Tag: vaccine injury

Death rate after Covid vaccines is much higher than flu shots, says Sen. Johnson

“Using the midpoint assumption that 70% of distributed flu vaccines were administered, the 25.5 deaths per million doses of the COVID-19 vaccine represents a 55 fold increase over the flu vaccine deaths per million doses. This is a shocking difference and only adds to the growing evidence of safety signals that are screaming to be taken seriously.”Sen. Ron Johnson (R-Wisconsin)

Sen. Ron Johnson (R-Wisconsin) has sent a letter to Health and Human Services (HHS) Secretary Xavier Becerra, FDA Commissioner Robert Califf, and CDC Director Mandy Cohen regarding concerning information on the safety of the Covid-19 vaccines. According to an analysis conducted by the senator’s office, Covid vaccines are far deadlier than flu shots.

Johnson also questioned the health agency officials on their awareness of a recently released study that researchers claimed raises additional safety concerns about Covid-19 vaccines relating to the production of “off-target” or incorrect proteins.

And Johnson reiterated his previous requests for the agencies to produce data on the safety of the Covid-19 vaccines.

“When it comes to responding to my data requests on the adverse events associated with the Covid-19 vaccines, your arrogant lack of transparency has been unprecedented, irresponsible, and completely unacceptable. Over the course of the last 32 months, I have raised questions, sent formal requests, and conducted oversight on the safety and efficacy of the Covid-19 vaccines,” wrote Johnson. “Instead of addressing my legitimate questions and requests for information, you and other public health officials continue to promote the Covid-19 vaccines as safe and effective and often use the number of vaccine doses administered as support for that misleading claim.” 

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Landmark Case Means Americans Can Now Sue Big Pharma for Vaccine Injuries

Up until now, the drug companies have been shielded from liability for all the COVID vaccine injuries and deaths that they have caused. They’re protected by something called the PREP Act, which stands for Public Readiness and Emergency Preparedness. A judge in a landmark Michigan case, however, has now ruled that the PREP Act does not shield the Big Pharma companies from liability if their medicines are contaminated.

That’s it. The floodgates are finally open. If you were hurt by a COVID shot or if one of your loved ones died from it, you can now sue the Big Pharma companies.

The Michigan case was brought by Dan Nowacki, an elderly man who was hospitalized with COVID. Mr. Nowacki was treated with Remdesivir, which is a COVID treatment drug made by pharmaceutical company Gilead. Remdesivir is a relatively new treatment, so it’s shielded under the PREP Act.

Mr. Nowacki was treated with Remdesivir intravenously. His attorneys just proved in court that at least two of the vials that Mr. Nowacki was administered were contaminated with shards of glass. It caused him to have two catastrophic strokes in the hospital. He’s now permanently bedridden. About 55,000 vials of Remdesivir were recalled in November of 2021 due to glass contamination.

The judge ruled that the pharmaceutical companies’ liability shielding does not protect them in the case of contamination. If the Big Pharma companies are being protected from being sued, then they still have to meet basic safety standards. They can’t just inject their medicines into people if they know that those medicines are contaminated with shards of glass, arsenic, or… just to name one possible contaminant off the top of our head… cancer-causing monkey viruses.

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Study Finds COVID Vaccination Independently Associated With Long COVID Syndrome

People who receive two doses of a COVID-19 vaccine may be more likely to develop long-COVID, a new study finds.

In the study published in PLOS One, researchers examined data from 487 and 371 individuals at four weeks and six months post-SARS-CoV-2 infection, respectively, to estimate the incidence, characteristics, and predictors of long COVID among patients. Long COVID symptoms were reported by 29.2 percent of participants four weeks following infection. This number dropped to 9.4 percent at six months, indicating symptoms may diminish over time.

Researchers found that the greater the severity of infection a patient had, the more likely they were to experience long COVID. The incidence of long COVID at four weeks of follow-up in those who experienced mild/moderate disease was 23.4 percent compared with 62.5 percent in those with severe cases.

At six months, the incidence of long COVID was considerably lower. For those with mild/moderate infection, only 7.2 percent reported symptoms compared with 23.1 percent in those with severe/critical cases. The most commonly reported symptom was fatigue. Other symptoms included cough, cognitive dysfunction or brain fog, and loss of taste and smell.

