific Literature
While counter-intuitive to those who uncritically accept the official marketing copy of the vaccine industry and their cheerleaders within government and the mainstream media, the research community and general public is beginning to appreciate how prevalent and well-documented vaccine failure really is, especially in the case of measles, hepatitis B, chickenpox, pertussis (whooping cough), HIV, polio, HPV, and influenza vaccines that do not work as advertised.
We live in a time when many medical interventions are decided not by the weight of the evidence itself, but by ‘science by proclamation,’ i.e. the public, and the regulatory agencies legally responsible for protecting them, simply accept pleas to authority or vague references to ‘the Science,’ without any acknowledgement of the reality of how vaccine research is manipulated or simply selectively published to serve economic and socio-political agendas. For example, of the billions of dollars (much of which is funded by you, the taxpayer) funneled into proving vaccines safe and effective thus far, not a single published study exists to date that compares vaccinated subjects to non-vaccinated ones. The obvious reason is that if the results of such a study demonstrated better health or immunity in the non-vaccinated group (as many suspect), the entire house of cards supporting our present-day, globally coordinated pro-vaccine agenda would fall to pieces.
Médecine et Maladies Infectieuses
Volume 44, Issues 11–12, December 2014, Pages 502-508
Original article Epidemic of complicated mumps in previously vaccinated young adults in the South-West of France Épidémie de formes compliquées d’oreillons chez de jeunes adultes vaccinés dans le Sud-Ouest de la France et revue de la littérature
Abstract
Objective
We report the features and diagnosis of complicated mumps in previously vaccinated young adults.
Patients and methods
We retrospectively studied 7 cases of complicated mumps managed during 1 year at the Bordeaux University Hospital. The diagnosis was suggested by the clinical presentation and confirmed using specific RT-PCR.
Results
Five cases of meningitis, 1 of orchitis, and 1 of unilateral hearing impairment were identified. Each of the 7 patients had been previously vaccinated with MMR, 4 had received 2 doses of this vaccine. Blood tests revealed high rates of IgG antibodies, usually considered as sufficient for immunological protection, and every patient had at least 1 positive RT-PCR test for mumps.
Conclusion
Outbreaks of complicated mumps may still occur despite a broad coverage of MMR vaccination. The clinical presentation suggested mumps but the final diagnosis could only be confirmed by genomic detection of the virus. Unusual viral strains with increased neurovirulence, insufficient population coverage associated with immunity decrease over time may explain outbreaks of complicated mumps. A full vaccine scheme of contact people or a third injection of vaccine for previously vaccinated people who are at risk of developing mumps are required to prevent further spreading of the disease during the outbreak.
Aluminum Should Now Be Considered a Primary Etiological Factor in Alzheimer’s Disease
Posted by Professor Chris Exley on Jun 13, 2017 3:59:38 PM
The following paper was published by the Journal of Alzheimer’s Disease Reports. References may be found here.
Abstract: In this paper, I have summarized the experimental and largely clinical evidence that implicates aluminum as a primary etiological factor in Alzheimer’s disease. The unequivocal neurotoxicity of aluminum must mean that when brain burdens of aluminum exceed toxic thresholds that it is inevitable that aluminum contributes toward disease. Aluminum acts as a catalyst for an earlier onset of Alzheimer’s disease in individuals with or without concomitant predispositions, genetic or otherwise. Alzheimer’s disease is not an inevitable consequence of aging in the absence of a brain burden of aluminum.
Study – Aluminum Should Now Be Considered a Primary Etiological Factor in Alzheimer’s Disease
EVIDENCE NOW POINTS TO ALUMINUM AS A CONTRIBUTORY FACTOR IN ALL FORMS OF ALZHEIMER’S DISEASE
Aluminum is unquestionably neurotoxic [1] and it is accepted as the cause of encephalopathies in, for example, individuals undergoing renal dialysis [2] and similarly in individuals who have received aluminum-based prostheses [3]. There are myriad ways by which aluminum can exert toxicity; its Al3 + (aq) ion is highly biologically reactive, but to do so and thereby bring about change in a biochemical system, the aluminum content of any compartment, such as a tissue, must achieve a toxic threshold or burden [4]. However, aluminum-induced encephalopathies are not Alzheimer’s disease, though they may share some similar neuropathological hallmarks [5]; they are acute conditions whereas Alzheimer’s disease might now be considered as an acute response to chronic intoxication byaluminum [1].
