Let me get this straight about the COVID-19 vaccine
Let me get this straight about the COVID-19 vaccine
Yoda
JF-Expert Member
- Jul 22, 2018
- 48,475
- 70,102
1. Chanjo za COVID-19 ni SALAMA na zimefanyiwa majaribio ya kutosha ya usalama wake.
2.Chanjo za Covid zote za Marekani, Ulaya, Russia na China HAZIGUSI DNA kabisa, zote ni kwa ajili ya mRNA.
3.Chanjo za COVID-19 zimewahi kutengezewa kwa sababu ya maendeleo makubwa ya teknolojia ya madawa karne ya 21 na ufadhili mkubwa wa haraka wa kifedha
4.
2.Chanjo za Covid zote za Marekani, Ulaya, Russia na China HAZIGUSI DNA kabisa, zote ni kwa ajili ya mRNA.
3.Chanjo za COVID-19 zimewahi kutengezewa kwa sababu ya maendeleo makubwa ya teknolojia ya madawa karne ya 21 na ufadhili mkubwa wa haraka wa kifedha
4.
Pendaelli
JF-Expert Member
- Feb 13, 2014
- 11,050
- 31,412
Mpaka huu ugonjwa uje uishe tutasikia na kuona mengi sana.
Lakini mimi binafsi nadhani hakuna mwenye taarifa kamilifu kati yetu sote, sana tunasikia kisha kuchambua kwa tafsiri zetu na kuja na hitimisho na kulifanya sahihi.
Ni vizuri lakini tunaweza kuwa tupo kwenye udanganyifu kwa tafsiri zetu wenyewe au tupo sahihi.
Muda ndio unaweza kutupa majibu sahihi kwamba ni nani mwenye usahihi au upotoshaji.
Tokea huu ugonjwa utokee ni karibu mwaka wa pili sasa, na kwa namna hiyo kwamba haupo ni uwongo.
Ni karibu sasa mwaka mmoja tokea matumizi ya cha chanjo dhidi ya huu ugonjwa, kama kungekuwa na athari za muda mfupi mpaka sasa zingekuwa Zimesha kutokeza na hapo ndipo tungepata kujua huwenda kukawepo na athari za muda mrefu.
Baada yake matokeo ya athari yameripotiwa kwa uchache sana ambayo katika hali yoyote lazima iwe hivyo kwa sababu mwanadamu siyo mkamilifu kwa hivyo ni nadra kufanya kitu kikawa kikamilifu moja kwa moja.
Kwa hivyo kwa kua muda bado upo na maisha bado yapo, tuendelee kujifunza na sio kuwa na hitimisho lililotafsiriwa na mitazamo yetu.
Lakini mimi binafsi nadhani hakuna mwenye taarifa kamilifu kati yetu sote, sana tunasikia kisha kuchambua kwa tafsiri zetu na kuja na hitimisho na kulifanya sahihi.
Ni vizuri lakini tunaweza kuwa tupo kwenye udanganyifu kwa tafsiri zetu wenyewe au tupo sahihi.
Muda ndio unaweza kutupa majibu sahihi kwamba ni nani mwenye usahihi au upotoshaji.
Tokea huu ugonjwa utokee ni karibu mwaka wa pili sasa, na kwa namna hiyo kwamba haupo ni uwongo.
Ni karibu sasa mwaka mmoja tokea matumizi ya cha chanjo dhidi ya huu ugonjwa, kama kungekuwa na athari za muda mfupi mpaka sasa zingekuwa Zimesha kutokeza na hapo ndipo tungepata kujua huwenda kukawepo na athari za muda mrefu.
Baada yake matokeo ya athari yameripotiwa kwa uchache sana ambayo katika hali yoyote lazima iwe hivyo kwa sababu mwanadamu siyo mkamilifu kwa hivyo ni nadra kufanya kitu kikawa kikamilifu moja kwa moja.
Kwa hivyo kwa kua muda bado upo na maisha bado yapo, tuendelee kujifunza na sio kuwa na hitimisho lililotafsiriwa na mitazamo yetu.
Mathanzua
JF-Expert Member
- Jan 4, 2017
- 17,251
- 22,929
- Thread starter
- #626
Updates:
Over 32,000 People DEAD in Brazil Following COVID-19 Vaccines According to Official Media Report
Posted on August 22, 2021 by State of the Nation
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A COVID-19 ward in a hospital in Londrina, Brazil. Elderly are frequently hospitalized after two doses of the COVID-19 vaccine. Source.
by Brian Shilhavy
Editor, Health Impact News
A Health Impact News reader from Brazil has alerted us to official media reports stating that during a 5-month period, over 32,000 people in Brazil have died following a COVID-19 injection.
Currently in Brazil, the following vaccines are authorized for use: AstraZeneca/Oxford, Pfizer/BioNTech, Coronavac (also called Sinovac), J&J/Janssen, and Butanvac.
The report was published on uol.com.br, which reportedly has about the same number of pageviews as CNN.com, according to data from SimilarWeb. It is so big, that ICANN has given its own domain: .uol.
Despite these high amounts of deaths following vaccination, the report states:
“Vaccination is still the best way to control the disease.”
But even these cases of deaths following COVID-19 injections might be under-reported, as the country’s state news agency reported in July that in the small state of Distrito Federal, at least 711 died after taking the first experimental vaccine, while another 263 people died after taking two doses of the experimental vaccines. (Source.)
Brazil’s state news agency reports:
Vaccination does not prevent re-infection or the evolution to more serious conditions, including death. Therefore, the Health Secretary stressed the importance of keeping the prevention measures against the new coronavirus.
“We are always alerting people to wear masks, wash their hands, use alcohol gel, and avoid crowds. Even if we are vaccinated, we can acquire the virus and have complications”, he declared. (Source.)
Parts of this article were translated by DeepL.
Over 32,000 People DEAD in Brazil Following COVID-19 Vaccines According to Official Media Report
Posted on August 22, 2021 by State of the Nation
FacebookTwitterPinterestRedditEmailShare
A COVID-19 ward in a hospital in Londrina, Brazil. Elderly are frequently hospitalized after two doses of the COVID-19 vaccine. Source.
by Brian Shilhavy
Editor, Health Impact News
A Health Impact News reader from Brazil has alerted us to official media reports stating that during a 5-month period, over 32,000 people in Brazil have died following a COVID-19 injection.
Currently in Brazil, the following vaccines are authorized for use: AstraZeneca/Oxford, Pfizer/BioNTech, Coronavac (also called Sinovac), J&J/Janssen, and Butanvac.
The report was published on uol.com.br, which reportedly has about the same number of pageviews as CNN.com, according to data from SimilarWeb. It is so big, that ICANN has given its own domain: .uol.
Despite these high amounts of deaths following vaccination, the report states:
“Vaccination is still the best way to control the disease.”
But even these cases of deaths following COVID-19 injections might be under-reported, as the country’s state news agency reported in July that in the small state of Distrito Federal, at least 711 died after taking the first experimental vaccine, while another 263 people died after taking two doses of the experimental vaccines. (Source.)
Brazil’s state news agency reports:
Vaccination does not prevent re-infection or the evolution to more serious conditions, including death. Therefore, the Health Secretary stressed the importance of keeping the prevention measures against the new coronavirus.
“We are always alerting people to wear masks, wash their hands, use alcohol gel, and avoid crowds. Even if we are vaccinated, we can acquire the virus and have complications”, he declared. (Source.)
Parts of this article were translated by DeepL.
Mathanzua
JF-Expert Member
- Jan 4, 2017
- 17,251
- 22,929
- Thread starter
- #629
Updates:
The FDA Just Granted FULL APPROVAL to the Exceedingly Dangerous and Deadly Pfizer-BioNTech Covid ‘Vaccines’!
Posted on August 23, 2021 by State of the Nation
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FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
Berkeley Lovelace Jr.
CNBC
KEY POINTS
The FDA granted Pfizer and BioNTech full U.S. approval of their Covid-19 vaccine.
