Editor's Note:  RISK-BENEFIT ANALYSIS  . . . Injecting this poisonous crap into yourself is INSANE!  The risks are devastating, the benefits don't exist!

TrialSiteNews.com

Are the COVID-19 mRNA vaccines durability improving? No, they are not, and in fact, even if an individual followed public health instructions, getting three doses of the primary series to bolster protection with a mutating virus and a vaccine truly lacking in durability such as the Pfizer BNT162b2 product consumers are afforded absolutely no protection against hospitalization unless they get annual boosters. This is the clear message taken from the latest research led by researchers at Kaiser Permanente, Department of Research & Evaluation, Pasadena and other locations.

The team of physicians and epidemiologists pondered whether administration of the Pfizer BNT162b2 XBB vaccine offers additional protection against COVID-19 hospital admissions and ambulatory visits for US adults compared with not receiving a BNT162b2 XBB vaccine of any kind and whether older versions of the COVID-19 vaccine still provide any protection compared with being unvaccinated. Executing a case-control study targeting 2854 cases and 15, 345 controls, the Pfizer BNT162b2 XBB vaccine provided statistically significant additional protection against a range of COVID-19 outcomes during the early part of the 2023 to 2024 viral respiratory season according to the study outcomes. Older versions of COVID-19 vaccines offered no additional protection compared with being unvaccinated, including against COVID-19 hospital admissions, regardless of the number or type of prior doses received. Sara Y. Tartof, PhD, MPH and colleagues report their study outcomes support the current recommendations of the Centers for Disease Control and Prevention (CDC) for annual updates. Put another way, the COVID-19 mRNA vaccine durability continues to be a challenge, with waning effectiveness, necessitating the recommendation of an annual booster for any protection of hospitalization whatsoever. What is not contemplated are the potential long-term consequences of repeated mRNA boosters, year after year. This impact has not been studied.

TheGatewayPundit.com

Kansas Attorney General Kris Kobach announced Monday he is suing pharmaceutical giant Pfizer for misleading Kansas residents about the safety and efficacy of its COVID-19 vaccine.

During a press conference in Topeka, alongside Deputy Attorney General Fran Oleen and Assistant Attorneys General Kaley Schrader and Melanie Jack, Kobach detailed the allegations lodged against Pfizer.

“Pfizer made multiple misleading statements to deceive the public about its vaccine at a time when Americans needed the truth,” said Kobach.

The complaint, lodged today in Thomas County District Court, accuses Pfizer of misleading Kansans about the vaccines’ risks, including potential harm to pregnant women and the risk of myocarditis. The suit further alleges that Pfizer falsely claimed its vaccine was effective against COVID variants, despite evidence to the contrary.

Infowars.com

A study published this month has found that the Pfizer mRNA Covid ‘vaccine’ gene therapy injections contain DNA contamination at over 500 times allowable levels, raising fears that the DNA may integrate into the vaccinated person’s own DNA, causing mutations that can lead to diseases such as cancer.

“The available information and data indicate that the ready-to-use mRNA vaccine Comirnaty contains DNA impurities that exceed the permitted limit value by several hundred times and, in some cases, even more than 500 times,” the study said in the ‘Conclusions’ section.

Revolver.news

What should be splashed across headlines nationwide is oddly quiet. In a muffled bombshell, Pfizer, a titan in Big Pharma, has just settled a shocking 10,000 lawsuits linked to cancer and the antacid Zantac. Yes, you heard that right—banishing heartburn could now be a deadly choice, thanks to Big Pharma. These are the same so-called “experts” who rushed to declare their sketchy COVID vaccine was perfectly safe even before it was properly tested. Now it’s clear why so many people were skeptical—and rightly so.

Scientists have uncovered startling evidence that a substantial portion of the batches of the Pfizer-BioNTech COVID-19 vaccine deployed in the European Union may in fact have consisted of placebos – and that the German regulator knew this and did not subject them to quality-control testing.

Infowars.com

A Pfizer whistleblower has raised the alarm that Pfizer workers were offered a “separate and distinct” COVID-19 vaccine and were told their jab would “not impact supply to national governments in any way.”

A leaked email from January 2021, provided exclusively to Infowars, explained to colleagues and contractors at Pfizer’s Pearl River research site that site-essential workers would be offered COVID-19 vaccinations that are “separate and distinct” from the doses Pfizer committed to governments worldwide.

“I am pleased to inform you that we will begin offering COVID-19 vaccinations to eligible on-site essential colleagues and contractors over the next several weeks,” reads the leaked Email. “Eligible on-site essential contractors will be notified, either by e-mail or by their Pfizer sponsor, and will receive instructions for registering for an on-site appointment as well.”

Editor's Note:  These two psychopaths could not be more EVIL.  First they deliberately inject the global population with POISON COVID JABS that are now known to be causing cancer rates to explode, now they expect people to line up for more deadly jabs to treat the cancer they caused!

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Alex Jones breaks down alarming remarks by Bill Gates and Pfizer CEO Albert Bourla essentially admitting plans to conduct MORE global mRNA and oncological experiments on the human population.

The first post-authorization safety analysis of Pfizer’s Abrysvo RSV vaccine
found the average time between vaccination and preterm birth was three days.
Two-thirds of reported cases occurred within a week.

ChildrenHealthDefense.org

A new preprint study shows a statistically significant safety signal for preterm birth associated with Pfizer’s respiratory syncytial virus (RSV) vaccine, Abrysvo.

The first post-authorization safety analysis of Pfizer’s RSV vaccine — RSV prefusion F protein (RSVPreF) — found the average time between vaccination and preterm birth was three days.

Two-thirds of reported cases occurred within a week.

“This study highlights ongoing concern about preterm birth among pregnant individuals following RSVPreF vaccination,” the authors wrote.

Canadian researchers at the University of Ottawa School of Epidemiology and Public Health assessed all adverse events reported to the Vaccine Adverse Event Reporting System (VAERS) database following RSV immunization between Sept. 1, 2023, and Feb. 23, 2024.

Infowars.com

Dr. Naomi Wolf joined a panel of experts at the Wellness Company’s Spike Symposium last June to break down Pfizer’s attempts to cover up adverse effects of its experimental COVID mRNA vaccines on fertility and newborns.

“There’s a section in the Pfizer documents where there’s an 80% miscarriage rate of the women whom they’re following to term,” Wolf said.

Pfizer knew what would happen to newborns pic.twitter.com/AsjF9nuleX

— illuminatibot (@iluminatibot) April 28, 2024

“It shows that Pfizer knew that babies in utero were being exposed to the vaccine,” she said. “In their words, the babies were dying through ‘transplacental exposure.’ But they knew that and they knew that they were poisoning breastmilk and that the lipid nanoparticles, the mRNA, and presumably the spike [protein] was making it into the breastmilk and causing convulsions and deaths.”

TheEpochTimes.com

Pfizer’s COVID-19 drug did not work for many vaccinated people, according to a new paper from the company’s scientists.

There was not a statistically significant difference between Paxlovid and placebo recipients in terms of time to alleviation of symptoms, the scientists reported in the new paper.