Former Pfizer Employee Whistleblower Alleges Falsified Data in COVID Biologic Trial
A former testing site researcher in Texas has alleged that Pfizer’s pre-licensure BNT162b2 (also known as “Comirnaty”) COVID-19 biologic trials included falsification of data, unblinding patients, employing inadequately trained vaccinators, and delays in following up on experimental COVID vaccine adverse reaction reports.1 According to clinical trial researcher Brook Jackson, the incidences occurred during the phase […]
Young Man in New Zealand Dies of Myocarditis 12 Days After Getting Pfizer COVID Biologic
A 26-year-old man in Dunedin, New Zealand died on Nov. 17, 2021 unexpectedly, 12 days after getting the first dose of Pfizer/BioNTech’s experimental messenger RNA (mRNA) BNT162b2 (also known as “Comirnaty”) biologic for COVID-19. Rory James Nairn was vaccinated on Nov. 5 and reportedly began to feel heart palpations or “flutters” a few hours after […]
CDC Opts for mRNA Biologics Over J&J COVID Vaccine Following Nine Blood Clotting Deaths
Based on concerns over a growing number of reports of a blood clotting disorder known as thrombosis with thrombocytopenia syndrome (TTS) following vaccination with Johnson & Johnson/Janssen’s experimental human adenovirus vectored Ad26.COV2.S vaccine, the Advisory Committee on Immunization Practices (ACIP) voted 15-0 on Dec. 16, 2021 to recommend the experimental messenger RNA (mRNA) COVID-19 biologics […]
Ohio Jury Found Pharmacies Liable for Fueling the Opioid Crisis
On Nov. 23, 2021, a federal jury in Ohio held pharmacies liable for their role in the epidemic of opioid use in America. The jury found that CVS, Walgreens and Walmart were responsible for inappropriately dispensing large amounts of opioid drugs prescribed by doctors that caused hundreds of deaths from overdoses. Rite Aid and Giant […]
Some Physicians Warn Against Warp Speed COVID Vaccinations for Children
On Oct. 29, 2021 the U.S Food and Drug Administration (FDA) approved the use of Pfizer/BioNTech COVID-19 vaccine by five- to 11-year-old children under federal Emergency Use Authorization (EUA) guidelines. As California became the first state to announce that COVID vaccine will be required for children to attend school, districts in several other states plan […]
Merck and Pfizer Seek Approval for COVID-19 Antiviral Drugs
Merck and Pfizer have submitted Emergency Use Authorization (EUA) applications to the U.S. Food and Drug Administration (FDA) to authorize distribution of what would be the first antiviral drug specifically designed to treat COVID-19 disease.1 Merck/Ridgeback Biotherapeutics are seeking EUA approval for Molnupiravir (MK-4482/EIDD-2801), an investigational oral antiviral drug originally developed to treat influenza.2 Pfizer […]