The move may encourage some unvaccinated Americans to get the shots as well as give more private businesses across the nation greater confidence to implement vaccine mandates.
Up until now, the mRNA vaccine was on the U.S. market under an Emergency Use Authorization.
The Food and Drug Administration on Monday granted full approval to Pfizer and BioNTech Covid-19 vaccine – becoming the first in the U.S. to win the coveted designation and giving even more businesses, schools and universities greater confidence to adopt vaccine mandates.
Up until now, the mRNA vaccine, which will be marketed as Comirnaty, was on the U.S. market under an Emergency Use Authorization that was granted by the FDA in December. Since then, more than 204 million of the Pfizer shots have been administered, according to data compiled by the Centers for Disease Control and Prevention.
Federal health officials had been under mounting pressure from the scientific community and advocacy groups to fully approve Pfizer and BioNTech’s vaccine ever since the drugmakers submitted their application to the agency in early May. The companies submitted a Biologics License Application, which secures full approval, to the FDA on May 7 for patients age 16 and up.
FDA scientists evaluated “hundreds of thousands of pages” of vaccine data from 40,000 trial participants, according to the U.S. agency. The vaccine was found to be 91% effective in preventing Covid – slightly lower than the 95% efficacy rate trial data showed when the shot was authorized late last year and before the delta variant took hold in the U.S.
Pfizer’s vaccine met the agency’s “high standards for safety, effectiveness, and manufacturing quality,” acting FDA Commissioner Janet Woodcock said in a statement. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated.”
The FDA held a media briefing at 11 a.m. Monday to discuss the approval.
Although more than 60% of the total U.S. population has had at least one dose of a Covid vaccine, many Americans say they are still hesitant about getting vaccinated, even as the highly contagious delta variant spreads. Full approval may convince some Americans that the shots are safe, doctors and epidemiologists say. In fact, a survey from the Kaiser Family Foundation found 3 in 10 unvaccinated adults said they would be more likely to get vaccinated if one of the vaccines receives full approval.
Full approval is “more psychological than anything else,” said Dr. Paul Offit, a voting member of the agency’s Vaccines and Related Biological Products Advisory Committee. “I mean you already have more than 320 million doses administered that are out there. The vaccines already have an enormous safety and efficacy profile.”
U.S. approval is also likely to spur a new wave of vaccine mandates from corporate America. Major companies – from Walt Disney to Walmart – have already told some or all of their employees that they must get fully vaccinated against Covid this fall. Still, some private businesses may have felt hesitant about requiring the shots, before full approval, even though they had the legal authority to do so, said Dorit Reiss, a professor of law at UC Hastings College of the Law.
The Pentagon said it would make vaccinations mandatory for service members “no later” than the middle of September, or sooner if the FDA grants full approval earlier.
“You’re going to see the empowerment of local enterprises, giving mandates that could be colleges, universities, places of business, a whole variety and I strongly support that,” White House chief medical officer Dr. Anthony Fauci said Aug 8, when asked about full approval of the vaccines. “The time has come. … We’ve got to go the extra step to get people vaccinated.”
Pfizer’s shot is the first Covid vaccine to receive full regulatory approval in the U.S. Federal regulators had previously said they would work as quickly as possible to clear Pfizer’s vaccines.
The vaccine is still under emergency use authorization for children 12 to 15 as the company continues to collect data. Dr. Peter Marks, the FDA’s top vaccine regulator, said Monday the agency would move as “swiftly” as possible on approving the shot for kids under 12 once the company submits the data.
“Currently, there are still trials ongoing and so the agency has to wait for the company to submit the data for those trials,” he said during a briefing. “We certainly want to make sure that we get it right.”
Standard vaccine reviews generally take several months to a year or more to determine whether they are safe and effective for use in the general public. But due to the pandemic, which has killed more than 628,000 Americans, the FDA permitted the use of the shots under an EUA.
In a public health emergency, the manufacturing and approval of vaccines can be streamlined through emergency authorizations. Former Health Secretary Alex Azar declared a public health emergency on Jan. 31, 2020. The health emergency has been renewed several times, most recently in late July. The FDA allowed the use of the shots with just two months of safety data under an EUA. It’s not the same as a Biologic License Application, or a request for full approval, which requires at least six months of data.
Before granting full approval, FDA scientists must painstakingly look through the companies’ clinical trial data, including for any discrepancies or safety concerns, said Offit, who is also director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
It’s a lot of data, Offit said. He previously said when Merck submitted its data from its 70,000-person rotavirus vaccine trial, the pages that were generated could have exceeded the height of the Sears Tower — a 1,450-foot skyscraper in Chicago that’s now known as Willis Tower.
“The FDA will do what it thinks it needs to do to make sure that the American public is safe,” he said.
Full approval is also very beneficial to companies that submit an application, former FDA Commissioner Dr. Robert Califf said in a phone interview in May.
With it, Pfizer and BioNTech are now able to market the shots directly to U.S. consumers. Companies can’t promote their products under an EUA, he said. It also allows the shot to stay on the market once the pandemic is over and the U.S. is no longer considered in an “emergency.”
“The vaccines will still have to be administered under the supervision of a professional who’s qualified,” Califf said. “It’s not like they can send the vaccines to people’s homes. However, they can advertise on TV and promote their products under the watchful eye of the FDA.”
Pfizer and BioNTech have said they expect to generate billions from the vaccine. Under full approval, the companies could also decide to charge more for the vaccines, health experts say.
The companies have already raised the price of their vaccine in the European Union, according to the Financial Times. They are now charging $23 per dose, up from their previous price of $18.40, according to the report.
Pfizer and BioNTech also plan to ask the FDA to approve a third dose as a booster shot following full approval. Last week, the Biden administration said it was preparing to offer booster shots to all eligible Americans beginning the week of Sept. 20.
___
www.cnbc.com
The FDA Just Granted FULL APPROVAL to the Exceedingly Dangerous and Deadly Pfizer-BioNTech Covid ‘Vaccines’!
Posted on August 23, 2021 by State of the Nation
FacebookTwitterPinterestRedditEmailShare
FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
Berkeley Lovelace Jr.
CNBC
KEY POINTS
The FDA granted Pfizer and BioNTech full U.S. approval of their Covid-19 vaccine.
The move may encourage some unvaccinated Americans to get the shots as well as give more private businesses across the nation greater confidence to implement vaccine mandates.
Up until now, the mRNA vaccine was on the U.S. market under an Emergency Use Authorization.
The Food and Drug Administration on Monday granted full approval to Pfizer and BioNTech Covid-19 vaccine – becoming the first in the U.S. to win the coveted designation and giving even more businesses, schools and universities greater confidence to adopt vaccine mandates.
Up until now, the mRNA vaccine, which will be marketed as Comirnaty, was on the U.S. market under an Emergency Use Authorization that was granted by the FDA in December. Since then, more than 204 million of the Pfizer shots have been administered, according to data compiled by the Centers for Disease Control and Prevention.
Federal health officials had been under mounting pressure from the scientific community and advocacy groups to fully approve Pfizer and BioNTech’s vaccine ever since the drugmakers submitted their application to the agency in early May. The companies submitted a Biologics License Application, which secures full approval, to the FDA on May 7 for patients age 16 and up.
FDA scientists evaluated “hundreds of thousands of pages” of vaccine data from 40,000 trial participants, according to the U.S. agency. The vaccine was found to be 91% effective in preventing Covid – slightly lower than the 95% efficacy rate trial data showed when the shot was authorized late last year and before the delta variant took hold in the U.S.
Pfizer’s vaccine met the agency’s “high standards for safety, effectiveness, and manufacturing quality,” acting FDA Commissioner Janet Woodcock said in a statement. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated.”
The FDA held a media briefing at 11 a.m. Monday to discuss the approval.
Although more than 60% of the total U.S. population has had at least one dose of a Covid vaccine, many Americans say they are still hesitant about getting vaccinated, even as the highly contagious delta variant spreads. Full approval may convince some Americans that the shots are safe, doctors and epidemiologists say. In fact, a survey from the Kaiser Family Foundation found 3 in 10 unvaccinated adults said they would be more likely to get vaccinated if one of the vaccines receives full approval.
