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Re: Coronavirus
https://www.bitchute.com/video/8GmmR...andomize=false
MASS DEATH INCOMING? CDC Data Show over 100K DEAD from the Vaccine
First published at 06:46 UTC on February 19th, 2022.
https://static-3.bitchute.com/live/c...ko_320x180.jpg
The Red Elephants - Vincent James
The Red Elephants
24:44 video runtime
Also see article at
https://www.dailyveracity.com/2022/0...pted-as-truth/
Three Things That Were Considered ‘Dangerous Misinformation’ Last Year Which are Now Widely Accepted as Truth
byDaily Veracity Staff
February 7, 2022
8 minute read
No comments
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Dachsie comment:
at 15:43
"we all got COVID, or whatever it is"
Vincent James in this video seems to indicate that his older sister who did not also join the family Christmas get-together happened to "get COVID" too and that this older sister of his who is a teacher in Chicago got more serious symptoms of the illness than he and his other family members got while on their Christmas holiday gathering.
That is an important insight. People ARE catching something. It is convenient to refer to " it " as "COVID" but technically that is not accurate and precise as far as the science is concerned. COVID has never been a thing that is scientifically identified. It's not a thing.
Vincent James were not overly scared when the family all caught "COVID." They just regarded it as an uneventful case of something like "the flu" or "a cold" and they took some vitamin C and Zinc (no ivermectin) and they all went on with their Christmas gathering and all got over a brief mild illness with no problems.
But his sister is said to have contracted "COVID" with more severe symptoms (@ 19:42 ) and she was the only person in his family who was "vaccinated". The symptoms of whatever is contracted seems to hit vaccinated people harder and they have more severe symptoms. That seems to sum things up very nicely.
I would go on to say that the "vaccines" especially the mRNA ones, really seem to immediately change the person's immune system's anibodies defenses so that natural immunity to mild pathogens going around is substantially impaired from the first 2-shot doses of "the vaccine." His sister had the 2-shot vaccine plus one booster. But apparently she pulled through OK, which many people do, especially younger people.
Getting the vaccine is when big problems can start, however, when older people get the shot, and/or people of any age who already have some other medical condition when already causes them to have somewhat weakened immune systems.
We still can't "follow the science" on this illness because the Devil has written the "genetic code" for this illness.
_________________________
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Re: Coronavirus
https://static-3.bitchute.com/live/c...X9_320x180.jpg
Dachsie comment:
Janice McGheachin, current Lt. Gov. of Idaho, is running as Republican candidate for Idaho governor. She has an excellent record of fighting current Idaho governor Little on mask mandates, lockdowns and other PLANdemic evil.
I hope she wins the candidacy and I hope true patriots get out and vote for her in the primary election voting day of May 17, 2022.
I try to avoid politics as much as possible but I believe this lady will fight for all true American patriots know is most important in this crucial time.
Run for office NOW.
Political candidates for any office, federal, state or local, need to take advantage of the awakening that is happening right now in the USA regarding how
how The masks are a joke and do not work and never did work and the science proves it...
how the VACCINES are what are causing the serious serious sickness that some people are getting,
The Vaccines don't work and do not meet the scientific definition of what a vaccine is.
Many truths coming out in the mainstream media right now blowing the lid off all the lives of the fake pandemic , PLANdemic, that Michael Yeadon, reired Pfizer top executive, says are logically only for the purpose of
DEPOPULATION.
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https://static-3.bitchute.com/live/c...X9_320x180.jpg
https://rumble.com/vv1emi-live-trude...cs-drug-b.html
LIVE: Trudeau Declares War on God, McGeachin Fights to Save Idaho, Docs Drug Babies
Janice McGheachin was running for Idaho governor and was in the Republican primary election, but do not know how this excellent politician did in that primary election.
The Idaho primary voting day will occur on May 17, 2022. The general election will occur on November 8, 2022. Additional general election candidates will be added here following the primary.
Republican primary election
Republican primary for Governor of Idaho
The following candidates are running in the Republican primary for Governor of Idaho on May 17, 2022.
