Questionable Data Used for New Covid Vaccine Approvals - Interview with David Wiseman, PhD
Ordinarily, the Food and Drug Administration’s (FDA) approval of a drug is generally followed by the Center for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices (ACIP) recommending that the public take it. In the case of the latest COVID-19 vaccine, this took only one day. In a September 11 press release, FDA reported on that day’s approvals for updated mRNA vaccines. Importantly the agency used an “Accelerated Approvals Program.” More specifically the agency issued an emergency use authorization for the under 12-year-old cohort, while granting formal approvals for all else under the Accelerated Approvals Program, based on a surrogate endpoint. This means they used an exception they have to rush when there are serious unmet needs—and they don’t have to have comprehensive clinical evidence.
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Free Speech on Adverse Effects Awaken India vs Serum Institute
The right to free speech in the public interest is contentious. During Covid-19, this right is under intense scrutiny with proponents for and against making robust arguments, depending on which side of the medical industrial complex fence they stand, and what value is attributed to free speech in difficult times.
A case in point is the TNI case, which includes including Trialsite News and others as applicants. Another groundbreaking case is Missouri vs Biden, where the judge compelled government to stop colluding with social media companies that suppress the flow of information related to Covid-19.
Another critical case of extreme importance takes us to India. It is a battle between the Awaken India Movement (AIM) and the Serum Institute of India (SII) - where a recent court judgement raises questions about free speech, public interest and health. Our guest is health advocate and researcher Yoga
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47-year-old Vaccine Injured Mother files $10.5 Million Lawsuit against the Canadians Government
47-year-old Vaccine Injured Mother files $10.5 Million Lawsuit against the Canadian Government and the CBC.
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TrialSite News Founder Speaks to Vaccination as a Significant Tool Utilized in Public Health
TrialSite News Founder Daniel O’Connor discusses the false dichotomy of the pro-vaccination, vs anti-vaccination stances. Why vaccines are an important tool, just as honesty of potential vaccination issues are necessary for the public discourse.
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Pioneer Dr Paul Marik: Repurposed Medicines
In a riveting interview with Shabnam Palesa Mohamed, Dr Paul Marik talks about:
How living in South Africa trained him for excellence, resilience and innovation
Why Big Pharma is in a full spectrum war with repurposed medicines that would benefit health in low to middle income countries the most.
Losing trust in the WHO, referencing a documentary called Trust WHO: "We couldn't trust the WHO 15 years ago, we can't trust the WHO now, and we can never trust the WHO. "Their name is World Health Organisation, but they have nothing to do with health. The WHO preserves the economic, interests of the people that support them." - like Big Pharma, who he critiques for "obscene" price gouging on essential drugs. He says "this cartel must be broken."
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The Challenge Of Rare Adverse Effects In Low Income Patients
In a human interest episode of Medical Files, Shabnam Palesa Mohamed talks to two South African doctors treating people with post-C19 injection adverse effects. The patients interviewed, Mrs Mulder and Mrs Wagner, bravely describe their painful experiences, how their lives were changed, that previous doctors failed to help them, and their financial struggles since. The doctors, both members of the Stop The Shots court case, share low cost treatments they are trying to alleviate symptoms, and issue an appeal to other doctors to not ignore people who need help. Both women want the world to know that their lives matter. South African are reporting adverse effects to independent platform SAVAERS.co.za
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Patrick Girondi Sues Biotech and Venture Capitalist Firm over charges of violating RICO Act
A civil action has been filed, charging violations of the Federal Racketeering and Corrupt Organizations Act (RICO), fraudulent inducement and unfair business practices in the United States District Court in Massachusetts. The defendants are Nick Leschly, Mitchell Finer, Phillip Reilly, Third Rock Ventures, bluebird bio Inc., and 2seventy Bio Inc. This lawsuit is linked to the TrialSite’s ongoing tracking of the San Rocco Therapeutics (SRT), formerly Errant Gene Therapeutics, and bluebird legal conflict. See “A FamilyMan’s battle against the forefront of capitalist medicine: the case of Errant Gene Therapeutics.”
