(Just the News) The CDC and FDA on Tuesday recommended a “pause” in administering single-dose Johnson & Johnson COVID-19 vaccine in the United State until they can fully investigate reports of potentially dangerous blood clots.
(Brian Shilhavy) As can be expected when new experimental “vaccines” that are not approved by the FDA are given emergency use authorization to fight a “pandemic” that is now over a year old, reported deaths following the injections of these shots have now skyrocketed in the U.S. population by over 6000% here at the end of the first quarter of 2021, as compared to recorded deaths following FDA-approved vaccines at the end of the first quarter of 2020.
(100 Percent Fed Up) In a rush to produce and distribute millions of COVID vaccines, Johnson & Johnson’s manufacturing facilities have fallen under intense scrutiny for their significant FDA violations. After having to dispose of 15 million vaccines that had been contaminated due to human error, attention is being brought to the prior infractions of the production companies being used.
(Lance D Johnson) In the beginning of the “pandemic,” the Food and Drug Administration (FDA) approved fraudulent, high-cycle threshold PCR test kits that produced a high percentage of false positives — up to 97 percent. As more false positives turned up, Americans were told that they could be perfectly well, yet be “asymptomatic carriers” who also transmit infections. This was an ELABORATE LIE, a mass deception that permeated the population with fear. The spiking number of cases was based on fraudulent covid-19 testing kits that were designed to show a high percentage of positives based on the high number of amplification cycles used. These tests could not decipher infectious virus material and were not designed to determine viral load. This is why inanimate objects tested positive. This is why thousands of deaths were mis-attributed as covid-19 fatalities.
(Cassie B.) The natural health community experienced a huge loss when the FDA claimed that all homeopathic products are unapproved “new drugs” and must be withdrawn from the marketplace in 2019 in a move that has made it more challenging for people seeking homeopathic remedies to get the help they need.
(Robert L. Kinney, Pharm.D., M.A.) There are ongoing reports of the COVID-19 vaccine causing severe allergic reactions in recipients throughout the world. There is information that suggests that such allergic reactions, along with other dangers, were known to be associated with the COVID-19 vaccines but were covered up or wrongly downplayed prior to and during the emergency use authorization process.
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(CHRIS ENLOE) A top FDA official says the ‘culprit’ behind the reaction may have been identified
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(Franz Walker) For the past months, government agencies such as the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA) have been relying on Wuhan coronavirus (COVID-19) testing results to track the spread of the pandemic.
(B.N. Frank) The FDA is supposed to protect Americans from harmful products before they are made available to the public AND recall harmful products quickly when there is evidence that they are unsafe. They have a long history of failing to do so. Some examples include opioids, countless other medications, medical devices (see 1, 2, 3) and even hand sanitizers.
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(Sophie Mann) The White House has overruled new guidelines from the Food and Drug Administration that would likely have prevented introducing potential coronavirus vaccines to the market, prior to the Nov. 3 election. Related Trump’s Condition Substantially Improved, But He’s “Not Out Of The Woods Yet”, Doctor Says Source – Just the News by Sophie […]
(Mayukh Saha) Do you regularly lather yourself up with sunscreen every time you go out? Are you one of those people who express shock when someone doesn’t wear sunscreen? Well, we have got bad news for you. A recent test done by the FDA showed that sunscreen chemicals may be doing you more harm than good.
(Tal Axelrod) The Food and Drug Administration (FDA) halted a coronavirus testing program promoted by billionaire Bill Gates and Seattle health officials pending reviews.
(Nathaniel Weixel) The Trump administration is fast-tracking authorization of the drug remdesivir as a treatment for COVID-19.
(Eric A. Blair) The antimalarial drug hydroxychloroquine has been deemed the most highly rated treatment for the novel coronavirus in an international poll of more than 6,000 doctors.
(Andy Corbley) As the U.S. Food and Drug Administration (FDA) works to facilitate expedited access to several investigative drug interventions to treat COVID-19 patients, one particularly promising treatment is now set to enter clinical trials in New York.