Candidate
Image of https://s3.amazonaws.com/ballotpedia...nBradshaw2.jpg
Steven Bradshaw
Image of https://s3.amazonaws.com/ballotpedia...mmonBundy2.jpg
Ammon Bundy
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Chris Hammond
Image of https://s3.amazonaws.com/ballotpedia...umphreysed.jpg
Ed Humphreys
Image of https://s3.amazonaws.com/ballotpedia...Lisa-Marie.jpg
Lisa Marie
Image of https://s3.amazonaws.com/ballotpedia...cGeachin41.jpg
Janice McGeachin
Silhouette Placeholder Image.png
Cody Usabel
Stew Peters Show
Published February 15, 2022 18,415 Views
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Re: Coronavirus
This ENTIRE Stew Peters show of Feb. 15. 2022 is EXTREMELY IMPORTANT.
WATCH IT NOW.
https://rumble.com/vv1emi-live-trude...cs-drug-b.html
https://static-3.bitchute.com/live/c...MM_320x180.jpg
Watch guest Ali Schultz J.D. tell about a USA hospital kidnapping a new born baby and Life Flighting the baby to another hospital without telling the mother and then trying to give baby on Remdesivir. but that atrocity killshot had not happened at time of this stew Peters show.
This is RACKETEERING and multiple felony CRIMES !!!!!!!
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Re: Coronavirus
https://christianresearchnetwork.org...e-catastrophe/
https://christianresearchnetwork.org...crn-header.png
CDC data signaling vaccine catastrophe
CDC data signaling vaccine catastrophe
https://i0.wp.com/christianresearchn...00%2C201&ssl=1
Posted by Marsha West ∙ February 16, 2022 ∙ In News ∙ Coronavirus - COVID-19, Cover up, Death, Democrat, Health, Research, Science, Truth, United States Government, Vaccine, Vaccine Adverse Event Reporting System-VAERS, Biden Joe ∙ Bookmark permalink
(Art Moore – WND) In 1976, after 32 deaths were attributed to the swine flu vaccine, the U.S. government halted the mass vaccination campaign.
But now, despite the VAERS database run by the CDC and the FDA reporting more than 23,000 deaths related to the COVID-19 vaccines, the messaging from establishment media and top health officials such as Dr. Rochelle Walensky and Dr. Anthony Fauci essentially is that no one has died or suffered severe adverse effects from the largest rollout of an experimental vaccine in world history.
When confronted more than one month ago in a Senate hearing, Walensky and Fauci both dodged a direct question about the number of vaccine deaths and injuries by undermining the validity of the VAERS data, which is compiled to monitor vaccine safety. And “fact checkers” repeatedly have cited the CDC saying it can’t be proved that any of the deaths record in VAERS were caused by the vaccines. To date, as WND reported, Walensky still has not fulfilled her promise to a Republican senator to provide the American people with the government’s evidence-based estimate of vaccine-related deaths and adverse events.
https://www.wnd.com/wp-content/uploa...ky-hearing.jpg
CDC Director Dr. Rochelle Walensky during a Jan. 11 Senate hearing (Video screenshot)
View article →
https://www.wnd.com/2022/02/cdc-data-signaling-vaccine-catastrophe/
WND EXCLUSIVE
CDC data signaling vaccine catastrophe
It took only 32 deaths to halt 1976 shot campaign
Art Moore By Art Moore
Published February 14, 2022 at 7:14pm
DISCLAIMER: This news story is posted for informational and research purposes and is not in any way intended as an endorsement of WND.
The conservative voice and Christian content are being silenced more and more. CRN offers a lifeline to conservative people of faith who are disgusted with Facebook, Twitter and the MSM for failing to report, even blocking, important news stories that don’t comport with the far left’s narrative. We urge you to sign up to receive our FREE need to read articles. NO ADS! NO VIDEOS! NO POPUPS! JUST STRAIGHT NEWS.
Join Marsha West on MeWe
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Dachsie comment:
See full hyperlinks at original posted site...
https://christianresearchnetwork.org...e-catastrophe/
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Re: Coronavirus
https://rumble.com/vuxr6i-phd-biolog...tastrophe.html
Video of Dr. Rose,
PHD : CDC figures signal vaccine catastrophe
arthurdmoore Published February 14, 2022
1:02:33 video runtime
in reference to this artcle
https://www.wnd.com/2022/02/cdc-data...e-catastrophe/ also containing this embedded video
excerpt from last part of WND article
"There is something going on'
Rose gave testimony in October to an FDA panel in which members said they reluctantly approved the shots for children 5-11 because they wanted high-risk children to have access. Panel member Dr. Eric Rubin, editor-in-chief of the New England Journal of Medicine, famously said: "We're never going to learn about how safe the vaccine is unless we start giving it. That's just the way it goes."
In testimony in September to the Vaccines and Related Biological Products Advisory Committee when it was considering Pfizer's request for authorization of booster shots, Rose emphasized that there are more VAERS death reports in 2biological data analyst021 than the last 10 years combined.
The FDA's vaccine panel was scheduled to vote this Tuesday on whether to recommend authorization of the shot for children under 5. But the FDA announced last Friday that the decision will be postponed for at least two months because more data is needed.
That’s a significant sign, Rose said, that the tide may be turning.
"There is something going on there. We are all holding our breath hoping that maybe we have presented enough data now and maybe enough people have said said the right things to the right people," she said.
"Or maybe some people's consciences are starting to wake up."
Rose said children, who have zero chance statistically of dying from COVID-19, do not need to be vaccinated for the virus.
“Ask any immunologist, any vaccinologist, any person who knows anything about epidemiology, immunology, viral dynamics. Anyone who knows what herd immunity actually means," she said. "I mean, come on!"
Pointing to the Canadian trucker protest, she sees "a groundswell of people who are united in wanting this to end."
"They're not going to be able to keep hiding the adverse event data," she said.
"It's going to be so in your face soon – I think probably by the fall of this year – that nobody's going to be able to hide this."
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Re: Coronavirus
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Re: Coronavirus
Dachsie comment:
The case of whistleblower Brook Jackson
and
Pfraudulent Pfizer marches on.
Pfizer provides half of the funding for the FDA and a large number of the FDA, NIH, NIAID and CDC top level executives and administrators own vaccine-related patents and stocks which greatly personally enriches this gang of criminals.
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https://www.youtube.com/watch?v=0BXrz91nHms
https://www.youtube.com/watch?v=0BXrz91nHms
16:14 video runtime
15:26 / 16:14
COVID-19 vaccine
Get the latest information from the CDC.
See more resources on Google
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EXCLUSIVE: Pfizer Clinical Trial Whistleblower's Lawsuit Presses Ahead Without Government’s Help
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Premiered Feb 16, 2022
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Re: Coronavirus
Dachsie comment:
I notice in this report that they consistently use the term "lab leak" with no explanation of the term.
There is an[B] leak , which implies accidental leak /B]or escape of the pathogen from a lab,
and there is a [B]release, which implies intentional release /B] of a pathogen in a deliberate way as to place and time of release.
Both a "leak" and a "release" imply the "virus" or pathogen is outside / not confined of the laboratory where it is supposed to be.
I still think this unfolding narrative and aspect of the origins of the "COVID-19 virus" is a story that is not about FACT and TRUTH. (Epoch Times is careful in their reporting so everything they report is founded in fact and delivered objrctively, but the overall effect of this reporting appears to support the political narrative that is being built or developed now to make is appear that Fouci's dismissal ("firing") look like a "feather in the cap" of Biden and congress.
It does appear that Fauci story is being "set up" so as to set up Fauci for his fall, his dismissal by what will appear in the media as his "firing."
This will be a very useful distraction media story as well, distracting from the total collapse of the Biden administration debacle. (I also found it very telling that Fauci, in ore of his contentious political theater episodes with Senator Rand Paul , countered with something about the January 6 2021 Pelosi "insurrection" false event as being true and what Senator Paul's real problem was /is. That placed Fauci firmly in the Deep State Destroy the USA Republic camp, in my opinion.)
One other important "take-away" ---
It is indisputably possible for secret government laboratories to create lethal pandemic-level pathogens and to deliberately release them on the populace. This capability to make and use bioweapons and to make "medicines" and "vaccines" for puposes of killing people can be used any time again in the future. What is also knowable from this "PLANdemic" is that it is possible to permanently change the genetic make-up of humans with synthetic lab-created substances and products so that a human can become an owned and controlled patented entity, no longer homo sapiens.
______________________
https://www.youtube.com/watch?v=ZR5r...jSoEDkp8Ze9Hxm
https://www.youtube.com/watch?v=ZR5rUzdrKe0&list=PLM3fq8FbhwLzd6_5ZZBjSoED kp8Ze9Hxm
13:47 video runtime
Fauci Knew About Virus Lab Origin Via Secret Teleconference, Pushed Alternate Narrative
Fauci Knew About Virus Lab Origin Via Secret Teleconference, Pushed Alternate Narrative
Crossroads Highlights
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Re: Coronavirus
Dachsie comment:
Just to archive one of Pfizer's communications with the FDA. Note how "vaccines" in children age 6 months through 4 years of age age are considered to be needed "to address the urgent public health need".
This is pure E V I L
The meeting that was recently scheduled to discuss and approve these Emergency Use Authorization "vaccines" for very young children was canceled and it is unknown why but we can hope and pray that these evildoers will grow a conscience and never follow through with this evil plan.
____________
Excerpt:
https://investors.pfizer.com/Investo...A/default.aspx
Investor Relations > News > News Details
Pfizer and BioNTech Initiate Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age Following Request From U.S. FDA
02.01.2022 "to address the urgent public health need."
[B]With pediatric COVID-19 cases surpassing 10 million and at the request of the FDA, the companies have submitted available data on the safety and efficacy of two 3 µg doses as part of a three-dose primary series for this age group to address the urgent public health need[/B]
Companies plan to submit additional data on a third 3 µg dose in this age group in the coming months
If authorization is granted, the Pfizer-BioNTech vaccine would be the first COVID-19 vaccine available for pediatric populations under 5 years of age
NEW YORK & MAINZ, Germany--(BUSINESS WIRE)-- Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that following a request from the U.S. Food and Drug Administration (FDA) the companies have initiated a rolling submission seeking to amend the Emergency Use Authorization (EUA) of the Pfizer-BioNTech COVID-19 Vaccine to include children 6 months through 4 years of age (6 months to <5 years of age), in response to the urgent public health need in this population. The companies expect to complete the EUA submission in the coming days. This application is for authorization of the first two 3 µg doses of a planned three-dose primary series in this age group. Data on a third dose given at least 8 weeks after completion of the second dose are expected in the coming months and will be submitted to the FDA to support a potential expansion of this requested EUA.
Since the pandemic began, more than 10.6 million children have tested positive for COVID-19 in the U.S.,1 with children under 4 accounting for more than 1.6 million of those cases.2 Further, reported COVID-19 cases and related hospitalization among children have spiked dramatically across the United States during the Omicron variant surge. For the week ending January 22, children under 4 accounted for 3.2% of the total hospitalizations due to COVID-19.2 If authorization is granted, the Pfizer-BioNTech COVID-19 Vaccine would be the first vaccine available to help protect children under 5 years of age from this disease, potentially including future emerging variants of concern.
“As hospitalizations of children under 5 due to COVID-19 have soared, our mutual goal with the FDA is to prepare for future variant surges and provide parents with an option to help protect their children from this virus,” said Albert Bourla, Chairman and Chief Executive Officer, Pfizer. “Ultimately, we believe that three doses of the vaccine will be needed for children 6 months through 4 years of age to achieve high levels of protection against current and potential future variants. If two doses are authorized, parents will have the opportunity to begin a COVID-19 vaccination series for their children while awaiting potential authorization of a third dose.”
“Our vaccine has already demonstrated a favorable safety, tolerability and efficacy profile in multiple clinical trials and real-world studies for all age groups starting from 5 years old,” said Ugur Sahin, M.D., CEO and Co-founder of BioNTech. “If authorized, we are very excited about the prospect of offering parents the opportunity to help protect their children 6 months through 4 years of age from COVID-19 and the potentially severe consequences of infection.”
The request to amend the EUA is based on the totality of data on the safety, tolerability, immunogenicity, and available efficacy of two doses of the Pfizer-BioNTech COVID-19 Vaccine. The companies also plan to share these data with the European Medicines Agency and other regulatory agencies around the world.
The companies plan to provide ample supply of the 3 µg dose to meet demand should the FDA approve the EUA application. The companies previously announced planned global supply capacity of approximately four billion doses of the Pfizer-BioNTech COVID-19 Vaccine in 2022. The companies continue to supply the vaccine under their existing supply agreement with the U.S. government, which continues through April 2022.
About the Phase 1/2/3 Trial in Children
The Phase 1/2/3 trial initially enrolled 4,500 children ages 6 months to under 12 years of age in the United States, Finland, Poland, and Spain from more than 90 clinical trial sites. Additional children have been enrolled in all age groups following study amendments and the trial currently includes approximately 8,300 children. It was designed to evaluate the safety, tolerability, and immunogenicity of the Pfizer-BioNTech vaccine on a two-dose schedule (approximately 21 days apart) in three age groups: ages 5 to under 12 years; ages 2 to under 5 years; and ages 6 months to under 2 years. Based on the Phase 1 dose-escalation portion of the trial, children ages 5 to under 12 years received a two-dose schedule of 10 µg each while children under age 5 received a lower 3 µg dose for each injection in the Phase 2/3 study. The trial enrolled children with or without prior evidence of SARS-CoV-2 infection. On December 17, 2021, Pfizer and BioNTech announced the companies would test a third 3 µg dose given at least two months after the second dose in children under age 5 and a third dose of the 10 µg formulation in children 5 to under 12 years of age.
The Pfizer-BioNTech COVID-19 Vaccine, which is based on BioNTech’s proprietary mRNA technology, was developed by both BioNTech and Pfizer. BioNTech is the Marketing Authorization Holder in the United States, the European Union, the United Kingdom, Canada and other countries, and the holder of emergency use authorizations or equivalents in the United States (jointly with Pfizer) and other countries. Submissions to pursue regulatory approvals in those countries where emergency use authorizations or equivalent were initially granted are planned.
U.S. Indication & Authorized Use
HOW IS THE VACCINE GIVEN?
The vaccine will be given as an injection into the muscle.
Primary Series:
In individuals 5 years of age and older, the vaccine is administered as a 2-dose series, 3 weeks apart. In individuals 5 years of age and older, a third primary series dose may be administered at least 28 days after the second dose to individuals who are determined to have certain kinds of immunocompromise.
Booster Dose:
A single booster dose of the vaccine may be administered at least 5 months after completion of a primary series of the Pfizer-BioNTech COVID-19 Vaccine or COMIRNATY® (COVID-19 Vaccine, mRNA) to individuals 12 years of age and older
A single booster dose of the vaccine may be administered to individuals 18 years of age and older who have completed primary vaccination with a different authorized COVID-19 vaccine. Individuals should check with their healthcare provider regarding timing of the booster dose
WHAT IS THE INDICATION AND AUTHORIZED USE?
The Pfizer-BioNTech COVID-19 Vaccine has received EUA from FDA to provide:
a 2-dose primary series to individuals 5 years of age and older
a third primary series dose to individuals 5 years of age and older who have been determined to have certain kinds of immunocompromise
a single booster dose to individuals 12 years of age and older who have completed a primary series with Pfizer-BioNTech COVID-19 Vaccine or COMIRNATY® (COVID-19 Vaccine, mRNA)
a single booster dose to individuals 18 years of age and older who have completed primary vaccination with a different authorized COVID-19 vaccine. The booster schedule is based on the labeling information of the vaccine used for the primary series
COMIRNATY® (COVID-19 Vaccine, mRNA) is an FDA-approved COVID-19 vaccine made by Pfizer for BioNTech.
It is approved as a 2-dose series for prevention of COVID-19 in individuals 16 years of age and older
It is also authorized under EUA to provide:
a 2-dose primary series to individuals 12 through 15 years of age
a third primary series dose to individuals 12 years of age and older who have been determined to have certain kinds of immunocompromise
a single booster dose to individuals 12 years of age and older who have completed a primary series with Pfizer-BioNTech COVID-19 Vaccine or COMIRNATY® (COVID-19 Vaccine, mRNA)
a single booster dose to individuals 18 years of age and older who have completed primary vaccination with a different authorized COVID-19 vaccine. The booster schedule is based on the labeling information of the vaccine used for the primary series
EUA Statement
Emergency uses of the vaccine have not been approved or licensed by FDA, but have been authorized by FDA, under an Emergency Use Authorization (EUA) to prevent Coronavirus Disease 2019 (COVID-19) in individuals 5 years of age and older. The emergency uses are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of the medical product under Section 564(b)(1) of the FD&C Act unless the declaration is terminated or authorization revoked sooner. Please see EUA Fact Sheets at www.cvdvaccine-us.com.
IMPORTANT SAFETY INFORMATION
Individuals should not get the vaccine if they:
had a severe allergic reaction after a previous dose of this vaccine
had a severe allergic reaction to any ingredient of this vaccine
Individuals should tell the vaccination provider about all of their medical conditions, including if they:
have any allergies
have had myocarditis (inflammation of the heart muscle) or pericarditis (inflammation of the lining outside the heart)
have a fever
have a bleeding disorder or are on a blood thinner
are immunocompromised or are on a medicine that affects the immune system
are pregnant, plan to become pregnant, or are breastfeeding
have received another COVID-19 vaccine
have ever fainted in association with an injection
The vaccine may not protect everyone.
Side effects reported with the vaccine include:
There is a remote chance that the vaccine could cause a severe allergic reaction
A severe allergic reaction would usually occur within a few minutes to 1 hour after getting a dose of the vaccine. For this reason, vaccination providers may ask individuals to stay at the place where they received the vaccine for monitoring after vaccination
Signs of a severe allergic reaction can include difficulty breathing, swelling of the face and throat, a fast heartbeat, a bad rash all over the body, dizziness, and weakness
If an individual experiences a severe allergic reaction, they should call 9-1-1 or go to the nearest hospital
Myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart) have occurred in some people who have received the vaccine, more commonly in males under 40 years of age than among females and older males. In most of these people, symptoms began within a few days following receipt of the second dose of the vaccine. The chance of having this occur is very low. Individuals should seek medical attention right away if they have any of the following symptoms after receiving the vaccine:
chest pain
shortness of breath
feelings of having a fast-beating, fluttering, or pounding heart
Additional side effects that have been reported with the vaccine include:
severe allergic reactions; non-severe allergic reactions such as rash, itching, hives, or swelling of the face; myocarditis (inflammation of the heart muscle); pericarditis (inflammation of the lining outside the heart); injection site pain; tiredness; headache; muscle pain; chills; joint pain; fever; injection site swelling; injection site redness; nausea; feeling unwell; swollen lymph nodes (lymphadenopathy); decreased appetite;diarrhea; vomiting; arm pain; fainting in association with injection of the vaccine
These may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The possible side effects of the vaccine are still being studied in clinical trials. Call the vaccination provider or healthcare provider about bothersome side effects or side effects that do not go away
Data on administration of this vaccine at the same time as other vaccines have not yet been submitted to FDA. Individuals considering receiving this vaccine with other vaccines, should discuss their options with their healthcare provider.
