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Lawsuit to stop the uses of c***d v*****es
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Jul 23, 2021 08:39:48   #
Redangel62
 
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es

Secretary of Health and Human Services Xavier Becerra speaks to the press in Washington on May 5, 2021. (Drew Angerer/Getty Images)MORE
V*****ES & SAFETY
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es
Lawsuit citing whistleblower's claim that the true deaths following v******tion are much higher than reported
BY LI HAI
July 22, 2021 Updated: July 22, 2021

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the e*******y use a***********n (EUA) of C****-** v*****es for three groups of Americans: anyone under the age of 18, anyone who has recovered from C****-**, and those who haven’t given informed consent as defined by federal law.

The motion was filed against Xavier Becerra, Secretary of the Department of Health and Human Services (HHS), and other defendants in a federal district court in the Northern District of Alabama.

“The emergency declaration and its multiple renewals are illegal,” the complaint (pdf) alleges.

According to the Federal Food, Drug, and Cosmetic Act, when the HHS secretary declares that an emergency use is appropriate, the FDA (Food and Drug Administration) may then authorize unapproved use or EUA of a v*****e.

On Feb. 4, 2020, then-HHS Secretary Alex Azar declared a public health emergency, saying that existing circumstances justify the EUA.

The complaint alleges that the legal requirements to issue and maintain C****-** v*****e EUAs aren’t being met.

Department of Health and Human Services in Washington on Sept. 16, 2011. (Susan Stierch/CC 4.0)
MOST READ

Pennsylvania Decertifies County’s V****g System, Cites Violation of E******n Code
First, there’s no underlying emergency and no “serious or life-threatening disease or condition,” the complaint states.

According to the defendants’ data, the CCP v***s has an overall survivability rate of 99.8 percent globally, “on a par with the seasonal flu.”

However, the defendants’ data is deliberately inflated, the complaint alleges. It claims that HHS has changed the rules applicable to people responsible for writing death certificates and requires them to make cause of death determinations primarily attributable to C****-**. From last March, death certificates indicated “C****-** [as] being the underlying cause more often than not.”

RELATED

FDA Grants Eli Lilly’s Experimental C****-** Antibody-Drug E*******y Use A***********n
The way in which C****-** is diagnosed, using magnified values from PCR tests that were also authorized for emergency use, guarantees “an unacceptably high number of false-positive results,” the complaint states.

Second, C****-** v*****es aren’t effective in diagnosing, treating, or preventing a disease or condition, which fails another requirement for issuing and maintaining EUAs.

The complaint cites data from the Centers for Disease Control and Prevention (CDC) that says a total of 10,262 CCP v***s breakthrough infections (detection of SARS-COV-2 within 14 or more days after receiving required dosages of a C****-** v*****e) were reported between Jan. 1 and April 30.

“It is important to note that the v*****es were only shown to reduce symptoms—not block t***smission,” the complaint reads.

Third, the benefits don’t outweigh the known and potential risks of each v*****e. Those risks are especially increased in reproductive health, potential death, neurological damage, more virulent strains, and others.

And lastly, there are adequate, approved, and available alternatives to the v*****es, such as Ivermectin, Budesonide, Hydroxychloroquine, and others.

Not Adequately Informed
The plaintiffs also allege that health care professionals and v*****e candidates aren’t being adequately informed about the v*****es, as the federal law requires.

“No one ever provided me with any information regarding possible adverse reactions, nor did they provide me with any information regarding alternative treatments. I did not understand this was gene therapy rather than a traditional v*****e. Again, I also did not understand that the v*****es were not ‘approved’ by the FDA,” plaintiff Angelia Deselle said in a declaration included in the lawsuit.

The V*****e A*****e E***t Reporting System (V***S) was established to provide information regarding a*****e e***ts potentially caused by v*****es. The complaint states that V***S isn’t accurate and that the federal government is failing to provide data from other sources, such as the military, Medicare, and Medicaid.

According to the complaint, a patient can’t give informed consent without an understanding of the risks.

Under-18 Age Group and Those Recovered From C****-**
“CDC data indicates that children under 18 have a 99.998 percent C****-** recovery rate with no treatment,” the complaint reads. “Injecting this under-18 subpopulation with the V*****es threatens them with immediate, potentially life-threatening harm.”

Last month, the CDC said that more than 1,200 cases of heart inflammation in adolescents and young adults were reported following the administration of P****r’s or M*****a’s two-dose v*****es.

“There is no public interest in subjecting children to experimental v******tion programs, to protect them from a disease that does not threaten them,” Dr. Angelina Farella, a pediatrician who has actively practiced for over 25 years, said in a statement. Farella is an expert for America’s Frontline Doctors.


Syringes with the P****r-BioNTech v*****es lie on a tray during a program without an appointment, in Sant Vicenc de Castellet, north of Barcelona, Spain, on July 6, 2021. (Albert Gea/Reuters)
The complaint also asserts that Americans who have recovered from C****-** shouldn’t get v******ted.

It cites a recent Cleveland Clinic study that demonstrates that natural immunity through prior infection is stronger than any benefit conferred by a C****-** v*****e. Another study, published in the New England Journal of Medicine, shows that of those with preexisting C****-** immunity, 89 percent reported adverse side-effects after receiving the first v*****e injection.