Nick Leschly, the former CEO of bluebird bio, profited $24,000,000, alone in 2018, making him the highest compensated pharma CEO in the world. The complaint alleges that his earnings were a direct result of fraudulent and corrupt RICO violations at the expense of the health of patients. Bluebird bio’s gene therapy was approved in August 2022 to treat Thalassemia for $2.8 million per patient. SRT has a safer gene therapy product that will cost over $2,000,000 less at $700,000.
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AFRICAN GOVT ACCUSED OF COVID CORRUPTION
With Africa being a favourite playground for the pharmaceutical industry, it became critical for scientist, researcher and activist Fahrie Hassan to not only investigate blatant and hidden conflicts of interest in South Africa (and globally), but to expose the complex dynamics that lead to often shocking decisions about health, especially during the last three years.
In this Conflicts of Interest Masterclass, he talks to Shabnam Palesa Mohamed about conflicts of interest in the South African Department of Health, and the economic hitmen role of organisations like the Bill and Melinda Gates Foundation, the CDC, US AID, PEPFAR, and the Clinton Health Access Initiative (CHAI), in capturing health and democracy.
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Brooke Jackson Vs Pfizer Case Dismissed. What Next?
In this rivetting conversation, Shabnam Palesa Mohamed engages Katherine Watt and Sasha Latypova about the hotly debated dismissal of Brook Jackson's court case against Pfizer, Ventavia and ICON. Were they surprised at Judge Michael's Truncale's judgment? What did they think about the judgment as it relates to false claims, defrauding government and democracy? What are the prospects of success in other cases against the controversial Pfizer INC? Or should the public exercise its vote in protest?
The information presented is solely for educational purposes. Never disregard professional medical advice. It is not intended to be a substitute for professional medical advice, diagnosis, or treatment in regards to any patient.
Treatment for an individual patient should rely on the judgment of your physician or another qualified health provider. Always seek their advice with any questions you may have regarding your health or medical condition.
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FDA Authorizes Changes to Simplify Use of Bivalent mRNA COVID-19 Vaccines. Ignores VAERS Data
Dr. Wiseman discusses the U.S. Food and Drug Administration's amendment of the emergency use authorizations (EUAs) of the Moderna and Pfizer-BioNTech COVID-19 bivalent mRNA vaccines. This action includes authorizing the current bivalent vaccines (original and omicron BA.4/BA.5 strains) to be used for all doses administered to individuals 6 months of age and older, including for an additional dose or doses for certain populations. The monovalent Moderna and Pfizer-BioNTech COVID-19 vaccines are no longer authorized for use in the United States.
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Dr. Mobeen discusses Magic Mushrooms VS Pharma Drugs
Can psychedelics like psylocybins ('magic mushrooms') heal depression, cure addiction, and reduce age related cognitive decline? What would be the impact on Big Pharma's blockbuster drugs be, if more people had access to cost-effective psychedelics? Shabnam Palesa Mohamed engages Dr Mobeen Syed (a popular clinician, software engineer and a health educator) on fascinating psychedelic studies.
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Conflicts of Interest - A Case Study of Canada
Conflicts of interest erupted into a critical focus area in understanding drugs, politics and power, especially during the last three years. We invite scientist Deanna McCleod to a Conflicts of Interest Masterclass - and engage her definitions, how this controversial issue plays out in Health Canada, and whether awareness will lead to evolution for informed consent and ethical decision making.
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OBGYN reveals damning data on miscarriage and fertility rates in bombshell interview
I had the pleasure of interviewing Dr Kim Biss, a practicing obstetrician & and gynaecologist from St. Petersburg, Florida, one of the very few OBGYNs speaking out against the COVID-19 vaccines for pregnant women. During the interview, she revealed damning data with regards to miscarriage and fertility rates seen in her practice, post mRNA vaccine roll-out.
