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--"Humanized Mice" Project; Agency Wanted "Fresh, Shipped on Wet Ice" Fetal Organs
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Former Food and Drug Administration Commissioner Scott Gottlieb said that the six-foot social distancing mandate that was employed across much of the United States and the world to deal with the CCP virus pandemic "wasn't based on clear science.
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In the U.S., vaccines granted Emergency Use Authorization by the FDA, as is the case with the Pfizer and Moderna COVID vaccines, are considered experimental. Administrators of emergency use vaccines are required by law to inform vaccine recipients of
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Moms across America and Demon Hunter -- Makes sense, the guy that ran the company that made Roundup was moved over to head up the FDA a few years ago. I assume he is still there protecting us right?
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Source: Moms across America and Demon Hunter -- Makes sense, the guy that ran the company that made Roundup was moved over to head up the FDA a few years ago. I assume he is still there protecting us right?
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...Cow registration mandates
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The FDA is holding up a cheap, durable vaccine currently in use in other countries even as thousands of Americans die from the virus every day.
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Distilleries just learned that to cap off a brutal year, the FDA is charging them a fee normally reserved for drug manufacturing facilities.
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Anthony Fauci's criminal big pharma sidekick, former FDA commissioner Scott Gottlieb, writes in The Wall Street Journal: The novel coronavirus is about to make its last major stand, so prepare for the most difficult six weeks yet. But things w
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Investigation reveals FDA's failure to account for the cumulative effect of chemicals on public health, particularly for communities already facing significant health and socio-economic disparities and for children who are uniquely susceptible to d
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The US has already begun to roll out 2.9-million doses of the Pfizer vaccine, and on Friday, the FDA authorized a second COVID-19 vaccine from Moderna for emergency use and plans to ship 7.9-million doses to 3,700 locations this week. Neither the Pfi
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There is clear evidence that its edicts are actually harming the American population, especially with its overreach into the Expanded Access program which allows doctors to choose experimental drugs for their patients.
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Genetically engineering pigs so they lack a certain sugar on the surface of their cells that triggers meat allergies or organ rejection won approval from the Food and Drug Administration Monday.
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U.S. Food and Drug Administration staff recommends monitoring people who get Pfizer or Moderna's Covid-19 vaccine shots for possible cases of Bell's Palsy, saying it's not necessarily a side effect but worth watching out for, reports CNBC.
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In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.
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In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.
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The Food and Drug Administration (FDA) on Friday night approved the first coronavirus vaccine for emergency use in the United States, several media outlets reported, clearing the way for U.S. officials to begin vaccinating millions of Americans as ea
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In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.
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In a letter to Peter Marks, director of the Center for Biologics Evaluation and Research, Robert F. Kennedy, Jr. asks the U.S. Food and Drug Administration to take a cautious approach in approving COVID-19 vaccines that have been developed at "warp
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A former FDA employee-turned-whistleblower says the agency downgraded his report on safety violations at a Merck vaccine plant. The allegation raises questions about how the FDA will monitor safety of COVID vaccine manufacturers.
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...for human consumption. Cotton plants and their seeds normally contain a toxic organic compound called gossypol, which can damage human red blood cells, causing anemia and death in people who consume it.
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The FDA announced on the 17th that the first at-home COVID test which provides rapid results has been approved in the United States.
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After declaring its own experimental Wuhan coronavirus (Covid-19) vaccine to be "safe," "effective," and ready to go, drug giant Pfizer is now planning to file for emergency use authorization from the U.S. Food and Drug Administration (FDA).
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As far back as April, U.S. National Institute of Allergy and Infectious Diseases (NIAID) Director Dr. Anthony Fauci was touting Gilead's antiviral remdesivir as "the standard of care for patients with COVID-19."
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The agency itself certainly tries to present itself as independent from the industries it regulates but, in reality, legal loopholes have led to the FDA receiving money from, and being captured and corrupted by, private interests.