“C***D recovered patients are at extremely high risk to a v*****e,” plaintiffs’ expert Dr. Richard Urso said in a statement. “They have all the requisite components of immune memory. V******tion may activate a hyperimmune response leading to a significant tissue injury and possibly death.”

Whistleblower Testimony: 45,000 Deaths Following V******tions
Jane Doe, a computer programmer with expertise in the health care data analytics field, filed a sworn statement indicating that the actual number of deaths following the C****-** v******tion is about 45,000.

“It is my professional estimate that V***S database, while extremely useful, is under-reported by a conservative factor of at least 5. On July 9, 2021, there were 9,048 deaths reported in V***S,” Jane Doe said in her statement (pdf).

“I queried data from CMS medical claims with regard to v*****es and patient deaths, and have assessed that the deaths occurring within 3 days of v******tion are higher than those reported in V***S by a factor of at least 5. This would indicate the true number of v*****e-related deaths was at least 45,000.”

Jane Doe noted that the swine flu v*****e was taken off the market because of 53 deaths reported following v******tion.

“The evidence makes it irrefutable that Plaintiffs and others in the public will suffer irreparable injury … if this motion is denied,” the plaintiffs asserted. “Finally, the evidence tilts the balance of hardships and public interest … decisively in favor of Plaintiffs.”

In an email to The Epoch Times, HHS declined to comment on the lawsuit, saying, “As a matter of policy, we do not comment on pending litigation.”

President Joe Biden has praised the v*****es as safe and effective.

“You know, some people have questions about how quickly the v*****es were developed. They say they’ve been developed so quickly, they can’t be that good. Well, here’s what you need to know: V*****es were developed over a decade of research in similar v***ses, and they’ve gone through strict FDA clinical trials,” Biden said last month.

“The bottom line is this—I promise you: They are safe. They are safe. And even more importantly, they’re extremely effective.”

The Biden administration announced earlier this month that it would begin a door-to-door outreach campaign in targeted communities to boost C****-** v******tion rates.

Reply
Jul 23, 2021 08:54:32   #
Sonny Magoo Loc: Where pot pie is boiled in a kettle
 
Thank you for sharing this information.
It confirms much of what I have already been shown, experienced, or had understood.
Big Pharma =big lies and big profits.
..and F***i is right in the middle.

Reply
Jul 23, 2021 09:06:44   #
lpnmajor Loc: Arkansas
 
Redangel62 wrote:
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es

Secretary of Health and Human Services Xavier Becerra speaks to the press in Washington on May 5, 2021. (Drew Angerer/Getty Images)MORE
V*****ES & SAFETY
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es
Lawsuit citing whistleblower's claim that the true deaths following v******tion are much higher than reported
BY LI HAI
July 22, 2021 Updated: July 22, 2021

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the e*******y use a***********n (EUA) of C****-** v*****es for three groups of Americans: anyone under the age of 18, anyone who has recovered from C****-**, and those who haven’t given informed consent as defined by federal law.

The motion was filed against Xavier Becerra, Secretary of the Department of Health and Human Services (HHS), and other defendants in a federal district court in the Northern District of Alabama.

“The emergency declaration and its multiple renewals are illegal,” the complaint (pdf) alleges.

According to the Federal Food, Drug, and Cosmetic Act, when the HHS secretary declares that an emergency use is appropriate, the FDA (Food and Drug Administration) may then authorize unapproved use or EUA of a v*****e.

On Feb. 4, 2020, then-HHS Secretary Alex Azar declared a public health emergency, saying that existing circumstances justify the EUA.

The complaint alleges that the legal requirements to issue and maintain C****-** v*****e EUAs aren’t being met.

Department of Health and Human Services in Washington on Sept. 16, 2011. (Susan Stierch/CC 4.0)
MOST READ

Pennsylvania Decertifies County’s V****g System, Cites Violation of E******n Code
First, there’s no underlying emergency and no “serious or life-threatening disease or condition,” the complaint states.

According to the defendants’ data, the CCP v***s has an overall survivability rate of 99.8 percent globally, “on a par with the seasonal flu.”

However, the defendants’ data is deliberately inflated, the complaint alleges. It claims that HHS has changed the rules applicable to people responsible for writing death certificates and requires them to make cause of death determinations primarily attributable to C****-**. From last March, death certificates indicated “C****-** [as] being the underlying cause more often than not.”

RELATED

FDA Grants Eli Lilly’s Experimental C****-** Antibody-Drug E*******y Use A***********n
The way in which C****-** is diagnosed, using magnified values from PCR tests that were also authorized for emergency use, guarantees “an unacceptably high number of false-positive results,” the complaint states.

Second, C****-** v*****es aren’t effective in diagnosing, treating, or preventing a disease or condition, which fails another requirement for issuing and maintaining EUAs.

The complaint cites data from the Centers for Disease Control and Prevention (CDC) that says a total of 10,262 CCP v***s breakthrough infections (detection of SARS-COV-2 within 14 or more days after receiving required dosages of a C****-** v*****e) were reported between Jan. 1 and April 30.

