Statistics and data manipulation

Dr. Theresa Long, medical officer with the United States military, has testified in court that she was ordered by a superior to suppress Covid-19 vaccine injuries following the Biden regime’s mandate

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.

If fraud did take place, Pfizer can (and likely will) be held liable for the more than one million injuries its injection has caused in the U.S. alone, and we all look forward to that reckoning.

And the lack of FDA oversight

ICAN demands that the FDA immediately release the identity of a secret ingredient in the Pfizer vaccine.

ICAN’s lead attorney, Aaron Siri, is representing a broad group of scientists from major universities across the country in a lawsuit seeking to obtain the documents Pfizer provided the FDA to license its COVID-19 vaccine. As you may have seen, the FDA’s response was to ask the judge for a total of 55 years to fully produce these documents!

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!

For the second time, the FDA has avoided answering very simple questions about discrepancies concerning the numbers of deaths in Pfizer’s clinical trial, citing “resource constraints” and blaming its workload, in part, on ICAN’s FOIA requests.

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 has repeatedly demanded that CDC and other “health” agencies appropriately attribute deaths from COVID vs deaths with COVID.

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

In July, ICAN uncovered highly concerning case report forms from individuals in Pfizer’s clinical trial. The August batch contains even more.

ICAN-obtained presentation indicates CDC, FDA and NIH higher-ups knew about shocking levels of waning immunity and breakthrough infection.

The September batch of COVID vaccine trial documents covers a range of information, inc. interesting correspondence between FDA and Pfizer

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.

The Many, Many Faces of Fraud

Here are some indisputable facts about the challenge of assessing the ‘efficacy’ – in particular, benefits and risks, of Covid-19 vacci...

Three participants in the Pfizer Covid vaccine trial died shortly after vaccination and their deaths were not fully investigated, the latest trial documents released under court order reveal.

There are ways to ensure any trial will give you the results you want. Here are the top six methods used to manipulate covid research results.

From the 4/6 FDA VRBPAC Meeting

In Canada, informed consent to medical interventions - including vaccines - is the law. The Canadian Covid Care Alliance supports Informed Consent. References Contained in Video: Supreme Court of Canada Judgment - Cuthbertson vs Rasouli https://scc-csc.lexum.com/scc-csc/scc-csc/en/item/13290/index.do “The patient’s consent must be given voluntarily and must be informed.” The Ontario Health Care Consent Act https://www.ontario.ca/laws/statute/96h02 Elements of Consent CDC Risk for COVID-19 Infection, Hospitalization, and Death By Age Group https://www.cdc.gov/coronavirus/2019-ncov/covid-data/investigations-discovery/hospitalization-death-by-age.html The New England Journal of Medicine Pfizer Vaccine Phase 2 Trial Results https://www.nejm.org/doi/full/10.1056/nejmoa2034577 FDA - Communicating Risks and Benefits https://www.fda.gov/files/about%20fda/published/Communicating-Risk-and-Benefits---An-Evidence-Based-User%27s-Guide-%28Printer-Friendly%29.pdf Consent - A Guide for Canadian Physicians (Canadian Medical Protective Association) https://www.cmpa-acpm.ca/en/advice-publications/handbooks/consent-a-guide-for-canadian-physicians "Further, even uncommon risks of great potential seriousness should be disclosed.” Reported side effects following COVID-19 vaccination in Canada (Government of Canada) https://health-infobase.canada.ca/covid-19/vaccine-safety/ Vaccine Adverse Event Reporting System https://vaers.hhs.gov British Medical Journal Sixty seconds on… Vitamin D https://www.bmj.com/content/371/bmj.m3872/rr-5 CCCA Evaluation of Ivermectin as an Effective Prophylactic, and for Treatment in Hospitalized Patients with COVID-19 https://www.canadiancovidcarealliance.org/media-resources/evaluation-of-ivermectin/ National Centre for Biotechnology Information Ivermectin, ‘Wonder drug’ from Japan: the human use perspective https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/ Pfizer Fact Sheet for Recipients and Caregivers https://www.fda.gov/media/144414/download US National Library of Medicine Study to Describe the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaccine Candidates Against COVID-19 in Healthy Individuals https://clinicaltrials.gov/ct2/show/NCT04368728 Moderna Product Monograph, Including Patient Medication Information - COVID-19 Vaccine Moderna https://www.modernacovid19global.com/ca/product-monograph.pdfSupreme Court of Canada Judgment - Cuthbertson vs Rasouli https://scc-csc.lexum.com/scc-csc/scc-csc/en/item/13290/index.do “The patient’s consent must be given voluntarily and must be informed.” The Ontario Health Care Consent Act https://www.ontario.ca/laws/statute/96h02 Elements of Consent CDC Risk for COVID-19 Infection, Hospitalization, and Death By Age Group https://www.cdc.gov/coronavirus/2019-ncov/covid-data/investigations-discovery/hospitalization-death-by-age.html The New England Journal of Medicine Pfizer Vaccine Phase 2 Trial Results https://www.nejm.org/doi/full/10.1056/nejmoa2034577 FDA - Communicating Risks and Benefits https://www.fda.gov/files/about%20fda/published/Communicating-Risk-and-Benefits---An-Evidence-Based-User%27s-Guide-%28Printer-Friendly%29.pdf Consent - A Guide for Canadian Physicians (Canadian Medical Protective Association) https://www.cmpa-acpm.ca/en/advice-publications/handbooks/consent-a-guide-for-canadian-physicians "Further, even uncommon risks of great potential seriousness should be disclosed.” Reported side effects following COVID-19 vaccination in Canada (Government of Canada) https://health-infobase.canada.ca/covid-19/vaccine-safety/ Vaccine Adverse Event Reporting System https://vaers.hhs.gov British Medical Journal Sixty seconds on… Vitamin D https://www.bmj.com/content/371/bmj.m3872/rr-5 CCCA Evaluation of Ivermectin as an Effective Prophylactic, and for Treatment in Hospitalized Patients with COVID-19 https://www.canadiancovidcarealliance.org/media-resources/evaluation-of-ivermectin/ National Centre for Biotechnology Information Ivermectin, ‘Wonder drug’ from Japan: the human use perspective https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/ Pfizer Fact Sheet for Recipients and Caregivers https://www.fda.gov/media/144414/download US National Library of Medicine Study to Describe the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaccine Candidates Against COVID-19 in Healthy Individuals https://clinicaltrials.gov/ct2/show/NCT04368728 Moderna Product Monograph, Including Patient Medication Information - COVID-19 Vaccine Moderna https://www.modernacovid19global.com/ca/product-monograph.pdf

But it's actually worse than it sounds

By Maryanne Demasi, PhD

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: