Showing posts with label Europe. Show all posts
Showing posts with label Europe. Show all posts

6 EU countries suspended Moderna COVID-19 vaccine for young people

side effects reported

France, Finland, Germany, Sweden, Iceland and Denmark no longer recommend the Moderna Covid-19 vaccine

More countries suspended Moderna COVID-19 vaccine for young people

News breaking: This morning, the Moderna vaccine has been banned by another country. The German Vaccination Committee (STIKO) advises people under 30 not to use this COVID-19 vaccine because it is rare. Risk of heart disease!

And just yesterday, the French and Swedish governments have just announced that people under the age of 30 will stop using the Moderna vaccine.

The highest health advisory body in France officially announced yesterday that it would not recommend that people under the age of 30 in the country be vaccinated with the COVID-19 vaccine produced by the American Moderna Pharmaceutical Factory.

The reason is that the vaccine has a higher risk of side effects in people of this age group, which will cause Heart-related diseases.

Immediately, the Swedish health officer also quickly decided to suspend indefinitely the Moderna vaccine for people under 30.

At the same time, the Nordic countries Finland, Iceland and Denmark have also taken similar measures-Norway is encouraging men under the age of 30 not to get the vaccine, but it has not yet made mandatory requirements because the country already has data showing that it is vaccinated. Of young men are at increased risk of myocarditis and pericarditis.

As of today, a total of six countries including France, Finland, Germany, Sweden, Iceland and Denmark no longer recommend the Moderna Covid-19 vaccine to people under the age of 30, because it will cause them to have a higher risk of developing myocarditis.

The following figure shows the number and proportion of deaths, injuries and various disabilities in the vaccine adverse reaction system as of October 8, 2021:

We must know that the German decision to stop the Moderna vaccine was made at a time when the number of new coronavirus cases reported in the country hit a record high. Because Moderna vaccine has caused myocarditis in young people in Germany one after another, the German permanent vaccination committee, therefore, only recommends Pfizer vaccine for people under 30 years old.

And just yesterday, the French and Swedish governments have just announced that people under the age of 30 will stop using the Moderna vaccine.

The highest health advisory body in France officially announced yesterday that it would not recommend that people under the age of 30 in the country be vaccinated with the COVID-19 vaccine produced by the American Moderna Pharmaceutical Factory.

However, for people over the age of 30, STIKO said that even if they were vaccinated with Moderna, the risk of heart disease did not increase. However, it is still recommended that pregnant women, regardless of whether they are above or below 30 years old, choose only to vaccinate Pfizer. 

It is reported that these data are released by Paul Ehrlich Insitute, a government agency responsible for monitoring and evaluating vaccine side effects and complications.Not only these European countries, the United States is also delaying the approval of the Moderna childhood vaccine. The Pfizer vaccine is recommended for children 5-11 years old. According to the VAERS website, nearly 4,000 Americans in the United States have died after being vaccinated with Moderna’s COVID-19 vaccine.

Dr. McCullough, an American cardiologist and former deputy director of the Department of Internal Medicine at Baylor University Medical Center, said: The number of heart inflammation cases in the United States has increased by 21,000% within 4 months, mainly affecting young men. “In June 2021, the Centers for Disease Control said there were 200 Cases of myocarditis. But by October, we have 10,304 cases.”

Vaccines For Kids Potentially More Dangerous than Virus, German Gov’t Reports

Germany Study

According to a safety report published by the Federal Institute for Vaccines and Biomedicines in Germany, the number of reported cases of suspected adverse effects following COVID-19 vaccination in children aged 12 to 17 has now exceeded the total number of COVID-related hospitalizations for children within the same age group since the beginning of the pandemic.

The report, which was published on September 20 by the PEI (Paul-Ehrlich-Institut), a German federal agency and medical regulatory body in charge of promoting drug and vaccine safety, has released new data on COVID-19 vaccines adverse effects, particularly among children aged 12 to 17.

The data, which was collected from the beginning of the vaccination campaign until August 31, shows that 1,228 vaccinated children aged 12 to 17 reported one or several suspected adverse effects following vaccination. This comes only three months after the beginning of the vaccination campaign for that age group, and just two weeks following a recommendation by the STIKO, the German Standing Committee on Vaccination.

By comparison, the total number of children aged 12 to 17 who were admitted to the hospital for COVID-19 between March 2020 and July 2021 is 1,225. In other words, within just 3 months, the number of cases of vaccinated children suffering from potential vaccine-related adverse effects exceeded the number of COVID-related hospitalizations within the same age group over a period of 16 months.

This new data seems to indicate that more children are suffering from the vaccine meant to protect them from COVID-19, than from the virus itself.

The most serious adverse effects reported include heart diseases such as myocarditis and pericarditis, as well as other serious health conditions such as thrombosis, pulmonary embolism, and the Guillain-Barré Syndrome.