Patients should always ask their healthcare providers for medical advice about adverse events. Individuals are encouraged to report negative side effects of vaccines to the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). Visit https://www.vaers.hhs.gov or call 1‐800‐822‐7967. In addition, side effects can be reported to Pfizer Inc. at www.pfizersafetyreporting.com or by calling 1-800-438-1985.
Click for
Fact Sheets and Prescribing Information for individuals 12 years of age and older
Full Prescribing Information (16 years of age and older) DILUTE BEFORE USE, Purple Cap
Full Prescribing Information (16 years of age and older) DO NOT DILUTE, Gray Cap
EUA Fact Sheet for Vaccination Providers (12 years of age and older), Purple Cap
EUA Fact Sheet for Vaccination Providers (12 years of age and older), Gray Cap
Recipients and Caregivers Fact Sheet (12 years of age and older)
Fact Sheets for individuals 5 through 11 years of age
EUA Fact Sheet for Vaccination Providers (5 through 11 years of age), Orange Cap
Recipients and Caregivers Fact Sheet (5 through 11 years of age)
About Pfizer: Breakthroughs That Change Patients’ Lives
At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 170 years, we have worked to make a difference for all who rely on us. We routinely post information that may be important to investors on our website at www.Pfizer.com. In addition, to learn more, please visit us on www.Pfizer.com and follow us on Twitter at @Pfizer and @Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook.com/Pfizer.
Pfizer Disclosure Notice
The information contained in this release is as of February 1, 2022. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.
SNIP
A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2020 and in its subsequent reports on Form 10-Q, including in the sections thereof captioned “Risk Factors” and “Forward-Looking Information and Factors That May Affect Future Results”, as well as in its subsequent reports on Form 8-K, all of which are filed with the U.S. Securities and Exchange Commission and available at www.sec.gov and www.pfizer.com.
SNIP
For a discussion of these and other risks and uncertainties, see BioNTech’s Annual Report as Form 20-F for the Year Ended December 31, 2020, filed with the SEC on March 30, 2021, which is available on the SEC’s website at www.sec.gov. All information in this press release is as of the date of the release, and BioNTech undertakes no duty to update this information unless required by law.
_____________________________
1 Children and COVID-19: State-Level Data Report. American Academy of Pediatrics. https://www.aap.org/en/pages/2019-no...l-data-report/. Updated January 20, 2022. Accessed January 28, 2022.
2 Laboratory-Confirmed COVID-19-Associated Hospitalizations. Centers for Disease Control and Prevention. https://gis.cdc.gov/grasp/covidnet/covid19_5.html. Updated January 22, 2022. Accessed January 28, 2022.
Pfizer:
Media Relations
+1 (212) 733-7410
PfizerMediaRelations@pfizer.com
Investor Relations
+1 (212) 733-4848
IR@pfizer.com
BioNTech:
Media Relations
Jasmina Alatovic
+49 (0)6131 9084 1513
Media@biontech.de
Investor Relations
Sylke Maas, Ph.D.
+49 (0)6131 9084 1074
Investors@biontech.de
Source: Pfizer Inc.
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Re: Coronavirus
Dachsie comment:
I have been counting the instances of cover-up and non-response to FOIA requests and other kinds of unprofessional and dishonest practices of the CDC HHS / NIH / NIAID, and FDA.
My list of such instances is growing rapidly.
"shot cover-up shows the FILL IN THE BLANK is politicized and corrupt" sums up the general tone and demeanor of these federal Justin-Castro -style "federal public health agencies."
I regret to say this practice of keeping the public locked out of information about their individual health care matters is now manifesting in our contacts with our local doctors' offices and hospitals, the same totalitarian style and treatment of the patients.
The quality of medical care in the USA has deteriorated substantially and is widely noticeable for the reason that the entire "pandemic" and "virus" and COVID-19 narrative was full of big lies from the beginning. This has put our entire healthcare system in the position of having to lie and lock the patients out of information and "non-protocol" care of their health issues.