NHF Sweden – Swedish open letter to the Italian Parliament about the unconstitutional Vaccine Decret
Swedish open letter to the Italian Parliament, Senate and Government about the unconstitutional Vaccine Decret
The Italian Vaccine Decret (n 73/2017) is unconstitutional and you must not approve. We will take legal actions against anti democratic Governments that are violating international laws.
As of November 2013 there have been 31,741 adverse effects, including 6248 permanent injuries and 144 deaths recorded following Gardasil vaccines. Pharmaceutical companies which make the vaccine, as well as the Department of Health and Human Services which holds patents and earns profits from the vaccine, say that they are all a coincidence. The mainstream media is even worse: they are in denial that these events are even happening.
Watch the video above and listen to the stories of girls who have become disabled and died, and ask yourself why their stories are not being told, and why the mainstream media is trying to censor them as much as possible.
Johns Hopkins Scientist Reveals Shocking Report on Flu Vaccines
by SYLVIA BOOTH HUBBARD
A Johns Hopkins scientist has issued a blistering report on influenza vaccines in the British Medical Journal (BMJ). Peter Doshi, Ph.D., charges that although the vaccines are being pushed on the public in unprecedented numbers, they are less effective and cause more side effects than alleged by the Centers for Disease Control and Prevention (CDC). Further, says Doshi, the studies that underlie the CDC’s policy of encouraging most people to get a yearly flu shot are often low quality studies that do not substantiate the official claims.
Promoting influenza vaccines is one of the most visible and aggressive public health policies in the United States, says Doshi of the Johns Hopkins School of Medicine. Drug companies and public officials press for widespread vaccination each fall, offering vaccinations in drugstores and supermarkets. The results have been phenomenal. Only 20 years ago, 32 million doses of influenza vaccine were available in the United States on an annual basis. Today, the total has skyrocketed to 135 million doses.
“The vaccine may be less beneficial and less safe than has been claimed, and the threat of influenza seems to be overstated,” Doshi says. Mandatory vaccination polices have been enacted, often in healthcare facilities, forcing some people to take the vaccine under threat of losing their jobs.
The main assertion of the CDC that fuels the push for flu vaccines each year is that influenza comes with a risk of serious complications which can cause death, especially in senior citizens and those suffering from chronic illnesses. That’s not the case, said Doshi.
BMJ – Influenza: marketing vaccine by marketing disease
BMJ 2013; 346 doi: https://doi.org/10.1136/bmj.f3037 (Published 16 May 2013)
The CDC pledges “To base all public health decisions on the highest quality scientific data, openly and objectively derived.” But Peter Doshi argues that in the case of influenza vaccinations and their marketing, this is not so
Promotion of influenza vaccines is one of the most visible and aggressive public health policies today. Twenty years ago, in 1990, 32 million doses of influenza vaccine were available in the United States. Today around 135 million doses of influenza vaccine annually enter the US market, with vaccinations administered in drug stores, supermarkets—even some drive-throughs. This enormous growth has not been fueled by popular demand but instead by a public health campaign that delivers a straightforward, who-in-their-right-mind-could-possibly-disagree message: influenza is a serious disease, we are all at risk of complications from influenza, the flu shot is virtually risk free, and vaccination saves lives. Through this lens, the lack of influenza vaccine availability for all 315 million US citizens seems to border on the unethical. Yet across the country, mandatory influenza vaccination policies have cropped up, particularly in healthcare facilities,1 precisely because not everyone wants the vaccination, and compulsion appears the only way to achieve high vaccination rates.2 Closer examination of influenza vaccine policies shows that although proponents employ the rhetoric of science, the studies underlying the policy are often of low quality, and do not substantiate officials’ claims. The vaccine might be less beneficial and less safe than has been claimed, and the threat of influenza appears overstated.
La Lorenzin ha appena ammesso che tutela gli interessi delle farmaceutiche The has just admitted that it protects the interests of the pharmaceutical companies
Dott. Franco Trinca: il suo studio sulla pericolosità dei vaccini Dr… Franco Trinca: His study on the dangers of vaccines
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