V-Safe Has More Vaccine Adverse Reaction Data Than VAERS but CDC Keeps It Absolutely Secret. Why?

By now, most of our everyday readers are very familiar with the Vaccine Adverse Event Reporting System (VAERS). It’s a portal that allows Americans to report adverse reactions to vaccines. It has been the topic of many stories here as it shows currently around 11,000 deaths following the so-called Covid “vaccines.”

A lawsuit that we covered yesterday laid down the bombshell that a CDC whistleblower claims the actual post-vaccine death estimates from the CDC are around 45,000. This bit of information dominated conversations regarding the lawsuit, but there was an important gem also described that needs as much attention, if not more.

According to the lawsuit, the V-Safe database has much more data about vaccine adverse reactions than VAERS. It’s a mobile app that allows the tens of millions of vaxxed in America to easily report adverse reactions. As their website notes, “Use your smartphone to tell CDC about any side effects after getting the COVID-19 vaccine. You’ll also get reminders if you need a second vaccine dose.”

With VAERS data, one must proactively find the database and fill out a long questionnaire for their information to be registered. This is one of the reasons experts estimate between 1%-10% sampling; in other words, whatever the number of reactions are reported on VAERS should be multiplied by 10-100 in order to get a more accurate picture.

V-Safe is the opposite. Instead of making it difficult to report, it makes it very easy. Instead of being challenging to find (doctors have been told not to refer their patients to VAERS if they have a reaction), it is proactive and actually sends push notifications to the vaccinated to inquire about their conditions.  The CDC has built a vast repository of data that is smartphone-confirmed, meaning nobody’s sitting in their basement with a VPN making false reports. This is the most accurate recording of information about the adverse effects of Covid-19 vaccines.

And it’s locked away with cybersecurity protocols that would make the NSA sweat. Why?

The answer is obvious. They are very well aware that there are mountains of adverse reactions to the Covid-19 “vaccines” but if they reveal it, any of it, they will verify what countless doctors, scientists, and whistleblowers have been saying for month. They have a mission of injecting every American with the experimental drugs and any data that hurts their agenda is suppressed. It must be.

Megan Redshaw details the lawsuit and asks more questions about V-Safe in this article cross-posted from Children’s Health Defense:

Federal Lawsuit Seeks Immediate Halt of COVID Vaccines, Cites Whistleblower Testimony Claiming CDC Is Under-Counting Vaccine Deaths

America’s Frontline Doctors filed a motion to stop the use of Emergency Use Authorization (EUA) COVID vaccines for anyone under 18, anyone with natural immunity or anyone who hasn’t received informed consent.

America’s Frontline Doctors (AFLDS) filed a motion July 19, seeking immediate injunctive relief in Alabama Federal District Court to stop the use of Emergency Use Authorization (EUA) COVID vaccines — Pfizer/BioNTech, Moderna and Johnson & Johnson (J&J) — for three groups of Americans.

According to a press release, AFLDS is asking to immediately stop administration of experimental COVID vaccines in anyone 18 and younger, all those who have recovered from COVID and acquired natural immunity, and every other American who has not received informed consent as defined by federal law.

The 67-page motion requests the judge issue a preliminary injunction pursuant to § 360bbb–3(b)(1)(C) for the following reasons:

• There is no emergency, which is a prerequisite to issuing EUA and EUA renewals for COVID vaccines.
• There is “no serious or life-threatening disease or condition.”
• Vaccines do not diagnose, treat or prevent SARS-CoV-2 or COVID.
• Known and potential risks of the vaccine outweigh their known and potential benefits.
• There are adequate, approved and available alternatives to vaccines.
• Healthcare professionals and vaccine candidates are not adequately informed.

The authors of the motion attached a declaration by a whistleblower who came forward alleging deaths occurring within 72 hours of receiving a COVID vaccine are significantly under-reported in the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Events Reporting System (VAERS) maintained by the U.S. Food and Drug Administration (FDA).

As of July 9, reported deaths in the VAERS totaled 10,991. Of those, 4,593 occurred within 72-hours of vaccination.

The whistleblower — a computer programmer who developed more than 100 distinct healthcare fraud algorithms, and who has expertise in healthcare data analytics that allows her to access Medicare and Medicaid data obtained by the Centers for Medicare and Medicaid Systems (CMS) — filed a sworn statement under penalty of perjury alleging the actual number of COVID vaccine-related deaths is closer to 45,000.

The whistleblower alleged that VAERS, while extremely useful, is under-reported by a conservative factor of at least five.

In her statement, she said:

“On July 9, 2021, there were 9,048 deaths reported in VAERS. I verified these numbers by collating all of the data from VAERS myself, not relying on a third party to report them. In tandem, I queried data from CMS medical claims with regard to vaccines and patient deaths, and have assessed that the deaths occurring within 3 days of vaccination are higher than those reported in VAERS by a factor of at least 5. This would indicate the true number of vaccine-related deaths was at least 45,000. Put in perspective, the swine flu vaccine was taken off the market which only resulted in 53 deaths.”

AFLDS said the findings were shocking, and informed consent is impossible when safety data is not accurate.