“It is important to note that the v*****es were only shown to reduce symptoms—not block t***smission,” the complaint reads.

Third, the benefits don’t outweigh the known and potential risks of each v*****e. Those risks are especially increased in reproductive health, potential death, neurological damage, more virulent strains, and others.

And lastly, there are adequate, approved, and available alternatives to the v*****es, such as Ivermectin, Budesonide, Hydroxychloroquine, and others.

Not Adequately Informed
The plaintiffs also allege that health care professionals and v*****e candidates aren’t being adequately informed about the v*****es, as the federal law requires.

“No one ever provided me with any information regarding possible adverse reactions, nor did they provide me with any information regarding alternative treatments. I did not understand this was gene therapy rather than a traditional v*****e. Again, I also did not understand that the v*****es were not ‘approved’ by the FDA,” plaintiff Angelia Deselle said in a declaration included in the lawsuit.

The V*****e A*****e E***t Reporting System (V***S) was established to provide information regarding a*****e e***ts potentially caused by v*****es. The complaint states that V***S isn’t accurate and that the federal government is failing to provide data from other sources, such as the military, Medicare, and Medicaid.

According to the complaint, a patient can’t give informed consent without an understanding of the risks.

Under-18 Age Group and Those Recovered From C****-**
“CDC data indicates that children under 18 have a 99.998 percent C****-** recovery rate with no treatment,” the complaint reads. “Injecting this under-18 subpopulation with the V*****es threatens them with immediate, potentially life-threatening harm.”

Last month, the CDC said that more than 1,200 cases of heart inflammation in adolescents and young adults were reported following the administration of P****r’s or M*****a’s two-dose v*****es.

“There is no public interest in subjecting children to experimental v******tion programs, to protect them from a disease that does not threaten them,” Dr. Angelina Farella, a pediatrician who has actively practiced for over 25 years, said in a statement. Farella is an expert for America’s Frontline Doctors.


Syringes with the P****r-BioNTech v*****es lie on a tray during a program without an appointment, in Sant Vicenc de Castellet, north of Barcelona, Spain, on July 6, 2021. (Albert Gea/Reuters)
The complaint also asserts that Americans who have recovered from C****-** shouldn’t get v******ted.

It cites a recent Cleveland Clinic study that demonstrates that natural immunity through prior infection is stronger than any benefit conferred by a C****-** v*****e. Another study, published in the New England Journal of Medicine, shows that of those with preexisting C****-** immunity, 89 percent reported adverse side-effects after receiving the first v*****e injection.

“C***D recovered patients are at extremely high risk to a v*****e,” plaintiffs’ expert Dr. Richard Urso said in a statement. “They have all the requisite components of immune memory. V******tion may activate a hyperimmune response leading to a significant tissue injury and possibly death.”

Whistleblower Testimony: 45,000 Deaths Following V******tions
Jane Doe, a computer programmer with expertise in the health care data analytics field, filed a sworn statement indicating that the actual number of deaths following the C****-** v******tion is about 45,000.

“It is my professional estimate that V***S database, while extremely useful, is under-reported by a conservative factor of at least 5. On July 9, 2021, there were 9,048 deaths reported in V***S,” Jane Doe said in her statement (pdf).

“I queried data from CMS medical claims with regard to v*****es and patient deaths, and have assessed that the deaths occurring within 3 days of v******tion are higher than those reported in V***S by a factor of at least 5. This would indicate the true number of v*****e-related deaths was at least 45,000.”

Jane Doe noted that the swine flu v*****e was taken off the market because of 53 deaths reported following v******tion.

“The evidence makes it irrefutable that Plaintiffs and others in the public will suffer irreparable injury … if this motion is denied,” the plaintiffs asserted. “Finally, the evidence tilts the balance of hardships and public interest … decisively in favor of Plaintiffs.”

In an email to The Epoch Times, HHS declined to comment on the lawsuit, saying, “As a matter of policy, we do not comment on pending litigation.”

President Joe Biden has praised the v*****es as safe and effective.

“You know, some people have questions about how quickly the v*****es were developed. They say they’ve been developed so quickly, they can’t be that good. Well, here’s what you need to know: V*****es were developed over a decade of research in similar v***ses, and they’ve gone through strict FDA clinical trials,” Biden said last month.

“The bottom line is this—I promise you: They are safe. They are safe. And even more importantly, they’re extremely effective.”

The Biden administration announced earlier this month that it would begin a door-to-door outreach campaign in targeted communities to boost C****-** v******tion rates.
Nonprofit Sues HHS to Immediately Stop E*******y U... (show quote)



Reply
 
 
Jul 23, 2021 09:38:14   #
microphor Loc: Home is TN
 
Redangel62 wrote:
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es

Secretary of Health and Human Services Xavier Becerra speaks to the press in Washington on May 5, 2021. (Drew Angerer/Getty Images)MORE
V*****ES & SAFETY
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es
Lawsuit citing whistleblower's claim that the true deaths following v******tion are much higher than reported
BY LI HAI
July 22, 2021 Updated: July 22, 2021

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the e*******y use a***********n (EUA) of C****-** v*****es for three groups of Americans: anyone under the age of 18, anyone who has recovered from C****-**, and those who haven’t given informed consent as defined by federal law.

The motion was filed against Xavier Becerra, Secretary of the Department of Health and Human Services (HHS), and other defendants in a federal district court in the Northern District of Alabama.

“The emergency declaration and its multiple renewals are illegal,” the complaint (pdf) alleges.

According to the Federal Food, Drug, and Cosmetic Act, when the HHS secretary declares that an emergency use is appropriate, the FDA (Food and Drug Administration) may then authorize unapproved use or EUA of a v*****e.

On Feb. 4, 2020, then-HHS Secretary Alex Azar declared a public health emergency, saying that existing circumstances justify the EUA.

The complaint alleges that the legal requirements to issue and maintain C****-** v*****e EUAs aren’t being met.

Department of Health and Human Services in Washington on Sept. 16, 2011. (Susan Stierch/CC 4.0)
MOST READ

Pennsylvania Decertifies County’s V****g System, Cites Violation of E******n Code
First, there’s no underlying emergency and no “serious or life-threatening disease or condition,” the complaint states.

According to the defendants’ data, the CCP v***s has an overall survivability rate of 99.8 percent globally, “on a par with the seasonal flu.”

However, the defendants’ data is deliberately inflated, the complaint alleges. It claims that HHS has changed the rules applicable to people responsible for writing death certificates and requires them to make cause of death determinations primarily attributable to C****-**. From last March, death certificates indicated “C****-** [as] being the underlying cause more often than not.”

RELATED

FDA Grants Eli Lilly’s Experimental C****-** Antibody-Drug E*******y Use A***********n
The way in which C****-** is diagnosed, using magnified values from PCR tests that were also authorized for emergency use, guarantees “an unacceptably high number of false-positive results,” the complaint states.

Second, C****-** v*****es aren’t effective in diagnosing, treating, or preventing a disease or condition, which fails another requirement for issuing and maintaining EUAs.

The complaint cites data from the Centers for Disease Control and Prevention (CDC) that says a total of 10,262 CCP v***s breakthrough infections (detection of SARS-COV-2 within 14 or more days after receiving required dosages of a C****-** v*****e) were reported between Jan. 1 and April 30.

“It is important to note that the v*****es were only shown to reduce symptoms—not block t***smission,” the complaint reads.

Third, the benefits don’t outweigh the known and potential risks of each v*****e. Those risks are especially increased in reproductive health, potential death, neurological damage, more virulent strains, and others.

And lastly, there are adequate, approved, and available alternatives to the v*****es, such as Ivermectin, Budesonide, Hydroxychloroquine, and others.

Not Adequately Informed
The plaintiffs also allege that health care professionals and v*****e candidates aren’t being adequately informed about the v*****es, as the federal law requires.

“No one ever provided me with any information regarding possible adverse reactions, nor did they provide me with any information regarding alternative treatments. I did not understand this was gene therapy rather than a traditional v*****e. Again, I also did not understand that the v*****es were not ‘approved’ by the FDA,” plaintiff Angelia Deselle said in a declaration included in the lawsuit.

The V*****e A*****e E***t Reporting System (V***S) was established to provide information regarding a*****e e***ts potentially caused by v*****es. The complaint states that V***S isn’t accurate and that the federal government is failing to provide data from other sources, such as the military, Medicare, and Medicaid.

According to the complaint, a patient can’t give informed consent without an understanding of the risks.

Under-18 Age Group and Those Recovered From C****-**
“CDC data indicates that children under 18 have a 99.998 percent C****-** recovery rate with no treatment,” the complaint reads. “Injecting this under-18 subpopulation with the V*****es threatens them with immediate, potentially life-threatening harm.”

Last month, the CDC said that more than 1,200 cases of heart inflammation in adolescents and young adults were reported following the administration of P****r’s or M*****a’s two-dose v*****es.

“There is no public interest in subjecting children to experimental v******tion programs, to protect them from a disease that does not threaten them,” Dr. Angelina Farella, a pediatrician who has actively practiced for over 25 years, said in a statement. Farella is an expert for America’s Frontline Doctors.


Syringes with the P****r-BioNTech v*****es lie on a tray during a program without an appointment, in Sant Vicenc de Castellet, north of Barcelona, Spain, on July 6, 2021. (Albert Gea/Reuters)
The complaint also asserts that Americans who have recovered from C****-** shouldn’t get v******ted.

It cites a recent Cleveland Clinic study that demonstrates that natural immunity through prior infection is stronger than any benefit conferred by a C****-** v*****e. Another study, published in the New England Journal of Medicine, shows that of those with preexisting C****-** immunity, 89 percent reported adverse side-effects after receiving the first v*****e injection.

“C***D recovered patients are at extremely high risk to a v*****e,” plaintiffs’ expert Dr. Richard Urso said in a statement. “They have all the requisite components of immune memory. V******tion may activate a hyperimmune response leading to a significant tissue injury and possibly death.”

