Rebuttal letter to European Medicines Agency from Doctors for Covid Ethics, April 1, 2021

From Doctors for Covid Ethics

Emer Cooke, Executive Director, European Medicines Agency, Amsterdam, The Netherlands

April 1st, 2021

Ladies and Gentlemen,

FOR THE URGENT PERSONAL ATTENTION OF: EMER COOKE, EXECUTIVE DIRECTOR OF THE EUROPEAN MEDICINES AGENCY

We acknowledge receipt of your March 23 reply to our letter dated February 28, seeking reassurance that foreseeable risks of gene-based COVID-19 “vaccines” had been ruled out in animal trials prior to human use. Our concerns arise from multiple lines of evidence, including that the SARS-CoV-2 “spike protein” is not a passive docking protein, but its production is likely to initiate blood coagulation via multiple mechanisms.

Regrettably, your reply of March 23 is unconvincing and unacceptable. We are dismayed that you choose to respond to our request for crucially important information in a dismissive and unscientific manner. Such a cavalier approach to vaccine safety creates the unwelcome impression that the EMA is serving the interests of the very pharmaceutical companies whose products it is your pledged duty to evaluate. The evidence is clear that there are some serious adverse event risks & that a number of people, not at risk from SARS-CoV-2, have died following vaccination.

1. You concede that the “vaccines”, which are more accurately described as investigational gene-based agents, enter the bloodstream but you can obviously provide no quantitative data. In the absence of the latter, any scientific assessment you purport to have undertaken lacks foundation.

2. Your statement that non-clinical studies do not indicate any detectable uptake of the vaccines into endothelial cells lacks credibility. We demand to see the scientific evidence. If not available, it must be assumed that endothelial cells are targeted.

3. Auto-attack could not have been excluded in animals unless they had been immunologically primed beforehand. We demand evidence that such experiments had been performed. Similar experiments have been undertaken before with previous, unsuccessful candidate vaccines, and fatal, antibody-dependent enhancement of disease was observed.

4. We requested scientific evidence, not a vague description of what was purportedly seen in non-valid animal experiments. Your cursory mention of laboratory findings in humans is cynical. In view of the plausible connection between production of spike protein and the emergence of thromboembolic serious adverse events (SAEs), we demand to see the results of D-dimer determinations. As you are aware, D-dimer is a very good test as an aid to diagnose thrombosis.

After delivery of our letter to you on March 1, events followed that debunk your response to our last three queries to an extent that can only be termed embarrassing. As we feared, severe and fatal coagulopathies occurred in young individuals following “vaccination”, leading 15 countries to suspend their AZ-“vaccination” program. An official investigation by the EMA into the cases of afflicted younger individuals followed, the results of which were announced by the WHO on March 17, 2021, stating: “At this time, WHO considers that the benefits of the AstraZeneca vaccine outweigh its risks and recommends that vaccinations continue.”

What was this decision based upon? The WHO is not a competent body for formally evaluating drug safety. That is explicitly the role of the agency you lead.

In your press release, you disclosed the following information to support your conclusion. You had scrutinized data on two mortally dangerous conditions that had followed within 14 days of “vaccination”: DIC, disseminated intravascular coagulation; and CSVT, cerebral sinus vein thrombosis. 5 DIC and 18 CSVT were on record, with a total death toll of 9. Most cases were <55 year-old individuals. 5 DIC and 12 CSVT were under 50 years of age. None were reported as having had serious pre-existing illness.

You stated numbers that “normally” would be expected : DIC <1, CSVT 1.3.

(Continued …)

Source: Rebuttal letter to European Medicines Agency from Doctors for Covid Ethics, April 1, 2021

15 million J&J COVID Vaccines Thrown Away After Ingredient Mix-Up With AstraZeneca • Children’s Health Defense

The mix-up at a Baltimore manufacturing plant forced regulators to delay authorization of the plant’s production lines and prompted an FDA investigation.

By Megan Redshaw

Fifteen million doses of Johnson & Johnson (J&J’s) vaccine failed quality control after workers at a Baltimore manufacturing plant negligently combined ingredients from AstraZeneca and J&J’s COVID vaccine.

The mix-up forced regulators to delay authorization of the plant’s production lines and prompted an investigation by the U.S. Food and Drug Administration (FDA).

According to The New York Times, the plant is run by Emergent BioSolutions, a manufacturing partner with J&J and AstraZeneca, whose vaccine has yet to be authorized for use in the U.S.

Emergent has been cited repeatedly by the FDA for problems such as poorly trained employees, cracked vials and mold around one of its facilities, according to records obtained by the Associated Press through the Freedom of Information Act.