Full approval is “more psychological than anything else,” said Dr. Paul Offit, a voting member of the agency’s Vaccines and Related Biological Products Advisory Committee. “I mean you already have more than 320 million doses administered that are out there. The vaccines already have an enormous safety and efficacy profile.”
U.S. approval is also likely to spur a new wave of vaccine mandates from corporate America. Major companies – from Walt Disney to Walmart – have already told some or all of their employees that they must get fully vaccinated against Covid this fall. Still, some private businesses may have felt hesitant about requiring the shots, before full approval, even though they had the legal authority to do so, said Dorit Reiss, a professor of law at UC Hastings College of the Law.
The Pentagon said it would make vaccinations mandatory for service members “no later” than the middle of September, or sooner if the FDA grants full approval earlier.
“You’re going to see the empowerment of local enterprises, giving mandates that could be colleges, universities, places of business, a whole variety and I strongly support that,” White House chief medical officer Dr. Anthony Fauci said Aug 8, when asked about full approval of the vaccines. “The time has come. … We’ve got to go the extra step to get people vaccinated.”
Pfizer’s shot is the first Covid vaccine to receive full regulatory approval in the U.S. Federal regulators had previously said they would work as quickly as possible to clear Pfizer’s vaccines.
The vaccine is still under emergency use authorization for children 12 to 15 as the company continues to collect data. Dr. Peter Marks, the FDA’s top vaccine regulator, said Monday the agency would move as “swiftly” as possible on approving the shot for kids under 12 once the company submits the data.
“Currently, there are still trials ongoing and so the agency has to wait for the company to submit the data for those trials,” he said during a briefing. “We certainly want to make sure that we get it right.”
Standard vaccine reviews generally take several months to a year or more to determine whether they are safe and effective for use in the general public. But due to the pandemic, which has killed more than 628,000 Americans, the FDA permitted the use of the shots under an EUA.
In a public health emergency, the manufacturing and approval of vaccines can be streamlined through emergency authorizations. Former Health Secretary Alex Azar declared a public health emergency on Jan. 31, 2020. The health emergency has been renewed several times, most recently in late July. The FDA allowed the use of the shots with just two months of safety data under an EUA. It’s not the same as a Biologic License Application, or a request for full approval, which requires at least six months of data.
Before granting full approval, FDA scientists must painstakingly look through the companies’ clinical trial data, including for any discrepancies or safety concerns, said Offit, who is also director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
It’s a lot of data, Offit said. He previously said when Merck submitted its data from its 70,000-person rotavirus vaccine trial, the pages that were generated could have exceeded the height of the Sears Tower — a 1,450-foot skyscraper in Chicago that’s now known as Willis Tower.
“The FDA will do what it thinks it needs to do to make sure that the American public is safe,” he said.
Full approval is also very beneficial to companies that submit an application, former FDA Commissioner Dr. Robert Califf said in a phone interview in May.
With it, Pfizer and BioNTech are now able to market the shots directly to U.S. consumers. Companies can’t promote their products under an EUA, he said. It also allows the shot to stay on the market once the pandemic is over and the U.S. is no longer considered in an “emergency.”
“The vaccines will still have to be administered under the supervision of a professional who’s qualified,” Califf said. “It’s not like they can send the vaccines to people’s homes. However, they can advertise on TV and promote their products under the watchful eye of the FDA.”
Pfizer and BioNTech have said they expect to generate billions from the vaccine. Under full approval, the companies could also decide to charge more for the vaccines, health experts say.
The companies have already raised the price of their vaccine in the European Union, according to the Financial Times. They are now charging $23 per dose, up from their previous price of $18.40, according to the report.
Pfizer and BioNTech also plan to ask the FDA to approve a third dose as a booster shot following full approval. Last week, the Biden administration said it was preparing to offer booster shots to all eligible Americans beginning the week of Sept. 20.
___
FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
The FDA's approval of the Pfizer and BioNTech Covid shot will likely spur more businesses to adopt vaccine mandates for workers.
Mathanzua
JF-Expert Member
- Jan 4, 2017
- 17,251
- 22,929
- Thread starter
- #630
Updates:
The FDA Just Granted FULL APPROVAL to the Exceedingly Dangerous and Deadly Pfizer-BioNTech Covid ‘Vaccines’!
Posted on August 23, 2021 by State of the Nation
FacebookTwitterPinterestRedditEmailShare
FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
Berkeley Lovelace Jr.
CNBC
KEY POINTS
The FDA granted Pfizer and BioNTech full U.S. approval of their Covid-19 vaccine.
The move may encourage some unvaccinated Americans to get the shots as well as give more private businesses across the nation greater confidence to implement vaccine mandates.
Up until now, the mRNA vaccine was on the U.S. market under an Emergency Use Authorization.
The Food and Drug Administration on Monday granted full approval to Pfizer and BioNTech Covid-19 vaccine – becoming the first in the U.S. to win the coveted designation and giving even more businesses, schools and universities greater confidence to adopt vaccine mandates.
Up until now, the mRNA vaccine, which will be marketed as Comirnaty, was on the U.S. market under an Emergency Use Authorization that was granted by the FDA in December. Since then, more than 204 million of the Pfizer shots have been administered, according to data compiled by the Centers for Disease Control and Prevention.
Federal health officials had been under mounting pressure from the scientific community and advocacy groups to fully approve Pfizer and BioNTech’s vaccine ever since the drugmakers submitted their application to the agency in early May. The companies submitted a Biologics License Application, which secures full approval, to the FDA on May 7 for patients age 16 and up.
FDA scientists evaluated “hundreds of thousands of pages” of vaccine data from 40,000 trial participants, according to the U.S. agency. The vaccine was found to be 91% effective in preventing Covid – slightly lower than the 95% efficacy rate trial data showed when the shot was authorized late last year and before the delta variant took hold in the U.S.
Pfizer’s vaccine met the agency’s “high standards for safety, effectiveness, and manufacturing quality,” acting FDA Commissioner Janet Woodcock said in a statement. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated.”
The FDA held a media briefing at 11 a.m. Monday to discuss the approval.
Although more than 60% of the total U.S. population has had at least one dose of a Covid vaccine, many Americans say they are still hesitant about getting vaccinated, even as the highly contagious delta variant spreads. Full approval may convince some Americans that the shots are safe, doctors and epidemiologists say. In fact, a survey from the Kaiser Family Foundation found 3 in 10 unvaccinated adults said they would be more likely to get vaccinated if one of the vaccines receives full approval.
Full approval is “more psychological than anything else,” said Dr. Paul Offit, a voting member of the agency’s Vaccines and Related Biological Products Advisory Committee. “I mean you already have more than 320 million doses administered that are out there. The vaccines already have an enormous safety and efficacy profile.”
U.S. approval is also likely to spur a new wave of vaccine mandates from corporate America. Major companies – from Walt Disney to Walmart – have already told some or all of their employees that they must get fully vaccinated against Covid this fall. Still, some private businesses may have felt hesitant about requiring the shots, before full approval, even though they had the legal authority to do so, said Dorit Reiss, a professor of law at UC Hastings College of the Law.
The Pentagon said it would make vaccinations mandatory for service members “no later” than the middle of September, or sooner if the FDA grants full approval earlier.
“You’re going to see the empowerment of local enterprises, giving mandates that could be colleges, universities, places of business, a whole variety and I strongly support that,” White House chief medical officer Dr. Anthony Fauci said Aug 8, when asked about full approval of the vaccines. “The time has come. … We’ve got to go the extra step to get people vaccinated.”
Pfizer’s shot is the first Covid vaccine to receive full regulatory approval in the U.S. Federal regulators had previously said they would work as quickly as possible to clear Pfizer’s vaccines.