Whistleblower Testimony: 45,000 Deaths Following V******tions
Jane Doe, a computer programmer with expertise in the health care data analytics field, filed a sworn statement indicating that the actual number of deaths following the C****-** v******tion is about 45,000.

“It is my professional estimate that V***S database, while extremely useful, is under-reported by a conservative factor of at least 5. On July 9, 2021, there were 9,048 deaths reported in V***S,” Jane Doe said in her statement (pdf).

“I queried data from CMS medical claims with regard to v*****es and patient deaths, and have assessed that the deaths occurring within 3 days of v******tion are higher than those reported in V***S by a factor of at least 5. This would indicate the true number of v*****e-related deaths was at least 45,000.”

Jane Doe noted that the swine flu v*****e was taken off the market because of 53 deaths reported following v******tion.

“The evidence makes it irrefutable that Plaintiffs and others in the public will suffer irreparable injury … if this motion is denied,” the plaintiffs asserted. “Finally, the evidence tilts the balance of hardships and public interest … decisively in favor of Plaintiffs.”

In an email to The Epoch Times, HHS declined to comment on the lawsuit, saying, “As a matter of policy, we do not comment on pending litigation.”

President Joe Biden has praised the v*****es as safe and effective.

“You know, some people have questions about how quickly the v*****es were developed. They say they’ve been developed so quickly, they can’t be that good. Well, here’s what you need to know: V*****es were developed over a decade of research in similar v***ses, and they’ve gone through strict FDA clinical trials,” Biden said last month.

“The bottom line is this—I promise you: They are safe. They are safe. And even more importantly, they’re extremely effective.”

The Biden administration announced earlier this month that it would begin a door-to-door outreach campaign in targeted communities to boost C****-** v******tion rates.
Nonprofit Sues HHS to Immediately Stop E*******y U... (show quote)


Nobody come to my door, you will have some hurt feelings when you leave and remember "if you hurt a Dems feelings, they are going to need a crying room and some therapy!

Reply
Jul 23, 2021 09:38:56   #
microphor Loc: Home is TN
 
Sonny Magoo wrote:
Thank you for sharing this information.
It confirms much of what I have already been shown, experienced, or had understood.
Big Pharma =big lies and big profits.
..and F***i is right in the middle.


agree

Reply
Jul 23, 2021 09:54:36   #
Redangel62
 
microphor wrote:
Nobody come to my door, you will have some hurt feelings when you leave and remember "if you hurt a Dems feelings, they are going to need a crying room and some therapy!


In Michigan if you hurt a libs feeling soon will be doing 20 years in jail. They are attempting to pass that law!

Reply
Jul 23, 2021 10:54:46   #
SGM B Loc: TEXAS but live in Alabama now
 
Redangel62 wrote:
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es

Secretary of Health and Human Services Xavier Becerra speaks to the press in Washington on May 5, 2021. (Drew Angerer/Getty Images)MORE
V*****ES & SAFETY
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es
Lawsuit citing whistleblower's claim that the true deaths following v******tion are much higher than reported
BY LI HAI
July 22, 2021 Updated: July 22, 2021

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the e*******y use a***********n (EUA) of C****-** v*****es for three groups of Americans: anyone under the age of 18, anyone who has recovered from C****-**, and those who haven’t given informed consent as defined by federal law.

The motion was filed against Xavier Becerra, Secretary of the Department of Health and Human Services (HHS), and other defendants in a federal district court in the Northern District of Alabama.

“The emergency declaration and its multiple renewals are illegal,” the complaint (pdf) alleges.

According to the Federal Food, Drug, and Cosmetic Act, when the HHS secretary declares that an emergency use is appropriate, the FDA (Food and Drug Administration) may then authorize unapproved use or EUA of a v*****e.

On Feb. 4, 2020, then-HHS Secretary Alex Azar declared a public health emergency, saying that existing circumstances justify the EUA.

The complaint alleges that the legal requirements to issue and maintain C****-** v*****e EUAs aren’t being met.

Department of Health and Human Services in Washington on Sept. 16, 2011. (Susan Stierch/CC 4.0)
MOST READ

Pennsylvania Decertifies County’s V****g System, Cites Violation of E******n Code
First, there’s no underlying emergency and no “serious or life-threatening disease or condition,” the complaint states.

According to the defendants’ data, the CCP v***s has an overall survivability rate of 99.8 percent globally, “on a par with the seasonal flu.”

However, the defendants’ data is deliberately inflated, the complaint alleges. It claims that HHS has changed the rules applicable to people responsible for writing death certificates and requires them to make cause of death determinations primarily attributable to C****-**. From last March, death certificates indicated “C****-** [as] being the underlying cause more often than not.”

RELATED

FDA Grants Eli Lilly’s Experimental C****-** Antibody-Drug E*******y Use A***********n
The way in which C****-** is diagnosed, using magnified values from PCR tests that were also authorized for emergency use, guarantees “an unacceptably high number of false-positive results,” the complaint states.

Second, C****-** v*****es aren’t effective in diagnosing, treating, or preventing a disease or condition, which fails another requirement for issuing and maintaining EUAs.

