Thrombosis

Karen Kingston joins Stew Peters to discuss revelations of fraud at a research company contracted to carry out Pfizer’s pivotal COVID-19 vaccine trial and how the FDA stepped in to conceal the high frequency of adverse reactions by removing these patients from the vaccine data. Kingston says this is criminal. “This is conspiring to commit aggravated assault against minors and adults in America. There’s no gray area, anymore.” On November 2nd, the British Medical Journal put out a report in which they announced that a whistleblower named Brooke Jackson, who works for the contract research organization, Ventavia had come forward to say that during one Pfizer trial of 1,000 vaccinated patients, nearly half were coached to alter the descriptions of their adverse events in their test diaries after 407 came down with COVID-19, versus 287 in the placebo group, which Karen describes as “A serious adverse event.” “They came down with it, Stew within a week of their first or second dose and they define COVID-19 as not just the mild or moderate symptoms, they define it as severe liver, kidney and neurological disorders, they define it as death and ICU admissions.  “So there could have been 407 people