Pfizer/Moderna clinical trials and safety studies

This nonprofit, made up of public health professionals, medical professionals, scientists, and journalists exists solely to obtain and disseminate the data

Four days after the Pfizer vaccine was approved for ages 16+, PHMPT submitted a Freedom of Information Act Request to the FDA for all of the data within Pfizer’s COVID-19 vaccine biological product file. PHMPT has now sued the FDA for not releasing the data. Click below for court documents and for productions of Pfizer’s documents from the FDA.

Buy The Pfizer Papers: Pfizer's Crimes Against Humanity by The WarRoom/DailyClout Pfizer Documents Analysts, Wolf, Naomi, Kelly, Amy, Bannon, Stephen K (ISBN: 9781648210372) from Amazon's Book Store. Everyday low prices and free delivery on eligible orders.

In collaboration with the Daily Clout, UKC has produced a summary of the #PfizerReports with links back to the full reports.

Motion for summary judgement filed 10/17/2024

The latest release by the U.S. Food and Drug Administration of Pfizer-BioNTech COVID-19 vaccine documents raises questions about how frequently adverse events experienced by clinical trial participants were reported as “unrelated” to the vaccine.

The "missing link" was there in Pradhan's paper all along, we just needed to ask the right question: "where are the genome sequences for the Gp-120 inserts"

According to Alexandra Latypova, an ex-pharmaceutical industry executive, documents obtained from the U.S. Department of Health and Human Services on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe.

New documents obtained by TrialSite News suggest routine quality testing issues were overlooked in the rush to authorize use of the Pfizer COVID vaccine.

In this work, we review the reports provided by Pfizer to the FDA for the trial's first interim analysis. The reports demonstrate severe flaws in the procedure of approving Pfizer's Covid-19 vaccine based on data from the vaccine’s phase III clinical trial.

This article reviews some of the publicly available documents on Pfizer’s non-clinical development program and points out its deficiencies, omissions and gaps, which were very obvious, yet were never questioned by the regulators or other health authorities.

Search, summarise, analyse and discover information from the Pfizer documents released under FOIA

Dr. Robert Malone is a leading expert in the field of mRNA vaccine technology, an immunologist and molecular biologist with more than 35 years of experienc...

A group of scientists and medical researchers sued the FDA under FOIA to force release of hundreds of thousands of documents related to licensing of the Pfizer-BioNTech Covid-19 vaccine. Plaintiff’s attorney Aaron Siri, who is representing the group, explains the fight that led a federal court to order expedited release of documents the agency claimed it would take decades to process.

The FDA has made public the first batch of documents it used to authorize Pfizer’s COVID shots, including a report detailing over 150,000 serious adverse events and more than 1,200 deaths connected to the jabs.

ICAN’s attorneys reviewed a startling report from June 2020 that Pfizer submitted to the FDA concerning its mRNA COVID-19 vaccine.

A Federal judge ordered FDA to release the documents it relied upon to license Pfizer and Moderna COVID-19 Vaccines for 12-15 yr-olds.

The latest batch of Pfizer COVID-19 Vaccine documents contain case report forms of 212 trial subjects, and many are highly concerning.

FDA says it has produced all documents in the biologic product file of Pfizer’s COVID-19 vaccine for ages 16 and up, 800 days after approval.

Documents with a large file size are provided in a .zip file and will need to be uncompressed after download.

Public Health and Medical Professionals for Transparency Documents Pfizer 12-15 and Moderna Court Documents

Public Health and Medical Professionals for Transparency Documents Pfizer 16+ Court Documents

Documents with a large file size are provided in a .zip file and will need to be uncompressed after download.

As of November 2023, FDA has represented that the production of the biologic product file for Comirnaty (16 years of age and older) is complete. PHMPT is

A great win for transparency that removes a stranglehold "health" authorities have had on data independent scientists need to offer solutions and address serious issues with the vaccine program.

Was it fraud? You tell me.

But first...why haven't you even heard of them?