The average month to month miscarriage rate in 2020 was 4%. In 2021, it jumped 7-8%, roughly doubling in 2022 to 15%. By December of that year, it reached 25%.
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C19: Public Health or Defense Operation?
A terrifying agenda around the C-19 shots is exposed by researcher and paralegal Katherine Watt: C-19 is a global 'kill box' operation that targeted informed consent, health, lives and democracy. In conversation with Shabnam Palesa Mohamed, she also draws a clear agenda between C-19, 911, and the Patriot Act - a creeping and profitable lockstep to deep state totalitarianism globally. Finally, she explains how and why anyone opposing a DOD-Corporate narrative regarded as an enemy of the state.
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Who was paid to ignore C19 injection effects?
Forced by his former employer to take the C-19 shot, Barend van Vuuren feels betrayed. He developed multiple illnesses, including hepatisis and dementia. With mounting medical bills, his wife Claressa helps him through this interview and makes a powerful statement: people were paid to inflict this kind of trauma, government and Big Pharma must be accountable, and so too should captured scientists and media. They also want the Department of Health to stay far away from the children they plan to inject.
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Covid-19 Shot Justice: We Won't Give Up
Amariska Oguz took the C19 shot to protect her family, she believed in the safe and effective narrative. Afflicted by Gullian Barre Syndrome (GBS), she lost her ability to walk and to do basic things for herself. Amariska was also psychologically abused when in a public hospital. Her treating doctor, Dr EV Rapiti, shares his fearless views on the lack of moral courage of doctors who sold out or refuse to speak out. Rapiti is part of the court case to stop the shots pending investigation into safety and conflicts of interest.
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FDA Discusses Ischemic Stroke, Future Of Vaccine Schedules at the VBRPAC Meeting
Join The Conversation! | https://trialsitenews.com/
David Wiseman, and TrialSite News Founder discuss the FDA's Vaccine and Biological Products Advisory Committee Meeting, where everything from Ischemic Stroke safety signals from the Covid Vaccine, to the future of the Covid Vaccine Schedule was covered.
David Wiseman Notes on the FDA Meeting | https://www.researchgate.net/publication/367433336_Annotations_on_FDA_Briefing_Document_for_VRBPAC_Meeting_January_26_2023_Future_Vaccination_Regimens_Addressing_COVID-19_FDA-2022-N-2810
David Wiseman Twitter | https://twitter.com/AdhesionsOrg
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Nick Hudson: "The citizens of the world are owed an explanation."
Sonia Elijah of Trial Site News catches up with South Africa-based, Nick Hudson, co-founder and chairman of PANDA- Pandemics Data & Analytics (pandata.org). The last time Elijah interviewed Hudson was in March 2022, the day after he was permanently suspended for 'violating the Twitter rules' for daring to question Pfizer's phase 3 clinical trials and their alleged mRNA vaccine efficacy of 95%. Thanks to Elon Musk's takeover of Twitter, Hudson's account was recently reinstated.
In the interview, Hudson effortlessly countered the many facets of the official Covid-19 narrative with factual evidence and observational data. He spoke about Big Tech's censorship of dissenting voices, particularly those of eminent scientists, medical experts and other academics. Hudson also shone a light on the major conflicts of interests at play and propaganda.
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Exploring "The Spirit Molecule": Interview with DMT Researcher Pascal Michael
Martha speaks to researcher and Psychology Lecturer Pascal Michael. Having completed the first field study comparing the potent, psychoactive, DMT, with near-death experiences, Pascal shares his research and discusses the neurology, phenomenology, and therapeuticpotentials of this profound psychedelic molecule.
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Psychedelics to Treat Cluster Headaches with Ainslie Course and Jonathan Leighton.