The vaccine is still under emergency use authorization for children 12 to 15 as the company continues to collect data. Dr. Peter Marks, the FDA’s top vaccine regulator, said Monday the agency would move as “swiftly” as possible on approving the shot for kids under 12 once the company submits the data.
“Currently, there are still trials ongoing and so the agency has to wait for the company to submit the data for those trials,” he said during a briefing. “We certainly want to make sure that we get it right.”
Standard vaccine reviews generally take several months to a year or more to determine whether they are safe and effective for use in the general public. But due to the pandemic, which has killed more than 628,000 Americans, the FDA permitted the use of the shots under an EUA.
In a public health emergency, the manufacturing and approval of vaccines can be streamlined through emergency authorizations. Former Health Secretary Alex Azar declared a public health emergency on Jan. 31, 2020. The health emergency has been renewed several times, most recently in late July. The FDA allowed the use of the shots with just two months of safety data under an EUA. It’s not the same as a Biologic License Application, or a request for full approval, which requires at least six months of data.
Before granting full approval, FDA scientists must painstakingly look through the companies’ clinical trial data, including for any discrepancies or safety concerns, said Offit, who is also director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
It’s a lot of data, Offit said. He previously said when Merck submitted its data from its 70,000-person rotavirus vaccine trial, the pages that were generated could have exceeded the height of the Sears Tower — a 1,450-foot skyscraper in Chicago that’s now known as Willis Tower.
“The FDA will do what it thinks it needs to do to make sure that the American public is safe,” he said.
Full approval is also very beneficial to companies that submit an application, former FDA Commissioner Dr. Robert Califf said in a phone interview in May.
With it, Pfizer and BioNTech are now able to market the shots directly to U.S. consumers. Companies can’t promote their products under an EUA, he said. It also allows the shot to stay on the market once the pandemic is over and the U.S. is no longer considered in an “emergency.”
“The vaccines will still have to be administered under the supervision of a professional who’s qualified,” Califf said. “It’s not like they can send the vaccines to people’s homes. However, they can advertise on TV and promote their products under the watchful eye of the FDA.”
Pfizer and BioNTech have said they expect to generate billions from the vaccine. Under full approval, the companies could also decide to charge more for the vaccines, health experts say.
The companies have already raised the price of their vaccine in the European Union, according to the Financial Times. They are now charging $23 per dose, up from their previous price of $18.40, according to the report.
Pfizer and BioNTech also plan to ask the FDA to approve a third dose as a booster shot following full approval. Last week, the Biden administration said it was preparing to offer booster shots to all eligible Americans beginning the week of Sept. 20.
The FDA Just Granted FULL APPROVAL to the Exceedingly Dangerous and Deadly Pfizer-BioNTech Covid ‘Vaccines’!
Posted on August 23, 2021 by State of the Nation
FacebookTwitterPinterestRedditEmailShare
FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
Berkeley Lovelace Jr.
CNBC
KEY POINTS
The FDA granted Pfizer and BioNTech full U.S. approval of their Covid-19 vaccine.
The move may encourage some unvaccinated Americans to get the shots as well as give more private businesses across the nation greater confidence to implement vaccine mandates.
Up until now, the mRNA vaccine was on the U.S. market under an Emergency Use Authorization.
The Food and Drug Administration on Monday granted full approval to Pfizer and BioNTech Covid-19 vaccine – becoming the first in the U.S. to win the coveted designation and giving even more businesses, schools and universities greater confidence to adopt vaccine mandates.
Up until now, the mRNA vaccine, which will be marketed as Comirnaty, was on the U.S. market under an Emergency Use Authorization that was granted by the FDA in December. Since then, more than 204 million of the Pfizer shots have been administered, according to data compiled by the Centers for Disease Control and Prevention.
Federal health officials had been under mounting pressure from the scientific community and advocacy groups to fully approve Pfizer and BioNTech’s vaccine ever since the drugmakers submitted their application to the agency in early May. The companies submitted a Biologics License Application, which secures full approval, to the FDA on May 7 for patients age 16 and up.
FDA scientists evaluated “hundreds of thousands of pages” of vaccine data from 40,000 trial participants, according to the U.S. agency. The vaccine was found to be 91% effective in preventing Covid – slightly lower than the 95% efficacy rate trial data showed when the shot was authorized late last year and before the delta variant took hold in the U.S.
Pfizer’s vaccine met the agency’s “high standards for safety, effectiveness, and manufacturing quality,” acting FDA Commissioner Janet Woodcock said in a statement. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated.”
The FDA held a media briefing at 11 a.m. Monday to discuss the approval.
Although more than 60% of the total U.S. population has had at least one dose of a Covid vaccine, many Americans say they are still hesitant about getting vaccinated, even as the highly contagious delta variant spreads. Full approval may convince some Americans that the shots are safe, doctors and epidemiologists say. In fact, a survey from the Kaiser Family Foundation found 3 in 10 unvaccinated adults said they would be more likely to get vaccinated if one of the vaccines receives full approval.
Full approval is “more psychological than anything else,” said Dr. Paul Offit, a voting member of the agency’s Vaccines and Related Biological Products Advisory Committee. “I mean you already have more than 320 million doses administered that are out there. The vaccines already have an enormous safety and efficacy profile.”
U.S. approval is also likely to spur a new wave of vaccine mandates from corporate America. Major companies – from Walt Disney to Walmart – have already told some or all of their employees that they must get fully vaccinated against Covid this fall. Still, some private businesses may have felt hesitant about requiring the shots, before full approval, even though they had the legal authority to do so, said Dorit Reiss, a professor of law at UC Hastings College of the Law.
The Pentagon said it would make vaccinations mandatory for service members “no later” than the middle of September, or sooner if the FDA grants full approval earlier.
“You’re going to see the empowerment of local enterprises, giving mandates that could be colleges, universities, places of business, a whole variety and I strongly support that,” White House chief medical officer Dr. Anthony Fauci said Aug 8, when asked about full approval of the vaccines. “The time has come. … We’ve got to go the extra step to get people vaccinated.”
Pfizer’s shot is the first Covid vaccine to receive full regulatory approval in the U.S. Federal regulators had previously said they would work as quickly as possible to clear Pfizer’s vaccines.
The vaccine is still under emergency use authorization for children 12 to 15 as the company continues to collect data. Dr. Peter Marks, the FDA’s top vaccine regulator, said Monday the agency would move as “swiftly” as possible on approving the shot for kids under 12 once the company submits the data.
“Currently, there are still trials ongoing and so the agency has to wait for the company to submit the data for those trials,” he said during a briefing. “We certainly want to make sure that we get it right.”
Standard vaccine reviews generally take several months to a year or more to determine whether they are safe and effective for use in the general public. But due to the pandemic, which has killed more than 628,000 Americans, the FDA permitted the use of the shots under an EUA.
In a public health emergency, the manufacturing and approval of vaccines can be streamlined through emergency authorizations. Former Health Secretary Alex Azar declared a public health emergency on Jan. 31, 2020. The health emergency has been renewed several times, most recently in late July. The FDA allowed the use of the shots with just two months of safety data under an EUA. It’s not the same as a Biologic License Application, or a request for full approval, which requires at least six months of data.
Before granting full approval, FDA scientists must painstakingly look through the companies’ clinical trial data, including for any discrepancies or safety concerns, said Offit, who is also director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
It’s a lot of data, Offit said. He previously said when Merck submitted its data from its 70,000-person rotavirus vaccine trial, the pages that were generated could have exceeded the height of the Sears Tower — a 1,450-foot skyscraper in Chicago that’s now known as Willis Tower.
“The FDA will do what it thinks it needs to do to make sure that the American public is safe,” he said.
Full approval is also very beneficial to companies that submit an application, former FDA Commissioner Dr. Robert Califf said in a phone interview in May.
With it, Pfizer and BioNTech are now able to market the shots directly to U.S. consumers. Companies can’t promote their products under an EUA, he said. It also allows the shot to stay on the market once the pandemic is over and the U.S. is no longer considered in an “emergency.”