Even more concerning are the first reported cases of fatalities following vaccination in that age-group. According to the PEI report, “three of the 1,228 reported cases of adverse effect have resulted in the death of the patients within two to twenty-four days following vaccination with [Pfizer/BioNTech].”

Based on the newly release data, if the vaccination campaign extends to all minors aged 12 to 17, as well as to other age groups, as is currently expected, the total number of vaccine-related deaths among minors could be triple or even four times that of COVID-related deaths in the same age group throughout the whole pandemic. In other words, the vaccines offered to protect children from COVID are potentially more dangerous to children than the virus itself, according to an analysis published by Susan Bonath of RT DE.

The report also showed a significant increase of reported cases of adverse effects in adults, including a staggering increase in severe adverse reactions. Data collected throughout the month of August shows a 15-fold increase with skyrocketing numbers of severe reactions going from 1,094 to 15,122 in just one month. A steady increase in the number of vaccine-related deaths can also be observed.

According to Bonath’s analysis of the report, the total number of reported vaccine-related injuries and deaths over a span of seven months far exceeds that of all other vaccines together over a span of twenty years, from 2000 to 2020, with the number of long-term effects almost four times higher and the number of deaths more than three times higher.

This remarkable discrepancy was pointed out by RT DE editor Florian Warweg at a press conference with the Federal Ministry of Health on September 8. Warweg, who referred at the time to data which is no longer up to date, asked Andreas Deffner, spokesperson of the Federal Health Ministry:

Japan Suspends Use of 1.63 million Moderna Vaccines

CONTAMINATION OF METAL PARTICLES

Japan on Thursday suspended the use of 1.63 million doses here shipped to 863 vaccination centers nationwide, more than a week after the domestic distributor, Takeda Pharmaceutical, received reports of contaminants in some vials.

The contaminant found in a batch delivered to Japan is believed to be a metallic particle, Japanese public broadcaster NHK reported, citing health ministry sources.

"Particulates.  Based on past experience, these are likely to be glass chips or stopper detritis, but this should help get to the bottom of the graphene hypothesis.  I have confidence in the Japanese. "  Says, Dr Robert Malone

The European Union drugs regulator said it was investigating the incident at the Spanish plant run by Rovi, but did not find reasons to seek a temporary suspension of production after an initial assessment.

“COVID-19 vaccine production in Rovi is able to continue, following a preliminary risk assessment,” the European Medicines Agency told Reuters in a statement.

“An investigation into the root cause is ongoing. EMA will be able to provide more information as the investigation progresses,” it added.

Moderna has so far delivered to the EU nearly 75 million doses of its COVID-19 vaccine, EU public data show. The company has two contracts with the 27-nation bloc for up to 460 million shots.

Spanish pharma company Rovi, which bottles Moderna vaccines for markets outside of the United States, said the contamination could be due to a manufacturing issue on a production line. A spokesperson said the company could not say anything more while it was investigating.

Moderna put the lot in question and two adjacent ones on hold.

NHK, in a report published late on Thursday, cited health ministry sources as saying the contaminant was believed to be a particle that reacted to magnets and was therefore suspected to be a metal. Moderna has described it as “particulate matter” that did not pose a safety or efficacy issue.

A Japanese health ministry official said the composition of the contaminant has not been confirmed. In a statement, Takeda said it asked Moderna to investigate the issue and that it would work with the ministry to replace the affected supply.

News of the contaminant could prove a fresh setback for Japan’s inoculation drive as it struggles to persuade many - particularly young people - to get vaccinated.

See Reuters story

The Best Vaccine Presentation From The Inventor of mRNA (2 Hours)

mRNA Inventor Dr. Robert Malone will tell you more about the COVID vaccine science and Government, CDC, FDA bureaucracy in the next 2 hours than you will ever hear.  Dr. Robert Malone emphasizes compassion and is trying to bend consensus to get governments to focus more on treatment!  Europe is far ahead of the USA in this thinking. 

The "Black Swan" event of 2020 — the SARS-CoV-2 pandemic — imposed disruptive stresses on virtually all local, national, and international systems. In response, many governments (Germany, England, America) chose to invest in, emphasize, and expedite deployment of non-traditional gene therapy-based vaccines, while excluding off-label drug use (i.e. famotidine, hydroxychloroquine, etc.).

One has to ask: Why?

Why would governments and governmental agencies purposefully ignore — and in many instances, ban — repurposed OTC drug therapies, while ramrodding at breakneck speed what some have called, at best, an "experimental drug?"

And in a country identified with the right to free speech, why would doctors, scientists, and everyday citizens who are questioning public policy regarding the vaccine be likewise ignored, censored, and — in many instances like Dr. Malone — banned?

