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Pfizer Asks FDA to Clear COVID Shots for Babies

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Children statistically have virtually no chance of death or serious illness from COVID-19, but, in any case, the experimental vaccines rushed to market under emergency use authorization have proven to be ineffective against the current SARS-CoV-2 variants while posing the risk of severe harm or death in proportions far higher than any vaccine in history.

Children also, according to studies, are at low risk of spreading COVID-19. Further, the CDC recently reported higher COVID-19 case rates have been recorded among fully vaccinated children than unvaccinated in the age group 5-11 since February 2022. And the U.K.’s Office for National Statistics found children are up to 52 times more likely to die following the COVID-19 injection than children who have not received it.

Nevertheless, Pfizer has submitted a request to the FDA – which tried to hide Pfizer’s clinical trial data for 75 years – to grant emergency use authorization to administer its COVID-19 vaccine to children from six months to 5 years of age.

The pharmaceutical giant declared in May that a three-shot regimen of its Pfizer-BioNTech vaccine was 80.3% effective in preventing COVID infections among children under 5, based on early results of its trial for that cohort. (Read more from “Pfizer Asks FDA to Clear COVID Shots for Babies” HERE)

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Pfizer Says COVID-19 Pill Cut Hospital, Death Risk by 90%

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Pfizer Inc. said Friday that its experimental antiviral pill for COVID-19 cut rates of hospitalization and death by nearly 90% in high-risk adults, as the drugmaker joins the race to bring the first easy-to-use medication against the coronavirus to the U.S. market.

Currently all COVID-19 treatments used in the U.S. require an IV or injection. Competitor Merck’s COVID-19 pill is already under review at the Food and Drug Administration after showing strong initial results, and on Thursday the United Kingdom became the first country to OK it.

Pfizer said it will ask the FDA and international regulators to authorize its pill as soon as possible, after independent experts recommended halting the company’s study based on the strength of its results. Once Pfizer applies, the FDA could make a decision within weeks or months. If authorized the company would sell the drug under the brand name Paxlovid. (Read more from “Pfizer Says COVID-19 Pill Cut Hospital, Death Risk by 90%” HERE)

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Pfizer Auditor Blows Lid on Vaccine Maker, Reveals Why She Decided To Come Forward; NBA Player Reveals Reaction To COVID Vaccine Ended His Season

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By Townhall. A Pfizer whistleblower said that she decided to expose her company after a decade of working for them because she feels that people are not making informed decisions about what goes into their body.

Melissa McAtee told The Daily Wire’s Candace Owens that she had damming information on Pfizer, which recently had their COVID-19 vaccine approved by the Food and Drug Administration, but did not elect to reveal it until another whistleblower for the company spoke on why they had come forward. . .

McAtee, who was a quality auditor at Pfizer, noticed that the vaccine was glowing under a certain light and, even after alerting the company, the issue was still ignored. She also noted that fellow employees who had worked at the company for upwards of 40 years had never seen what was going on with this vaccine.

She said in a Project Veritas interview made public last week that internal Pfizer emails from high-level employees instructed workers not to reveal to the public the role aborted fetal cells played in the development of its coronavirus vaccine. . .

She also noted that the company engaged in secrecy, such as shutting down hallways and certain processes, when they knew that the FDA would be coming to the plant. (Read more from “Pfizer Auditor Blows Lid on Vaccine Maker, Reveals Why She Decided To Come Forward” HERE)

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NBA Player Reveals Adverse Reaction to COVID Vaccine Ended Season

By WND. Amid the controversy over basketball superstar Kyrie Irving’s refusal to take a COVID-19 vaccine, a former NBA player says his season ended early last year after he developed blood clots he attributes to a COVID shot.

Brandon Goodwin, who was a point guard for the Atlanta Hawks, recently told his side of the story on a Twitch stream, SB Nation reported. . .
“I got sick and I never quite recovered from it,” Goodwin said on the stream, as posted on YouTube. “I would always have back pain, I was just super tired in the games.”

“That’s when I found out I had blood clots. That all within the span of a month,” he said.

“I was fine until then,” Goodwin said. “I was fine up until I took the vaccine, I was fine.” (Read more from “NBA Player Reveals Adverse Reaction to COVID Vaccine Ended Season” HERE)

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