A Pfizer subcontractor is being accused of falsifying data, unblinding patients, hiring inadequately trained vaccinators and failing to follow up on adverse events during the company’s Wuhan coronavirus (Covid-19) “vaccine” clinical trials.
A paper published in the British Medical Journal (BMJ) reveals that the company, called Ventavia Research Group, heavily manipulated the phase III study for Pfizer’s Chinese Virus injection during the fall of 2020, just months before it was rushed into production and distribution at “warp speed” by the Trump administration.
A company whistleblower came forward with the revelations, which prompted a group of 16 Swedish doctors and researchers to circulate a petition calling on the Pfizer jab to no longer be administered in the Nordic country.
“The staff who performed quality checks were reportedly overwhelmed by the amount of problems they discovered,” reported Sputnik News. “The BMJ (study) concluded that the trial raised questions about data integrity and regulatory oversight.”
The 16 signatories of the petition called the revelations “extremely serious,” adding that the side effects associated with Pfizer’s injections are “gigantic.”
“For instance, in Sweden alone during the ten months that vaccination has taken place wholly 83,744 suspected side effects have been reported – which is more than ten times more than all side effects reported for all drugs and vaccines per year in the immediately preceding years, for a total of about 25,000 substances, the authors emphasized,” Sputnik explained.
Pfizer does whatever it wants because the FDA lets it