The complaint cites data from the Centers for Disease Control and Prevention (CDC) that says a total of 10,262 CCP v***s breakthrough infections (detection of SARS-COV-2 within 14 or more days after receiving required dosages of a C****-** v*****e) were reported between Jan. 1 and April 30.

“It is important to note that the v*****es were only shown to reduce symptoms—not block t***smission,” the complaint reads.

Third, the benefits don’t outweigh the known and potential risks of each v*****e. Those risks are especially increased in reproductive health, potential death, neurological damage, more virulent strains, and others.

And lastly, there are adequate, approved, and available alternatives to the v*****es, such as Ivermectin, Budesonide, Hydroxychloroquine, and others.

Not Adequately Informed
The plaintiffs also allege that health care professionals and v*****e candidates aren’t being adequately informed about the v*****es, as the federal law requires.

“No one ever provided me with any information regarding possible adverse reactions, nor did they provide me with any information regarding alternative treatments. I did not understand this was gene therapy rather than a traditional v*****e. Again, I also did not understand that the v*****es were not ‘approved’ by the FDA,” plaintiff Angelia Deselle said in a declaration included in the lawsuit.

The V*****e A*****e E***t Reporting System (V***S) was established to provide information regarding a*****e e***ts potentially caused by v*****es. The complaint states that V***S isn’t accurate and that the federal government is failing to provide data from other sources, such as the military, Medicare, and Medicaid.

According to the complaint, a patient can’t give informed consent without an understanding of the risks.

Under-18 Age Group and Those Recovered From C****-**
“CDC data indicates that children under 18 have a 99.998 percent C****-** recovery rate with no treatment,” the complaint reads. “Injecting this under-18 subpopulation with the V*****es threatens them with immediate, potentially life-threatening harm.”

Last month, the CDC said that more than 1,200 cases of heart inflammation in adolescents and young adults were reported following the administration of P****r’s or M*****a’s two-dose v*****es.

“There is no public interest in subjecting children to experimental v******tion programs, to protect them from a disease that does not threaten them,” Dr. Angelina Farella, a pediatrician who has actively practiced for over 25 years, said in a statement. Farella is an expert for America’s Frontline Doctors.


Syringes with the P****r-BioNTech v*****es lie on a tray during a program without an appointment, in Sant Vicenc de Castellet, north of Barcelona, Spain, on July 6, 2021. (Albert Gea/Reuters)
The complaint also asserts that Americans who have recovered from C****-** shouldn’t get v******ted.

It cites a recent Cleveland Clinic study that demonstrates that natural immunity through prior infection is stronger than any benefit conferred by a C****-** v*****e. Another study, published in the New England Journal of Medicine, shows that of those with preexisting C****-** immunity, 89 percent reported adverse side-effects after receiving the first v*****e injection.

“C***D recovered patients are at extremely high risk to a v*****e,” plaintiffs’ expert Dr. Richard Urso said in a statement. “They have all the requisite components of immune memory. V******tion may activate a hyperimmune response leading to a significant tissue injury and possibly death.”

Whistleblower Testimony: 45,000 Deaths Following V******tions
Jane Doe, a computer programmer with expertise in the health care data analytics field, filed a sworn statement indicating that the actual number of deaths following the C****-** v******tion is about 45,000.

“It is my professional estimate that V***S database, while extremely useful, is under-reported by a conservative factor of at least 5. On July 9, 2021, there were 9,048 deaths reported in V***S,” Jane Doe said in her statement (pdf).

“I queried data from CMS medical claims with regard to v*****es and patient deaths, and have assessed that the deaths occurring within 3 days of v******tion are higher than those reported in V***S by a factor of at least 5. This would indicate the true number of v*****e-related deaths was at least 45,000.”

Jane Doe noted that the swine flu v*****e was taken off the market because of 53 deaths reported following v******tion.

“The evidence makes it irrefutable that Plaintiffs and others in the public will suffer irreparable injury … if this motion is denied,” the plaintiffs asserted. “Finally, the evidence tilts the balance of hardships and public interest … decisively in favor of Plaintiffs.”

In an email to The Epoch Times, HHS declined to comment on the lawsuit, saying, “As a matter of policy, we do not comment on pending litigation.”

President Joe Biden has praised the v*****es as safe and effective.

“You know, some people have questions about how quickly the v*****es were developed. They say they’ve been developed so quickly, they can’t be that good. Well, here’s what you need to know: V*****es were developed over a decade of research in similar v***ses, and they’ve gone through strict FDA clinical trials,” Biden said last month.

“The bottom line is this—I promise you: They are safe. They are safe. And even more importantly, they’re extremely effective.”

The Biden administration announced earlier this month that it would begin a door-to-door outreach campaign in targeted communities to boost C****-** v******tion rates.
Nonprofit Sues HHS to Immediately Stop E*******y U... (show quote)


I believe Bribem is a liar, and so are his “handlers”, oh - and he is not only full of himself, he is full of crap!
By the way, if you come to my door without prior permission or a warrant, you are trespassing on private by property - ignore the NO TRESPASSING signs at your own peril.

