Steve Kirsch – New VAERS analysis reveals hundreds of serious adverse events that the CDC and FDA never told us about

They missed hundreds of serious adverse events that are more elevated than myocarditis. A new VAERS analysis done by Albert Benavides blows the doors off the “safe and effective” narrative.

Source: https://stevekirsch.substack.com/p/new-vaers-analysis-reveals-hundreds

The CDC and FDA have said the vaccines are “safe and effective.” They haven’t found any serious issues with the COVID vaccines. Zero. Zip. Nada. It was the DoD that found myocarditis.

The evidence in plain sight shows that they are either lying or incompetent. Or both. But of course, the medical community is never going to call them on this.

C19 count
This is the raw number of VAERS events in 2020 and 2021 due to the COVID vaccines for that symptom. The key here is that this count should be multiplied by 41 (known as the underreporting factor or URF to estimate the absolute number of events that occurred). See this article for how that is computed.

Baseline count
The baseline rate is the # of incidents occurring in a 5 year period from 2015-2019 for all vaccines given in that time period.

X-factor
The X-factor is the (C19 count*5/Baseline count). This is because the baseline is 5 years so we compare the COVID counts in a year vs. the average count in a typical year. So an X-factor of 10 or more would mean that the symptom is very likely to be caused by the vaccine since it is highly elevated from the “normal” rate.

Now let’s tackle the tabs. There are two tabs:

match tab
On the match tab are symptoms where the baseline count !=0

no match tab
On the “no match” tab are symptoms where the baseline count=0. So these are quite extraordinary since these symptoms are not typically seen even once in 5 years. So here, even a small value in the “count” field is very significant, e.g., 2 or more would be comparable to a 10X or more on the “match tab.”

Now here are some screenshots of the first page of the two tabs:

And the no match tab:

What the data tells us

Here are a few quick observations from the complete data set (see next section for downloading):

  1. Female reproductive issues top the list. These are strongly elevated by these vaccines. Many of the top symptoms are all related to the menstrual process.
  2. There are an enormous number of cardiovascular and neurological events that are strongly elevated, many of them serious.
  3. Fibrin D dimer increased is #53 on the list, elevated by a factor of over 400x above baseline. Charles Hoffe discovered D-dimer was elevated in over 60% of the patients he measured. This is very serious as D-dimer is a lagging indicator of blood clots.
  4. Troponin increased was #130, elevated by a factor of 205. Troponin indicates heart damage and it is elevated to extreme levels (10X heart attack levels or more) and can stay elevated for months at a time (with a heart attack, the levels start returning back to normal immediately after the incident)
  5. Death as a symptom (which is pretty unusual coding since it isn’t a symptom), is #433 and elevated by 96X. Hardly a “safe” vaccine.
  6. Brain herniation at #405 is elevated by a factor of 100X over baseline. However, this is not considered a big deal at the CDC (perhaps because many people there don’t use their brain).
  7. Cardiac arrest at #450 is elevated by 93X. This is when your heart stops. This is a relatively serious condition since you don’t last for too long after that. It’s a bit surprising that the CDC missed that one. Perhaps because they don’t have a heart?
  8. Pulmonary embolism #24 is elevated by 954 times normal. How the CDC can miss that one is simply astonishing! This was the cause of death of 2 of the 14 kids that the CDC looked at in their death analysis. Mainstream press will never ask them that question as to why the CDC would not find causality here. They wrote: “CDC reviewed 14 reports of death after vaccination. Among the decedents, four were aged 12–15 years and 10 were aged 16–17 years. All death reports were reviewed by CDC physicians; impressions regarding cause of death were pulmonary embolism (two), …” 954 times normal is hard to explain, isn’t it? So no causality? That’s hard to explain, so they didn’t. They just moved on as if there is nothing to see.
  9. Intracranial haemorrhage (their spelling) is at #604 and is elevated by 79X. Two of the 14 kids from the CDC analysis died from that. How could that not be causal? They never explained that.
  10. Tinnitus at #362 is elevated by 105X. This can be so bad that people can kill themselves from this alone. One of the people who work at Vaccine Safety Research Foundation (VSRF) had to talk a friend out of suicide.
  11. There are many many more issues to be concerned with, but I wanted to get the list out quickly so there can be more eyes on this.
  12. For months, I’ve offered to discuss our data and analyses to both the FDA and CDC outside committees as well as the CDC and FDA themselves, but nobody wanted to see it. Most hit delete on my emails. A few told me to wait for the public comment period and submit it then (which I’ve done). Nobody followed up.

