Two Massachusetts attorneys, Patricia B. Doherty and Julie A. Piantedosi, wrote a letter to the Massachusetts Attorney General (AG), Andrea Campbell, stating: The Federal Government, Food and Drug Administration (FDA), and the Centers for Disease Control and Prevention (CDC) hid the Pfizer mRNA COVID vaccine’s known adverse event details – […]
Report 52: Nine Months Post-COVID mRNA “Vaccine” Rollout, Substantial Birth Rate Drops in 13 European Countries, England/Wales, Australia, and Taiwan.
Robert W. Chandler, MD, completed extensive research to write the article below. Some of the highlights of this important piece include: Nine months following the rollout of the COVID-19 mRNA “vaccines,” substantial birth rate drops were seen in 13 of 19 European countries, England and Wales (one entity based on how […]
Letter to Five Utah County or District Attorneys: Screen for State Prosecution of CDC Officials for Reckless Endangerment of County Residents
On December 27, 2022, Attorney Edward A. Berkovich sent a letter to the county or district attorneys for Utah’s five most populous counties, encouraging them to consider investigation and prosecution of Centers for Disease Control and Prevention (CDC) officials for reckless endangerment of their county residents, under Utah Code § 76-5-112, […]
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 […]
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 […]
Letter to Wisconsin Attorney General: Request for State Criminal Investigation of CDC Officials for Recklessly Endangering Safety
On December 13, 2022, a War Room/DailyClout Pfizer Documents Analysis Project volunteer attorney sent a letter to Wisconsin Attorney General Josh Kaul requesting that his office investigate Centers for Disease Control and Prevention (CDC) officials for recklessly endangering safety of Wisconsinites when they delayed for three months reporting the incidence […]
Letter to California AG: Criminal Investigation of CDC Officials for Child Endangerment
On December 9, 2022, War Room/DailyClout volunteer attorney Virginia E. Stewart wrote a letter to California Attorney General (AG), Rob Bonta, requesting that his office investigate the Centers for Disease Control and Prevention (CDC) officials for child endangerment pursuant to California Penal Code 273(a), which states: Any person who, under […]
“170 Patients That Changed Everything” – Spectator | Australia
Few people realise that the Emergency Use Authorisation (EUA) of the Pfizer-BioNTech Covid-19 Vaccine/BNT162b2 was granted on the efficacy data of 170 patients. The 162 who received a placebo and 8 patients who were vaccinated formed the basis of the 95 per cent efficacy claims. There has not been much […]
UK Public Health Agency Approves COVID-19 vaccine for Babies Age Six Months- Four Years
The Medicines and Healthcare products Regulatory Agency (MHRA), a public health agency in the UK has signed its approval on administering COVID mRNA vaccines to babies from the age of six months old. The mRNA vaccine will be given at a smaller dose than the older age groups, and still […]
Pfizer Broke Its Own Rules to Obtain EUA
War Room/DailyClout Research Team Finds Pfizer Broke Its Own Clinical Trial Rules Dishonestly to Obtain mRNA COVID Vaccine EUA 95% Vaccine Efficacy Out of the tens of thousands of trial participants, the efficacy rate was determined by just 170 participants who contracted COVID-19 in the time frame set after Dose […]
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 46: How Many Pregnant Women Received LNP/mRNA via COVID-19 Vaccine During the Year 2021? Only Estimates Are Available.
Shockingly, as 2022 comes to a close and the world reaches the two-year mark of experimental COVID-19 vaccines being available to the general public, the scientific and medical communities, as well as everyday citizens, still have very little information about the effects of mRNA COVID-19 vaccines on pregnant women and […]
Letter to Florida Attorney General: Consider State Criminal Prosecution of CDC Officials for Reckless Endangerment of Citizens
Attorney Edward A. Berkovich wrote a November 17, 2022, letter to Florida Attorney General, Ashley B. Moody, copying State Surgeon General, Joseph Ladapo, MD, asking her to consider screening for prosecution of the Centers for Disease Control and Prevention (CDC) officials for violating Florida’s culpable negligence criminal code section. Please […]
United Kingdom Health Agency Gets FOIA Requesting All AstraZeneca COVID-19 Vaccine Data
A legally-produced, effective Freedom of Information Act (FOIA) request was sent to Dame June Raine, Chief Executive of Medicines and Healthcare Products Regulatory Agency (MHRA), on behalf of the Health Advisory and Recovery Team (HART), requesting that the MHRA fully produce all the data, information and documents submitted to them by AstraZeneca […]
A Drug Safety Physician’s Correspondence with the FDA: A Quest for Accuracy in Investigational Bivalent mRNA COVID-19 ‘Vaccine’ Adverse Event Reporting
Introduction On November 4, 2022, the Centers for Disease Control and Prevention (CDC) and U.S. Food and Drug Administration (FDA) concluded that, based on Vaccine Adverse Events Reporting System (VAERS) and v-safe data received between August 31, 2022, and October 23, 2022, “Health care providers and patients can be […]
Documentary: “Safe and Effective: A Second Opinion”
“Safe and Effective: A Second Opinion” shines a light on Covid-19 vaccine injuries and bereavements, but also takes an encompassing look at the systemic failings that appear to have enabled them. We look at leading analysis of pharmaceutical trials, the role of the Medicines and Healthcare Regulatory Agency (MHRA) in […]
Report 42: Pfizer’s EUA Granted Based on Fewer Than 0.4% of Clinical Trial Participants. FDA Ignored Disqualifying Protocol Deviations to Grant EUA.
Locations of the 170 Pfizer Clinical Trial Patients Used to Gain Emergency Use Authorization (EUA) for Its COVID mRNA Vaccine. Courtesy of OPENVAET.org For audio-visual explanations of this report, please see these videos. So much has been written about the pivotal Pfizer Trial for COVID-19 (C4591001), that it is sometimes […]
Report 41: 2021 CDC and FDA Misinformation – Retroactive Editing, Erroneous Spontaneous Abortion Rate Calculation, Obfuscation in the New England Journal of Medicine
The following article is a follow-up to Dr. Chandler’s report, “Data Do Not Support Safety of mRNA COVID Vaccination for Pregnant Women,” which reviewed “Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant Persons,” New England Journal of Medicine, April 21, 2021, and June 17, 2021. To best understand this […]
Report 40: Data Do Not Support Safety of mRNA COVID Vaccination for Pregnant Women
Commentary on “Preliminary Findings of mRNA Covid Vaccine Safety in Pregnant Persons” as Reported by the Centers for Disease Control and Prevention and the Food and Drug Administration, June 17, 2021, New England Journal of Medicine Note: On September 26, 2022, Dr. Chandler published a follow-up report to the report […]
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, […]