Reply
 
 
Jul 23, 2021 11:54:36   #
microphor Loc: Home is TN
 
SGM B wrote:
I believe Bribem is a liar, and so are his “handlers”, oh - and he is not only full of himself, he is full of crap!
By the way, if you come to my door without prior permission or a warrant, you are trespassing on private by property - ignore the NO TRESPASSING signs at your own peril.



Reply
Jul 23, 2021 12:08:27   #
Redangel62
 
SGM B wrote:
I believe Bribem is a liar, and so are his “handlers”, oh - and he is not only full of himself, he is full of crap!
By the way, if you come to my door without prior permission or a warrant, you are trespassing on private by property - ignore the NO TRESPASSING signs at your own peril.


I want them to come! Have a ton of questions to ask them about their health! Like do you have hiv? Whens the last time you had sex with your partner? Hepatitis? Yeast infection?

Reply
Jul 23, 2021 17:00:31   #
SGM B Loc: TEXAS but live in Alabama now
 
Redangel62 wrote:
I want them to come! Have a ton of questions to ask them about their health! Like do you have hiv? Whens the last time you had sex with your partner? Hepatitis? Yeast infection?


Or, when was the last time you had sex with your dead brothers wife? When was the first time, was he dead then???

Reply
Jul 23, 2021 17:56:12   #
Redangel62
 
SGM B wrote:
Or, when was the last time you had sex with your dead brothers wife? When was the first time, was he dead then???


Also good questions. If they can knock in my door asking about my personal info, ill ask back

Reply
 
 
Jul 24, 2021 16:48:38   #
BBZ Loc: Long Island, NY
 
Redangel62 wrote:
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es

Secretary of Health and Human Services Xavier Becerra speaks to the press in Washington on May 5, 2021. (Drew Angerer/Getty Images)MORE
V*****ES & SAFETY
Nonprofit Sues HHS to Immediately Stop E*******y Use A***********n of C****-** V*****es
Lawsuit citing whistleblower's claim that the true deaths following v******tion are much higher than reported
BY LI HAI
July 22, 2021 Updated: July 22, 2021

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the e*******y use a***********n (EUA) of C****-** v*****es for three groups of Americans: anyone under the age of 18, anyone who has recovered from C****-**, and those who haven’t given informed consent as defined by federal law.

The motion was filed against Xavier Becerra, Secretary of the Department of Health and Human Services (HHS), and other defendants in a federal district court in the Northern District of Alabama.

“The emergency declaration and its multiple renewals are illegal,” the complaint (pdf) alleges.

According to the Federal Food, Drug, and Cosmetic Act, when the HHS secretary declares that an emergency use is appropriate, the FDA (Food and Drug Administration) may then authorize unapproved use or EUA of a v*****e.

On Feb. 4, 2020, then-HHS Secretary Alex Azar declared a public health emergency, saying that existing circumstances justify the EUA.

The complaint alleges that the legal requirements to issue and maintain C****-** v*****e EUAs aren’t being met.

Department of Health and Human Services in Washington on Sept. 16, 2011. (Susan Stierch/CC 4.0)
MOST READ

Pennsylvania Decertifies County’s V****g System, Cites Violation of E******n Code
First, there’s no underlying emergency and no “serious or life-threatening disease or condition,” the complaint states.

According to the defendants’ data, the CCP v***s has an overall survivability rate of 99.8 percent globally, “on a par with the seasonal flu.”

However, the defendants’ data is deliberately inflated, the complaint alleges. It claims that HHS has changed the rules applicable to people responsible for writing death certificates and requires them to make cause of death determinations primarily attributable to C****-**. From last March, death certificates indicated “C****-** [as] being the underlying cause more often than not.”

RELATED

FDA Grants Eli Lilly’s Experimental C****-** Antibody-Drug E*******y Use A***********n
The way in which C****-** is diagnosed, using magnified values from PCR tests that were also authorized for emergency use, guarantees “an unacceptably high number of false-positive results,” the complaint states.

Second, C****-** v*****es aren’t effective in diagnosing, treating, or preventing a disease or condition, which fails another requirement for issuing and maintaining EUAs.

The complaint cites data from the Centers for Disease Control and Prevention (CDC) that says a total of 10,262 CCP v***s breakthrough infections (detection of SARS-COV-2 within 14 or more days after receiving required dosages of a C****-** v*****e) were reported between Jan. 1 and April 30.

“It is important to note that the v*****es were only shown to reduce symptoms—not block t***smission,” the complaint reads.

Third, the benefits don’t outweigh the known and potential risks of each v*****e. Those risks are especially increased in reproductive health, potential death, neurological damage, more virulent strains, and others.

And lastly, there are adequate, approved, and available alternatives to the v*****es, such as Ivermectin, Budesonide, Hydroxychloroquine, and others.

Not Adequately Informed
The plaintiffs also allege that health care professionals and v*****e candidates aren’t being adequately informed about the v*****es, as the federal law requires.

“No one ever provided me with any information regarding possible adverse reactions, nor did they provide me with any information regarding alternative treatments. I did not understand this was gene therapy rather than a traditional v*****e. Again, I also did not understand that the v*****es were not ‘approved’ by the FDA,” plaintiff Angelia Deselle said in a declaration included in the lawsuit.

