3 Reasons to Doubt COVID Vaccine Safety

Unassailable proof that the COVID vaccines are the most deadly vaccines in human history

Just for the record…Just because the FDA, CDC and the Public Health Agency of Canada have found no issues with the vaccines, doesn’t mean they are safe. Here’s unassailable proof they aren’t.

We have to stop blindly trusting our trusted authorities that they are giving us good information. It isn’t warranted. We should always insist on hearing both sides of the story.

We should be extremely suspicious when not a single leading medical advocate of the vaccine is willing to debate a team of qualified scientists who disagree with the narrative.

For example, it is well known that Merck received approval from the FDA to give Vioxx to 2 year old children just 3 weeks before Merck pulled the drug for safety issues.

We’re doing it again now with our kids and this time the drug companies aren’t going to pull it even though there is compelling evidence is in plain sight of everyone.

Here are three pieces of unassailable proof that the COVID vaccines are the most dangerous in history and should be immediately pulled:

  1. The VAERS data shows 8,456 deaths in the US (note: if you are using openvaers, be sure to “flip the switch” to show domestic only). Even using the most conservative assumptions of 223 background deaths (the highest annual death toll in VAERS history for domestic deaths), this is 8,233 “excess” deaths. Something caused those deaths. That’s a HUGE number. It’s a public health disaster. If it wasn’t the vaccine, then what did the CDC find caused all these excess deaths? Nothing! Absolutely nothing! Note that I didn’t even have to multiply by the VAERS under-reporting factor (URF) of 41 (calculated via the CDC’s own methodology). There are only 226M vaccinated people. That’s a death rate from the vaccine of at least 36 deaths per million vaccinated (assuming the most conservative possible URF of 1). That’s 36 times more deadly than the deadliest vaccine in human history, a vaccine that is too unsafe to use. It has no business being on the market. Note that all reports in VAERS are validated by HHS before they are allowed to appear in VAERS. Mistakes do happen. There are at least 2 records of the 1.6M in VAERS that were gamed, one by Dr. David Gorski (who is proud of breaking Federal law to do that).

  2. A prominent group of neurologists with 20,000 patients has had around 2,000 patients with vaccine-related adverse reactions. In the 11 year history of the practice, they’ve never had a patient with a vaccine-related adverse reaction. While this could happen just by bad luck, the chance of it happening by “bad luck” is less than 1 in 10**100, i.e., impossible. This is a huge increase in significant neurological events that is inexplicable if the vaccines are safe. This is further evidence that the increase in the events reported in VAERS is not “stimulated reporting.” NOTE: The doctors won’t come forward publicly for fear of retribution (loss of medical license). That’s why nobody knows. With the doctors’ permission, I’m happy to disclose it to the NY Times or other allegedly reputable news source under NDA if they want to do a story on it.
  3. And then there is the 60-fold increase in the rates of adverse events happening in front of our eyes. Hard to explain since it never happened before the vaccines rolled out.

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From Steve Kirsch, here.

Corona Vaccine Trials: ‘Open and Transparent’?

Wait what? FDA wants 55 years to process FOIA request over vaccine data

That’s how long the Food & Drug Administration in court papers this week proposes it should be given to review and release the trove of vaccine-related documents responsive to the request. If a federal judge in Texas agrees, plaintiffs Public Health and Medical Professionals for Transparency can expect to see the full record in 2076.

The 1967 FOIA law requires federal agencies to respond to information requests within 20 business days. However, the time it takes to actually get the documents “will vary depending on the complexity of the request and any backlog of requests already pending at the agency,” according to the government’s central FOIA website.

Justice Department lawyers representing the FDA note in court papers that the plaintiffs are seeking a huge amount of vaccine-related material – about 329,000 pages.

The plaintiffs, a group of more than 30 professors and scientists from universities including Yale, Harvard, UCLA and Brown, filed suit in September in U.S. District Court for the Northern District of Texas, seeking expedited access to the records. They say that releasing the information could help reassure vaccine skeptics that the shot is indeed “safe and effective and, thus, increase confidence in the Pfizer vaccine.”

But the FDA can’t simply turn the documents over wholesale. The records must be reviewed to redact “confidential business and trade secret information of Pfizer or BioNTech and personal privacy information of patients who participated in clinical trials,” wrote DOJ lawyers in a joint status report filed Monday.

The FDA proposes releasing 500 pages per month on a rolling basis, noting that the branch that would handle the review has only 10 employees and is currently processing about 400 other FOIA requests.

“By processing and making interim responses based on 500-page increments, FDA will be able to provide more pages to more requesters, thus avoiding a system where a few large requests monopolize finite processing resources and where fewer requesters’ requests are being fulfilled,” DOJ lawyers wrote, pointing to other court decisions where the 500-page-per-month schedule was upheld.

Civil division trial lawyer Courtney Enlow referred my request for further comment to the DOJ public affairs office, which did not respond.

Plaintiffs’ lawyers argue that their request should be top priority, and that the FDA should release all the material no later than March 3, 2022.

