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(NaturalHealth365) Fact check from Reuters: Moderna and Pfizer were allowed to run animal testing and human testing of their COVID injection simultaneously, which is not a standard protocol in drug safety trials. Additionally, clinical trials for Modern and Pfizer will not end until October 2022 and January 2023, respectively.
These drugs are, without question, still in their experimental phase, and everyone who receives a shot should be considered part of a clinical trial – something that even a representative from Moderna admitted to during a recent phone call with a COVID shot victim.
(NaturalHealth365) Earlier this month, a Pfizer executive stated during a virtual symposium with Johns Hopkins University that the pharmaceutical company hopes their experimental mRNA drug will be in the arms of children as young as 5 years old by September or October. They’re also hoping to get a COVID booster shot out soon in order to protect against the so-called Delta variant of the pandemic virus – even though the U.S. Centers for Disease Control and Prevention (CDC) insist booster shots aren’t needed.
As a parent, do you have questions about your young child getting an experimental mRA shot? Are you aware that many medical experts also question giving these shots to kids, too?
(NaturalHealth365) The speed of the COVID shot program is unprecedented. Never before has the world seen such a rapid rollout and heavy promotion of an unapproved drug. To date, millions of doses of the experimental injection have been administered, even though the full extent of jab-related health risks remains unknown.
As you know, even children as young as 12 are eligible to receive these experimental drugs thanks to Pfizer’s successful bid to earn Emergency Use Authorization (EUA) for this age group. But one Israeli researcher and professor claims the drug company used questionable tactics to obtain the FDA’s green light.
(NaturalHealth365) Since at least April 2021, officials (including the Pfizer CEO himself) have hinted at the eventual need for a COVID shot booster, thanks to so-called virus variants and the waning effectiveness of these experimental drugs.
But as Pfizer prepares to seek Emergency Use Authorization (EUA) for its booster mRNA jab, a stunning revelation from a team of Spanish researchers sheds a worrisome light on these jabs’ true ingredients. So what have millions of people been unknowingly exposed to as a result of this massive drug trial?
(NaturalHealth365) After announcing that the effectiveness of its controversial and highly profitable COVID shot declines six months after injection, pharmaceutical company Pfizer now states it will be seeking Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for a third “booster” shot in August.
(NaturalHealth365) Americans aren’t the only ones with concerns about the COVID injection. In the United Kingdom – where currently just 46 percent of the population are considered fully vaxxed against the virus that causes COVID-19 – a team of independent researchers recently sounded the alarm on what is known about adverse effects from the available shots.
(NaturalHealth365) In recent headlines, COVID shot producer Moderna claims that its experimental drug is “100% effective” in preventing COVID in teens aged 12 to 17.
Now, as parents around the country worry that the shot will be mandated for kids, adolescents, and teens before returning to school in the fall, concerning reports of heart inflammation post-jab are now calling the safety and effectiveness of these drugs into serious question.
(NaturalHealth365) $26 billion: that’s how much money Pfizer expects to make in 2021 thanks to its COVID shot, accounting for more than one-third of the pharmaceutical giant’s sales.
But even as Pfizer reportedly plans to file for full FDA approval of its experimental drug this month, doctors and individuals are beginning to raise serious questions over the possibility that this experimental drug could be shedding or causing harm to people who are choosing to remain shot-free, including severely altered menstruation.
A group of 57 leading scientists, doctors, and policy experts has released a report calling in to question the safety and efficacy of the current Covid-19 vaccines and are now calling for an immediate end to all vaccine programs.
(NaturalHealth365) Did you know “healthcare providers are required by law” to report certain adverse events to the Vaccine Adverse Event Reporting System (VAERS) operated by the U.S. Department of Health and Human Services (HHS)? The emphasis above — underlined and bolded — comes directly from the HHS website, which has become immensely popular since the COVID shot rollout began in the United States.