The death certificates for every death that took place in Minnesota between 2015 and the present were made available by someone (who must remain anonymous), which gave us the chance to check the CDC’s accuracy in reporting US death statistics. Naturally, the CDC isn’t.
As we will show, the CDC is hiding references to the COVID vaccine on Minnesota death certificates, which are already extremely uncommon due to the widespread denial of vaccine side effects by the medical establishment.
In almost every death certificate that identifies a covid vaccine as a cause of death, the CDC committed data fraud by not assigning the ICD 10 code for vaccine side effects to the causes of death listed on the death certificate.
Background
When someone dies, there is a death certificate that is filled out for official/legal purposes. Death certificates contain a lot of information (some states include more than others), including the causes of death (CoD).
The term “causes of death” refers to the medical conditions that ultimately contributed to the decedent’s passing. A condition does not have to be the direct cause of death for it to be considered a CoD; it only needs to have some effect on the decedent’s medical decline. CoD would apply if a person had high blood pressure, then experienced a heart attack, followed by cardiac arrest, which resulted in death. However, since it had nothing to do with their passing, this unfortunate person’s ingrown toenail cannot be considered a cause of death.
This is from the CDC’s own guidance explaining how to properly fill out CoD’s on a death certificate (you don’t need to understand the difference between Cause A, B, etc for this article):
The critical thing to keep in mind is that the person filling out the death certificate writes a text description of the CoD’s, but doesn’t assign the ICD 10 codes for the CoD’s.
That’s the CDC’s job.
ICD 10 Coding System for CoD’s
There is a fancy coding system that is used to classify the many thousands of medical conditions that can play a role in death known as the International Classification of Diseases. Every few years, it is updated/revised to keep up with new medical (or bureaucratic) developments, as new conditions are discovered and old conditions are reorganized or reclassified.
The current iteration of the ICD that was used for the deaths we’re looking at is the ICD 10 (that’s the 10th version). It is basically a hierarchical classification system:
There are codes for practically every random weird thing you can think of:
These are categories themselves – a code can go as 7 characters long:
(There are other ICD 10 codes for various specific complications or side effects of vaccines, but the point remains that an ICD 10 code for vaccine side effects exists.)
CDC – Centers for Data Concealment
The CDC assigns ICD 10 codes after receiving the death certificates from the various states. When the algorithm is unable to confidently assign an ICD code to the text description written on the actual death certificate (for example, due to confusing spelling or a text description that does not make much sense), a small percentage of cases are decided by CDC staff. I verified this with a biostatistician employed by the Department of Health in a US state (I’m withholding the name in order to maintain my persona grata status). The person who obtained the Minnesota death certificates also confirmed with state officials that the CDC assigned the ICD codes to their data.
What a death certificate identifying a covid vaccine as a CoD *should* look like
In the MN tranche, there are three death certificates that either have T88.1 or Y59.0 on them. Surprisingly, the other two are for a covid vaccine while the first is for a flu vaccine reaction.
Note – when used below:
UCoD (Underlying Cause of Death) refers to “the disease or injury that initiated the train of events leading directly to death, or the circumstances of the accident or violence which produced the fatal injury.”
MCoD (Multiple Causes of Death) refers to “the immediate cause of death and all other intermediate and contributory conditions listed on the death certificate.” (everything else)
The first death certificate contains a covid vaccine ICD (below), and it looks like the CDC was trapped and could not avoid putting it on without fundamentally rewriting the death certificate, because the vaccine complication is unambiguously listed as the UCoD (this death certificate is saying the person was killed by a heart attack caused by the covid vaccine within minutes of injection):
The second death certificate the CDC deigned to assign a vaccine ICD (and not only one but *BOTH* vaccine ICD codes(!!)) feels like perhaps a rogue CDC employee was working that day and snuck it in:
In any event, as we can clearly see, both T88.1 and Y59.0 are indeed appropriate for when a covid vaccine is listed as a CoD. Thus the CDC cannot claim that there was no official ICD 10 code that could be used to designate covid vaccines (or any other excuse).
The FRAUD:
With that introduction, below are 7 death certificates from Minnesota that identify a covid vaccine as a cause of death where the CDC omitted the corresponding ICD 10 code identifying a vaccine side effect when the CDC assigned ICD codes to the death certificates.
The first death certificate that was falsely completed provides a crucial detail emphasizing both the fraud and the blatant double standards for assigning CoDs.