As the leading scientist in cutting-edge vaccine technology development and being at the forefront of public health responses over 30 years, Dr. Robert Malone, MD, MS is uniquely qualified to discuss the origins of these preferentially treated genetic vaccine platforms and current government implementation policies. Today, public policy, bioethics, traditional-, social- and other media censorship, academia, "Big Pharma," tech, and myriad sectors interact under unprecedented stress. Are the governmental responses we are witnessing — that reveal emergent threats to individual rights and good government — all part of the "Noble Lie?"

ABOUT OUR SPEAKER: Robert W. Malone MD, MS is an internationally recognized scientist (virology, immunology, molecular biology) and the original inventor of mRNA- and DNA-vaccination, and multiple non-viral DNA and RNA/mRNA delivery technologies.

Dr. Malone has assembled and managed expert teams focused on solving complicated biodefense challenges to meet US government requirements, and were instrumental in enabling the PHAC/rVSV ZEBOV (“Merck Ebola”) vaccine to move quickly to licensure.

Since January 10, 2020, Dr. Malone has been focused on clinical research including the COVID-19 disease mechanism, drug development, non-invasive treatments, and repurposed COVID-19 drug treatments, such as mast cells, celecoxib, dexamethasone, and famotidine.

He is a US-based physician-scientist consultant specializing in developing medical countermeasures (vaccines and drugs) for infectious diseases. He has served as an Assistant and Associate Professor of Pathology and Surgery at UC Davis, the University of Maryland, and the Armed Forces University of the Health Sciences. Among Dr. Malone's many core competencies are clinical development and regulatory affairs. He was scientifically trained at the Salk Institute of Molecular Biology and Virology Laboratories, among other prestigious institutions.

dr malone mrna vaccine inventor

EU looks into Pfizer, Moderna Vaccine Side Effects

 EU flag covid

CAN YOU BELIEVE THE MAINSTREAM MEDIA ACTUALLY REPORTED THIS?  YOU KNOW THIS IS ONLY A FRACTION OF THE WHOLE STORY. 

Three new conditions reported by a small number of people after vaccination with COVID-19 shots from Pfizer (PFE.N) and Moderna (MRNA.O) are being studied to assess if they may be possible side effects, Europe's drugs regulator said on Wednesday.

Erythema multiforme, a form of allergic skin reaction; glomerulonephritis or kidney inflammation; and nephrotic syndrome, a renal disorder characterized by heavy urinary protein losses, are being studied by the safety committee of the European Medicines Agency (EMA), according to the regulator.

Pfizer, by far the biggest supplier of COVID-19 vaccines to the European Union, and Moderna did not immediately respond to Reuter's requests for comment.

Just over 43.5 million doses of Moderna's vaccine, Spikevax, have been administered in the European Economic Area as of July 29, the EMA said, compared to more than 330 million doses of the Pfizer shot, Comirnaty, developed with Germany's BioNTech (22UAy.DE).

Last month, the EMA found a possible link between very rare heart inflammation and the mRNA vaccines. However, the European regulator and the World Health Organization have stressed that the benefits from these vaccines outweigh any risks.

The watchdog did not give details on Wednesday on how many cases of the new conditions were recorded but said it had requested more data from the companies. The EMA did not recommend changes to the labeling of the vaccines.

It disclosed the new assessments as part of routine updates to the safety section of all authorized vaccines' databases and added menstrual disorders as a condition it was studying for vaccines, including those from AstraZeneca (AZN.L) and J&J (JNJ.N), after the EMA's update last week.

Moderna's shares, which have climbed more than 75% to Tuesday's close since mid-July when it joined the S&P 500 index (.SPX), fell about 16% to $384 on Wednesday.

Fight For Your Freedom Against COVID Passes

This is why we should NEVER accept their use!  Join the challenge against COVID passes!

Divisive. Discriminatory. Wrong. We need YOU to join the fight against COVID passes.

Why we must stop COVID passes

The UK Government has released the NHS COVID pass and is now "strongly encouraging" businesses to restrict access using them, leading anyone from bouncers to bosses to conduct health ID checks. 

They're planning to make COVID passes mandatory - and are even threatening to make vaccine-only passes mandatory for nightclubs and universities.

COVID certificates would be the first attempt at segregation in Britain for many decades, dividing communities without reducing risks. We are in real danger of becoming a checkpoint nation.

We cannot, and will not, let this Government create a two-tier nation of division, discrimination and injustice.

Our common goal is to exit lockdown - healthy, safe and free. But we can't arrive at freedom through exclusion. 

The effect of the scheme would be to create a society where the poorest, the most marginalised, and anyone who does not comply with unprecedented demands for medical interventions could be denied basic socio-economic opportunities and afforded fewer liberties than their neighbours, colleagues and fellow citizens. 

The prospect of internal health passports signals a grave unbalancing of the relationship between not only citizens and the state but citizens and employers, business owners, managers, marshals, and anyone else dressed with authority.

The Government’s push for COVID-status certificates puts Britain in the midst of one of the greatest civil liberties battles we have faced in modern times. This is a time to stand up and take action.

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