By Dr. Joseph Mercola and Dr. Robert Malone
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 âper protocolâ treatment group (those who completed all doses and were fully compliant with the study design) as opposed to âintent to treatâ 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 âper protocolâ 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 itâs 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…
