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Dr. Robert Malone, an internationally recognized scientist and holder of the original patents for mRNA and DNA vaccines, spent decades learning how to develop a safe and efficient drug or a vaccine by following the proper processes and regulations.
On a recent episode of CHD.TV’s “Doctors and Scientists,” Malone shared his views on the key problems with gene therapy and how “bad science gets played” between medical agencies and large universities.
Malone performs threat assessments, makes health recommendations and acts as a liaison between government and intelligence communities during disease outbreaks.
Malone told “Doctors and Scientists” host Brian Hooker, Ph.D., that on Jan. 4, 2020, he received a call from Michael Callahan, a CIA officer and biowarfare expert who was in Wuhan, China. Callahan told Malone there was a problem with the coronavirus and they needed to “pay attention to it.”
Malone said he made the same assessment for COVID-19 as he made for the Zika virus.
“I felt there was no way a vaccine would be available in a safe and effective and well-regulated fashion, and in a timely fashion, so I got my team spun up on drug repurposing,” he said.
That’s when he discovered the over-the-counter drug, famotidine, a drug that reduces stomach acid. Marketed under the brand name Pepcid, the drug also is useful for treating COVID-19, Malone said.
“There are several different strategies for the early treatment of COVID to save lives,” Malone said. “And the sick, sad thing is they’ve all been suppressed intentionally because if the FDA [U.S. Food and Drug Administration] acknowledges [these strategies] … then by law, it would not be able to apply the Emergency Use Authorization to the vaccines.”
Malone and Hooker discussed the FDA’s latest moves: authorization of the COVID-19 shots for children and infants as young as 6 months old and authorization of a change to the mRNA vaccines without requiring additional data showing a bivalent vaccine — containing both the original 2019 Wuhan variant and one of the Omicron variants — is safe and effective for those age groups that are already authorized to receive a booster dose.
Malone explained how the FDA bypasses important clinical trials designed to ensure the new vaccine is effective and does not cause any adverse effects.
“The FDA and the CDC [Centers for Disease Control and Prevention] are completely corrupt,” Malone said. “The fraud is deep and broad, it is transparent to much of the world.”
Malone revealed the moment he had an epiphany and decided to expose the corruption within the FDA, CDC, Big Pharma and other higher medical and governmental agencies.
“There is no way that humans, patients — however you want to define them — vaccine recipients, have received informed consent,” Malone said. “Because the CDC has actively blocked anyone’s ability to be able to access the actual information about adverse events and risks.”
Is there hope?
Malone described what needs to happen to reverse the fascism that has been integrated into our governmental system.
He said:
“We have a grossly corrupted system. It is corrupted at every single level. We are one of the only nations in the world in which the pharmaceutical industry is allowed to directly market to people.
“We are one of the only nations in the world in which there are no regulations on pharmaceutical pricing. We have got to pay attention to this hot mess that got us here.”
Watch the full episode here:
