According to Moderna’s ‘ongoing Trial 3’ of their vaccine, as of November 2020, of a total efficacy analysis population 28,207, 185 of the placebo group became contaminated with “CoVid”. That would represent 1.3% of the population. Adverse reactions among a group of 15,185 participants and included: pain at site 92%, fatigue 70%, headache 64%, myalgia 61.5%, arthralgia 46%, chills, 45%, vomiting 24%, axillary swelling 20%, fever 15%. I would venture those numbers incredibly significant!
Moderna states that their trials are wholly funded by NIH…
All participants in the study were high risk. Those younger than 65 had a risk factor disease per the CDC guidelines including; severe obesity, cardiac disease, bronchitis, emphysema, cystic fibrosis, etc… In other words, the study did NOT include healthy non-risk populations.
Oddly, November 2020 would appear to be the last time clinical trial information was made available.
Emergency Use rules state that the unapproved vaccines may only have authorized use if there is no approved available alternative. According to the FDA: “In phase 3, the vaccine is generally administered to thousands of people in randomized, controlled studies involving broad demographic groups (i.e., the population intended for use of the vaccine)”.
Given that the Moderna Phase 3 Trial was only conducted on ‘at-risk’ population only – that would mean the vaccine is only authorized for the at-risk population!
Despite media language, Fauci determinations, CDC altered guidelines, the FDA would appear to be doing little to nothing regarding any Vaccine:
The last time the FDA held a committee meeting (virtually) to discuss the vaccines was June 10th in order to determine pediatric use. Prior to that, a meeting was held on February 26th to discuss allowing Biotech authorized use. There has been NO followup on updated Trials… NONE.
In order to get actual “approval” Phase IV trials must be conducted over a period of 2 years tracking VAERS and by law one safeguard implemented by the FDA requires “Informed Consent and Assent”. In other words, a mandate is illegal per FDA regulations.