Dr. Robert Malone, the inventor of mRNA and DNA vaccines, slammed health regulatory agencies for not informing people about potential plasmid DNA contamination in mRNA COVID-19 vaccines.
The Food and Drug Administration is asking a judge to give it 75 years to produce data concerning the Pfizer and BioNTech vaccine, up 20 years from a previous request.
Though the World Health Organization declared smallpox, a contagious and sometimes fatal infectious disease, eradicated in 1980, there have been longstanding concerns that smallpox could be used as a bioweapon.
The US Food and Drug Administration has issued "the most serious type of recall" for popular home testing kits that show if one is infected with coronavirus. At least 2.2 million products may have been showing false positives.
The FDA started the "horse dewormer" fallacy based on a Mississippi health department report that said 70% of poison control calls were related to veterinary ivermectin. It was actually 70% of ivermectin-related calls, six in all, four of which w
• http://www.ronpaulinstitute.org by mary l. g. ther
Fact-checkers screening for "misinformation," please note: everything that follows are direct quotes from the FDA Authorization Letter for COMIRNATY, the FDA-approved COMIRNATY package insert, as well as direct quotes of Diana Bianchi, director o
While the media has spent more than a year ridiculing the widely-prescribed drug Ivermectin to treat Covid-19 ?" branding it a 'horse dewormer for idiots,' they've kept oddly silent about another widely prescribed drug that's also used in ho
The Food and Drug Administration on Monday approved Pfizer and BioNTech's request to allow their Covid-19 vaccine to be given to kids ages 12 to 15 on an emergency use basis, allowing states to get middle school students vaccinated before the fall.
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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