“The vaccines will still have to be administered under the supervision of a professional who’s qualified,” Califf said. “It’s not like they can send the vaccines to people’s homes. However, they can advertise on TV and promote their products under the watchful eye of the FDA.”
Pfizer and BioNTech have said they expect to generate billions from the vaccine. Under full approval, the companies could also decide to charge more for the vaccines, health experts say.
The companies have already raised the price of their vaccine in the European Union, according to the Financial Times. They are now charging $23 per dose, up from their previous price of $18.40, according to the report.
Pfizer and BioNTech also plan to ask the FDA to approve a third dose as a booster shot following full approval. Last week, the Biden administration said it was preparing to offer booster shots to all eligible Americans beginning the week of Sept. 20.
Mathanzua
JF-Expert Member
- Jan 4, 2017
- 17,251
- 22,929
- Thread starter
- #631
Updates:
The FDA Just Granted FULL APPROVAL to the Exceedingly Dangerous and Deadly Pfizer-BioNTech Covid ‘Vaccines’!
Posted on August 23, 2021 by State of the Nation
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FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
Berkeley Lovelace Jr.
CNBC
KEY POINTS
The FDA granted Pfizer and BioNTech full U.S. approval of their Covid-19 vaccine.
The move may encourage some unvaccinated Americans to get the shots as well as give more private businesses across the nation greater confidence to implement vaccine mandates.
Up until now, the mRNA vaccine was on the U.S. market under an Emergency Use Authorization.
The Food and Drug Administration on Monday granted full approval to Pfizer and BioNTech Covid-19 vaccine – becoming the first in the U.S. to win the coveted designation and giving even more businesses, schools and universities greater confidence to adopt vaccine mandates.
Up until now, the mRNA vaccine, which will be marketed as Comirnaty, was on the U.S. market under an Emergency Use Authorization that was granted by the FDA in December. Since then, more than 204 million of the Pfizer shots have been administered, according to data compiled by the Centers for Disease Control and Prevention.
Federal health officials had been under mounting pressure from the scientific community and advocacy groups to fully approve Pfizer and BioNTech’s vaccine ever since the drugmakers submitted their application to the agency in early May. The companies submitted a Biologics License Application, which secures full approval, to the FDA on May 7 for patients age 16 and up.
FDA scientists evaluated “hundreds of thousands of pages” of vaccine data from 40,000 trial participants, according to the U.S. agency. The vaccine was found to be 91% effective in preventing Covid – slightly lower than the 95% efficacy rate trial data showed when the shot was authorized late last year and before the delta variant took hold in the U.S.
Pfizer’s vaccine met the agency’s “high standards for safety, effectiveness, and manufacturing quality,” acting FDA Commissioner Janet Woodcock said in a statement. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated.”
The FDA held a media briefing at 11 a.m. Monday to discuss the approval.
Although more than 60% of the total U.S. population has had at least one dose of a Covid vaccine, many Americans say they are still hesitant about getting vaccinated, even as the highly contagious delta variant spreads. Full approval may convince some Americans that the shots are safe, doctors and epidemiologists say. In fact, a survey from the Kaiser Family Foundation found 3 in 10 unvaccinated adults said they would be more likely to get vaccinated if one of the vaccines receives full approval.
Full approval is “more psychological than anything else,” said Dr. Paul Offit, a voting member of the agency’s Vaccines and Related Biological Products Advisory Committee. “I mean you already have more than 320 million doses administered that are out there. The vaccines already have an enormous safety and efficacy profile.”
U.S. approval is also likely to spur a new wave of vaccine mandates from corporate America. Major companies – from Walt Disney to Walmart – have already told some or all of their employees that they must get fully vaccinated against Covid this fall. Still, some private businesses may have felt hesitant about requiring the shots, before full approval, even though they had the legal authority to do so, said Dorit Reiss, a professor of law at UC Hastings College of the Law.
The Pentagon said it would make vaccinations mandatory for service members “no later” than the middle of September, or sooner if the FDA grants full approval earlier.
“You’re going to see the empowerment of local enterprises, giving mandates that could be colleges, universities, places of business, a whole variety and I strongly support that,” White House chief medical officer Dr. Anthony Fauci said Aug 8, when asked about full approval of the vaccines. “The time has come. … We’ve got to go the extra step to get people vaccinated.”
Pfizer’s shot is the first Covid vaccine to receive full regulatory approval in the U.S. Federal regulators had previously said they would work as quickly as possible to clear Pfizer’s vaccines.
The vaccine is still under emergency use authorization for children 12 to 15 as the company continues to collect data. Dr. Peter Marks, the FDA’s top vaccine regulator, said Monday the agency would move as “swiftly” as possible on approving the shot for kids under 12 once the company submits the data.
“Currently, there are still trials ongoing and so the agency has to wait for the company to submit the data for those trials,” he said during a briefing. “We certainly want to make sure that we get it right.”
Standard vaccine reviews generally take several months to a year or more to determine whether they are safe and effective for use in the general public. But due to the pandemic, which has killed more than 628,000 Americans, the FDA permitted the use of the shots under an EUA.
In a public health emergency, the manufacturing and approval of vaccines can be streamlined through emergency authorizations. Former Health Secretary Alex Azar declared a public health emergency on Jan. 31, 2020. The health emergency has been renewed several times, most recently in late July. The FDA allowed the use of the shots with just two months of safety data under an EUA. It’s not the same as a Biologic License Application, or a request for full approval, which requires at least six months of data.
Before granting full approval, FDA scientists must painstakingly look through the companies’ clinical trial data, including for any discrepancies or safety concerns, said Offit, who is also director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
It’s a lot of data, Offit said. He previously said when Merck submitted its data from its 70,000-person rotavirus vaccine trial, the pages that were generated could have exceeded the height of the Sears Tower — a 1,450-foot skyscraper in Chicago that’s now known as Willis Tower.
“The FDA will do what it thinks it needs to do to make sure that the American public is safe,” he said.
Full approval is also very beneficial to companies that submit an application, former FDA Commissioner Dr. Robert Califf said in a phone interview in May.
With it, Pfizer and BioNTech are now able to market the shots directly to U.S. consumers. Companies can’t promote their products under an EUA, he said. It also allows the shot to stay on the market once the pandemic is over and the U.S. is no longer considered in an “emergency.”
“The vaccines will still have to be administered under the supervision of a professional who’s qualified,” Califf said. “It’s not like they can send the vaccines to people’s homes. However, they can advertise on TV and promote their products under the watchful eye of the FDA.”
Pfizer and BioNTech have said they expect to generate billions from the vaccine. Under full approval, the companies could also decide to charge more for the vaccines, health experts say.
The companies have already raised the price of their vaccine in the European Union, according to the Financial Times. They are now charging $23 per dose, up from their previous price of $18.40, according to the report.
Pfizer and BioNTech also plan to ask the FDA to approve a third dose as a booster shot following full approval. Last week, the Biden administration said it was preparing to offer booster shots to all eligible Americans beginning the week of Sept. 20.
___
www.cnbc.com
The FDA Just Granted FULL APPROVAL to the Exceedingly Dangerous and Deadly Pfizer-BioNTech Covid ‘Vaccines’!
Posted on August 23, 2021 by State of the Nation
FacebookTwitterPinterestRedditEmailShare
FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
Berkeley Lovelace Jr.
CNBC
KEY POINTS
The FDA granted Pfizer and BioNTech full U.S. approval of their Covid-19 vaccine.
The move may encourage some unvaccinated Americans to get the shots as well as give more private businesses across the nation greater confidence to implement vaccine mandates.
Up until now, the mRNA vaccine was on the U.S. market under an Emergency Use Authorization.
The Food and Drug Administration on Monday granted full approval to Pfizer and BioNTech Covid-19 vaccine – becoming the first in the U.S. to win the coveted designation and giving even more businesses, schools and universities greater confidence to adopt vaccine mandates.
Up until now, the mRNA vaccine, which will be marketed as Comirnaty, was on the U.S. market under an Emergency Use Authorization that was granted by the FDA in December. Since then, more than 204 million of the Pfizer shots have been administered, according to data compiled by the Centers for Disease Control and Prevention.
