Updated: 4 days ago
New release of court ordered document shows the company is AGAIN engaging in criminal misrepresentation of drug product -
Pfizer has doubled down, requesting the court extend time frame for full release of Covid-19 vaccine documents to 2096 - media continues to ignore evidence of severe safety issues coming from the pharmaceutical company's own evidence:
Young population groups not at risk for Covid-19 attributed severe outcomes:
Last week, the United States moved to expand Pfizer Covid-19 vaccine booster for ages 17 & 18, at the same time Taiwan ceased to administer the drug at all to under 18s due to myocarditis risks (same drug administered in US).
Taiwan (following US data and evidence around myocarditis risks in youth, end Pfizer vaccines in this age group):
"TAIPEI (Taiwan News) — Central Epidemic Command Center (CECC) head Chen Shih-chung (陳時中) said on Wednesday (Nov. 10) that a panel of experts has decided to suspend administering second doses of the Pfizer-BioNTech (BNT) COVID vaccine to children 12-17 years old amid concerns it may increase the risk of myocarditis.
Cases of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer lining of the heart) have been reported after BNT vaccination of children between 12 and 17 years of age. According to U.S. statistics, the risk of youths experiencing myocarditis after receiving the second BNT dose is 10 times higher than after the first dose, CNA reported"
This approval comes in the midst of global safety signals for mRNA vaccinations, not only flashing red, but screaming scarlet and major research publications red flagging dramatic increase in heart inflammation:
American Hearth Association abstract issues warning for dramatically increased risk of heart inflammation post mRNA vaccine.
American Heart Association Journal: Journal/CirculationAbstract Steven R Gundry Physician, American Hearth and Lung Institute Abstract of report finding: https://www.ahajournals.org/doi/10.1161/circ.144.suppl_1.10712
Abstract 10712: Mrna COVID Vaccines Dramatically Increase Endothelial Inflammatory Markers and ACS Risk as Measured by the PULS Cardiac Test: a Warning
"At the time of this report, these changes persist for at least 2.5 months post second dose of vac.We conclude that the mRNA vacs dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle and may account for the observations of increased thrombosis, cardiomyopathy, and other vascular events following vaccination.
British Physician Whistleblower documents major British research institution has duplicated the above California group's finding, sitting on data/fear of loss of pharmaceutical research funding:
In addition to the UK excess deaths reported in the above news interview, Indiana life insurance CEO says deaths are up 40% among people ages 18-64:
"Davison said the increase in deaths represents “huge, huge numbers,” and that’s it’s not elderly people who are dying, but “primarily working-age people 18 to 64” who are the employees of companies that have group life insurance plans through OneAmerica.
“And what we saw just in third quarter, we’re seeing it continue into fourth quarter, is that death rates are up 40% over what they were pre-pandemic,” he said......
Most of the claims for deaths being filed are not classified as COVID-19 deaths, Davison said:
In the midst of these alarming headlines, Pfizer released by court order, documents the pharmaceutical company attempted to keep confidential, after a group filed a Freedom of Information request for release of all Pfizer Covid-19 vaccination trial and contract documentation:
Public Health and Medical Professionals for Transparent Vs Pfizer: Original Court Document HERE
Judging by the first release of documents, it is clear Pfizer is requesting this time frame, as attempt to cover up how the company has failed to disclose key safety information for FDA approval of Pfizer's Corminaty Covid-19 vaccine (an act which may implicate the company in criminal misrepresentation of its product and criminal fraud, a behavior for which this corporation has a long documented record (refer to second half of this article to review documentation of Pfizer's criminal history)
A highlight article in New Zealand's Daily Telegraph highlighted this recent release of evidence:
Document released by Pfizer apparently as a result of a Freedom Of Information court order in the USA reveals a vast array of previously unknown vaccine adverse effects compiled from official sources around the world.
Pfizer concedes this is ‘a large increase’ in adverse event reports and that even this huge volume is under reported.
Over 100+ diseases are listed, many very serious.
This document was compiled by Pfizer in the very early days of the vaccine rollout in NZ but was possibly not supplied to our government.