AstraZeneca and J&J’s COVID vaccines employ the same technology which uses a version of a virus — known as a vector — that is transmitted into cells to make a protein that then stimulates the immune system to produce antibodies.

However, J&J’s and AstraZeneca’s vectors are biologically different and not interchangeable. (Continued …)

Source: 15 million J&J COVID Vaccines Thrown Away After Ingredient Mix-Up With AstraZeneca • Children’s Health Defense

PERSONAL RESPONSIBILITY — #ME FIRST MOVEMENT, Peggy Hall

I filmed this video more than a year BEFORE all this hogwash started!! Who knew my message would have even MORE value than ever!

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THE VANDEN BOSSCHE CONTROVERSY | The Highwire with Del Bigtree

THE VANDEN BOSSCHE CONTROVERSY

Allegations of ‘astroturfing’ emerged over The HighWire’s coverage of virologist Geert Vanden Bossche and his public plea to halt all #Covid19 vaccination. Del addresses the allegations with a response including important dialogues with RFK Jr. and Dr. Andrew Wakefield.

#DelBigtree #TheHighwire #TheDefender #RFKJr #AndyWakefield #GeertVandenBossche

POSTED: March 29, 2021

Source: THE VANDEN BOSSCHE CONTROVERSY

The Forbidden COVID-19 Chronicles | The Makers of COVID-19 Vaccines: Pfizer | Pamela A. Popper, President | Wellness Forum Health

Since the year 2000, Pfizer has been charged 74 times with criminal and civil violations and paid a total of $4,660,896,333 in fines. The top offenses to which the company pled guilty are unapproved marketing of products, bribery, making false claims, safety violations, environmental violations, racketeering, and violations of the Foreign Corrupt Practices Act.[1]

In spite of a very long list of criminal convictions, Pfizer and BioNTech were given an emergency use authorization for a COVID-19 vaccine on December 1, 2020.

Here are just a few of the episodes in which Pfizer and its subsidiaries have been found guilty of egregious acts:

In 2001, thirty Nigerian families sued Pfizer, claiming that the company conducted an unauthorized clinical trial of an untested antibiotic on their children without their consent in 1996 during a meningitis epidemic. Eleven children died as a result, and others had brain damage or became partially paralyzed or deaf.[2] In 2009 the company reached an out-of-court settlement with the Kenyan government for $75 million dollars, and in August 2011 the company paid $175,000 to each family to settle the claims.[3]

In 2004, Pfizer’s Warner-Lambert subsidiary paid $430 million to settle criminal and civil charges that it paid doctors to prescribe Neurontin, an epilepsy drug, for conditions for which it was never approved.[4] In 2008 it was discovered that Pfizer suppressed research showing that Neurontin did not work for these conditions and that the company routinely spun negative data about the drug to place it a more positive light. Additionally, the company combined negative studies with positive studies to neutralize negative findings and hide the fact that Neurontin did not work for unapproved uses.[5] A judge ordered the company to pay $142 million to settle racketeering charges.[6]

In 2005, Pfizer agreed to stop advertising Celebrex on television and subsequently admitted that a 1999 clinical trial showed that Celebrex increased the risk of heart disease in elderly patients.[7]

Pfizer and its subsidiary company Pharmacia and Upjohn can boast that in 2009 it paid the largest criminal fine ever in the history of the U.S. (at that time) for any matter – $1.195 billion dollars. The reason for the fine – the company’s reps were marketing Bextra, a pain reliever, for uses and doses specifically prohibited by the FDA. Additionally, the company was forced to forfeit $105 million which brought the total settlement of criminal charges to $1.3 billion.

In addition, Pfizer agreed to pay $1 billion more to resolve charges brought under the False Claims Act that the company illegally promoted four drugs – Bextra, Geodon (an anti-psychotic), Zyvox (an antibiotic) and Lyrica (an anti-epileptic drug) for off-label uses. The company was also found to have bribed doctors, paying kickbacks as incentives to prescribe these and other drugs.[8]

Subsequently, Bextra was withdrawn from the market after the FDA mandated a black box warning about cardiovascular and gastrointestinal side effects.[9] The company set aside $894 million dollars to settle claims for both Bextra and Celebrex.[10]

One of Pfizer’s biggest scandals involved defective heart valves sold through one of its subsidiaries that killed over 100 people. An investigation of this matter showed that the company deliberately misled regulators while seeking approval for the product. The company agreed to stop making the valves, but they had already been implanted in tens of thousands of people who were now at risk.[11] In 1994, the company paid $10.75 million to settle charges brought by the Justice Department that it lied to regulators about risks associated with these valves.