Federal health officials had been under mounting pressure from the scientific community and advocacy groups to fully approve Pfizer and BioNTech’s vaccine ever since the drugmakers submitted their application to the agency in early May. The companies submitted a Biologics License Application, which secures full approval, to the FDA on May 7 for patients age 16 and up.
FDA scientists evaluated “hundreds of thousands of pages” of vaccine data from 40,000 trial participants, according to the U.S. agency. The vaccine was found to be 91% effective in preventing Covid – slightly lower than the 95% efficacy rate trial data showed when the shot was authorized late last year and before the delta variant took hold in the U.S.
Pfizer’s vaccine met the agency’s “high standards for safety, effectiveness, and manufacturing quality,” acting FDA Commissioner Janet Woodcock said in a statement. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated.”
The FDA held a media briefing at 11 a.m. Monday to discuss the approval.
Although more than 60% of the total U.S. population has had at least one dose of a Covid vaccine, many Americans say they are still hesitant about getting vaccinated, even as the highly contagious delta variant spreads. Full approval may convince some Americans that the shots are safe, doctors and epidemiologists say. In fact, a survey from the Kaiser Family Foundation found 3 in 10 unvaccinated adults said they would be more likely to get vaccinated if one of the vaccines receives full approval.
Full approval is “more psychological than anything else,” said Dr. Paul Offit, a voting member of the agency’s Vaccines and Related Biological Products Advisory Committee. “I mean you already have more than 320 million doses administered that are out there. The vaccines already have an enormous safety and efficacy profile.”
U.S. approval is also likely to spur a new wave of vaccine mandates from corporate America. Major companies – from Walt Disney to Walmart – have already told some or all of their employees that they must get fully vaccinated against Covid this fall. Still, some private businesses may have felt hesitant about requiring the shots, before full approval, even though they had the legal authority to do so, said Dorit Reiss, a professor of law at UC Hastings College of the Law.
The Pentagon said it would make vaccinations mandatory for service members “no later” than the middle of September, or sooner if the FDA grants full approval earlier.
“You’re going to see the empowerment of local enterprises, giving mandates that could be colleges, universities, places of business, a whole variety and I strongly support that,” White House chief medical officer Dr. Anthony Fauci said Aug 8, when asked about full approval of the vaccines. “The time has come. … We’ve got to go the extra step to get people vaccinated.”
Pfizer’s shot is the first Covid vaccine to receive full regulatory approval in the U.S. Federal regulators had previously said they would work as quickly as possible to clear Pfizer’s vaccines.
The vaccine is still under emergency use authorization for children 12 to 15 as the company continues to collect data. Dr. Peter Marks, the FDA’s top vaccine regulator, said Monday the agency would move as “swiftly” as possible on approving the shot for kids under 12 once the company submits the data.
“Currently, there are still trials ongoing and so the agency has to wait for the company to submit the data for those trials,” he said during a briefing. “We certainly want to make sure that we get it right.”
Standard vaccine reviews generally take several months to a year or more to determine whether they are safe and effective for use in the general public. But due to the pandemic, which has killed more than 628,000 Americans, the FDA permitted the use of the shots under an EUA.
In a public health emergency, the manufacturing and approval of vaccines can be streamlined through emergency authorizations. Former Health Secretary Alex Azar declared a public health emergency on Jan. 31, 2020. The health emergency has been renewed several times, most recently in late July. The FDA allowed the use of the shots with just two months of safety data under an EUA. It’s not the same as a Biologic License Application, or a request for full approval, which requires at least six months of data.
Before granting full approval, FDA scientists must painstakingly look through the companies’ clinical trial data, including for any discrepancies or safety concerns, said Offit, who is also director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
It’s a lot of data, Offit said. He previously said when Merck submitted its data from its 70,000-person rotavirus vaccine trial, the pages that were generated could have exceeded the height of the Sears Tower — a 1,450-foot skyscraper in Chicago that’s now known as Willis Tower.
“The FDA will do what it thinks it needs to do to make sure that the American public is safe,” he said.
Full approval is also very beneficial to companies that submit an application, former FDA Commissioner Dr. Robert Califf said in a phone interview in May.
With it, Pfizer and BioNTech are now able to market the shots directly to U.S. consumers. Companies can’t promote their products under an EUA, he said. It also allows the shot to stay on the market once the pandemic is over and the U.S. is no longer considered in an “emergency.”
“The vaccines will still have to be administered under the supervision of a professional who’s qualified,” Califf said. “It’s not like they can send the vaccines to people’s homes. However, they can advertise on TV and promote their products under the watchful eye of the FDA.”
Pfizer and BioNTech have said they expect to generate billions from the vaccine. Under full approval, the companies could also decide to charge more for the vaccines, health experts say.
The companies have already raised the price of their vaccine in the European Union, according to the Financial Times. They are now charging $23 per dose, up from their previous price of $18.40, according to the report.
Pfizer and BioNTech also plan to ask the FDA to approve a third dose as a booster shot following full approval. Last week, the Biden administration said it was preparing to offer booster shots to all eligible Americans beginning the week of Sept. 20.
___
FDA grants full approval to Pfizer-BioNTech’s Covid shot, clearing path to more vaccine mandates
The FDA's approval of the Pfizer and BioNTech Covid shot will likely spur more businesses to adopt vaccine mandates for workers.
mwengeso
JF-Expert Member
- Nov 27, 2014
- 9,227
- 6,670
Kama wako jasiri waliochanjwa wakapime iwapo miili yao imezalisha kinga dhidi ya UVIKO-19
Yawezekana wanaotoa taarifa kuhusu chanjo za UVIKO-19 si wanasayansi ila ni walevi wa gongo na mataputapu. Ina maana wewe ni mtaalamu amvaye baada ya kuwa umezisikiliza umefikia hitimisho lako hilo.
Mimi niliyesikiliza kuna moja hii. https://z-28b3jxzl1og7.bitchute.com/gCBOKmrTndsE/NZU2pSlZiI5M.mp4
Hiyo video clip ni mahojiano ya Mtaalamu wa chanjo, anayeshimika duniani. Anasema chanjo yoyote ya virusi hutengenezwa kwa ajili ya aina hiyo ya kirusi tu. Kirusi cha korona kinabadilika kila kukicha kiasi kutengeneza chanjo ni changamoto (muda na gharama). Hivyo chanjo zilizipo zimeidhinishwa kwa hati ya dharura kwa kuwa ufanisi na usalama wake haujathibitishwa.
Je, kwa hoja hizo wewe, MTAALAMU, una maoni gani?
mwengeso
JF-Expert Member
- Nov 27, 2014
- 9,227
- 6,670
Kulingana na chapisho na mahojiano na wanasayansi ya virusi na chanjo, chanjo za mRNA zimetengenezwa mfano wa kirusi cha korona ambacho hutumia "protein spike" kupenya kwenye seli za kinga ndani ya mwili wa binadamu. Lakini imethibitishwa ndani ya maabara kuwa "protein spike" ni sumu mwilini. Itakuwaje pale chanjo hizo, zilizotengenezwa kwa jinsi hiyo "protein spike" zitakaposambaa mwilini mwa aliyechanjwa?
Mathanzua
JF-Expert Member
- Jan 4, 2017
- 17,251
- 22,929
- Thread starter
- #635
Updates:
Data: Most in new surge of Israel’s Covid cases were vaccinated
By World Tribune
The vast majority of new serious cases of Covid in Israel are vaccinated individuals, author and independent journalist Alex Berenson noted.
Serious cases of the virus “have risen 10-fold since the beginning of July — from roughly five a day to about 40 over the last week,” Berenson said in an Aug. 3 report. “The overall number of patients has soared too — from 30 to more than 200.”
Israel and the UK “are much better at providing data than the United States — they provide updates every day, which limits their opportunities to manipulate it,” he noted.
