FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal

The Defender | 12 July 2022 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. According to an ex-pharmaceutical…

Government Officials Pressured EU Regulators to Rush Authorization of Pfizer Vaccine, Leaked Documents Reveal

Michael Nevradakis | 11 July 2022 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. 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…

Uruguay Halts COVID-19 Vaccine for Kids Under 13, Judge Demands Government Officials Turn Over Pfizer Contracts

The Defender | 8 July 2022 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. Uruguay suspended COVID-19 vaccines for children under 13 after a judge on Thursday issued an injunction halting vaccinations in that…

Uruguayan Judge Demands Government, Pfizer Turn Over Documents as Court Considers Request to Halt COVID Vaccines for Kids

The Defender | 6 July 2022 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. Uruguayan government officials and Pfizer on Wednesday appeared in court after a judge gave them 48 hours to present detailed…

‘Why the Rush for Toddler Vaccines?’ Asks Wall Street Journal Editorial Board Member

Susan C. Olmstead | 5 July 2022 Allysia Finley, a member of Wall Street Journal’s editorial board, Monday called into question the motives behind the U.S. Food and Drug Administration’s decision to extend emergency use of Pfizer and Moderna’s COVID-19 vaccines to infants and toddlers. A Wall Street Journal (WSJ) editorial board member Monday called into…

Pfizer Asks Court to Dismiss Whistleblower Lawsuit Because Government Was Aware of Fraud

The Defender | 5 July 2022 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. A lawsuit filed by whistleblower…

From FDA to MHRA: are drug regulators for hire?

BMJ | 29 June 2022 Patients and doctors expect drug regulators to provide an unbiased, rigorous assessment of investigational medicines before they hit the market. But do they have sufficient independence from the companies they are meant to regulate? Maryanne Demasi investigates Over the past decades, regulatory agencies have seen large proportions of their budgets funded by…