The FDA daily adverse event dashboard updates are designed to provide faster access to safety information for drugs and biologics. By offering FDA daily adverse event dashboard updates, the agency aims to reduce delays and improve the transparency of reported data. Background on the FAERS System The FDA Adverse Event […]
COVID-19 Vaccines and Neuropsychiatric Risks: Study Insights
The potential link between COVID-19 vaccination and neuropsychiatric conditions has sparked significant interest in recent medical research. A peer-reviewed study, “View of Association Between COVID-19 Vaccination and Neuropsychiatric Conditions,” published in the International Journal of Innovative Research in Medical Science investigates this connection, offering insights into post-mRNA COVID vaccination adverse […]
Report 97: Pfizer Obscured Myocarditis Safety Signal Specific to Young Men. FDA Took Five Months to Notice Pfizer’s Obfuscation.
Career scientists are struggling with attention to detail in fulfilling their vaccine safety duties. Their conclusions, marked by errors and oversights, have led to lives lost and debilitating disorders, as proven by the government scientists’ own review documents. In spring 2021, the US Food and Drug Administration (FDA) granted emergency […]
V-Safe Voices: Tachycardia Post-COVID Vaccination
DailyClout Introduces a New Series: “V-Safe Voices” The Centers for Disease Control and Prevention (CDC) uses V-safe to monitor vaccine safety. After signing up, V-safe participants share, through an app, with the CDC how they or their dependent(s) feel after getting a participating vaccine, including the COVID-19 vaccines. The app presents […]
Report 94: Pfizer Secretly Studied a Heart Damage Marker, Troponin I, in Five- to 15-Year-Olds, Following mRNA COVID Vaccination in 2021.
We warned that there was proof that the Pfizer BNT162b2 mRNA COVID vaccine caused heart damage in teens and young adults, as early as May of 2021. As more information surfaces from the court-mandated release of Pfizer clinical trial documents by the FDA, and via FOIA’d emails, the CDC’s cover-up […]
Report 87: In Early 2021, Pfizer Documented Significant Harms and Deaths Following Vaccination with Its mRNA COVID Vaccine. The FDA Did Not Inform the Public.
INTRODUCTION “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021,” Pfizer’s post-marketing report, a required U.S. Food and Drug Administration (FDA) compliance document, is one of the ways in which the FDA assessed patients’ risks associated with Pfizer’s COVID-19 vaccine, BNT162b2. The data within the […]
“To Evaluate the Safety, Tolerability, and Immunogenicity of BNT162b2 Against COVID-19 in Healthy Pregnant Women 18 Years of Age and Older” – Latest version (submitted July 14, 2023) on ClinicalTrials.gov
“The Safety of BNT162b2 Against COVID-19 in Healthy Pregnant Women 18 Years of Age and Older,” eh? Hmm. I was under the impression that if you are pregnant, or hoping to be, you shouldn’t do certain things like drink alcohol, smoke cigarettes, and get injected with experimental transfecting agents. You […]
International Experts Testify Again, This Time in Brazil (Porto Alegre Seminar)
The brave representative Fernanda Barth led the hearing in the Municipality of Porto Alegro along with John Kage. Many of the names you have come to love and respect were there, and I was asked by Dr Naomi Wolf to represent the 3,500 volunteers of the WarRoom/DailyClout Pfizer Document Investigations. […]
Carol Taccetta, MD: “Boxed Warning,” the FDA’s Most Serious Warning, Is Absent from All COVID-19 Vaccine Fact Sheets
Introduction There are some adverse reactions in a product label that are so serious, and possibly even preventable, that special labeling is required to highlight this warning information: a “BOXED WARNING.” https://www.fda.gov/media/71866/download https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?fr=201.57 This boxed warning information, “critical for a prescriber to consider,” is commonly referred to as a […]
Report 77: Women Suffered 94% of Dermatological Adverse Events Reported in First 90 Days of Pfizer COVID “Vaccine” Rollout. 80% of These Adverse Events Were Categorized As “Serious.”
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt – produced a report about Dermatological Adverse Events of Special Interest (AESIs) found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 […]
Report 65: In the First Three Months of Pfizer’s mRNA “Vaccine” Rollout, Nine Patients Died of Anaphylaxis. 79% of Anaphylaxis Adverse Events Were Rated as “Serious.”
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt – produced an shocking review of anaphylaxis (severe allergy reaction) adverse events found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 […]
Losing Control of the Controlled Clinical Trial in These Times of Emergency Use Authorization (EUA) Vaccines
Do you remember your high school science teacher explaining what a controlled experiment is? It is when just one thing is changed in the group receiving the experimental intervention (compared to the “control” group receiving standard or no treatment), then one waits to see if there is a difference in […]
Report 54: Infants and Children Under 12 Given the Pfizer mRNA COVID “Vaccine” Seven Months BEFORE Pediatric Approval. 71% of Adverse Event Cases Classified as Serious.
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt – produced a shocking review of the pediatric data found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through […]