Related: Repercussions of Pfizer vaccine debated in Israel, out of the public eye, July 28, 2021
That data shows that, throughout July, most new Covid patients at hospitals were vaccinated.
The trend among serious illness in older vaccinated people “is terrible,” Berenson noted. “The rate of cases has risen 12-fold IN A MONTH. On July 4, fewer than 1 older vaccinated person in 100,000 became seriously ill. Today the rate is 10 in 100,000.”
Berenson continued: “It is worth noting that rates of serious illness among the vaccinated are now as high as they were among the unvaccinated only TWO WEEKS AGO. Perhaps that’s why the Israeli government is now predicting a further quadrupling of new serious cases by the end of August.”
A quadrupling would represent 800 serious cases. That would approaching the peak of the winter surge, which Berenson noted was “probably fueled by a spike in cases following the first vaccine dose.”
Israel can’t blame the unvaccinated for the surge in new cases, Berenson noted, as around 85 percent of adults over 30 are fully vaccinated, well above the range experts said would provide herd immunity.
“And yet instead of pulling back and at least considering a pause on vaccinations as it digests the disaster of the last month, Israel is going the other way — pushing a third dose on the elderly,” Berenson wrote.
“Meanwhile the cry to mandate or quasi-mandate vaccinations in the United States is only getting louder.”
www.jamiiforums.com
Data: Most in new surge of Israel’s Covid cases were vaccinated
By World Tribune
The vast majority of new serious cases of Covid in Israel are vaccinated individuals, author and independent journalist Alex Berenson noted.
Serious cases of the virus “have risen 10-fold since the beginning of July — from roughly five a day to about 40 over the last week,” Berenson said in an Aug. 3 report. “The overall number of patients has soared too — from 30 to more than 200.”
Israel and the UK “are much better at providing data than the United States — they provide updates every day, which limits their opportunities to manipulate it,” he noted.
Related: Repercussions of Pfizer vaccine debated in Israel, out of the public eye, July 28, 2021
That data shows that, throughout July, most new Covid patients at hospitals were vaccinated.
The trend among serious illness in older vaccinated people “is terrible,” Berenson noted. “The rate of cases has risen 12-fold IN A MONTH. On July 4, fewer than 1 older vaccinated person in 100,000 became seriously ill. Today the rate is 10 in 100,000.”
Berenson continued: “It is worth noting that rates of serious illness among the vaccinated are now as high as they were among the unvaccinated only TWO WEEKS AGO. Perhaps that’s why the Israeli government is now predicting a further quadrupling of new serious cases by the end of August.”
A quadrupling would represent 800 serious cases. That would approaching the peak of the winter surge, which Berenson noted was “probably fueled by a spike in cases following the first vaccine dose.”
Israel can’t blame the unvaccinated for the surge in new cases, Berenson noted, as around 85 percent of adults over 30 are fully vaccinated, well above the range experts said would provide herd immunity.
“And yet instead of pulling back and at least considering a pause on vaccinations as it digests the disaster of the last month, Israel is going the other way — pushing a third dose on the elderly,” Berenson wrote.
“Meanwhile the cry to mandate or quasi-mandate vaccinations in the United States is only getting louder.”
Most people in new surge of Israel’s Covid cases are vaccinated.
By World Tribune The vast majority of new serious cases of Covid in Israel are vaccinated individuals, author and independent journalist Alex Berenson noted. Serious cases of the virus “have risen 10-fold since the beginning of July — from roughly five a day to about 40 over the last week,”...
mwengeso
JF-Expert Member
- Nov 27, 2014
- 9,227
- 6,670
Mfano wa Israel, nchi iliyo mbali na Tz hauwezi kuwaamsha usingizini mashabiki wa chanjo. Nchi jirani, ambazo zimekuwa zikichujua hatua kali dhidi ya UVIKO-19 na sasa kulazimisha chanjo, maambukizi na vifo ni kama kawaUpdates:
Data: Most in new surge of Israel’s Covid cases were vaccinated
By World Tribune
The vast majority of new serious cases of Covid in Israel are vaccinated individuals, author and independent journalist Alex Berenson noted.
Serious cases of the virus “have risen 10-fold since the beginning of July — from roughly five a day to about 40 over the last week,” Berenson said in an Aug. 3 report. “The overall number of patients has soared too — from 30 to more than 200.”
Israel and the UK “are much better at providing data than the United States — they provide updates every day, which limits their opportunities to manipulate it,” he noted.
Related: Repercussions of Pfizer vaccine debated in Israel, out of the public eye, July 28, 2021
That data shows that, throughout July, most new Covid patients at hospitals were vaccinated.
The trend among serious illness in older vaccinated people “is terrible,” Berenson noted. “The rate of cases has risen 12-fold IN A MONTH. On July 4, fewer than 1 older vaccinated person in 100,000 became seriously ill. Today the rate is 10 in 100,000.”
Berenson continued: “It is worth noting that rates of serious illness among the vaccinated are now as high as they were among the unvaccinated only TWO WEEKS AGO. Perhaps that’s why the Israeli government is now predicting a further quadrupling of new serious cases by the end of August.”
A quadrupling would represent 800 serious cases. That would approaching the peak of the winter surge, which Berenson noted was “probably fueled by a spike in cases following the first vaccine dose.”
Israel can’t blame the unvaccinated for the surge in new cases, Berenson noted, as around 85 percent of adults over 30 are fully vaccinated, well above the range experts said would provide herd immunity.
“And yet instead of pulling back and at least considering a pause on vaccinations as it digests the disaster of the last month, Israel is going the other way — pushing a third dose on the elderly,” Berenson wrote. “Meanwhile the cry to mandate or quasi-mandate vaccinations in the United States is only getting louder.”
Most people in new surge of Israel’s Covid cases are vaccinated.
By World Tribune The vast majority of new serious cases of Covid in Israel are vaccinated individuals, author and independent journalist Alex Berenson noted. Serious cases of the virus “have risen 10-fold since the beginning of July — from roughly five a day to about 40 over the last week,”...
Mathanzua
JF-Expert Member
- Jan 4, 2017
- 17,251
- 22,929
- Thread starter
- #639
Updates:Most covid deaths now occurring in “fully vaccinated” people
by: Ethan Huff
(Natural News) The government of the United Kingdom has released new data showing that the vast majority of “delta variant” deaths are occurring among people who got “fully vaccinated” for the Wuhan coronavirus (Covid-19).
Only one third of all deaths supposedly caused by the delta variant are occurring in people who did not get the jab, which clearly shows that “Operation Warp Speed” is an utter failure – assuming that “saving lives” was the goal, anyway.
From February 1 through August 2, the U.K. recorded 742 deaths allegedly caused by the delta variant. Of these, 402 were fully vaccinated while 79 had received just one shot. The remaining 253 cases were unvaccinated.
You can view the official government report outlining the data at this link.
“If you get covid having been vaccinated, according to this data, you are much more likely to die than if you were not vaccinated!” writes Chris Waldburger on his Substack.
“Obviously some allowance must be made for more elderly people being vaccinated, but not enough to change the bottom line: This vaccine is not nearly as effective as advertised.”
Covid vaccinations must stop in the best interest of public health
In every country where Fauci Flu shot uptake is high, including in Israel, deaths and hospitalizations are soaring.
A whopping 60 percent of all new hospitalizations in Israel are “fully vaccinated” patients who are now being told by their government that they need a third “booster” shot in order to stay “safe” against vaccine-caused mutations.
“The powers that be will not admit there is something terribly wrong,” Waldburger adds, calling for “a complete recalibration of global policy” as “the only moral option” here.
“They will not acknowledge the clear science that people with natural immunity, and the young and healthy, do not need to take the risks of these injections.”
Waldburger also explains that natural immunity, meaning real immunity, is the best way to go. Vaccine-induced “immunity,” if you can even call it that, lasts for only a very short time at best. At worst, it destroys natural immunity forever, leaving a person prone to a lifetime of disease.
You can learn more about natural immunity and why it is superior to vaccine-induced “immunity.”
How many more new “variants” will emerge from the booster shots?