This death certificate identifies both a covid vaccine and covid itself as contributory CoD’s (in the last row highlighted in yellow, vaccine underlined in green, covid in blue):
“covid vaccine second dose 10 hrs prior to death”
“history of covid infection in May 2020” (about 7-8 months prior to death)
Any remotely objective person would presume that if a condition that occurred 7 months prior without any clear link to the actual death still nevertheless meets the standard for being identified as a CoD, then surely a condition or event that occurred a mere TEN HOURS before death identified by the doctor filling out the death certificate merits inclusion as a CoD.
Yet, the CDC assigned U70.1 – “COVID-19, virus identified” – for covid, but neglected to assign T88.1 or Y59.0 for the covid vaccine.
A second point to highlight is that we see that anything mentioned as a CoD, even in the context of “history of” that had (presumably) been long resolved, is a legitimate CoD insofar as assigning an ICD 10 code and epidemiological data are concerned.
This decedent suffered a cardiac arrest that ultimately led to her death *ONE DAY* after being vaccinated.
(For the record, I am not bothered by the “though it’s not clear as to any mechanism for how the vaccine could have led to the cardiac arrest” line. This death occurred February 24, 2021 – well before there was any sort of public awareness about the multiple plausible mechanisms by which the vaccine could cause heart damage. So to me, whoever filled out the death certificate was a gutsy fellow willing to identify a covid vaccine on a death certificate that had his name on it.)
Fraudulent Death Certificate #3
This death certificate doesn’t merely identify a covid vaccine, it explains that the decedent “felt sick after the vaccine” and died 4 days later from a heart attack. Yet, no T88.1 or Y59.0.
This death certificate provides that the decedent received her second dose of Pfizer 18 days prior to her death.
Here we have a 65-year-old male who was killed by a heart attack 12 days after getting vaccinated.
This particular instance is noteworthy. The family had to exert pressure on the coroner to include the most recent COVID booster on the death certificate, according to someone involved with this death. In addition, a family member submitted a VAERS report on their own behalf after the patient’s medical professionals refused.
Furthermore, the CDC applied W34 as the UCoD. What is W34 for?
‘accidental discharge and malfunction from other and unspecified firearms and guns.’
There is no mention of any firearms mishaps on the death certificate.
Especially on a death certificate with other ICD 10 misdemeanors, one would have to wonder how such an incorrect code came to be. It is unlikely that “Y590” or “T881” would be “misspelled” or mistaken for “W34” by an algorithm.
Perhaps the failure to include T88.1 or Y59.0 here could be excused if there were no other instances of fraudulent omission of vaccine ICD codes on other death certificates and the CDC didn’t regularly assign U07.1 for a covid infection that resolved a year ago.
At minimum, this death certificate should contain T88.0 – ‘Infection following immunization’ – to document the breakthrough infection (which is a subject for a separate article as this seems to be fairly widespread).
Additional Observations
The following table shows the date of death and age for all 9 death certificates shown above that identified a covid vaccine as a CoD:
It is striking that 7/9 died before May 2021. This is odd – if anything, the deaths should skew later, not earlier. Vaccine adverse events were denied – with maximum prejudice and then some – for many months before the medical mainstream has finally (begrudgingly) started to acknowledge that the covid vaccines can trigger potentially lethal pathologies (in exceedingly rare instances to be sure).
Coroners may have been discouraged from including a covid vaccine on death certificates due to “administrative” interference, as evidenced by the concentration of death certificates that did so at the start of the rollout.
Another noteworthy tidbit here is the age of the decedents: every single one is a senior citizen, and the average age of the decedents is 80. This is important to highlight because whereas young people “dying suddenly” stands out, there has been much less attention or acknowledgement of the covid vaccine’s devastating toll upon the old and frail, where deaths – even those that occur in close proximity to vaccination – are readily attributed to prior health conditions.
Finally, the CDC’s actions raise the question of whether it is completely qualified or reliable enough to be the custodian of the country’s epidemiological data. Many of the datasets that support entire fields of study are managed by the CDC. All data under the control of the CDC is potentially suspect if the CDC is willing to fraudulently alter the data (or even if the CDC is simply too incompetent to prevent data corruption). This is especially true if the data relates to a contentious political or social issue. To put it mildly, the implications of this are disturbing.
If the US had a functional Depts., Justice the CDC personnel would be tried for 1st degree murder for EVERY death in association with the experimental mNRA gene therapy Death Shot.
The CDC is nothing more than a subsidiary of Big Pharma’s genocidal dollar machine.
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SACRAMENTO, CA — Former Los Angeles Mayor and current California gubernatorial candidate Antonio Villaraigosa has publicly alleged that Kamala Harris and Xavier Becerra were involved in concealing former President Joe Biden’s mental and physical decline during his time in office.
Villaraigosa, a Democrat, made the claim amid a heated California gubernatorial race. Becerra, the former Secretary of Health and Human Services, is also a candidate, while speculation continues over a potential Harris bid. The race comes as current Governor Gavin Newsom reaches the end of his second and final term, per California’s two-term limit.
In a statement referencing recent reporting and excerpts from the book Original Sin, Villaraigosa stated:
“What I’ve seen in news coverage and excerpts from the new book ‘Original Sin’ is deeply troubling. At the highest levels of our government, those in power were intentionally complicit or told outright lies in a systematic cover up to keep Joe Biden’s mental decline from the public.”
Both Harris and Becerra previously served as California Attorney General. Villaraigosa emphasized their past leadership roles, stating:
“Now, we have come to learn this cover up includes two prominent California politicians who served as California Attorney General – one who is running for Governor and another who is thinking about running for Governor.”
He added:
“Those who were complicit in the cover up should take responsibility for the part they played in this debacle, hold themselves accountable, and apologize to the American people. I call on Kamala Harris and Xavier Becerra to do just that – and make themselves available to voters and the free press because there’s a lot of questions that need to be answered.”
Becerra responded in a statement, saying:
“It’s clear the President was getting older, but he made the mission clear: run the largest health agency in the world, expand care to millions more Americans than ever before, negotiate down the cost of prescription drugs, and pull us out of a world-wide pandemic. And we delivered.”
Kamala Harris has not issued a public response. Fox News Digital reported that it reached out to the offices of Harris and the Bidens but had not received a reply at the time of publication.
The allegations come as discussions about Biden’s cognitive and physical health continue. Earlier this month, during an appearance on The View, Biden dismissed claims of cognitive decline during his presidency.
In related developments, Biden’s personal office recently confirmed that he had been diagnosed with prostate cancer characterized by a high Gleason score and metastasis to the bone.
Villaraigosa’s comments are the latest in a growing list of concerns raised within the Democratic Party about leadership transparency and accountability in the final years of the Biden administration.
A newly released interim report from Senator Ron Johnson’s office claims top U.S. health officials in the Biden administration withheld critical information in early 2021 about potential heart-related side effects associated with mRNA COVID-19 vaccines. The 54-page report alleges that despite receiving multiple warnings about the risks—particularly cases of myocarditis and related conditions in young people—federal agencies delayed issuing formal alerts for several months.
According to the report, health officials at the Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) were informed as early as February 2021 about international concerns, including an attempt by Israel’s Ministry of Health to raise alarm over roughly 40 myocarditis cases tied to the Pfizer vaccine. At that time, Israel’s vaccination campaign was further along than the U.S.’s, offering an early view of potential adverse effects.
In response to Israel’s outreach, FDA officials acknowledged limitations in existing data and asked for further information. However, despite growing domestic reports of heart inflammation—more than 158 cases by April—the agencies did not formally update the public until late June. The vaccine was nonetheless approved for adolescents in May.
By late May, internal deliberations began over whether to issue a Health Alert Network (HAN) message, which is typically used by the CDC to quickly notify clinicians and public health departments of emerging health threats. Some officials reportedly feared sounding “alarmist.” Others questioned whether the data truly warranted a full-scale warning. Ultimately, the HAN alert was shelved in favor of a more subdued website notice issued on May 28.
In the interim, internal talking points continued to describe the condition as rare and urged continued vaccination. The official FDA label for both the Pfizer and Moderna vaccines wasn’t updated to reflect the myocarditis risk until June 25.
The report, while critical, notes that many individuals who developed myocarditis, pericarditis, or myopericarditis after vaccination experienced a resolution of symptoms, a finding consistent with CDC data.
Senator Johnson, a frequent critic of the federal pandemic response, has argued that transparency was lacking during this period. “The full extent of the Biden administration’s failure to immediately warn the public about all COVID-19 vaccine adverse events must be completely exposed,” the report concludes.
Health officials involved in the decisions, including then-FDA commissioner Dr. Janet Woodcock and then-CDC director Dr. Rochelle Walensky, have not yet publicly responded to the findings in the interim report.
The release comes amid ongoing political scrutiny over pandemic-era decision-making and the future of public health communications in the wake of COVID-19. The Biden administration and health agencies have consistently maintained that the benefits of mRNA vaccines outweigh the risks, particularly during the height of the pandemic when COVID-19 posed a significant public health threat.
As investigations continue, Johnson’s subcommittee says it plans to further examine the internal communications and decision-making processes of the nation’s top health agencies.
A newly released analysis is raising serious questions about the safety profile of mifepristone, the drug responsible for over half of abortions in the United States. While abortion-rights advocates, corporate media outlets, and the U.S. Food and Drug Administration (FDA) maintain that the drug is “safe and effective,” a comprehensive study based on real-world insurance claims paints a far more concerning picture.
Described as the “largest known study of the abortion pill,” the report was conducted by Ethics and Public Policy Center President Ryan Anderson and Director of Data Analysis Jamie Bryan Hall. Using a massive dataset that included Medicaid, TRICARE, Medicare, Department of Veterans Affairs, and private insurance claims, the researchers analyzed 865,727 prescriptions of mifepristone distributed to 692,873 women between 2017 and 2023.
The findings are striking: approximately 10.9 percent of those chemical abortions—about 94,605 cases—involved potentially life-threatening “serious adverse events” within 45 days of taking the drug. These complications included emergency room visits, hemorrhage, sepsis, infection, and follow-up surgeries. This complication rate is at least 22 times higher than the <0.5 percent figure cited by the FDA on the Mifeprex label.
The researchers noted that some patients experienced complications in multiple categories, and that the 45-day window used for measurement was “conservative,” especially considering that the FDA has relied on studies using a timeframe of up to 72 days.
One chart from the study revealed that among women who sought post-abortion care within 45 days:
15.1% visited the emergency room,
8.5% required surgical treatment,
2.5% experienced hemorrhage,
1.9% suffered infections, and
0.9% were diagnosed with sepsis.
“These outcomes were drawn from actual claims data,” the researchers emphasized, “not modeled projections or self-reported surveys.” In Anderson’s words to The Federalist: “This study is the statistical equivalent of a category 5 hurricane hitting the prevailing narrative of the abortion industry. It reveals, based on real-world data, the shocking number of women who suffer serious medical consequences because of the abortion pill.”
The FDA originally approved mifepristone in 2000 based on 10 clinical trials involving only 30,966 patients—women who were described as “prescreened,” “generally healthy,” and treated in controlled environments. The authors of the new study argue that those trials are both outdated and unrepresentative of today’s broad and diverse patient base.
“The women in our dataset receive (or fail to receive) pre- and post-abortion healthcare of the real-world quality that prevails in the U.S. today, not the carefully controlled regimen of care that ordinarily prevails in a clinical trial,” the study says.
Despite repeated petitions from pro-life medical groups to revisit the approval of mifepristone, the FDA has consistently declined to take action. Critics argue the agency failed to meet its legal obligation to address the concerns. Meanwhile, regulatory oversight has continued to loosen. By 2016, the FDA under the Obama administration had altered the drug’s dosing, cut down the number of in-person doctor visits required, broadened who could prescribe it, and eliminated requirements to report non-fatal complications.
The Biden administration went further. In 2021, the FDA permanently allowed mifepristone to be delivered by mail, bypassing the need for a clinic visit. Pharmacies like Walgreens and CVS were later authorized to dispense the pill. As of 2023, a woman can obtain mifepristone with just one telehealth appointment with “any approved healthcare provider (not necessarily a physician)” and self-administer the drug at home. Alarmingly, prescribers are not required to report adverse events unless they learn the patient has died.
The study recommends that the FDA reinstate its original safety protocols. These would include requiring multiple in-person visits, physician-only prescribing, ultrasound confirmation of gestational age and the absence of ectopic pregnancy, and mandatory reporting of complications. The goal, according to the authors, is not only to reduce immediate harm but also to facilitate better long-term safety tracking.
“The FDA should further investigate the harm this drug causes to women and, based on objective safety criteria, reconsider its approval altogether. Women deserve better than the abortion pill,” the study concludes.
While legal efforts to challenge the pill’s availability have so far been unsuccessful, the issue remains live. In 2023, the Supreme Court declined to weigh in on the merits of mifepristone’s approval, ruling that the plaintiffs lacked standing. However, Justice Brett Kavanaugh’s opinion left open the possibility for the Court to consider a more suitable challenge in the future.
Cliff Taylor
July 3, 2023 at 11:55 pm
If the US had a functional Depts., Justice the CDC personnel would be tried for 1st degree murder for EVERY death in association with the experimental mNRA gene therapy Death Shot.
The CDC is nothing more than a subsidiary of Big Pharma’s genocidal dollar machine.
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