In 2012 the company settled charges related to a multi-million-dollar bribery scheme involving payments to government officials, health regulators, doctors, and hospital administrators in Bulgaria, Croatia, Kazakhstan and Russia. Pfizer used sham consulting contracts, exclusive distributorships and improper travel and cash payments in order to gain market share, and earned over $7 million in profits as a result of its illegal behavior. The fine – only $15 million.[12]

During one 3-year period, Pfizer Italy provided free cell phones, copy machines, printers and televisions to doctors; gave them paid vacations with companions; and made direct cash payments to doctors which were falsely categorized as speaker fees and professional training. The company paid a fine of $60.2 million which represents about one half of one percent of the company’s annual profits.[13]

And this is the problem. For Pfizer and other drug companies, paying billions of dollars in criminal and civil fines for misrepresentation and hurting and killing people is just a cost of doing business. Employees of Pfizer and its subsidiaries are not indicted and prosecuted, so there really is no reason for the company’s management to stop doing these things.

Would you purchase any product made by this company? I wouldn’t – not even mouth wash. Why? Because Pfizer could not even play it straight with a product like this. The company paid $70,000 in fines to 10 states to settle charges concerning misleading advertising for a mouth rinse called Plax in 1991.[14]

What on earth would possess regulators to allow a company like this to continue to do business in the United States? Or to grant an Emergency Use Authorization to a Pfizer vaccine? Regulators would not allow it, but business partners, of course, would. And it is abundantly clear that U.S. government agencies like the FDA and CDC are not regulators, but rather business partners for drug and vaccine makers.

[1] https://violationtracker.goodjobsfirst.org/parent/pfizer
[2] Tamar Lewin. Families Sue Pfizer on Test of Antibiotic. New York Times August 30 2001
[3] David Smith. Pfizer pays out to Nigerian families of meningitis drug trial victims. The Guardian August 12 2011
[4] https://www.justice.gov/archive/opa/pr/2004/May/04_civ_322.htm
[5] Stephanie Saul. Experts Concluded Pfizer Manipulated Studies. New York  Times Oct 8 2008
[6] Jef Feeley and Janelle Lawrence. Pfizer to Pay $142.1 Million Over Neurontin Marketing. Bloomberg Jan 28 2011
[7] Alex Berneson and Gardiner Harris. Pfizer Says 1999 Trials Revealed Risks With Celebrex. New York Times Feb 1 2005
[8] https://www.justice.gov/opa/pr/justice-department-announces-largest-health-care-fraud-settlement-its-history
[9] Anna Wilde Mathews and Scot Hensley. FDA Stiffens Painkiller Warnings, Pushes Pfizer to Suspend Bextra. Wall Street Journal April 8 2005
[10] Stephanie Saul. Pfizer to Settle Claims Over Bextra and Celebrex. New York Times Oct 17, 2008
[11] Manufacturer Ends Production of Heart Valve. New York Times November 28 1986
[12] https://www.justice.gov/opa/pr/pfizer-hcp-corp-agrees-pay-15-million-penalty-resolve-foreign-bribery-investigation
[13] Paul Knaggs. Coronavirus: what do we know about ‘Pfizer’ and can we trust them with a vaccine. Labour Heartlands November 10 2020
[14] The Media Business: Advertising; Pfizer’s Pact on Plax Ads. New York Times Feb 21 1991

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CDC’s Vaccine Excipient Summary-Excipients Included in U.S. Vaccines, by Vaccine

[Forwarded from OFFICIAL CHARLIE WARD SHOW 💥 XRP QFS 💥]

“I gathered all vaccine ingredients into a list and contacted Poison Control. After intros and such, and asking to speak with someone tenured and knowledgeable, this is the gist of that conversation.

Me: My question to you is how are these ingredients categorized? As benign or poison? (I ran a few ingredients, formaldehyde, Tween 80, mercury, aluminum, phenoxyethanol, potassium phosphate, sodium phosphate, sorbitol, etc.)

He: Well, that’s quite a list… But I’d have to easily say that they’re all toxic to humans… Used in fertilizers… Pesticides… To stop the heart… To preserve a dead body… They’re registered with us in different categories, but pretty much poisons. Why?

Me: If I were deliberately to feed or inject my child with these ingredients often, as a schedule, obviously I’d put my daughter in harm’s way… But what would legally happen to me?

He: Odd question… But you’d likely be charged with criminal negligence… perhaps with intent to kill… and of course child abuse… Your child would be taken away from you… Do you know of someone’s who’s doing this to their child? This is criminal…

Me: An industry… These are the ingredients used in vaccines… With binding agents to make sure the body won’t flush these out… To keep the antibody levels up indefinitely…

He: WHAT?!

Your conclusion?

