By Mychal Massie November 4, 2021 @ Daily Rant
April 24, 2019, I wrote a syndicated article referencing an article by Susan Scutti and Elizabeth Cohen on the then new admissions (April 19, 2019) by the Centers for Disease Control (CDC) that vindicated me per what I had been warning since 2014 about disease threats from illegal aliens:
“I was attacked and ridiculed by the jack-booted, storm troopers from George Soros funded cultural-Marxist front groups, such as People for the American Way, Daily Kos and Con Web Watch. Any one of these groups would have been highly praised by Hitler, Stalin, Marx, Mao or Lenin. … The incestuous exogamy of these groups resembled that of an elapid and a phyllobates terribilis, i.e., the golden poison frog. In brief they are deadly toxins whose only purpose is to sow discord and advance neo-Leninism. … But, as my track record continues to prove, I’m right and those androgynous species of Erebusic commonality continue to be proven wrong. Just don’t hold your breath waiting for them to admit they’re wrong.”
This brings me once again to a position of deriving no pleasure from saying: “I told you so!!”
The article following on “falsified data per Pfizer drug” further confirms what I have been speaking in public and private. People motivated by fear and misinformation are highly susceptible to being massively deceived; the injurious part of said deceit, is that by the time the truth is revealed it’s typically too late for those who bought the lie. It happened with obamacare; remember:
you can keep your doctor and the repeated lies about the price of coverage not increasing, etc?
The truth ultimately always comes out, but even then the deceived are frequently too embarrassed to admit they were played for fools, choosing instead to publicly attack the messenger(s). Others sign onto class-action lawsuits for their pound of compensation for not listening, while still others lay awake at night waiting for the proverbial other shoe to drop.
The government con-game is always the same: Scare and bully as many as possible into obeying whatever satanic scam they are pushing (for, as we’re told, our own protection), before the truth becomes too obvious to ignore. Once again, I point to obamacare as an example.
The global public has been lied to from the beginning, when we were told nearly two-years ago that things would be shut down for two weeks to flatten the curve. Then came the vaccine that wasn’t a vaccine but an experimental drug with life-threatening side-effects, including death. The actual numbers of deaths from the covid flu are inflated and falsely identified: remember the people who died in automobile accidents and motorcycle accidents being identified as covid deaths? Remember the public was told the toxic-drug was safe for pregnant women and nursing mothers, until the truth could no longer be hidden and/or denied? After being assured that the drug was safe for 3 and 5 year olds, Dr. Ben Carson warns the drug is making guinea-pigs out of children.
Now as indicated below those of us who were warning about falsification of efficacy and the danger in taking the toxins – the truth is coming out that these toxic pharmaceuticals are neither effective nor safe.
I repeat, that I’m not telling you what to do. I’m saying make informed decisions
based upon facts, not motivated by fear; because making decisions based
upon coercion and lies, can and will bring about deadly consequences.
By Adina Kutnicki, November 3, 2021
THOUGH it has been amply evidenced, over and over again, that Pfizer has gone to great lengths to push their covid vax on every living human being, come what may, there are countless who should know better than to fall for their jive-talk, but, nevertheless, are snowed. Regardless, pharma greed + leadership’s quest for power and control are a deadly cocktail. Literally.
CONSIDER:- EXPLOSIVE REVELATION: Indian Television Exposes How Pfizer Bullies and Blackmails Countries for COVID Shots – “Desperate Countries force to Make Humiliating Concessions” (VIDEO)
- Harvard, Stanford Scientists Show How Fauci Fooled America +
- Massive Flight Cancellations Due to Vaccine Deaths and Employee Resignations – Biden Regime’s Purposeful Destructive Swathe Across America. Beyond.
- Half-dozen FDA vaccine panel members are tied to Pfizer
and so on and so forth.
THUS, it is alongside this very same duplicitous trajectory that more of the same has come to light. Inexorably, beyond the pale.
ZERO HEDGE | By Tyler Durden | November 2, 2021
A whistleblower involved in Pfizer’s pivotal phase III Covid-19 vaccine trial has leaked evidence to a notable peer-reviewed medical publication that poor practices at the contract research company she worked for raise questions about data integrity and regulatory oversight.
Brook Jackson, a now-fired regional director at Ventavia Research Group, revealed to The BMJ that vaccine trials at several sites in Texas last year had major problems – including falsified data, broke fundamental rules, and were ‘slow’ to report adverse reactions.
When she notified superiors of the issues she found, they fired her.
A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails. -The BMJ
Poor laboratory management
Jackson, a trained clinical trial auditor with more than 15 years’ experience, says she repeatedly warned her superiors of poor laboratory management, patient safety concerns, and data integrity issues. After she was ignored, she started documenting problems with the camera on her mobile phone.
One photo, provided to The BMJ, showed needles discarded in a plastic biohazard bag instead of a sharps container box. Another showed vaccine packaging materials with trial participants’ identification numbers written on them left out in the open, potentially unblinding participants. Ventavia executives later questioned Jackson for taking the photos.
The unblinding was potentially far more severe as well. Per the trial’s design, unblinded staff prepared and administered either Pfizer’s Covid-19 vaccine or a placebo. This was done to preserve the blinding of trial participants and other staff – including the principal investigator. At Ventavia, however, Jackson says that drug assignments were left in participants’ charts and accessible to blinded personnel. The breach was corrected last September, two months into the trial at which point there were around 1,000 participants already enrolled.
Jackson recorded a September 2020 meeting with two Ventavia directors, at which an executive can be heard saying that the company couldn’t quantify the types and number of errors with their testing.
“In my mind, it’s something new every day,” they said, adding “We know that it’s significant.“
According to the report, Ventavia also failed to keep up with data entry – as a Sept. 2020 email from Pfizer partner ICON reveals.
