(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experienced a huge loss when the FDA claimed that all homeopathic products are unapproved “new drugs” and must be withdrawn from the marketplace in 2019 in a move that has made it more challenging for people seeking homeopathic remedies to get the help they need.
(CHRIS ENLOE) A top FDA official says the ‘culprit’ behind the reaction may have been identified
(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.
The post FDA & CDC Finally Admit That Covid-19 Tests Are Faulty appeared on Stillness in the Storm.
(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.
(Nathaniel Weixel) The Trump administration is fast-tracking authorization of the drug remdesivir as a treatment for COVID-19.
The post FDA to Authorize Emergency Use of New Coronavirus Treatment appeared on Stillness in the Storm.
(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.