In this interview, Martha speaks to Ainslie Course, a cluster headache survivor and Vice President of the charity Clusterbusters, and Jonathan Leighton,founder of OPIS (Organisation for the Prevention of Intense Suffering) - a Swiss think tank whose mission is to prioritise the alleviation of suffering. Together, they discuss the use of psychedelics in managing Cluster Headaches--including Ainslie's own personal life-changing journey--the unmet need for more effective treatments in cluster headache management, and political barriers to psychedelics access
https://clusterbusters.org/
https://www.preventsuffering.org/
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Ketamine-assisted Therapy and Medicalising Psychedelic: Interview with Dr Ben Sessa
For this special interview, Martha chats with Dr Ben Sessa - a Psychiatrist, MDMA, Psilocybin and Ketamine Psychotherapist, Psychedelic Researcher, Author, and Chief Medical Officer of AWAKNLife Sciences. In this interview, Dr Sessa chats about AWAKN - the UK's first ketamine-assisted psychotherapy clinic and psychedelic research centre, as well as the future of psychedelic research and medicalisation of these medicines.
https://awaknlifesciences.com/
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Interview with a Cluster Headaches survivor. Psilocybin use and the founder of OPIS
Ainslie Course - a Cluster Headaches survivor who describes her own experience using psilocybin to treat her condition, and Jonathan Leighton, founder of OPIS - an advocacy group.
In this interview, since Ainslie discusses her own experience with what's currently illegal in the UK, and this is made clear in the interview as we go on to discuss legislation
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Virologist Dr. Marc Johnson on Tracking Cryptic Lineages of COVID-19
Dr. Marc Johnson PhD is a virologist at the University of Missouri School of Medicine whose research focuses on retroviral assembly, a biological process that engages multiple viral and cellular actors. You can learn more about his research interests here.
You can read more about his work on tracking cryptic COVID lineages in wastewater in Nature Newsand follow him on Twitter here.
https://www.nature.com/articles/d41586-022-02996-y
https://twitter.com/SolidEvidence
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The advocate, the mother and the doctor raise concerns regarding the mRNA shots
Sonia Elijah of Trial Site News speaks to:
Kim Witczak, leading international drug safety advocate and consumer representative on the FDA’s advisory committee. Following the tragic event of her husband, Woody’s, suicide shortly after taking Pfizer’s anti-depressant medication, Zoloft, Wiczak filed a lawsuit against the behemoth drug company when she discovered, suicide was a known side effect, resulting in Pfizer adding a warning label issued as a black box warning by the FDA. Witczak speaks about her extensive research on the Big Pharma’s insidious influence over media; the legal system; medical journals and academic institutions to name but a few, culminating in her generating a map called the Spider’s Web.
Heather Hudson, mother of a severely mRNA vaccine injured young man, turned medical researcher, speaks openly about her son’s injuries (pulmonary embolisms, blood clotting and neuropathy) and how his condition, anti-phospholipid syndrome, which causes the immune system to attack the body’s own cells, is related to the lipid nanoparticles found in the Pfizer-BioNTech mRNA Covid-19 vaccine, particularly the modified phospholipids.
Dr Eduardo Balbona helped save Cody, Heather’s son, when he was on the brink of death, and when all the other doctors turned him away. Dr Balbona ran critical tests that showed the modified phospholipids found in the mRNA vaccine, caused Cody’s life-altering injuries.
Both Dr Balbona and Hudson’s ground-breaking research has led to the discovery of how the injectable modified phospholipids can cause serious adverse events in the human body.
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Immunologist David Ostrov Discusses Potential Use & Early Testing
Description: Repeat guest Dr. Ostrov is an immunologist and researcher at the University of Florida College of Medicine. You can learn more about him, "Lactovid", and contact him here.To learn more about participating in the Long COVID trial, you can https://pmr.med.ufl.edu/research/currently-enrolling-studies/registry-for-people-with-long-covid/
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