“This 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer’s COVID-19 vaccine,” wrote Aaron Siri of Siri & Glimstad in New York and John Howie of Howie Law in Dallas in court papers.

“The entire purpose of the FOIA is to assure government transparency,” they continued. “It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.”

They also argue that Title 21, subchapter F of the FDA’s own regulations stipulates that the agency “is to make ‘immediately available’ all documents underlying licensure of a vaccine.”

Given the intense public interest in the vaccine, the plaintiffs’ lawyers say that the FDA “should have been preparing to release (the data) simultaneously with the licensure. Instead, it has done the opposite.”

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From Reuters, here.

There Are Lies, Stats Lies… and Then There Are Corona Vaccine Lies

BREAKING: Israeli physicians, scientists advise FDA of ‘severe concerns’ regarding reliability and legality of official Israeli COVID vaccine data

An independent Israeli group of physicians, lawyers, scientists, and researchers called the Professional Ethics Front today advised the U.S. Food and Drug Administration (FDA) regarding the upcoming FDA discussion on administering COVID-19 vaccines to children aged 5-11, expressing “severe concerns” regarding the reliability and legality of official Israeli COVID vaccine data.

“We are aware that the state of Israel is perceived as ‘the world laboratory’ regarding the safety and efficacy of the Pfizer-BioNTech COVID-19 vaccine, as reflected by statements made by Dr. Albert Bourla, Dr. Anthony Fauci, and other senior figures in leading health authorities throughout the world,” the letter reads. “It is therefore our understanding that the data and information coming from Israel play a crucial role in critical decision-making processes in regards to COVID-19 vaccination policies. We thus see it of utmost importance to convey a message of warning and raise our major concerns regarding potential flaws in the reliability of the Israeli data with respect to the Pfizer-BioNTech COVID-19 vaccine, as well as many significant legal and ethical violations that accompany the data collection processes.”

The letter elaborates: “We believe that the significant failures underlying the Israeli database, which have been brought to our attention by numerous testimonies, impair its reliability and legality to such an extent that it should not be used for making any critical decisions regarding the COVID-19 vaccines.”

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From America’s Frontline Doctors, here.

The Corona Vaccine’s Risks for Women Are Being Suppressed

Amid rising reports of vaccine-related menstrual disruptions, the CDC and FDA are dismissing women’s concerns and denying them information while corporate media pathologizes them in sexist fashion.

This August 11, the US Center for Disease Control (CDC) overhauled its COVID-19 vaccine guidance for pregnant women, now “urging” them to accept their shots.

Just 23% of pregnant women in the US have received one dose of a COVID-19 vaccine. Only something like 11.1% have been fully vaccinated.

The CDC is seeking to drive these numbers up, but it is not doing the one thing that would, perhaps more than anything else, assuage the “hesitations” of these so-called “anti-vaxxers”: investigate and explain widespread reports of menstrual disruption post-Covid 19 vaccine – and, if necessary, add a warning about it.

Why?

I have five female friends who, after receiving Covid-19 vaccines, experienced disruption to their menstrual cycles. Their symptoms have included hemorrhagic bleeding lasting more than a month; heavy intermittent bleeding for four months; passing golf-ball size clots of blood; and extreme cramping, serious enough to land one friend in the ER.

Most of these women are in their 20s and 30s, and at least one of them thinks she might want to have children. She now worries that her symptoms might be the harbinger of long-term fertility problems. At least two of my friends have symptoms that have not resolved. All are feminists and have throughout the years been consistent Democratic Party voters.

Other women of childbearing age have reported becoming temporarily “postmenopausal” after their second mRNA shot; conversely, women in menopause are reporting suddenly beginning to bleed again; trans men on hormone therapy have also reported sudden bleeding. Apparently, the number of vaccinated women around the world reporting alarmingly disrupted menstruation is, to be conservative, in the tens of thousands.

The US Food and Drug Administration (FDA), however, does not warn women who get the shots that they may experience a disrupted menstrual cycle.

Why is this? In part because even though menstruation is sometimes called the sixth vital sign and directly implicates fertility, and the fact that women on average suffer higher rates of adverse reaction to vaccines of all sorts and medication in general, the effects of Covid vaccines on women’s health specifically, including the menstrual cycle, were not studied as part of the Emergency Use Authorization process.

Impacts on menstrual cycles are, it turns out, very rarely studied in clinical vaccine trials. Stated another way, the quality of COVID-19 vaccine safety data is better for men than it is for women, yet across the country, vaccine mandates make no sex-distinction and in practicality, actually fall more heavily on majority-women industries. In this way, it could be argued, women are not being treated equally under U.S. law.

And now, despite widespread reports of post-vaccine menstrual disruption, it does not appear the CDC or FDA are taking the issue seriously. I contacted the FDA press office with specific and detailed questions about widespread reports of menstrual dysregulation after Covid vaccination. After some back and forth, an FDA spokesperson responded with an official statement:  boilerplate jibber-jabber that did not even speak to the issue of menstruation, much less state that all such reports had been investigated and dismissed.