In a press release, AFLDS said:

“It is unlawful and unconstitutional to administer experimental agents to individuals who cannot make an informed decision as to the true benefits and risks to the vaccine on an independent basis. They must be of an age or a capacity to make informed decisions and have been provided with all of the risk/benefit information necessary to make an informed decision.”

One of the named plaintiffs, Deborah Sobczak, the mother of a 15- and 17-year-old, said in the press release:

“My child will not be the subject of an experiment. What kind of monsters are we allowing to control us? Perfectly healthy children have developed heart inflammation, brain bleeding and even died! I have had enough. I am not sacrificing my child so a pharmaceutical company can experiment on her. This madness has to stop.”

There is no emergency warranting EUA of COVID vaccines, plaintiffs allege

According to the complaint, the U.S. Department of Health and Human Services (HHS) secretary, named as one of the defendants in the lawsuit, declared on Feb. 4, 2020, pursuant to § 360bbb–3(b)(1)(C), that SARS-CoV-2 created a “public health emergency.”

This initial emergency declaration has been renewed repeatedly and remains in force today — a necessary legal prerequisite for the issuance of vaccine EUAs, the complaint states. EUA allowed the mass use of the vaccines by the American public before the completion of the standard regimen of clinical trials and FDA approval.

Plaintiffs allege the emergency declaration and its multiple renewals are illegal because there is no underlying emergency. Using HHS COVID death data, SARS CoV-2 has an overall survivability rate of 99.8% globally, which increases to 99.97% for persons under the age of 70. This is consistent with the seasonal flu, the complaint states.

Plaintiffs argue HHS deliberately inflated COVID case data

Plaintiffs allege HHS’ data is deliberately inflated. On March 24, 2020, HHS changed the rules applicable to coroners and others responsible for producing death certificates and making “cause of death” determinations exclusively for COVID.

The rule change states: “COVID-19 should be reported on the death certificate for all decedents where the disease caused or is assumed to have caused or contributed to death.”

According to the complaint, HHS statistics showed 95% of deaths classified as “COVID-19 deaths” involved an average of four additional comorbidities. Plaintiffs claim the CDC knew the rules for coding and selection of the underlying cause of death would result in COVID being the underlying cause more often than not.

Plaintiffs said the actual number of COVID cases is also far lower than the reported number due to emergency use of polymerase chain reaction (PCR) tests, which are used as a diagnostic tool for COVID. The PCR tests are themselves experimental products, authorized by the FDA under separate EUAs. The package inserts state PCR tests should not be used to diagnose COVID.

The complaint alleges the way in which the PCR tests are being administered knowingly guarantees an unacceptably high number of false positive results.

COVID vaccine risks undisclosed and under-reported, lawsuit says

AFLDS medico-legal researchers analyzed the accumulated COVID vaccine risk data and found migration of the pathogenic SARS-CoV-2 spike protein in the body. Yet vaccines were authorized without any studies demonstrating where the spike proteins traveled in the body following vaccination, how long they remain active and what effect they have, the complaint states.

AFLDS researchers analyzed VAERS and discovered an increased risk of death from COVID vaccines. The database indicated vaccine deaths in the first quarter of 2021 represented a 12,000% to 25,000% increase in vaccine deaths, year-on-year.

From 2009 to 2019, there were 1529 reported deaths associated with all vaccines reported to VAERS, according to the motion. In the first quarter of 2021, there were more than 4,000 reported deaths with 99% of all reported vaccine deaths in 2021 attributed to the COVID vaccine. Only 1% were attributed to other vaccines in the system.

Plaintiffs also disclosed evidence of reproductive harm, vascular disease, autoimmune disease, neurological damage and they highlighted an increased risk of harm for children with COVID vaccines to support their position.

Why the secrecy around V-Safe data?

The complaint called attention to the secrecy of the CDC’s V-Safe system — a parallel system used to track reported adverse events via a smartphone app controlled exclusively by the CDC.

Plaintiffs raised concerns that information in V-Safe exceeds that in VAERS. They claim VAERS is inaccurate because it potentially includes fewer than 1% of all vaccine adverse events, and the federal government is failing to provide data from other monitoring sources such as V-Safe, CMS and the military.

Plaintiffs stated informed consent cannot be given without understanding the risks. They said they can’t help but wonder why HHS would fail to disclose to the public critical information related to risk from it’s reporting systems, “particularly in light of the fact that they have had the time and resources to study and extend the authorizations on the vaccines, build an enormous vaccine marketing machine and roll out vaccine clinics all over the nation.”

The lawsuit was filed by several law firms, including RENZ Law. The complaint and whistleblower declaration can be read here.

© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

One final note: The government in general and the CDC in particular is fully aware that the drugs are dangerous. They have the data to prove they’re safe if the data showed it to be. Instead, they keep that data locked away. Wake up, folks.

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The slow and steady reopening of America is revealing there was a lot more economic hardship brought about from the Covd-19 lockdowns than most realize. While we continue to hope advertising dollars on the sites go up, it’s simply not enough to do things the right way. We are currently experiencing a gap between revenue and expenses that cannot be overcome by click-ads and MyPillow promos alone (promo code “NOQ” by the way).

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