[awakened53]

VAERS Data Show New Deaths, Injuries After ‘Covid’ Fake Vaccines, As CDC Signs Off on 3rd Shot for Kids 5-11

VAERS data released Friday by the Centers for Disease Control and Prevention show 1,268,008 reports of adverse events from all age groups following COVID-19 vaccines, including 28,141 deaths and 230,364 serious injuries between Dec. 14, 2020, and May 13, 2022.
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,268,008 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 13, 2022, to the Vaccine Adverse Event Reporting System (VAERS).
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 28,141 reports of deaths — an increase of 173 over the previous week — and 230,364 serious injuries, including deaths, during the same time period — up 1,887 compared with the previous week. There were 6,859 additional total adverse events reported to VAERS over the previous week.
Excluding “foreign reports” to VAERS, 817,538 adverse events, including 12,961 deaths and 82,544 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 13, 2022.
Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.
Of the 12,961 U.S. deaths reported as of May 13, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
Read More: VAERS Data Show New Deaths, Injuries After COVID Vaccines, As CDC Signs Off on 3rd Shot for Kids 5-11

[awakened53]

Young Boy Died of Myocarditis After Pfizer Fake Vaccine, Says CDC Before Signing Off on 3rd Shot for Kids 5-11

VAERS data released Friday by the Centers for Disease Control and Prevention show 1,277,980 reports of adverse events from all age groups following COVID-19 vaccines, including 28,312 deaths and 232,694 serious injuries between Dec. 14, 2020, and May 20, 2022.
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,277,980 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 20, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 9,972 adverse events over the previous week.
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 28,312 reports of deaths — an increase of 171 over the previous week — and 232,694 serious injuries, including deaths, during the same time period — up 2,330 compared with the previous week.
Excluding “foreign reports” to VAERS, 820,788 adverse events, including 13,045 deaths and 82,974 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 20, 2022.
Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.
Read More: Young Boy Died of Myocarditis After Pfizer Vaccine, Says CDC Before Signing Off on 3rd Shot for Kids 5-11

[awakened53]

More ‘Covid’ Cases in Kids Who Got 2 Shots Compared to Those Who Got None, CDC Reports

The U.S. Food and Drug Administration authorized the use of a COVID-19 booster shot in children ages 5 to 11, even though data from the Centers for Disease Control and Prevention show case rates among kids in this age group who got two shots are now higher than rates in children who did not get the shots.
The U.S. Food and Drug Administration (FDA) amended its emergency use authorization for the Pfizer-BioNTech COVID-19 shot to allow a booster dose for children ages 5 to 11.
The FDA’s “evaluation of safety” for the booster dose in young children was based on a study of only about 400 children, and no meeting was held with the Vaccines and Related Biological Products Advisory Committee.
The booster shot is intended to be given at least five months after the primary two-dose series has been completed, but less than one-third — only 28.8% — of U.S. children in this age group have received the first two doses of this experimental gene therapy.
“[G]iven that these children have the lowest coronavirus vaccination rate of all eligible Americans, [as most parents have wisely avoided giving their child the jab] public health experts are not expecting a rush for the booster,” The New York Times reported, and this is good news since multiple red flags have arisen regarding the use of these shots, particularly among children.
COVID shots’ dismal effectiveness wanes rapidly
Booster shots are typically released because the initial shots aren’t working as planned.
This is certainly the case with COVID-19 shots, which have been found to have dismally low effectiveness rates of 12%, according to research conducted by the New York State Department of Health.
Read More: More COVID Cases in Kids Who Got 2 Shots Compared to Those Who Got None, CDC Reports

[awakened53]

Cult-Owned Psychopaths at the FDA Recommend Moderna Two-Dose ‘Covid’ Fake Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns. Cult-owned psychopaths sanctioning a fake vaccine produced by Cult-owned psychopaths

