⁣28 July 2021



Dr. Mercola interviews Dr. Robert Malone, the inventor of the
messenger RNA (mRNA) vaccine platform. He is one of the most qualified
individuals to opine on the benefits and potential risks of this
technology.

• Safety data analysis and reporting in clinical trials of the COVID
jabs appear to have been manipulated in at least some cases. One method
for manipulating randomized clinical trial safety data is to only
analyze the “per protocol” treatment group (those who completed all
doses and were fully compliant with the study design) as opposed to
“intent to treat” which would include all patients that have signed
informed consent
• For example, if a participant only accepted one
dose and trial protocol called for two, under a “per protocol” analysis,
adverse events they experienced would be dismissed and not included in
the safety analysis. This is a classic way to manipulate safety data in
clinical research, and it's usually forbidden
• Since the COVID shots
only have emergency use authorization, they are experimental products
and, as such, they are not authorized for marketing
• Bioethics are
written into federal law. As an experimental trial participant, you have
the right to receive full disclosure of any adverse event risks. Full
disclosure of risks is not being done, and in fact is being suppressed
•Adverse event risks must also be communicated in a way that you can
comprehend what the risks are, and the acceptance of an experimental
product must be fully voluntary and uncoerced. Enticement is strictly
forbidden

Source: ⁣https://www.bitchute.com/video/blxYyst1apKY/


Copyright holder of this video is Dr. Mercola