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Covid Vaccines Are Harming Boys More Than Girls

Why FDA Should Not Authorize COVID Vaccines for Kids, Teens

The Covid-19 vaccines are disproportionately harming boys more than girls, as the jabs are six times more harmful to males in comparison to females, at least as far as cardiovascular events are concerned.

Research shows that teenage boys are 600 per cent more likely to suffer a heart attack or health problems after receiving the Covid vaccine compared to teenage girls around the same age.

Data from the US now confirms that the highest risk group of suffering a “cardiac adverse event” post-injection are boys between the ages of 12 and 15.

Meanwhile, Professor Chris Whitty, the UK’s chief medical officer, and the Joint Committee on Vaccination and Immunisation (JCVI) have concluded that the “margin of benefit” on giving vaccines to 12-to-15-year-olds is “considered too small.”

There is no scientifically valid reason to be giving young children the Covid jabs, even more so when you consider how children have been injured by these jabs. The Pfizer jab, which has been approved for emergency use on children in countries such as the US, actually caused 86% of children to suffer from an adverse event ranging from mild to severe during trials.

Whilst it has been decided that the Covid jabs should not be used on children in the UK, Health Secretary Sajid Javid, on the other hand, is all about sticking the experimental vaccines in the arms of young boys and girls. In his opinion, Scotland, Wales and Northern Island should “consider the vaccination of 12- to 15-year-olds from a broader perspective.”

Javid said: “[I will] consider the advice from the chief medical officers, building on the advice from the JCVI, before making a decision shortly.”

An investigation into the rate of cardiac myocarditis, heart inflammation and chest pain in children 12- 17-year-olds following their second dose of the vaccine was recently carried out by a team of researchers at the University of California. Data found was compared to that of children in the same group needing hospitalisation after testing “positive” for the virus.

Dr Tracey Hoeg and her fellow researchers found that injected children especially injected boys, fare much worse than children who do not get the jab.

Boys 12-15-years-old typically suffer the worst post-injection, followed by boys aged 16-17. After that, girls aged 12-15 are next in line for heart problems.

Despite the results of this shocking research, health experts continue to push the vaccine agenda on everyone, with their sights firmly set on children, regardless of the millions of people who are suffering from adverse reactions caused by the jabs.



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Susan Price
Susan Price
11 days ago

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Last edited 11 days ago by Susan Price
Richard Noakes
Richard Noakes
11 days ago

And then we have the 5 to 11 year olds: Vaccines emergency use in children ages 5 to 11 by the end of October 2021
Washington — Former Food and Drug Administration (FDA) Commissioner Dr. Scott Gottlieb predicted Sunday that the agency he helmed will authorize Pfizer’s coronavirus vaccine for emergency use in children ages 5 to 11 by the end of October.
In an interview with “Face the Nation,” Gottlieb, who serves on Pfizer’s board of directors, said the drug company is expecting to have data on its vaccines in young children before the end of September, which will then be filed with the FDA “very quickly.” The agency then has said it will be weeks, rather than months, before determining whether it will authorize the vaccine for kids ages 5 to 11.
“In a best-case scenario, given that timeline they’ve just laid out, you could potentially have a vaccine available to children aged 5 to 11 by Halloween,” Gottlieb said. “If everything goes well, the Pfizer data package is in order, and FDA ultimately makes a positive determination, I have confidence in Pfizer in terms of the data that they’ve collected. But this is really up to the Food and Drug Administration to make an objective determination.”
·   Transcript: Dr. Scott Gottlieb on “Face the Nation”
Pfizer has been conducting clinical trials of its two-dose vaccine in children 2 years and older, and its approval could be crucial to helping combat the spread of the highly contagious Delta variant in schools. Children represent 25% of new COVID-19 infections.
The shot has already been authorized for children ages 12 to 15, and Gottlieb said he believes COVID vaccines will eventually be among those required for children in public schools.
“I think you’re going to see more local school districts and governors make those recommendations,” he said. “Eventually ACIP is going to make a recommendation about whether this should be included in the childhood immunization schedule. My guess is they’re waiting for more of the vaccines to be fully licensed to make that kind of a recommendation. But I would expect this eventually to be required as part of the childhood immunization schedule.”
For parents who may be wary of their children receiving a vaccine that is under emergency use, rather than fully approved by the FDA for children, Gottlieb encouraged them to consult with their pediatricians, but stressed they are not facing a “binary decision” of getting their children vaccinated against COVID-19 or not.
“There’s different ways to approach vaccination. You could go with one dose for now. You could potentially wait for the lower dose vaccine to be available, and some pediatricians may make that judgment. If your child’s already had COVID, one dose may be sufficient. You could space the doses out more,” he said. “So, there’s a lot of discretion that pediatricians can exercise, making largely off-label judgments, but exercising discretion within the context of what an individual child’s needs are, their risk is, and what the parents’ concerns are.”
While the FDA is expected to make a decision on whether to authorize COVID vaccines in children in the coming weeks, federal health agencies are also weighing whether to approve booster shots for vaccinated Americans.
The Biden administration initially announced in August that it was prepared to begin offering the boosters the week of September 20, and Americans would need to get their additional shots eight months after receiving their second vaccine dose. But Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, told “Face Nation” last week that it may only be Pfizer’s booster that receives federal approval by September 20.
The FDA’s advisory committee is scheduled to meet Friday to discuss the booster shots, and Gottlieb said the agency is positioned to act “very quickly” depending on the outcome of the meeting. If the boosters are approved, he said a Centers for Disease Control and Prevention advisory committee would then recommend which populations would get them first, likely those who are at higher risk of severe illness or death from COVID-19 such as elderly Americans living in nursing homes.
Pfizer has already filed its application with the FDA for approval of its booster, and Gottlieb predicted Johnson & Johnson will likely be next to do so.
“They have very good data also looking at boosters. They’ve showed a good response,” he said of Johnson & Johnson. “And I think that vaccine also could be in a position to get authorized by FDA in short order.”
Coronavirus Crisis
First published on September 12, 2021 / 11:48 AM
© 2021 CBS Interactive Inc. All Rights Reserved.

