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ROBERT MALONE: Officials in the United States are misleading the public about the risks of the widely acknowledged DNA fragment contamination present in virtually all batches and lots of COMIRNATY and SPIKEVAX.
The U.S. Food and Drug Administration (FDA) has approved two revolutionary cell-based gene therapies, Casgevy and Lyfgenia, which could be a lifesaver for people dealing with the disease who are
The U.S. Food and Drug Administration fought back on Friday against what it calls “the proliferation of misinformation” by Florida’s Surgeon General Joseph Ladapo about the safety of COVID-19 vaccines. In a letter earlier this month to the FDA, Ladapo had questioned the agency’s drug approval and raised alarms about what he sees as the risk of potential cancer posed by COVID-19 mRNA vaccines. ...
On December 8, 2023, the FDA approved the first cell-based gene therapies for the treatment of sickle cell disease (SCD) in patients 12 years and older—Vertex’s CASGEVY and Bluebird’s...
The U.S. Food and Drug Administration fought back on Friday against what it calls “the proliferation of misinformation” by Florida’s Surgeon General Joseph Ladapo about the safety of COVID-19 vaccines.