CDC – Selected Adverse Events Reported after COVID-19 Vaccination

Source: https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/adverse-events.html

Serious adverse events after COVID-19 vaccination are rare but may occur.

For public awareness and in the interest of transparency, CDC is providing timely updates on the following serious adverse events of interest:

  • Anaphylaxis after COVID-19 vaccination is rare and has occurred in approximately 2 to 5 people per million vaccinated in the United StatesSevere allergic reactions, including anaphylaxis, can occur after any vaccination. If this occurs, vaccination providers can effectively and immediately treat the reaction. Learn more about COVID-19 vaccines and allergic reactions, including anaphylaxis.
  • Thrombosis with thrombocytopenia syndrome (TTS) after Johnson & Johnson’s Janssen (J&J/Janssen) COVID-19 vaccination is rare. As of October 27, 2021, more than 15.5 million doses of the J&J/Janssen COVID-19 Vaccine have been given in the United States. CDC and FDA identified 48 confirmed reports of people who got the J&J/Janssen COVID-19 Vaccine and later developed TTS.  Women younger than 50 years old especially should be aware of the rare but increased risk of this adverse event. There are other COVID-19 vaccine options available for which this risk has not been seen. Learn more about J&J/Janssen COVID-19 Vaccine and TTS.
    • To date, two confirmed cases of TTS following mRNA COVID-19 vaccination (Moderna) have been reported to VAERS after more than 401 million doses of  mRNA COVID-19 vaccines administered in the United States. Based on available data, there is not an increased risk for TTS after mRNA COVID-19 vaccination.
  • CDC and FDA are monitoring reports of Guillain-Barré Syndrome (GBS) in people who have received the J&J/Janssen COVID-19 Vaccine. GBS is a rare disorder where the body’s immune system damages nerve cells, causing muscle weakness and sometimes paralysis. Most people fully recover from GBS, but some have permanent nerve damage. After more than 15.5 million J&J/Janssen COVID-19 Vaccine doses administered, there have been around 244 preliminary reports of GBS identified in VAERS as of October 27, 2021. These cases have largely been reported about 2 weeks after vaccination and mostly in men, many 50 years and older. CDC will continue to monitor for and evaluate reports of GBS occurring after COVID-19 vaccination and will share more information as it becomes available.
  • Myocarditis and pericarditis after COVID-19 vaccination are rare. As of October 27, 2021, VAERS has received 1,784 reports of myocarditis or pericarditis among people ages 30 and younger who received COVID-19 vaccine. Most cases have been reported after mRNA COVID-19 vaccination (Pfizer-BioNTech or Moderna), particularly in male adolescents and young adults. Through follow-up, including medical record reviews, CDC and FDA have confirmed 1,005 reports of myocarditis or pericarditis. CDC and its partners are investigating these reports to assess whether there is a relationship to COVID-19 vaccination. Learn more about COVID-19 vaccines and myocarditis.
  • Reports of death after COVID-19 vaccination are rare. More than 423 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through November 1, 2021. During this time, VAERS received 9,367 reports of death (0.0022%) among people who received a COVID-19 vaccine. FDA requires healthcare providers to report any death after COVID-19 vaccination to VAERS, even if it’s unclear whether the vaccine was the cause. Reports of adverse events to VAERS following vaccination, including deaths, do not necessarily mean that a vaccine caused a health problem. A review of available clinical information, including death certificates, autopsy, and medical records, has not established a causal link to COVID-19 vaccines. However, recent reports indicate a plausible causal relationship between the J&J/Janssen COVID-19 Vaccine and TTS, a rare and serious adverse event—blood clots with low platelets—which has caused deaths pdf icon[1.4 MB, 33 pages].