Me: But what about kids 0-4, they will be next

Carmel
Carmel
Reply to  Richard Noakes
11 days ago

Thank you for sharing that latest very important information……have you a link for that news article?

Carmel
Carmel
11 days ago

Let’s leave aside for a moment the flawed covid swab RT-PCR tests (testing for a supposed Biosecurity Class 4 Lab category of virus) that have been spewing out false positives creating a global false positive casedemic plus the fact that hundreds of individual Freedom of Information (FOI’s) requests to labs around the world have revealed that SARS CoV 2 has never been isolated. Therefore is SARS CoV 2 and all of its mutated variants perhaps a phantom virus with phantom variants?

Biostatistician Christine Massey – Freedom of Informations (FOI’s) on the isolation of SARS CoV2 and variants.
https://www.fluoridefreepeel.ca/fois-reveal-that-health-science-institutions-around-the-world-have-no-record-of-sars-cov-2-isolation-purification/

‘Conservatively’ using official US government data there are clearly ZERO BENEFITS FOR CHILDREN aged 0-17 years of age of the covid injections and ALL OF THE RISKS OF ADVERSE EFFECTS and the medium to long term effects of the covid injections are unknown.
And the cumulative effects of multiple covid injections, covid boosters and perhaps covid injection supplemental covid pills are all unknown.
And the future inter generational effects of the covid injections are unknown.

See Slide 16/Page 16 of the following Food and Drugs Administration (FDA) Presentation on Vaccines and Related Biological Products Advisory Committee October 22, 2020 Meeting Presentation

FDA Safety Surveillance of COVID-19 Vaccines :
DRAFT Working list of possible adverse event outcomes
https://www.fda.gov/media/143557/download

According to the latest Centre for Disease Control (CDC) update of March 19, 2021 the CDC’s current Best Estimate for the Covid-19 Infection Fatality Ratio (IFR) per 1,000,000 infections for the 0-17 age group is 0.002% or 20 deaths per million cases.
https://www.cdc.gov/coronavirus/2019-ncov/hcp/planning-scenarios.html#

According to the latest CDC Covid Injection Reported Adverse Events published September 7, 2021 the covid injection fatality rate per 1,000,000 covid doses administered is increasing and is ‘to date’ currently 0.002% or 20 reported deaths per 1,000,000 covid doses administered.
(Note that the typical ‘initial’ covid injection protocol consists of 2 doses of a covid injection, perhaps a booster followed by perhaps subsequent 6 monthly doses of covid injections and perhaps combined with (Pfizer) twice daily covid treatment pills) https://cdn.pfizer.com/pfizercom/2021-09/First_Participant_Dosed_in_Phase_2_3.pdf?xngrygl6i_kDXWrJtM7ixP65qQ6ZXOK0

‘More than 375 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through September 7, 2021. During this time, VAERS received 7,439 reports of death (0.0020%) among people who received a COVID-19 vaccine.’
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/adverse-events.html

Carmel
Carmel
11 days ago

Teens 50X More Likely to Have Heart Disease After COVID Shots than All Other FDA Approved Vaccines in 2021 Combined – CDC Admits True but Still Recommends It
https://vaccineimpact.com/2021/teens-50x-more-likely-to-have-heart-disease-after-covid-shots-than-all-other-fda-approved-vaccines-in-2021-combined-cdc-admits-true-but-still

Lorra
Lorra
11 days ago

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Last edited 11 days ago by Lorra
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