The V*****e A*****e E***t Reporting System (V***S) was established to provide information regarding a*****e e***ts potentially caused by v*****es. The complaint states that V***S isn’t accurate and that the federal government is failing to provide data from other sources, such as the military, Medicare, and Medicaid.

According to the complaint, a patient can’t give informed consent without an understanding of the risks.

Under-18 Age Group and Those Recovered From C****-**
“CDC data indicates that children under 18 have a 99.998 percent C****-** recovery rate with no treatment,” the complaint reads. “Injecting this under-18 subpopulation with the V*****es threatens them with immediate, potentially life-threatening harm.”

Last month, the CDC said that more than 1,200 cases of heart inflammation in adolescents and young adults were reported following the administration of P****r’s or M*****a’s two-dose v*****es.

“There is no public interest in subjecting children to experimental v******tion programs, to protect them from a disease that does not threaten them,” Dr. Angelina Farella, a pediatrician who has actively practiced for over 25 years, said in a statement. Farella is an expert for America’s Frontline Doctors.


Syringes with the P****r-BioNTech v*****es lie on a tray during a program without an appointment, in Sant Vicenc de Castellet, north of Barcelona, Spain, on July 6, 2021. (Albert Gea/Reuters)
The complaint also asserts that Americans who have recovered from C****-** shouldn’t get v******ted.

It cites a recent Cleveland Clinic study that demonstrates that natural immunity through prior infection is stronger than any benefit conferred by a C****-** v*****e. Another study, published in the New England Journal of Medicine, shows that of those with preexisting C****-** immunity, 89 percent reported adverse side-effects after receiving the first v*****e injection.

“C***D recovered patients are at extremely high risk to a v*****e,” plaintiffs’ expert Dr. Richard Urso said in a statement. “They have all the requisite components of immune memory. V******tion may activate a hyperimmune response leading to a significant tissue injury and possibly death.”

Whistleblower Testimony: 45,000 Deaths Following V******tions
Jane Doe, a computer programmer with expertise in the health care data analytics field, filed a sworn statement indicating that the actual number of deaths following the C****-** v******tion is about 45,000.

“It is my professional estimate that V***S database, while extremely useful, is under-reported by a conservative factor of at least 5. On July 9, 2021, there were 9,048 deaths reported in V***S,” Jane Doe said in her statement (pdf).

“I queried data from CMS medical claims with regard to v*****es and patient deaths, and have assessed that the deaths occurring within 3 days of v******tion are higher than those reported in V***S by a factor of at least 5. This would indicate the true number of v*****e-related deaths was at least 45,000.”

Jane Doe noted that the swine flu v*****e was taken off the market because of 53 deaths reported following v******tion.

“The evidence makes it irrefutable that Plaintiffs and others in the public will suffer irreparable injury … if this motion is denied,” the plaintiffs asserted. “Finally, the evidence tilts the balance of hardships and public interest … decisively in favor of Plaintiffs.”

In an email to The Epoch Times, HHS declined to comment on the lawsuit, saying, “As a matter of policy, we do not comment on pending litigation.”

President Joe Biden has praised the v*****es as safe and effective.

“You know, some people have questions about how quickly the v*****es were developed. They say they’ve been developed so quickly, they can’t be that good. Well, here’s what you need to know: V*****es were developed over a decade of research in similar v***ses, and they’ve gone through strict FDA clinical trials,” Biden said last month.

“The bottom line is this—I promise you: They are safe. They are safe. And even more importantly, they’re extremely effective.”

The Biden administration announced earlier this month that it would begin a door-to-door outreach campaign in targeted communities to boost C****-** v******tion rates.
Nonprofit Sues HHS to Immediately Stop E*******y U... (show quote)


America's Frontline Doctors is an American right-wing political organization known for spreading misinformation about the C****-** p******c. Founded by Simone Gold and promoted by the Tea Party Patriots, it has opposed lockdowns and social distancing mandates during the C****-** p******c by citing alleged and unapproved treatments for C****-**.

In January 2021, Gold and the group's communications director John Strand were both arrested in connection with the 2021 United States Capitol attack.

Reply
Jul 24, 2021 17:02:45   #
Redangel62
 
BBZ wrote:
America's Frontline Doctors is an American right-wing political organization known for spreading misinformation about the C****-** p******c. Founded by Simone Gold and promoted by the Tea Party Patriots, it has opposed lockdowns and social distancing mandates during the C****-** p******c by citing alleged and unapproved treatments for C****-**.

In January 2021, Gold and the group's communications director John Strand were both arrested in connection with the 2021 United States Capitol attack.
America's Frontline Doctors is an American right-w... (show quote)



Reply
Jul 24, 2021 17:40:55   #
BBZ Loc: Long Island, NY
 
You are a true Trump Republican, facts do not matter. However, conspiracy theorists are to be believed.

Reply
Jul 24, 2021 17:51:54   #
Redangel62
 
BBZ wrote:
You are a true Trump Republican, facts do not matter. However, conspiracy theorists are to be believed.


Fact
So God so oved the wold much he sent his only begotten son, so whoever believes in him shall not die but have everlasting life

Reply
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