Governments have given blanket immunity to Pfizer without requiring full release of documentation and safety data by the company. Several European Parliamentarian members held a recent press conference opposing European Green Pass Vaccine mandate, partially on the basis of mass suppression and cover up of data:
European Parliamentarian Hold Up Covid-19 Vaccine Pharmaceutical Contract 'Disclosure' - nearly all pages are blacked out:
For months, the media has parroted public health officials & medical 'experts' false claims of 'safety' and 'efficacy' based on lack of evidence (no mid or long term safety data whatsoever) with VAERS report data documenting record adverse event and fatality reports submitted in association with Covid-19 vaccines. This ALONE is unethical and inaccurate reporting.
Now, we have direct documentation and evidence, the media chorus of safety and efficacy based was based on false and incomplete evidence:
Media Sells the Pitch (forgive the watermark, testing video software right now
Compilation of early media claims - claims recited AGAINST evidence available at the time
Public Health and Medical Professionals for Transparency
Review of Pfizer Document:
First, document discloses Pfizer needed to hire additional staff to handle the large volume of adverse events reported to their system. Pfizer REDACTED the number of employees hired to process reports:
Page 6, Confidential:
"Pfizer has also taken a multiple actions to help alleviate the large increase of adverse event reports. This includes significant technology enhancements, and process and workflow solutions, as well as increasing the number of data entry and case processing colleagues. To date, Pfizer has onboarded approximately additional fulltime employees (FTEs). More are joining each month with an expected total of more than additional resources by the end of June 2021".
So, as the media was touting the utter safety and lack of evidence as THE evidence Pfizer Covid-19 was safe, the company was forced to hire additional staff to handle large volume of adverse safety events -
This document discloses 1,200 fatalities in association with the Pfizer program & 42,000
'Confidential' Page 7
1,223 reported fatalities and 42,086 adverse events recorded (February 28, 2021)
Note, majority, 29,914 in females.
Pfizer document correlates to CDC VAERS adverse event system & agency backloading mass amounts of early data with number of recent reports for early months of program skyrocketing over real time submission of data:
*CDC VAERS Reports for period of December 2020 & Ending March 31, 2021 have increased from 56,869 to 433,318 with majority of occurrence date within real time reporting period
Total VAERS Report Submitted As of April 1, 2021 for all Covid-19 vaccinations:
(archived on Children'' Health Defense website):
VAERS Covid-19 Reports December through March 2021 as of December 3, 2021 release:
CDC is not including date of submission for nearly all reports:
CDC SUPPRESSED 149,000 INJURY Reports in First Six Weeks Covid-19 Vaccine Program, DEATHS SOAR (includes summary for four month review)
Anaphylactic Shock: 1,833 anaphylactic shock incidents (Pfizer vaccination contains Polyethylene Glycol, sensitivity to PEG is contraindication to Pfizer vaccination, up to 72% population have antibodies to PEG, majority unaware of sensitivity until reaction, see second half of report HERE).
Page 10. Confidential:
"Four individuals went into anaphylactic shock and died the same day - Pfizer dismissed this data due to underlying health conditions or 'appeared to have Covid related pneumonia' :
(severe anaphylactic shock induces pulmonary edema/ fluid overfill of the lungs. and this 'individual' is likely Drene Keyes, a black minister who died the same day of Pfizer administration and labeled a 'Covid-19 death' despite no evidence of Covid-19 attributed infection and autopsy, treating physician, and coroner evidence attributing Pfizer vaccine to cause of death)
Drene Keyes must not be allowed to be dismissed as a footnote in a Pfizer document, covered up by Covid-19 attribution against all evidence. Each number refers to a PERSON.
Haematological AESIs: Adverse Effect of Special Interest:
699 cases of severe blood disorders reported by February 28, 2021, 932 cases total:
Pfizer concluded nearly a thousand adverse blood reactions did not correlate to safety issue (but failed to disclose adverses reports, majority severe Haematological to public). Media only reported on 36 cases of thrombocytopenia last winter, highlight the 'rarity' of symptoms based on lack of disclosure.
Thrombocytopenia deaths post mRNA vaccination have been dismissed by CDC under a similar plausible deniability standard, with the death of Michael Gregory not correlated to Moderna vaccination despite autopsy confirmation he died from the blood disorder and no preexisting condition to explain sudden onset post vaccination:
96% of Covid-19 attributed deaths have four serious medical conditions, deaths attributed through symptom presentation (alone) or severe flawed testing methods - full attribution CDC/WHO Covid-19 case attribution standards HERE
788 severe autoimmune reactions reported through End of February:
Page 20, Confidential
Pregnancy/Breastfeeding: 75 serious cases: