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FDA Dumps More Pfizer Documents: Why Were So Many Adverse Events Reported as ‘Unrelated’ to Vaccine?
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.
Congressman Introduces Bill to Force FDA to Release Pfizer Documents Within 100 Days, Instead of 55 Years
U.S. Rep. Ralph Norman (R-S.C.) on Thursday introduced legislation to require the U.S. Food and Drug Administration (FDA) to release, within 100 days, all records of information related to Pfizer COVID vaccines. The FDA had asked to be allowed to take up to 55 years to release the documents.
Government Officials Pressured EU Regulators to Rush Authorization of Pfizer Vaccine, Leaked Documents Reveal
U.S. and EU government officials pressured European drug regulators to rush approval of Pfizer-BioNTech’s COVID-19 vaccine despite safety concerns, according to leaked documents from the European Medicines Agency.
Uruguayan Judge Demands Government, Pfizer Turn Over Documents as Court Considers Request to Halt COVID Vaccines for Kids
Uruguayan government officials and Pfizer were ordered to appear in court Wednesday to provide documents for review regarding vaccine ingredients, adverse effects and contracts shielding the pharma giant from liability.
Documents released April 1 by the U.S. Food and Drug Administration show the adverse event rate per dose for Pfizer’s mRNA jab, based on the company’s own studies, is nearly 1 in 800, and the myocarditis rate is 10 in 100,000 — far greater than the 2 in 100,000 rate previously reported.
Pfizer hired about 600 additional full-time employees to process adverse event reports during the three months following authorization of its COVID-19 vaccine, with plans to hire 1,800 more by June 2021, newly released documents reveal.
The evidence laid out in official, legal documents used to issue an Emergency Use Authorization for the Pfizer-BioNTech COVID-19 vaccine, and a license for Pfizer’s Comirnaty vaccine, clearly contradicts safety information provided to the public.
The U.S. Food and Drug Administration on Tuesday released a 10,000-page cache of documents pertaining to the Emergency Use Authorization of Pfizer’s COVID vaccine. An initial review shows the documents contain details about animal studies, adverse events experienced by trial participants, the makeup of Pfizer’s internal review committee … and more.
A document released by the U.S. Food and Drug Administration shows Pfizer’s own analysis of adverse events following its COVID vaccine revealed safety concerns yet the FDA refuses to acknowledge them.
“ … it is dystopian for the government to give Pfizer billions, mandate Americans to take its product, prohibit Americans from suing for harms, but yet refuse to let Americans see the data underlying its licensure.”
Newly released documents support whistleblower Brook Jackson’s claims she was directly involved in Pfizer’s COVID vaccine phase 3 clinical trials, but Pfizer contractor, Ventavia Research Group, and media refuse to retract statements to the contrary.
New documents obtained by TrialSite News suggest routine quality testing issues were overlooked in the rush to authorize use of the Pfizer COVID vaccine.
Michigan State Student Who Suffered Blood Clot After Pfizer COVID Vaccine Granted Reprieve From Mandate
A college student who suffered a blood clot after getting Pfizer’s COVID-19 vaccine has been given a temporary reprieve from his school’s COVID-19 vaccine mandate.
Moderna Sues Pfizer Over COVID Vaccine Patent Infringement, But Patents ‘Belong to the World,’ Says Dr. Robert Malone
Moderna today filed patent infringement lawsuits against Pfizer and BioNTech, alleging the two companies copied Moderna’s patented mRNA technology. However, in an interview with The Defender, Dr. Robert Malone said the patents are derived from his own work on mRNA technology and they are now expired.
Nearly 30,000 Deaths Reported to VAERS, Including 17-Year-Old Who Died of Myocarditis 5 Months After Pfizer Shot
VAERS data released Friday by the Centers for Disease Control and Prevention show 1,371,474 reports of adverse events from all age groups following COVID-19 vaccines, including 29,981 deaths and 249,116 serious injuries between Dec. 14, 2020, and July 29, 2022.
Not only did Pfizer’s COVID-19 vaccines double the company’s annual revenue, but they also gave the drugmaker unique weight in determining U.S. health policy — something that concerns even staunch vaccine-pushers like Dr. Paul Offit.
Latest FDA-Pfizer Document Dump: Why Did So Many Participants With ‘Minor’ Adverse Events Withdraw From Trial?
July’s release of U.S. Food and Drug Administration documents pertaining to the Emergency Use Authorization 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.
The Defender’s Big Brother NewsWatch brings you the latest headlines related to governments’ abuse of power, including attacks on democracy, civil liberties and use of mass surveillance.
This month’s release of Pfizer COVID-19 vaccine documents by the U.S. Food and Drug Administration reveals three more reports of deaths among vaccine trial participants and more instances of Pfizer listing injuries as “not related” to the vaccine.
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.
In a move Children’s Health Defense President Mary Holland called “head-spinning,” the U.S. Food and Drug Administration on Friday granted full approval of Pfizer-BioNTech’s Comirnaty COVID-19 vaccine for adolescents 12 through 15 years old.
Uruguay Halts COVID-19 Vaccine for Kids Under 13, Judge Demands Government Officials Turn Over Pfizer Contracts
Uruguay suspended COVID-19 vaccines for children under 13 after a judge on Thursday issued an injunction halting vaccinations in that age group until government officials turn over its contracts with Pfizer.
In an interview with The Defender, the lawyer representing whistleblower Brook Jackson said Pfizer is arguing the court should dismiss Jackson’s lawsuit alleging fraud in Pfizer’s COVID-19 clinical trials because the U.S. government knew about the wrongdoings but continued to do business with the vaccine maker.
Pfizer, Moderna Shots More Likely to Cause Serious Injury Than Reduce Risk of COVID-Related Hospitalization
A new analysis of Pfizer and Moderna COVID-19 vaccine trial data shows the risk of serious injury following the vaccine is greater than the reduction in COVID-19 hospitalizations, according to a study posted June 23 on Social Science Research Network.
Julian Scholefield was paralyzed from the waist down in July 2021, 12 days after his second Pfizer COVID-19 vaccine. Nearly a year later, he’s still waiting for the government to respond to his request for compensation.
A nonprofit group is suing the U.S. Food and Drug Administration in an effort to obtain documents relating to the FDA’s approval of Moderna’s Spikevax COVID-19 vaccine after the agency told the group there was “no compelling need” to expedite the release of the documents.
The authors of a study showing Pfizer’s COVID-19 vaccine reduces sperm quality concluded the reduction was temporary, but others who examined the data behind the study questioned that assertion.