New COVID vaccine approved by FDA for emergency use, but there's no emergency

Published: Aug 27, 2024 Duration: 00:06:21 Category: News & Politics

Trending searches: covid 19 vaccine
the United States Food and Drug Administration just approved a new covid-19 vaccine for anyone aged six months and up through emergency use authorization even though the state of emergency ended almost 2 years ago on Thursday August 22nd the United States Food and Drug Administration the FDA approved a new covid-19 vaccine under emergency use authorization even though there's no emergency and Biden himself ended the National Emergency more than a year and a half ago in the spring of 2023 nonetheless the FDA has granted emergency use authorization for updated mRNA covid-19 vaccines a 2024 2025 formula from Mna and fiser featuring a monovalent component targeting the Omicron variant KP do2 strain they say that this updated formula will more closely Target currently circulating variants and provide better protection against serious consequences of covid-19 including hospitalization and death but the evidence supporting this is negligible at best and researchers have repeatedly sounded the alarm the prevention of hospitalization or death wasn't the studied Endo in the clinical trial outcomes instead the end points were whether or not people who take the vaccines test positive for covid-19 Less often and every other approval or authorization of updated formulations or new variant development is based on the safety and efficacy or lack thereof of the original injections 6 months clinical trial data which revealed that the covid-19 injections actually caused more harm than good with misrepresented data misleading demographics and procedural flaws Frontline covid Critical Care Alliance senior fellow Dr Mary tally Bowden explains how this approval was even possible yesterday the FDA approved yet another covid shot and we're now up to 10 shots to be fully vaccinated they approved for all ages 6 months and older and they passed through under uh eua or emergency use authorization the reason they're allowed to do this is because the prep Act is still in place and the prep act doesn't expire till the end of the year so even though there is no emergency whatsoever pharmaceutical companies are able to push this through uh in expedited fashion without proper studies these shots are all risk and no benefit and they should have been pulled off the market a long time ago and I urge people not to get any more of these shots when the panel said listen give it to 6-month old babies with zero assurances this possibly would be safe I said where were you the day when the who came out and said do not use desar in the [Music] hospital I'm Dr Peter McCulla join me for an evening together tiets are on sale now in the fda's path from research to emergency use authorization they explicitly note that the manufacturer must submit an investigational new drug application without it clinical trial in humans is not permitted to proceed so these are clearly investigational new drugs making the public receiving them part of the investigation we used to call that experimental now even though it was well known by the spring of 2022 that the more injected and boosted one was the more likely they were to end up in hospital the cover up of that actually began in the summer of 2021 with so-called breakthrough infections because somehow in the depths of skewed reality and compromised science these breakthrough infections meant that the vaccines were well working of course they worked so well in this graph by an anonymous X account now notorious for accurate data compilations that the vaccin were still being hospitalized and dying in Greater amounts than the unvaccinated especially if you add all of the vaccinated categories together and then contrast it with the unvaccinated category might I add here that this is technically an inaccurate category since data was based on the definition of being fully vaccinated which only applied to those who received their final dose of the co9 vaccine at least 14 days ago so if you were hospitalized died or tested Ted positive for covid-19 within 2 weeks of your dose you were marked as unvaccinated or partially vaccinated which paints a skewed picture of the data from the onset yet the fact that provincial and territorial data across Canada were showing that the shots weren't stopping infection or preventing hospitalization or deaths remains true the data from public health jurisdictions were painting a picture at the time that more doses equated to poorer outcomes but these data sets and visualizations were swiftly removed when it didn't align with the safe and effective Mantra while the usfda clings to the benefits of the novel injections purportedly outweighing the risk I have repeatedly inquired with our federal health regulator that's Health Canada to ascertain that claim my requests asking what exactly is the benefit and how they're calculating risk continually falls on deaf ears so will Health Canada follow in the O So to be expected fda's footsteps it would be unsurprising although a troubling continued pattern of approving investigational drugs under the guise of emergency use even as mounting evidence reveals that they're doing more harm than good The Continuous push for these injections despite their dubious safety and efficacy claims underscores a failure to uphold Public Health standards and instead prioritize profit over people for Rebel news I'm tamary ugolini [Music] we've been calling on federal minister of Health Mark Holland to revoke Market authorization for these novel injections at Noor shots.com more shots.com

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