During the four-week follow-up, patients were more likely to experience long COVID if they had preexisting medical conditions, a higher number of symptoms during the acute phase of COVID-19 illness, if their infection was more severe or resulted in hospitalization, or if they had received two COVID-19 vaccine doses.

Although previous vaccination was associated with long COVID, the authors could not find “any interaction effect of COVID-19 vaccination and acute COVID-19 severity on causing Long COVID.”

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An explosive new study describing “unintended immune responses” from mRNA injections has dropped a tactical nuke on Pfizer

Pfizer must feel like it’s been one damned thing after another these days. In a year packed with horrible news for the jabs – not to mention poor jab recipients – yesterday saw a critical new discovery of jab problems, possibly the worst and most damning yet. How bad was it? It was so bad that, even though I almost never make predictions any more, I will predict this: The FDA will be forced to withdraw the mRNA covid shots because of this study.

I’m not even joking about that.

Our investigation begins with yesterday’s Telegraph article about a new study headlined: ‘One in four who had Moderna or Pfizer Covid jabs experienced unintended immune response’.

The explosive, new, peer-reviewed, gold-standard study is already making news even though it was only published yesterday, 6 December. And it published in the well-respected journal Nature, featuring the multisyllabic, incomprehensible title, ‘N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting’.

This study has twenty authors. There is safety in numbers.

Don’t let the mind-numbing title fool you. If Kevin McKernan’s SV40 monkey virus discovery tossed a hand grenade into Pfizer’s machine-gun bunker, this carefully-written study dropped a tactical nuke on Pfizer’s Pacific Fleet anchoring at Hawaii. The study’s implications are vast.

Since the science is a little thick – no, it’s very thick – I’ll start by telling you the end first.

Here’s how The Telegraph’s article defensively described the study’s results. Keep in mind, they were down-playing the results, as much as they possibly could:

No adverse effects were created by the error, data show, but Cambridge scientists found such vaccines were not perfect and sometimes led to nonsense proteins being made instead of the desired Covid “spike”, which mimics infection and leads to antibody production (and) an immune system flare-up.

The new study, published in Nature, found this occurred in around 25-30 per cent of people.

Hahaha! The vaccines were “not perfect!!” Oh my gosh! Please, stop! Hahahaha! It hurts to laugh! Whew. Alright, I’m okay now. Onwards.

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Some COVID Vaccines Produce ‘Unintended Immune Response’ in Recipients: Study

Researchers in a landmark new study have discovered a sequence within the Pfizer mRNA vaccine that produces an “unintended immune response” in the body, which experts are calling a massive “developmental and regulatory failure.”

Synthetic Messenger Ribonucleic Acid (mRNA), such as that used in Moderna and Pfizer vaccines, enables the body to create a specific spike protein mimicking SARS-CoV-2. The body reacts to the foreign protein and generates protective immunity, which theoretically neutralizes the real virus when it enters the body.

“Researchers from the Medical Research Council (MRC) Toxicology Unit have discovered that the cellular machinery that ‘reads’ mRNAs ‘slips’ when confronted with repeats of a chemical modification commonly found in mRNA therapeutics. In addition to the target protein, these slips lead to the production of ‘off-target’ proteins triggering an unintended immune response,” said a press release for the study published in Nature on Dec. 6.

The MRC team redesigned the mRNA vaccine to prevent further harmful immune responses from the spike proteins.

“The researchers identified that bases with a chemical modification called N1-methylpseudouridine—which are currently contained in mRNA therapies—are responsible for the ‘slips’ along the mRNA sequence.”

When the MRC team collaborated with researchers from the Universities of Kent, Oxford, and Liverpool, they found an unintended immune response occurred in one-third of the 21 patients in the study who were inoculated with the Pfizer mRNA vaccine.

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DNA Contamination In COVID-19 Vaccines May Explain Rise In Cancers, Clots, Autoimmune Diseases: Pathologist

Clinical pathologist Dr. Ryan Cole has said that DNA contamination in some COVID-19 vaccines may be related to an increase in cancers, micro-clotting, and autoimmune diseases.

“My big concern is the fact that billions of people across the earth have received a product that was overtly contaminated with something that should not have been in the product,” Dr. Cole, an anatomic clinical pathologist with postgraduate Ph.D. training in immunology, recently told the “American Thought Leaders” program.

