FreewestMedia.com

The reports of athletes who suddenly collapse have been increasing noticeably lately. Heart problems such as heart inflammation are often the cause – one of the known life-threatening side effects of Covid vaccines, which even the manufacturers themselves warn against.

The current phenomenon is also evident if you simply look on Wikipedia at the list of footballers who have collapsed and died. The year 2021 stands out with 13 entries so far. In no other year mentioned have more footballers died during a game. And this list goes back to the year 1889. So it really is a historical event.

The mainstream media is curiously uninterested in this major global story. The German online outlet Wochenblick compiled a referenced list of the cardiac incidents in October while another online outlet Granite Grok published a new list of sportsmen collapsing on the field. Other outlets also listed these incidents, with some cases overlapping.

But these do not include Filipino professional basketball star Roider Cabrera who on Wednesday collapsed during tournament play in Pasig City. The Tribune from the Philippines reported he had a cardiac arrest. Roider Cabrera later lost consciousness inside the locker room before he was immediately rushed to hospital where he was diagnosed with fatal arrhythmia according to a local news.

Attorney Releases First Pages from Subpoenaed FDA Files – Shows Pfizer Documented 158,893 Adverse Events with 25,957 Nervous System Disorders in First Few Months of Distribution

TheGatewayPundit.com

Attorney Aaron Siri, Managing Partner of Siri & Glimstad, published his first report on the information he received from the FDA.

Siri has extensive complex civil litigation experience, including civil rights involving mandated medicine.

Aaron Siri has a history of representing people for vaccination injury for quite a while he recently told a US panel discussion led by Senator Ron Johnson that during the COVID crisis their phones have received an avalanche of requests. Aaron added, “If we actually sued all of the pharmaceutical companies for all of the complaints it would actually impossible for all of the attorneys around the country, around 100, to handle all of those matters.”

Editor's Note: Since when is it okay for ANY PRODUCT to kill this many people, cause this much harm and still be allowed on the market, much less FORCED ON EVERYONE BY GOVERNMENT!?

TheGatewayPundit.com

The official European Union database of suspected drug reaction website is now reporting 30,551 fatalities and 1,163,356 from COVID vaccines Pfizer, Moderna, and Johnson & Johnson, and AztraZeneca through November 13, 2021 based on the data submitted to its system.

According to European Medicines Agency, an official website of the European Union, the data of adverse reaction from COVID-19 vaccines were posted in ADRreports.eu portal that “allows users to view the total number of individual suspected side effect reports (also known as Individual Case Safety Reports, or ICSRs).”

All the data shown in the website and individual case report forms were taken from EudraVigilance, “a system designed for collecting reports of suspected side effects, used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorization in the European Economic Area (EEA).”

The information were submitted electronically to EudraVigilance by “national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.”

by Brian Shilhavy
Health Impact News

Attorney Aaron Siri is a Vaccine Injury attorney, one of just a handful of such attorneys in the U.S.

Since the passage of the 1986 National Vaccine Injury Compensation law, one cannot sue pharmaceutical companies for vaccine injuries and deaths.

A special U.S. Vaccine Court handles all cases with select judges chosen by the U.S. Government, and there only about 100 lawyers in the United States that are even trained to litigate in this special “court.”

The irony with COVID-19 vaccine injuries and deaths, is that even this very highly specialized and controlled government court will not try vaccine injury cases related to the COVID-19 experimental shots, mainly because they are still under Emergency Use Authorization and not fully approved by the FDA yet.

So Aaron Siri’s firm is suing the FDA, since there is no avenue in place within the U.S. Judicial system to sue the drug companies, or anyone else for that matter, for damages caused by the experimental COVID-19 “vaccines.”

We have previously covered Aaron Siri’s lawsuit, which represents brave doctors who have chosen to put their careers on the line to dare to expose vaccine deaths and injuries caused by the experimental shots, and these physicians are the plaintiffs. See:

MIT Scientist and Professor on Exposing COVID-19 Vaccine Injuries: “You Have to be Careful Because You Could be Eliminated”

Today, Attorney Siri published an update on his case against the FDA, where he wrote:

The FDA has asked a federal judge to make the public wait until the year 2076 to disclose all of the data and information it relied upon to license Pfizer’s COVID-19 vaccine.   That is not a typo.   It wants 55 years to produce this information to the public.

So, let’s get this straight. The federal government shields Pfizer from liability.  Gives it billions of dollars.  Makes Americans take its product.  But won’t let you see the data supporting its product’s safety and efficacy.  Who does the government work for?