“The expectation for this study is that all queries are addressed within 24hrs.” ICON then highlighted over 100 outstanding queries older than three days in yellow. Examples included two individuals for which “Subject has reported with Severe symptoms/reactions … Per protocol, subjects experiencing Grade 3 local reactions should be contacted. Please confirm if an UNPLANNED CONTACT was made and update the corresponding form as appropriate.” According to the trial protocol a telephone contact should have occurred “to ascertain further details and determine whether a site visit is clinically indicated.”
FDA Inspection woes
Other documents provided to The BMJ reveal that Ventavia officials were worried about three employees . In an email in early August 2020, an executive identified three site staff members with whom they need to “Go over e-diary issue/falsifying data, etc.”
One of the employees was “verbally counseled for changing data and not noting late entry,” a note reveals.
During the September meeting, Ventavia executives and Jackson discussed the potential for the FDA to show up for an inspection. On former Ventavia employee told The BMJ that the company was petrified over the potential for an FDA audit, and were in fact expecting one over the Pfizer vaccine trial.
“People working in clinical research are terrified of FDA audits,” Jill Fisher told the journal, adding however that the agency rarely does anything except review paperwork – usually months after a trial is over. “I don’t know why they’re so afraid of them,” she added – saying that she was surprised that the agency failed to inspect Ventavia following an employee complaint.
“You would think if there’s a specific and credible complaint that they would have to investigate that.”
FDA notified
Jackson sent a Sept. 25 email to the FDA in which she wrote that Ventavia had enrolled over 1,000 participants at three sites, out of the full trial’s 44,000 participants across 153 sites which included various academic institutions and commercial companies. She raised concerns over issues she had witnessed, including:
- Participants placed in a hallway after injection and not being monitored by clinical staff
- Lack of timely follow-up of patients who experienced adverse events
- Protocol deviations not being reported
- Vaccines not being stored at proper temperatures
- Mislabeled laboratory specimens and,
- Targeting of Ventavia staff for reporting these types of problems.
Hours later, the FDA emailed her back, thanking her for her input but notifying her that they would not comment on any investigation which may result.
That said, in August of this year, the FDA published a summary of its inspections of Pfizer’s pivotal phase III trial. They looked at just nine out of the trial’s 153 sites, and did not look at any of Ventavia’s operations. Further, no inspections were conducted following the December 2020 emergency authorization of the vaccine.
Other employees corroborate Jackson’s complaints
Two former Ventavia employees spoke with The BMJ anonymously, and confirmed ‘broad aspects’ of Jackson’s account.
One said that she had worked on over four dozen clinical trials in her career, including many large trials, but had never experienced such a “helter skelter” work environment as with Ventavia on Pfizer’s trial.
“I’ve never had to do what they were asking me to do, ever,” she told The BMJ. “It just seemed like something a little different from normal—the things that were allowed and expected.”
She added that during her time at Ventavia the company expected a federal audit but that this never came.
After Jackson left the company problems persisted at Ventavia, this employee said. In several cases Ventavia lacked enough employees to swab all trial participants who reported covid-like symptoms, to test for infection. Laboratory confirmed symptomatic covid-19 was the trial’s primary endpoint, the employee noted. (An FDA review memorandum released in August this year states that across the full trial swabs were not taken from 477 people with suspected cases of symptomatic covid-19.)
“I don’t think it was good clean data,” the employee said of the data Ventavia generated for the Pfizer trial. “It’s a crazy mess.” -The BMJ
The second employee told The BMJ that working at Ventavia was unlike any environment she had experienced in 20 years of research.
Since her firing, Jackson has reconnected with several Ventavia employees who either left or were fired themselves. One of them sent her a text message, which reads “everything that you complained about was spot on.”
Meanwhile, since Jackson reported issues with Ventavia to the FDA in September 2020, Pfizer has contracted with the company for four other vaccine clinical trials.
One has to wonder – if the FDA is auditing less than 10% of trials, how many more potential whistleblowers could there be?
{ADDENDUM: Bear uppermost in mind — To stifle the truth-telling found at this site, Face Book's censors have “zeroed-out” all of my articles via their “Boom and Ban” censors ala their ubiquitous “Community Standards” — as they hunt me up and down the internet like rabid dogs to their prey! No kidding. This is just some of Face Book’s modus operandi, what is now deemed their “love notes” to yours truly:This URL goes against our Community Standards on
spam:adinakutnicki.files.wordpress.comACTIVITY
"About your post Today at 4:34 PM: No one else can see your post". And so on and so forth. In fact, just recently, each article at my “parent site”, ADINA KUTNICKI: A ZIONIST & CONSERVATIVE BLOG, had its Face Book registered shares go from the hundreds, with some up to the many thousands, to a big, fat ZERO. In other words, all my shares have gone down the rabbit hole. Just like that. Poof.
Gone. As such, take it to the bank that each and every conservative voice which reaches a wide readership will, sooner than later, be CENSORED. MUTED.} MESSAGE FAILED:This message contains content that has been blocked by our security systems.If you think you’re seeing this by mistake, please let us know. Yes, additional “proof-in-the pudding” as to why “BANNED: How Facebook Enables Militant Islamic Jihad” had to be written!}
About the Author
Mychal Massie
Mychal S. Massie is an ordained minister who spent 13 years in full-time Christian Ministry. Today he serves as founder and Chairman of the Racial Policy Center (RPC), a think tank he officially founded in September 2015. RPC advocates for a colorblind society. He was founder and president of the non-profit “In His Name Ministries.” He is the former National Chairman of a conservative Capitol Hill think tank; and a former member of the think tank National Center for Public Policy Research. Read entire bio here
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