The U.S. Food and Drug Administration’s vaccine advisory panel on Tuesday voted 22 – 0 to authorize Moderna’s COVID-19 vaccines for children ages 6 to 11 and 12 to 17 despite the lack of short- and long-term safety data and no evidence children are at risk of serious illness.
The U.S. Food and Drug Administration’s (FDA) vaccine advisory panel today voted unanimously to recommend Moderna’s COVID-19 vaccine for children ages 6 to 17 after determining the benefits of the vaccine outweigh the risks for use.
The Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted 22 to 0 to recommend Moderna’s two-dose vaccine for 6- to 11-year-olds at half the strength of the adult version, and 22 to 0 in favor of authorizing the shot for 12- to 17-year-olds at the same strength as adults.
The FDA’s vaccine advisors will meet again on Wednesday to discuss amending Emergency Use Authorization (EUA) for Moderna’s COVID-19 vaccine to include the “administration of the primary series to infants and children 6 months through 5 years of age.”
The committee tomorrow also will discuss amending EUA of the Pfizer-BioNTech vaccine to “include the administration of the primary series to infants and children 6 months through 4 years of age.”
After VRBPAC makes its recommendations, the FDA will then decide whether to authorize Moderna and Pfizer’s vaccines for the suggested age groups.
During the public comment session of the meeting, individuals expressed concern over recommending a vaccine for an age group that has an almost zero risk of experiencing severe illness or death from COVID-19 and has already acquired a high level of natural immunity.
Read More: Breaking: FDA Panel Recommends Moderna Two-Dose COVID Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns

[Steve]

Big Pharma desperate

 ... to get COVID Shots on Childhood Schedule before ‘Emergency’ ends
Once the COVID-19 vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in any age group, including adults.

By Dr. Joseph Mercola
Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.
Story at a glance:

• The rate of COVID-19-associated hospitalization among children aged 5 to 11 is just 0.0008%. In real-world terms, that’s so close to zero you basically cannot lower it any further.
  
  
• Despite that, the vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — of the U.S. Food and Drug Administration (FDA) on June 15 unanimously approved granting Emergency Use Authorization (EUA) to Pfizer’s and Moderna’s COVID shots for infants and young children.
  
  
• Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old; Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years.
  
  
• In granting this EUA, the FDA again ignored injury and death data and swept medical ethics aside.
  
  
• The drug companies need this last remaining age group to be included under the EUA, because once the emergency is finally declared “over,” the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices. Once the vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in any age group, including adults…
  

https://childrenshealthdefense.org/defen...bb1506055b

[awakened53]

13 reasons why you should not allow your Baby or Toddler to be given the ‘Covid’ fake vaccine

The U.S. Food & Drug Administration (FDA) has questionably authorised emergency use of both the Pfizer and Moderna mRNA Covid-19 injections for use among children aged 6 months and above.
Here are 13 reasons why not a single teenager or child, let alone a 6-month-old baby should be given the Covid-19 vaccine.
Reason No. 1
86% of Children suffered an Adverse Reaction to the Pfizer Covid-19 Vaccine in the Clinical Trial
The information is publicly available and contained within a US Food & Drug Administration (FDA) fact sheet which can be viewed here (see page 25, table 5 on-wards).
That fact sheet contains two tables that detail the alarming rate of side effects and damage experienced by 12 – 15- year-old children who were given at least one dose of the Pfizer mRNA injection.
The tables shows that 1,127 children were given one dose of the mRNA jab, but only 1,097 children received the second dose. This fact in itself raises questions as to why 30 children did not receive a second dose of the Pfizer jab.
Of the 1,127 children who received a first dose of the jab 86% experienced an adverse reaction. Of the 1,097 children who received a second dose of the jab 78.9% experienced an adverse reaction.
Read more: 13 reasons why you should not allow your Baby or Toddler to be given the ‘Covid’ fake vaccine

[awakened53]

Reading the script: ‘Deadly virus surging in children will be defeated within five years’, vows Oxford vaccine chief. Another ‘virus’, another vaccine, another condition caused by re-diagnosis and fake vaccines

A deadly virus that surged among young children after lockdown will be treated by preventive vaccines within five years, the director of the Oxford Vaccine Group has said.
Respiratory syncytial virus (RSV) causes mild, cold-like symptoms for most, but can be deadly for infants and the elderly.
In the UK, RSV is responsible for around 30,000 paediatric hospitalisations and 83 deaths every year, estimates suggest. Among adults, the figures are even higher with 175,000 GP appointments, 14,000 hospitalisations and 8,000 deaths.
Typically spiking for six weeks in the winter, RSV puts significant strain on paediatric units. But for the last two years the virus has surged earlier in the year, in the summer months.
Professor Andrew Pollard, chair of the Joint Committee on Vaccination and Immunisation and director of the Oxford Vaccine Group, said we are still in a “funny post-pandemic phase” when it comes to the spread of the virus.
Read more: Reading the script: ‘Deadly virus surging in children will be defeated within five years’, vows Oxford vaccine chief. Another ‘virus’, another vaccine, another condition caused by re-diagnosis and fake vaccines

[awakened53]

Dozens of children given higher dose of fake vaccine at clinic ‘by mistake’