Read the full article on his Substack page.

by JD Ruker
TheLibertyDaily.com

In compliance with the recent court rulings against Joe Biden’s vaccine mandate, OSHA has officially suspended all activities related to it pending further court actions.

From their website:

On November 12, 2021, the U.S. Court of Appeals for the Fifth Circuit granted a motion to stay OSHA’s COVID-19 Vaccination and Testing Emergency Temporary Standard, published on November 5, 2021 (86 Fed. Reg. 61402) (“ETS”). The court ordered that OSHA “take no steps to implement or enforce” the ETS “until further court order.” While OSHA remains confident in its authority to protect workers in emergencies, OSHA has suspended activities related to the implementation and enforcement of the ETS pending future developments in the litigation.

The Biden-Harris regime plan on taking this all the way up the judicial ladder, but the wording in the judgments so far bodes well for those opposed to medical tyranny. This information must be disseminated far and wide as many businesses are preemptively imposing mandates on their employees, claiming they have no other choice. They have a choice, and they must be shown that we’re all aware they’re doing it of their own accord if they embrace the mandates.

By Dr. Jospeph Mercoloa
 

STORY AT-A-GLANCE

• According to a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial, data were falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind
• Brook Jackson was the regional director of Ventavia Research Group, a research organization charged with testing Pfizer’s COVID jab at several sites in Texas. Jackson repeatedly “informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues,” and when her concerns were ignored, she finally filed a complaint with the U.S. Food and Drug Administration
• The FDA did not follow up on her complaint. Ventavia was not one of the nine trial locations audited, and Pfizer did not bring any of those issues up when applying for emergency use authorization for its COVID shot
• Documentation shared by Jackson shows a Ventavia executive had identified three site staff members who had falsified data
• After being notified of Jackson’s complaints, Pfizer contracted Ventavia to conduct four additional trials — one for COVID shots in children and young adults, one for the COVID jab in pregnant women, a booster shot trial, and an RSV vaccine trial

Yet again, mainstream media have completely ignored what should have been front-page news. According to a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial in the fall of 2020, data were falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind.

What makes the media’s silence all the more remarkable is that this revelation was published in The British Medical Journal. Paul Thacker, investigative journalist for The BMJ, writes in his November 2, 2021, report:¹

By CDMedia.com

The Fifth Circuit Court of Appeals rules *unanimously* to *permanently* block OSHA mandate from taking effect nationwide, effectively vacating Biden’s executive order.

The Ruling sides with Texas, but is a *nationwide* injunction.

One Reagan and two Trump Judges made the ruling.

In their ruling, the Judges cited a tweet by MSM re WH COS admitting Biden Admin was trying to circumvent Constitution to force people to be vaccinated.

Only appeal now is thru Justice Alito to SCOTUS.

You can read the ruling here.

Editor's Note: Big Pharma knows damned well these jabs cause serious blood clotting issues!!  What more proof do you need?!

NaturalNews.com

A newly released document shows that drug giant Pfizer added a secret heart attack drug to the children’s version of its Wuhan coronavirus (COVID-19) vaccine.

The Food and Drug Administration (FDA) Advisory Committee that voted 17-0 to approve the jabs for children as young as five was notified that the children’s formulation of the drug contains tromethamine (Tris), a chemical that reduces blood acidity and stabilizes people who have suffered a heart attack.

“Each dose of this formulation contains 10 ?g (micrograms) of a nucleoside-modified messenger RNA (mRNA) encoding the viral spike (S) glycoprotein of SARS-CoV-2 that is formulated in lipid particles and supplied as a frozen suspension in multiple dose vials,” the “vaccine formulation” page of the document explains.

“To provide a vaccine with an improved stability profile, the Pfizer-BioNTech COVID-19 Vaccine for use in children 5-11 years of age uses tromethamine (Tris) buffer instead of the phosphate-buffered saline (PBS) as used in the previous formulation and excludes sodium chloride and potassium chloride.”

This “new formulation,” the document further reads, must be stored at a different temperature than the adult version of the injection.

Without so much as a second thought concerning this ingredient change, the FDA granted emergency use authorization (EUA) for this new drug to be administered to children as young as five.

This FDA briefing document was titled “EUA amendment request for Pfizer COVID-19 vaccine for use in children 5 through 11 years of age,” and was given to the advisory committee prior to its vote.