“If I went and bought some meat at the grocery store and they had heavy metal or pesticide toxins, they would pull those from the shelves immediately,” he added.

Recently, researchers found that vaccine vials containing Pfizer’s COVID-19 vaccines had billions of residual DNA fragments, including molecules derived from Simian Virus 40 (SV40) used as “promoters” or “enhancers” that help produce the mRNA molecules that help human cells make proteins that trigger an immune response inside the body.

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Elevated risk of stroke in elderly patients who receive Covid and high dose flu shot at same time

On Jan. 13 2023, the U.S. Food and Drug Administration (FDA) and the U.S. Centers for U.S. Disease Control and Prevention (CDC)) issued a public statement regarding the identification of a preliminary safety signal for ischemic stroke among adults over the age of 65 that occurs between one to 21 days after receiving Pfizer/BioNTech’s monovalent Comirnaty messenger RNA (mRNA) Covid-19 shot and the WT/OMI BA.4/BA.5 bivalent version of it.

The safety signal was detected in the CDC’s Vaccine Safety Datalink (VSD), however, a primary analysis conducted by federal public health officials did not find elevated stroke risk following Covid bivalent shots.

The first CDC analysis evaluated the risk of the stroke following a Covid bivalent shot. The study’s sample population included 5,397,278 adults over 65 years old, who were given either the monovalent Comirnaty bivalent WT/OMI BA.4/BA.5 shot or Moderna/NIAID’s bivalent Spikevax shot.

There were 2,886 cases of NHS; 2,641 cases of transient ischemic attack (TIA); 4,788 cases of NHS/TIA, and 808 cases of hemorrhagic stroke (HS) across both manufacturers of the Covid shots.

Approximately 10-15 percent of the sample cases claimed they had Covid disease between 31 to 365 days prior to suffering a stroke, and 34-45 percent had been given a high-dose or adjuvanted influenza vaccination at the same time.

The findings from the primary analysis showed that there were no statistically significant associations of an increased risk of stroke following administration of the Covid bivalent shots.

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Getting flu and COVID shot together still reasonable amid safety review of potential stroke risk: Experts

Older adults who received last year’s COVID booster and a high-dose version of the flu vaccine in the same visit may have a potential increased risk of stroke, according to a new FDA-funded study.

Experts urged that the results were preliminary and may be explained by other factors such as the fact that older adults are already at a higher risk for stroke due to their age.

“There is no need for panic, and emphatically no need to stop giving COVID and flu shots at the same time to older adults,” said Dr. Peter Chin-Hong, an infectious diseases specialist at the University of California, San Francisco, while he reiterated that more research is needed.

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How Pfizer Hid Nearly 80% of COVID Vaccine Trial Deaths From Regulators

Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.

The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.

Together, these strategies kept regulators and the public ignorant of a 3.7-fold increase in cardiac deaths among subjects who received the vaccine, according to analysis in the International Journal of Vaccine Theory, Practice, and Research.

The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”

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FDA finds potential ‘safety signal’ of seizures in 2-5 yr olds after getting Covid-19 shots

A new preprint study led by the U.S. Food and Drug Administration (FDA) has detected a potential “safety signal” for seizures and convulsions in young children after receiving the monovalent Pfizer or Moderna mRNA Covid-19 vaccines.

Researchers observed the condition in children ages 2-4 for the Pfizer vaccine, and ages 2-5 for the Moderna vaccine.

The total number of cases was 72, with over 50% meeting the definition for febrile seizures.

The median time between vaccination and seizures or convulsions was two days, with 32% occurring the day of or the day after vaccination. All seizures and convulsions took place within seven days of vaccination.

The signal emerged through near real-time surveillance of more than 4 million vaccinated children.

The researchers of the preprint study cautioned that the results “should be interpreted carefully given study limitations.”

The study also identified a myocarditis/pericarditis safety signal in mostly male children 12-17 years old.

However, since each of these conditions were a “known adverse outcome,” according to the researchers, they did not conduct any further follow-up.

Data for the study were collected through health claims records from CVS Health, Optum and Carelon Research, which participate in the FDA’s Center for Biologics Evaluation and Research, and supplemented with data from state and local immunization information systems databases.

The study covered reports through January, February or March of this year — as little as 6 months after the approval of vaccinations for younger children.

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