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In response to a Freedom of Information Request submitted by Children’s Health Defense, the Centers for Disease Control and Prevention last week admitted it never analyzed the Vaccine Adverse Event Reporting System for safety signals for COVID-19 vaccines.

The attorneys that represent ICAN are representing the plaintiff in a lawsuit against the FDA to obtain Pfizer’s covid vaccine documents. They recently secured an unredacted copy of a previously produced post-authorization adverse event report. The lifted redactions reveal that within weeks of Pfizer’s vaccine being administered pursuant to emergency use authorization, Pfizer, apparently unexpectedly, had to hire 600 full time employees “to help alleviate the large increase of adverse event reports” being received by the company.

The v-safe protocol lists a series of 15 “Adverse Events of Special Interest” but, unbelievably, the v-safe program itself does not even track these adverse events!

Recently, we told you that vaccine manufacturers have to submit FOIA requests to the FDA to obtain additional information regarding serious adverse events, including deaths, following the use of their products that are submitted to VAERS. We know this because Janssen’s Chief Medical Officer (CMO) said so during his presentation at the CDC’s Advisory Committee on Immunization Practices (ACIP) meeting, convened to investigate the safety of the J&J/Janssen vaccine.

Vaccine manufacturers, like the rest of the public, must submit a FOIA to the FDA to obtain additional information regarding serious adverse events, including deaths, submitted to VAERS. The problem: they are not doing it.

ICAN discovered 1,102 deleted reports from the Vaccine Adverse Event Reporting System(VAERS). ICAN wrote CDC, FDA, and HHS demanding answers.

ICAN has obtained unreleased lot and dose data for the Moderna and Pfizer COVID-19 vaccines. OpenVAERS’ analyses of this data indicates several “hot lots.”

A federal judge has ordered the CDC to release all 7.8 million v-safe free text field entries over the next 12 months.

Judicial Watch announced today that it filed a Freedom of Information Act (FOIA) lawsuit against the U.S. Department of Defense for records and communications relating to the data contained in the Defense Medical Epidemiology Database (Judicial Watch, Inc. v. U.S. Department of Defense (No. 1:22-cv-03043)).The Armed Forces Health Surveillance Branch’s Defense Medical Epidemiology Database is a web-based tool designed to provide access to:

Comprehensive investigation and analysis by Mathew Crawford

The Vaccine Wars Part XXXIII

They missed hundreds of serious adverse events that are more elevated than myocarditis. A new VAERS analysis done by Albert Benavides blows the doors off the "safe and effective" narrative.

The DMED data exposed by attorney Tom Renz and Senator Johnson is a smoking gun. General Austin should order all military docs to speak the truth. But he isn't. Why not?

An independent derivation of the VAERS URF using the CMS death data leads to a URF of 44.64 which then leads to a 388K excess death estimate.

They never found any safety signals, because they didn't look for them

Vaccine manufacturers, like the rest of the public, must submit a FOIA to the FDA to obtain additional information regarding serious adverse events, including deaths, submitted to VAERS. The problem: they are not doing it.

Going back to where it all began for me...