A mother was “devastated” after her children were mistakenly given a higher than normal dose of the Covid vaccine at a clinic in Southampton.
A total of 36 children, aged between five and 11, received their vaccinations at the children’s only pop-up vaccine clinic at Start Point in Sholing, Southampton, on Wednesday.
The mother of two, who wishes to remain anonymous, received a call later that evening from Solent NHS Trust, informing her that her children were among those given a higher dose of the paediatric Covid vaccination.
Speaking to the BBC, she said that she was already concerned about her children getting the vaccination in the first place, but she “took them along as I’d do anything in my power to protect them”.
She was told that she “shouldn’t expect anything significant” to happen to her children, but that any reaction they had to the jab “would last longer”.
“I haven’t slept for 48 hours, my anxiety is through the roof,” she added. Her children have not experienced any side effects.
Solent NHS Trust has apologised for the error, saying it is taking the situation “very seriously” and has begun an investigation.
Chief medical officer for the trust, Dr Dan Baylis, said: “We are very sorry this error occurred and we have contacted the parents of the children involved to apologise for the mistake and share support and guidance should their child experience any mild side effects such as tiredness or a headache.
Read More: Covid: Dozens of children given higher dose of vaccine at clinic ‘by mistake’

[awakened53]

Covid-19 Jabs: Never before have we been in so much danger

So, they’re now going to give the useless and toxic covid-19 jab to infants. They’re going to add a jab that doesn’t work and isn’t safe to an aggressive, untested, officially promoted programme of mass medication; the most alarming, experimental and grandiose example of centrally approved child abuse in human history; a programme that I believe has done infinitely more harm than good; a drug administration mania that should have been halted decades ago by the medical profession, and would have been if the medical profession hadn’t been bought by the drug industry; an untested experimental schedule that would have warmed the evil heart of Josef Mengele. Is it more dangerous to give the mRNA jab to babies whose mothers were jabbed before or during pregnancy or while they are breastfeeding? No one knows.
In America, the Government recommends that babies and infants should be given the following vaccines before they are 15-months-old: three doses for hepatitis B, two doses for rotavirus, four doses for diphtheria, tetanus and pertussis, four doses for haemophilus influenza, four doses of pneumococcal conjugate, three doses for polio, another one for influenza, one for measles, mumps and rubella, one for varicella, one for hepatitis and so on and so on…the list never ends. And now add in the toxic covid-19 jab. Why they don’t just slaughter infants at birth is a mystery. After 18 months they receive endless armfuls of more stuff. How kids ever get time to go to school is a mystery. I’m surprised they’re able to get to school. And, of course, it’s all much the same the world over.
How much testing has been done to check that all these vaccines don’t interact badly in the developing human body? None would be a good answer. How much research is done to see how much damage is being done to the developing immune system? Again, try none as your answer. Nearly all the medical research done these days is done by drug companies. Why would they want to find out how much damage their junk is doing?

Read More: Covid-19 Jabs: Never before have we been in so much danger

[awakened53]

Never mind all the deaths and health destruction: Pfizer/BioNTech ‘Covid’ fake vaccine authorised by UK government for use in infants and children aged 6 months to 4 years

The Comirnaty COVID vaccine has met the MHRA’s required safety, quality and effectiveness standards to be authorised for use in this age group
Authorisation has today been granted for a new presentation of the Pfizer/BioNTech COVID-19 vaccine (Comirnaty) for use in infants and children aged 6 months to 4 years.
The Medicines and Healthcare products Regulatory Agency (MHRA) has authorised the vaccine in this new age group after it has been found to meet the UK regulator’s standards of safety, quality and effectiveness, with no new safety concerns identified. This decision has been endorsed by the Commission on Human Medicines, after a careful review of the evidence.
This presentation is specially designed for this new age group and given at a lower dose compared to that used in individuals aged 5 to 11 years (3 micrograms compared with 10 micrograms). It is given as three injections in the upper arm, with the first two doses given 3 weeks apart, followed by a third dose given at least 8 weeks after the second dose.
In reaching their decision, the MHRA’s experts carefully reviewed data from an ongoing clinical trial involving 4,526 participants. The common, expected side effects (reactogenicity) were in-keeping with what can be anticipated from a vaccine in this age group.
It will be for the Joint Committee on Vaccination and Immunisation (JCVI) to determine if the vaccine will be recommended for use in this age group as part of the UK’s COVID-19 vaccination programme.

Read More: Pfizer/BioNTech COVID-19 vaccine authorised for use in infants and children aged 6 months to 4 years