These documents are the first significant release of data from Moderna’s COVID-19 clinical trials. They reveal the causes of deaths, serious adverse events, and instances of neurological disorders (such as Bell’s Palsy and Shingles) potentially associated with Moderna’s COVID-19 vaccine.
Importantly, these records also demonstrate the utter lack of thoroughness of these studies. Many of those who died after receiving the Moderna vaccine were not given an autopsy. According to one study, 16 individuals died after being administered the Moderna vaccine. The study’s authors indicated that out of those 16 deaths, only two autopsies were performed, five of the dead were not autopsied, and the autopsy status of nine of the dead was “unknown”.
There were numerous examples of participants with post-vaccination Bell’s Palsy and Shingles (Herpes Zoster). One 44 year-old female had “left side facial paralysis” just eight days after the second dose. Numerous vaccinated participants saw the onset of Shingles less than 10 days after vaccination.
Other key observations during the Moderna “studies” involved serious adverse events for those in the vaccinated groups. A number of participants experienced: myocardial infarction (heart attack); pulmonary embolism; spontaneous abortion/miscarriage; transient ischemic attack (TIA); and lymphoma. Subsequent analyses of reports from the FDA VAERS database, the Department of Defense’s DMED database, and European regulators showed heightened rates of these illnesses following administration of the Moderna vaccine.
And similar to their treatment of deaths post-vaccination, the studies seemed predestined to conclude that these serious adverse events – many of them life-threatening – were not related to the Moderna vaccine. It didn’t matter whether the adverse event occurred within days of vaccination. This creates serious doubt concerning the safety of the Moderna vaccine and the FDA’s standards and approval of the Moderna vaccine.