Now that this is becoming widely apparent with Wuhan Flu shots, governments around the world are ramping up the booster shot propaganda, claiming that a semi-annual injection is necessary for the “fully vaccinated” to stay “immune” to disease.
This makes no sense, of course, as the first two jabs clearly did nothing to promote immunity while leaving the injected prone to disease. The apparent hope, however, is that the injected will turn off their brains and just obey the orders.
Once the booster shot campaign really gets going and additional needles are plunged into arms, we expect a slew of new “variants,” likely even more deadly than the last, which will drive calls for a fourth booster, and so on and so forth, forever.
The plan would seem to be to so destroy people’s immune systems with these shots that they are forever reliant upon Big Pharma and the government to give them their next hit of “immunity” every six months or so.
“The truth is probably that the 253 unvaccinated deaths were from other causes, not covid or delta,” speculated one commenter at Chris Waldburger’s blog.
“Historians will look back and call this the malignant hypochondria era,” wrote another. “So there really is something going around that’s far more pernicious than Covid-19.”
Chinese Virus injections are a death sentence. To keep up with the latest, visit ChemicalViolence.com.
Sources for this article include:
ChrisWaldburger.Substack.com
Gov.uk
NaturalNews.com
Biznews.com
by: Ethan Huff
(Natural News) The government of the United Kingdom has released new data showing that the vast majority of “delta variant” deaths are occurring among people who got “fully vaccinated” for the Wuhan coronavirus (Covid-19).
Only one third of all deaths supposedly caused by the delta variant are occurring in people who did not get the jab, which clearly shows that “Operation Warp Speed” is an utter failure – assuming that “saving lives” was the goal, anyway.
From February 1 through August 2, the U.K. recorded 742 deaths allegedly caused by the delta variant. Of these, 402 were fully vaccinated while 79 had received just one shot. The remaining 253 cases were unvaccinated.
You can view the official government report outlining the data at this link.
“If you get covid having been vaccinated, according to this data, you are much more likely to die than if you were not vaccinated!” writes Chris Waldburger on his Substack.
“Obviously some allowance must be made for more elderly people being vaccinated, but not enough to change the bottom line: This vaccine is not nearly as effective as advertised.”
Covid vaccinations must stop in the best interest of public health
In every country where Fauci Flu shot uptake is high, including in Israel, deaths and hospitalizations are soaring.
A whopping 60 percent of all new hospitalizations in Israel are “fully vaccinated” patients who are now being told by their government that they need a third “booster” shot in order to stay “safe” against vaccine-caused mutations.
“The powers that be will not admit there is something terribly wrong,” Waldburger adds, calling for “a complete recalibration of global policy” as “the only moral option” here.
“They will not acknowledge the clear science that people with natural immunity, and the young and healthy, do not need to take the risks of these injections.”
Waldburger also explains that natural immunity, meaning real immunity, is the best way to go. Vaccine-induced “immunity,” if you can even call it that, lasts for only a very short time at best. At worst, it destroys natural immunity forever, leaving a person prone to a lifetime of disease.
You can learn more about natural immunity and why it is superior to vaccine-induced “immunity.”
How many more new “variants” will emerge from the booster shots?
Now that this is becoming widely apparent with Wuhan Flu shots, governments around the world are ramping up the booster shot propaganda, claiming that a semi-annual injection is necessary for the “fully vaccinated” to stay “immune” to disease.
This makes no sense, of course, as the first two jabs clearly did nothing to promote immunity while leaving the injected prone to disease. The apparent hope, however, is that the injected will turn off their brains and just obey the orders.
Once the booster shot campaign really gets going and additional needles are plunged into arms, we expect a slew of new “variants,” likely even more deadly than the last, which will drive calls for a fourth booster, and so on and so forth, forever.
The plan would seem to be to so destroy people’s immune systems with these shots that they are forever reliant upon Big Pharma and the government to give them their next hit of “immunity” every six months or so.
“The truth is probably that the 253 unvaccinated deaths were from other causes, not covid or delta,” speculated one commenter at Chris Waldburger’s blog.
“Historians will look back and call this the malignant hypochondria era,” wrote another. “So there really is something going around that’s far more pernicious than Covid-19.”
Chinese Virus injections are a death sentence. To keep up with the latest, visit ChemicalViolence.com.
Sources for this article include:
ChrisWaldburger.Substack.com
Gov.uk
NaturalNews.com
Biznews.com
mwengeso
JF-Expert Member
- Nov 27, 2014
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This is very seriuosUpdates:Most covid deaths now occurring in “fully vaccinated” people
by: Ethan Huff
(Natural News) The government of the United Kingdom has released new data showing that the vast majority of “delta variant” deaths are occurring among people who got “fully vaccinated” for the Wuhan coronavirus (Covid-19).
Only one third of all deaths supposedly caused by the delta variant are occurring in people who did not get the jab, which clearly shows that “Operation Warp Speed” is an utter failure – assuming that “saving lives” was the goal, anyway.
From February 1 through August 2, the U.K. recorded 742 deaths allegedly caused by the delta variant. Of these, 402 were fully vaccinated while 79 had received just one shot. The remaining 253 cases were unvaccinated.
You can view the official government report outlining the data at this link.
“If you get covid having been vaccinated, according to this data, you are much more likely to die than if you were not vaccinated!” writes Chris Waldburger on his Substack.
“Obviously some allowance must be made for more elderly people being vaccinated, but not enough to change the bottom line: This vaccine is not nearly as effective as advertised.”
Covid vaccinations must stop in the best interest of public health
In every country where Fauci Flu shot uptake is high, including in Israel, deaths and hospitalizations are soaring.
A whopping 60 percent of all new hospitalizations in Israel are “fully vaccinated” patients who are now being told by their government that they need a third “booster” shot in order to stay “safe” against vaccine-caused mutations.
“The powers that be will not admit there is something terribly wrong,” Waldburger adds, calling for “a complete recalibration of global policy” as “the only moral option” here.
“They will not acknowledge the clear science that people with natural immunity, and the young and healthy, do not need to take the risks of these injections.”
Waldburger also explains that natural immunity, meaning real immunity, is the best way to go. Vaccine-induced “immunity,” if you can even call it that, lasts for only a very short time at best. At worst, it destroys natural immunity forever, leaving a person prone to a lifetime of disease.
You can learn more about natural immunity and why it is superior to vaccine-induced “immunity.”
How many more new “variants” will emerge from the booster shots?
Now that this is becoming widely apparent with Wuhan Flu shots, governments around the world are ramping up the booster shot propaganda, claiming that a semi-annual injection is necessary for the “fully vaccinated” to stay “immune” to disease.
This makes no sense, of course, as the first two jabs clearly did nothing to promote immunity while leaving the injected prone to disease. The apparent hope, however, is that the injected will turn off their brains and just obey the orders.
Once the booster shot campaign really gets going and additional needles are plunged into arms, we expect a slew of new “variants,” likely even more deadly than the last, which will drive calls for a fourth booster, and so on and so forth, forever.
The plan would seem to be to so destroy people’s immune systems with these shots that they are forever reliant upon Big Pharma and the government to give them their next hit of “immunity” every six months or so.
“The truth is probably that the 253 unvaccinated deaths were from other causes, not covid or delta,” speculated one commenter at Chris Waldburger’s blog.
“Historians will look back and call this the malignant hypochondria era,” wrote another. “So there really is something going around that’s far more pernicious than Covid-19.”
Chinese Virus injections are a death sentence. To keep up with the latest, visit ChemicalViolence.com.
Sources for this article include:
ChrisWaldburger.Substack.com
Gov.uk
NaturalNews.com
Biznews.com
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Most covid deaths now occurring in “fully vaccinated” people – NaturalNews.com
The government of the United Kingdom has released new data showing that the vast majority of “delta variant” deaths are occurring among people who got “fully vaccinated” for the Wuhan coronavirus (Covid-19). Only one third of all deaths supposedly caused by the delta variant are occurring in...www.naturalnews.com