The U.S. Food and Drug Administration (FDA) is reportedly refusing to cooperate on a request to provide critical data which could tell us how “safe” the COVID vaccines really are. What could they possibly be hiding?
Republican Sen. Ron Johnson requested that the FDA provide the results of Empirical Bayesian (EB) data mining analyses on data from the Vaccine Adverse Event Reporting System in January but the federal agency decided they weren’t interested in complying.
The CDC also ran an analyses of the same data using a different method and the first time they did so, hundreds of concerning safety signals were triggered. This time around they claimed that none of the safety signals identified were “unexpected.”
The two agencies have run different types of analyses on the system’s reports, which are primarily made by health care professionals.
Johnson sought answers over this, which prompted the CDC to refer him to the FDA where the request was blocked.
“FDA’s EB data mining analyses of adverse events contained in VAERS reports for COVID-19 vaccines are currently the subject of pending FOIA [Freedom of Information Act] litigation. FDA is unable to comment on pending litigation or provide information or data that is currently being considered in pending litigation,” the agency told the senator.
Johnson responded to the agency’s effort to coverup this data by telling them that the American people via Congress have a right to know the truth.
“As you are well aware, Congress has a right to information contained at U.S. federal agencies as it conducts its constitutional oversight responsibilities,” Johnson said.
“It is outrageous that FDA would assert that pending litigation, and particularly FOIA litigation, would allow your agency to obstruct my congressional oversight,” he added.
“Any pending litigation FDA may have relating to its EB data mining records has no bearing on its responsibility to comply with a congressional request.”
This is not the first time the agency has refused to provide data like this, begging the question: whose side are they really on?
The federal agency seems to be more concerned with keeping people from seeing data which could harm Big Pharma’s bottom line than they are with keeping people safe.
This is particularly concerning when you consider that Joe Biden has greenlit a new vaccine development program which focuses on creating an all-new COVID jab which he intends to recommend to everyone – regardless of previous vaccination status.
Federal regulators won’t tell us how dangerous the injection that’s been around for roughly 3 years and dished out more than 1.5 million times is, but we’re expected to believe that we can trust them when they tell us the next one is, again, “safe and effective?’