FDA Oversight of Clinical Trials is “Grossly Inadequate” Say Experts

Maryanne Demasi On 25 September 2020, the US Food and Drug Administration (FDA) received a complaint by Brook Jackson who had been working for Ventavia Research Group, a Texas based company hired to run clinical trials for Pfizer’s covid-19 mRNA vaccine. Jackson, a regional director, had witnessed problems at three trial sites she was overseeing […]

Vaccines for Preventing Influenza in healthy Adults

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Vittorio Demicheli et al. We found 52 clinical trials of over 80,000 adults. We were unable to determine the impact of bias on about 70% of the included studies due to insufficient reporting of details. Around 15% of the included studies were well designed and conducted. We focused on reporting of results from 25 studies […]

Let’s Bring the Informed Consent Process Out of the Shadows

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Misha Angrist The disclosures researchers use to obtain consent in clinical trials are rarely shared with the public. They should be. Since the long parade of ethics scandals that plagued biomedical research during the 20th century — from Nazi doctors’ experiments, to the Tuskegee Syphilis Study, to a Brooklyn hospital study that injected patients with […]

Evidence of Harm

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Steve Kirsch Here’s a high level collection of some of the most compelling pieces of evidence I’ve seen to date. This is not an exhaustive list, but just the key pieces of data that are impossible to explain if the vaccines are safe and effective. I’ve divided the collection into sections and I’ve tried to […]

Latest FDA-Pfizer Document Dump: Why Did So Many Participants With ‘Minor’ Adverse Events Withdraw From Trial?

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Michael Nevradakis July’s release of U.S. Food and Drug Administration (FDA) documents pertaining to the Emergency Use Authorization (EUA) granted to the Pfizer-BioNTech COVID-19 vaccine included reports of a significant number of participants who withdrew from the trials — and the reasons for these withdrawals. In some instances, participants withdrew or were withdrawn from the trial […]

Pfizer’s ‘Sensitive’ Document Reveals Alarming Facts about Trial Subjects

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Sonia Elijah A particular document that stood out to me in the latest July 1, Pfizer data dump, is the 3611-page document entitled, ‘C4591001-fa-interim-narrative-sensitive.’ It contains pertinent information on hundreds of Pfizer’s clinical trial subjects who whether due to death, serious adverse events, pregnancy, COVID-19 or just ‘no longer meeting eligible criteria,’ were withdrawn from […]