One of my friends says, “I probably would have still gotten the vaccine, but I wish there had been research, a warning, something. My symptoms have been unpleasant and disconcerting, and it doesn’t seem like public health officials care. I think the way this is being handled will haunt me forever.”

Another, who is trying hard to not “freak out,” says “I wish I would have known about these side effects prior to receiving the vaccine. I would have been more cautious about receiving it. I hope the FDA takes these reports seriously and warns others about these side effects – after all, safety and regulation is their main responsibility.”

The fact that there is no warning, nor any urgent research into whether there should be a warning, seems jarringly sexist when you consider that the FDA has established and does warn that the mRNA Covid vaccines may cause rather trivial short-term side effects including the following: rashes, itching, hives, injection site pain, tiredness, headache, muscle pain, chills, joint pain, fever, nausea, swollen lymph nodes, diarrhea, vomiting; plus the recently added and potentially lethal conditions myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart), which primarily affect young men.

In other words, the FDA sees fit to warn that you might get itchy after the shot but has not deemed it important to determine, and if necessary, tell women – women who might be trying to conceive – that getting the shot could, at least in the short term, scramble their cycle.

Spare a thought for the tens of thousands of women undergoing expensive, invasive fertility treatments like egg retrieval and in vitro fertilization. According to Pew Research, about one third of all American women will undergo fertility treatment at some point. Most health insurance plans do not cover these difficult procedures, so many women pay out-of-pocket, sometimes dropping tens of thousands of dollars. Surely such female medical consumers have a right to know if an mRNA vaccine can trigger, for example, spontaneous prolonged bleeding that disrupts their reproductive efforts.

Covid-19 is a real and potentially lethal virus. I do not need to be convinced of this. And I understand that any healthy society has the right to protect itself, and relatedly, to regulate its members. I have empathy for public officials charged with weighing competing interests and having to make difficult calls in navigating this crisis. Even more, I empathize with American families doing their very best to protect themselves, their loved ones, and their communities, often in the face of profound and disorienting loss.

But it is also true that members of any healthy society have the right to demand that such regulations be based on trustworthy evidence and moral reason; and where such regulations implicate fundamental liberties, to demand that they are no more invasive than absolutely necessary.

The severity of COVID-19 does not negate women’s need for a rigorous and trustworthy scientific appraisal of the benefits and risks they face if they accept a COVID-19 vaccine.

Women deserve an immediate and thorough investigation into reports of post-vaccine menstrual dysregulation, clear and honest explanations of the findings, medical guidance for restoring menstrual health, restitution where necessary, a redoubled commitment to the principle of informed consent moving forward, and (like everyone else) access to reasonable, clearly-communicated, non-punitive accommodations if they decline a COVID-19 vaccine at this time.

Instead, women concerned about the health effects of Covid-19 vaccines have been subjected to 1950’s-style dismissals and demonization in blatantly sexist terms that stand at odds with #MeToo era calls to “believe women.”

They now face the prospect of being barred from their educational institutions, prohibited from entering public accommodations, and losing their jobs unless they “choose” a medical therapy that has not even been fully approved by the Food & Drug Administration, which has left more than an insignificant number of their friends and loved ones struggling, alone, with surprise menstrual side effects, against which pharmaceutical industries enjoy a complete, multi-layered liability shield.

From a purely bioethical standpoint, this situation should be enough to give us pause, from those concerned with women’s health; to those concerned about fundamental civil liberties like the right to privacy, equal protection, free association, and free speech; to those concerned about fighting “vaccine hesitancy”; to those concerned about the continued (yet threatened) legitimacy of foundational U.S. institutions. But it seems many in our political class only care about or understand the DC horse race. So let us put it in those terms: this issue will show up in 2022.

Zero published studies on the effects of Covid vaccines on women’s reproductive systems

By early spring 2021, anecdotal testimonies of sudden, early, disturbingly prolonged, abruptly absent, extremely painful, or unusually heavy and clot-filled menstrual cycles post-Covid 19 vaccination were circulating on social media. By May 17th, the UK’s Medicines & Healthcare Products Regulatory Agency had received 4,000 reports of post-vaccine menstruation disruption. By early July, that agency had received 13,000 such reports. Similar reports emerged from other countries like Canada and India.

In the U.S., adverse reactions to vaccines are tracked by the Vaccine Adverse Event Reporting System (VAERS), which was created in 1987 and is co-managed by the FDA and the CDC. As of July 26, VAERS showed many thousands of reports of various menstruation disorders, most related to mRNA Covid-19 vaccines.

There had been 1,624 reports of “menstruation irregular” logged; 1,352 reports of “menstrual disorder”; 563 reports of “menstruation delayed”; 803 reports of “vaginal hemorrhaging”; 239 reports of “postmenopausal hemorrhage”; 95 reports of “hemorrhage urinary tract”; 57 reports of “abnormal uterine bleeding”; and 41 reports of “hemorrhage in pregnancy.” Even more seriously, there were 691 reports of “abortion spontaneous”; 88 reports of “fetal death”; and 25 reports of “stillbirth.” The CDC claims rates of miscarriage by vaccinated women is within the normal range.

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From The Gray Zone, here.