COVID-19 Vaccine Safety Updates
Advisory Committee on Immunization Practices (ACIP)
Oct 21, 2021
Tom Shimabukuro, MD, MPH, MBA
Vaccine Safety Team
CDC COVID-19 Vaccine Task Force

PDF: https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2021-10-20-21/06-COVID-Shimabukuro-508.pdf

FDA Knew About Numerous Adverse Events For Children ‘Related’ To Pfizer Vaccine, Approved It Anyway

by Patrick Howley | National File

The Food And Drug Administration (FDA) approved an emergency use authorization for the Pfizer-BioNTech vaccine for children as young as 5 years old despite the fact that its Pfizer-connected advisory committee knew about numerous adverse events that were reported in Pfizer’s clinical trials for children, including adverse events that were determined to be “related” to the clinical vaccine trial.

The Briefing Packet for the FDA advisory committee meeting shows that the FDA advisers used clinical studies sponsored by BioNTech and conducted by or supported by Pfizer to approve the vaccine for young children.

VRBPAC-10.26.21-Meeting-Briefing-Document-Sponsor-Pfizer-508-Waiver (1)

Vaccines and Related Biological Products Advisory Committee October 26, 2021 Meeting Document

Source: https://www.fda.gov/media/153409/download

ON PAGE 39 the FDA document states (emphasis added):

Lymphadenopathy is considered an adverse reaction to vaccine and is noted as such in the EUA Fact Sheet. Among approximately 2250 children 5 to <12 years of age randomized 2:1 to receive BNT162b2 or placebo, as of the data cutoff date (06 September 2021), 13 participants (0.9%) in the BNT162b2 group and 1 participant (0.1%) in the placebo group had events of lymphadenopathy.” Lymphadenopathy is a lymph nodes disease. On page 40 the document states that “Lymphadenopathy has been identified as related to BNT162b2 in individuals ≥12 years of age and it is also observed in the pediatric 5 to <12 years of age group.” The document states that “One participant in the BNT162b2 group had a related AE of mild arthralgia (right elbow joint pain), with an onset the same day as Dose 2 (administered in the left deltoid muscle), that was reported as resolved the next day.” The document states that “One participant in the BNT162b2 group had a related AE of moderate paresthesia (bilateral lower extremity tingling) with onset at 1 day post-Dose 2 and reported as recovered/resolved 3 days after onset.” The document states that “In the BNT162b2 group, a psychiatric disorder event of tic was reported in 1 participant: One participant in the BNT162b2 group had an AE of Grade 3 tic with onset at 7 days post Dose 2 and reported as recovering/resolving at the time of the data cutoff. The AE was considered by the investigator as related to study intervention.” The document later notes that “There were 6 participants (0.4%) in the BNT162b2 group and 3 participants (0.4%) in the placebo group had events of lymphadenopathy.”

On PAGE 42 the document states that a trial participant dropped out of the trial due to an Adverse Event, stating “One participant (0.1%) in the BNT162b2 group discontinued from the vaccination period due to an AE (details in Section 3.7.2) and two participants (0.1%) in the BNT162b2 group and 1 participant (0.1%) in the placebo group withdrew from the study before the 1-month post Dose 2 visit. Neither of these withdrawals was reported as due to an AE.”

One participant had blood that passed through his/her anus, which is known as hematochezia, characterized by bloody stool. The document states that “One participant in the BNT162b2 group had a non-serious related AE reported by the investigator as moderate hematochezia 4 days after Dose 2. The participant had heme occult positive stool; was seen in the emergency department, and had no further tests done; and went home and the event resolved the same day without sequelae. This participant had a medical history of asthma and nondrug allergy and had no other reported AEs.”

THAT IS IMPOSSIBLE – Why Is Nobody Talking About These Strange Events…!?

 

THAT IS IMPOSSIBLE – Why Is Nobody Talking About These Strange Events…!?

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Just News – A Call For An Uprising – YOU WON’T BELIEVE WHAT FRIGHTENING EVENTS TOOK PLACE AT THIS CIRCUS

A Call For An Uprising – YOU WON’T BELIEVE WHAT FRIGHTENING EVENTS TOOK PLACE AT THIS CIRCUS

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