The man was beside himself. He asked if I would email him all this information. He wanted to share it with his adult kids who are parents. He was horrified and felt awful he didn’t know… his kids are vaccinated and they have health issues…”

~  By  Iris Figueroa 🍃♥️🍃

✅INGREDIENTS TO VACCINES –  You CANNOT make an educated decision without being educated.

Here are just SOME vaccine ingredients.

These are being INJECTED into your kids;

◾️Formaldehyde/Formalin – Highly toxic systematic poison and carcinogen.

◾️Betapropiolactone – Toxic chemical and carcinogen. May cause death/permanant injury after very short exposure to small quantities. Corrosive chemical.

◾️Hexadecyltrimethylammonium bromide – May cause damage to the liver, cardiovascular system, and central nervous system. May cause reproductive effects and birth defects.

◾️Aluminum hydroxide, aluminum phosphate, and aluminum salts – Neurotoxin. Carries risk for long term brain inflammation/swelling, neurological disorders, autoimmune disease, Alzheimer’s, dementia, and autism. It penetrates the brain where it persists indefinitely.

◾️Thimerosal (mercury) – Neurotoxin. Induces cellular damage, reduces oxidation-reduction activity, cellular degeneration, and cell death. Linked to neurological disorders, Alzheimer’s, dementia, and autism.

◾️Polysorbate 80 & 20 – Trespasses the Blood-Brain Barrier and carries with it aluminum, thimerosal, and viruses; allowing it to enter the brain.

◾️Glutaraldehyde – Toxic chemical used as a disinfectant for heat sensitive medical equipment.

◾️Fetal Bovine Serum – Harvested from bovine (cow) fetuses taken from pregnant cows before slaughter.

◾️Human Diploid Fibroblast Cells – aborted fetal cells. Foreign DNA has the ability to interact with our own.

◾️African Green Monkey Kidney Cells – Can carry the SV-40 cancer-causing virus that has already tainted about 30 million Americans.

◾️Acetone – Can cause kidney, liver, and nerve damage.

◾️E.Coli – Yes, you read that right.

◾️DNA from porcine (pig) Circovirus type-1

◾️Human embryonic lung cell cultures (from aborted fetuses)

✳️You can view all of these ingredients on the CDCs website. I encourage everyone to do their own research. Look up the MSDS on these chemicals. Read the thousands of peer reviewed studies that have evaluated the biological consequences these chemicals can have on the body, especially when being injected.

✳️Fact check vaccine ingredients here:

http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf

Click to access excipient-table-2.pdf

Is It Contagious? | Jason Shurka

In this video, I share insights, studies and history which has been hidden from the masses that has led us down a path of misguidance. I encourage you all to do your own research and come down to your own conclusions. “The Rosenau Experiment” is a great place to start.

Divided we fall…
UNITED WE FLY 😇🙏🏽😇

SHARE, SHARE, SHARE!!

With Infinite Love,
Jason Shurka 🙏🏽🌎💜

Interview With Vanden Bossche: Should Mass COVID Vaccinations Be Stopped? • Children’s Health Defense

After several hours of discussion, Rob Verkerk, Ph.D., of Alliance for Natural Health International concludes it would be “scientifically, socially and ethically irresponsible” to dismiss Dr. Geert Vanden Bossche’s concerns about mass vaccination.

EDITOR’S NOTE: The Defender is committed to providing a space for scientific debate. This piece is an interview conducted by Rob Verkerk, Ph.D., with Geert Vanden Bossche, Ph.D. The interview follows Verkerk’s recent analysis of the ongoing debate (this piece + this piece) sparked by Bossche concerning immune escape and mass vaccination during a pandemic.

Welcome to the first episode of our new interview series, Speaking Naturally — Open Discourses in a Censored World. In it we have the great pleasure of providing an in-depth interview with Geert Vanden Bossche, Ph.D., whose name will be familiar to anyone with a keen interest in understanding the effects of the current COVID mass vaccination program.

About our guest

Vanden Bossche knows a thing or two about vaccines and is a self-declared pro-vaxxer. He is a seasoned vaccine developer (vaccinologist) with a track record with GSK Biologicals, Novartis Vaccines and Solvay Biologicals. He’s also worked with the Bill & Melinda Gates Foundation’s Global Health Discovery team in Seattle as senior program officer and as senior Ebola program manager with the Global Alliance for Vaccines and Immunization in Geneva.

However, in early March, Vanden Bossche put out a call to the World Health Organization, supported by a 12-page document on a dedicated website especially set up to communicate his concerns. We responded with a 4,000-word article that tried to steer an objective line through conflicting streams of information and consider the implications of what appeared to be a whistleblower.

Continue reading at Source: Interview With Vanden Bossche: Should Mass COVID Vaccinations Be Stopped? • Children’s Health Defense