Attorney Diane Protat is “counsel for the collective “Where is my cycle?,” which groups together tens of thousands of women in Europe who suffer from the undesirable effects of the Covid 19 vaccination on their menstrual cycle: amenorrhea, menorrhagia, adenomyosis, endometriosis, polycystic ovarian syndrome, miscarriage or even hysterectomy.” In October […]
“Where’s my cycle?” v. European Commission: Tens of Thousands of European Women Demand Answers Regarding Undesirable Menstrual Effects Following COVID-19 Vaccination.
Report 63: In Q3 2022, Pfizer Wrote Off $450 Million of Expired or Expiring COVID-19-Related Inventory.
Despite generating over $100 billion in revenue in 2022, Pfizer’s stock has dropped precipitously. Pfizer’s revenue was relatively flat, hovering between $41 billion and $51 billion, from 2014 to 2020. Then, its mRNA COVID-19 “vaccine” was awarded Emergency Use Authorization (EUA) by the Food and Drug Administration (FDA) on December […]
Report 56: Histopathology Series Part 1 – Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus
Summary: Dr. Arne Burkhardt is one of eight international pathologists, physicians and scientists who were asked to perform a second autopsy, requested by friends and family of the deceased who were not satisfied with the results of the first autopsy. Thirty autopsies and three biopsies were evaluated; 15 cases […]
Letter to the FDA: COVID-19 ‘Vaccines’ and COVID-19 Infection Linked to Myocarditis – What Do They Have in Common?
Peter Marks, MD, PhD Director, Center for Biologics Evaluation and Research U.S. Food and Drug Administration 10903 New Hampshire Avenue WO71-7232 Silver Spring, MD 20993 Peter.Marks@fda.hhs.gov December 18, 2022 Dear Dr. Marks, I am troubled by the following, and look forward to your studied response on my single […]
Report 39: Despite Incomplete Safety Trials, the Food and Drug Administration (FDA) Grants Full Approval to Pfizer-BioNTech’s COMIRNATY® for Adolescents 12-15 Years of Age
Without a completed safety study or expert committee review, the FDA issued a supplemental Biologics License Application (“sBLA”) approval letter granting full FDA approval to Pfizer-BioNTech’s COMIRNATY® COVID-19 mRNA vaccine for use in children ages 12-15. This was done even though safety study completion, on which approval should be based, […]
The Food and Drug Administration (FDA) Grants Full Approval to Pfizer-BioNTech’s COMIRNATY for Adolescents 12-15 Years of Age Despite Incomplete Safety Trials
Without having assembled an expert committee, the FDA issued a supplemental BLA (“sBLA”) approval letter granting full FDA approval to Pfizer-BioNTech’s COMIRNATY COVID-19 mRNA vaccine for use in children ages 12-15. They did this despite the fact that the safety study on which approval should be based will not be […]
Report 31: Pfizer-BioNTech “Equivalent” Half Truths or a “Lot” of Lies?
Pfizer-BioNTech FDA-Approved “Equivalent” Half Truths or a “Lot” of Lies? This Report was written exclusively for DailyClout by the Members of the Pfizer Analysis team. It should not be copied or republished without permission from DailyClout or a full credit and link toDailyClout.io Summary The public was not told […]
Report 14: Were We Lied to by the FDA?
What’s the difference between Pfizer’s FDA approved COMIRNATY and the emergency use authorized “vaccine?” Only the law, not science, says the FDA. Were we lied to by the U.S. Food and Drug Administration (FDA) and the media when they told us that, if we received the Pfizer “vaccine” after […]