The foreword below, written by Dr. Naomi R. Wolf, is being added to the Amazon Kindle version of the War Room / DailyClout Pfizer Documents Analysis Volunteers’ Reports eBook: Find Out What Pfizer, FDA Tried to Conceal. [Note: Kindle ebooks can only be purchased on the Amazon website in a […]
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 50: 20% of Post-Jab Strokes Fatal in the 90 Days Following Pfizer COVID mRNA Vaccine Rollout
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Team created the following Stroke System Organ Class (SOC) Review from data in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). The stroke category comprises the diagnoses of strokes attributed to either obstruction […]
Report 49: Clotting System-Related Adverse Events Following Pfizer COVID-19 mRNA Vaccination
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Team created the following Thromboembolic System Organ Class (SOC) Review from data in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). The thromboembolic system is the human body’s clotting system and includes general […]
Letter to Oklahoma Attorney General: Request for State Criminal Investigation of CDC for the Crime of Maiming
On December 13, 2022, a War Room/DailyClout Pfizer Documents Analysis Project volunteer attorney and former employee of the Office of the Oklahoma Attorney General wrote a letter to Oklahoma Attorney General (AG) John M. O’Connor requesting a state criminal investigation of the Centers for Disease Control and Prevention (CDC) based […]
Letters to 13 State Attorneys General to Consider Investigating and Prosecuting CDC Officials for Reckless Endangerment or Similar Crimes
Attorney Edward A. Berkovich recently sent letters to the attorneys general for Wyoming, New Hampshire, Kentucky, Kansas, Texas, Indiana, Alaska, Alabama, Arizona, Tennessee, Montana, Florida, and Utah, encouraging them to consider state-level action to investigate and prosecute Centers for Disease Control and Prevention (CDC) officials for reckless endangerment or similar […]
Report 48: VAERS – 76% of Vaccine-Related Miscarriages from the Past 30 Years Occurred Once Pregnant Women Started Receiving COVID-19 Vaccines
If you are pregnant, you are more likely to lose your baby in a miscarriage if you receive a COVID-19 vaccine than if you receive measles, mumps, flu, tetanus, or any other vaccine. This and other alarming facts about risks to babies of vaccinated mothers comes from the U.S. government’s […]
Report 47: Blood System-Related Adverse Events Following Pfizer COVID-19 mRNA Vaccination
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Team created the following two-page Hematological System Organ Class (SOC) Review from data in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). The hematological system is the human body’s blood system and includes […]
Impotence, Erectile Dysfunction, and Multiple Prostate Problems Appear as Adverse Events After Vaccination with Pfizer’s mRNA COVID Vaccine
Shocking harms to men’s reproduction and sexual function continue to surface. In this video, DailyClout’s COO and Program Director of the War Room/DailyClout Pfizer Documents Analysis Project, Amy Kelly, talks about prostate problems, erectile dysfunction, and functional impotence found in an untitled Pfizer adverse events document (filename: “125742_S1_M5_5351_c4591001-interim-mth6-adverse-events“). The document is […]
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, […]