The "Emergency Use Authorization" of procedure and vaccines and tests may technically removes your health and life insurance companies for paying on claims related to death or injury from anything related to "COVID." I think most insurance policy contracts have wording to the effect that they do not have to pay on claims where there is reckless or risky dehavior on the insured part, and taking EUA medical procedures (including the nasal swab test) that can cause injury and death could come under that rule.
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https://www.youtube.com/post/UgkxlSm...xny9TlKSvRT1mS
Judicial Watch 2 days ago
From Judicial Watch President @TomFitton: RELENTLESS: @JudicialWatch Sues HHS for Records of Communication from Top FDA Officials Who Resigned Reportedly over COVID Booster Shots "This booster shot cover-up shows the FDA is politicized and corrupt." https://judicialwatch.org/covid-boost...
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https://www.judicialwatch.org/covid-booster-shots/
February 10, 2022 | Judicial Watch
Judicial Watch Sues HHS for Records of Communication from Top FDA Officials Who Resigned Reportedly over COVID Booster Shots
https://www.judicialwatch.org/wp-con...-1-768x401.jpg
(Washington, DC) – Judicial Watch announced today that it filed a Freedom of Information Act (FOIA) lawsuit against the Department of Health and Human Services (HHS) for records of communication from Dr. Marion Gruber and Dr. Philip Krause, the former director and deputy director of the US. Food and Drug Administration’s (FDA) Office of Vaccines Research and Review, who reportedly resigned during the White House’s push to approve the COVID-19 “booster shot” (Judicial Watch v. U.S. Department of Health and Human Services (No. 1:22-cv-00292)).
The lawsuit was filed in the United States District Court of the District of Columbia after HHS failed to respond to a September 3, 2021, FOIA request for:
All emails sent to and from Center for Biologics Evaluation and Research Director Marion Gruber regarding the Centers for Disease Control and Prevention/CDC, the Advisory Committee on Immunization (ACIP), and/or “booster vaccines” for the prevention and/or treatment of SARS-CoV-2 and/or COVID-19.
All emails sent to and from Center for Biologics Evaluation and Research Deputy Director Phil Krause regarding the Centers for Disease Control and Prevention/CDC, the Advisory Committee on Immunization (ACIP), and/or “booster vaccines” for the prevention and/or treatment of SARS-CoV-2 and/or COVID-19.
On September 22, 2021, the FDA approved use of a booster dose of the Pfizer drug. According to the organization’s news release, the FDA, “amended the emergency use authorization (EUA) for the Pfizer-BioNTech COVID-19 Vaccine to allow for use of a single booster dose, to be administered at least six months after completion of the primary series” for people at “high risk” of “severe COVID-19.”
On September 13, 2021, Gruber and Krause were among a group of resigning doctors who agreed that, “Available evidence doesn’t yet indicate a need for COVID-19 vaccine booster shots among the general population …”
Also on September 13, 2021, The Lancet published a paper to which Gruber and Krause contributed that noted:
Careful and public scrutiny of the evolving data will be needed to assure that decisions about boosting are informed by reliable science more than by politics.… Widespread boosting should be undertaken only if there is clear evidence that it is appropriate.
“This booster shot cover-up shows the FDA is politicized and corrupt,” said Judicial Watch President Tom Fitton. “The American people have a right to know about the safety and efficacy of the COVID-19 vaccines – especially given that officials in the FDA seem to have objected to the agency’s recommendations about the vaccines.”
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https://www.linkedin.com/in/marion-gruber/
Marion F. Gruber, Ph.D., MS
Vaccine Regulation | Clinical Trial Design | Global Public Health | Leadership | Policy and Guidance Development
IAVI
The University of Kiel
United States
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https://www.linkedin.com/in/phil-krause-b9668875/
Phil Krause 3rd degree connection 3rd
Deputy Director at FDA/CBER/OVRR
Yale University School of Medicine
Bethesda, Maryland, United States
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https://www.thelancet.com/journals/l...046-8/fulltext
"Careful and public scrutiny of the evolving data will be needed to assure that decisions about boosting are informed by reliable science more than by politics.… Widespread boosting should be undertaken only if there is clear evidence that it is appropriate."
