Elon Releases It All ~ The Twitter/FBI Files

youtu.be/fnPGM5Ugpko

Elon Musk has exposed a coordinated effort by the intelligent community to influence the censorship of the Hunter Biden laptop story two weeks before the 2020 presidential election.

Elon Musk is known for being one of the most forward-thinking and innovative businessmen in the world. But what happens when he takes on the establishment? Watch this video to find out.

youtu.be/fnPGM5Ugpko

What Do the Records Reveal About Covid-19 Vaccine and Boosters?

Here’s just a few that have been uncovered

Rest assured, this is just the tip of the iceberg……there’s more

FOIA Judicial Watch has uncovered a substantial amount of information regarding COVID-19 issues:

  • In October 2020, Judicial Watch received FDA records that detailed pressure for COVID-19 vaccine booster approval and use.
  • NIH records revealed an FBI “inquiry” into the NIH’s controversial bat coronavirus grant tied to the Wuhan Institute of Virology. The records also show National Institute of Allergy and Infectious Diseases (NIAID) officials were concerned about “gain-of-function” research in China’s Wuhan Institute of Virology in 2016. The Fauci agency was also concerned about EcoHealth Alliance’s lack of compliance with reporting rules and use of gain-of-function research in the NIH-funded research involving bat coronaviruses in Wuhan, China.
  • HHS records revealed that from 2014 to 2019, $826,277 was given to the Wuhan Institute of Virology for bat coronavirus research by the NIAID.
  • NIAID records showed that it gave nine China-related grants to EcoHealth Alliance to research coronavirus emergence in bats and was the NIH’s top issuer of grants to the Wuhan lab itself. The records also included an email from the vice director of the Wuhan Lab asking an NIH official for help finding disinfectants for decontamination of airtight suits and indoor surfaces.
  • HHS records included an “urgent for Dr. Fauci ” email chain, citing ties between the Wuhan lab and the taxpayer-funded EcoHealth Alliance. The government emails also reported that the foundation of U.S. billionaire Bill Gates worked closely with the Chinese government to pave the way for Chinese-produced medications to be sold outside China and help “raise China’s voice of governance by placing representatives from China on important international counsels as high level commitment from China.”
  • HHS records included a grant application for research involving the coronavirus that appears to describe “gain-of-function” research involving RNA extractions from bats, experiments on viruses, attempts to develop a chimeric virus and efforts to genetically manipulate the full-length bat SARSr-CoV WIV1 strain molecular clone.
  • HHS records showed the State Department and NIAID knew immediately in January 2020 that China was withholding COVID data, which was hindering risk assessment and response by public health officials.
  • University of Texas Medical Branch (UTMB) records show the former director of the Galveston National Laboratory at the University of Texas Medical Branch (UTMB), Dr. James W. Le Duc warned Chinese researchers at the Wuhan Institute of Virology of potential investigations into the COVID issue by Congress.
  • HHS records regarding biodistribution studies and related data for the COVID-19 vaccines show a key component of the vaccines developed by Pfizer/BioNTech, lipid nanoparticles (LNPs), were found outside the injection site, mainly the liver, adrenal glands, spleen and ovaries of test animals, eight to 48 hours after injection.
  • Records from the Federal Select Agent Program (FSAP) reveal safety lapses and violations at U.S. biosafety laboratories that conduct research on dangerous agents and toxins.
  • HHS records include emails between National Institutes of Health (NIH) then-Director Francis Collins and Anthony Fauci, the director of National Institute of Allergy and Infectious Diseases (NIAID), about hydroxychloroquine and COVID-19.
  • HHS records show that NIH officials tailored confidentiality forms to China’s terms and that the World Health Organization (WHO) conducted an unreleased, “strictly confidential” COVID-19 epidemiological analysis in January 2020.
  • Fauci emails include his approval of a press release supportive of China’s response to the 2019 novel coronavirus.

A “Pharmacokinetics Written Summary” marked “Confidential,” indicates that the information it contains is related to the mRNA-1273 (Moderna vaccine) strain, however, much of the data comes from work with mRNA-1647. The study states:

The results of a biodistribution study of mRNA-1647 support the development of mRNA-1273.

***

The biodistribution of mRNA-1647 was evaluated in a non-Good Laboratory Practice (GLP), single-dose, intramuscular (IM) injection study in Sprague Dawley rats…. mRNAs that are within an LNP of the same composition (e.g., mRNA-1273 and mRNA-1647) are expected to distribute similarly.

  • No absorption studies with mRNA-1273 [used in Moderna’s COVID vaccine] have been performed.
  • No metabolism studies with mRNA-1273 have been performed.
  • No excretion studies with mRNA-1273 have been performed.
  • No PK [pharmacokinetic] studies with mRNA-1273 have been performed.
  • No other PK studies with mRNA-1273 have been performed.

The “Summary” indicates:

According to PubMed.gov, “Pharmacokinetics studies are performed to clarify the absorption, distribution, metabolism, and excretion of drug candidates…[and] are required for establishing the efficacy and safety in humans.”)

A separate study submitted to the FDA sponsored by Moderna Therapeutics Inc. and conducted by Charles River Laboratories in Montreal, Canada is titled “A Single Dose Intramuscular Injection Tissue Distribution Study of mRNA-1647 in Male Sprague-Dawley Rats” in which “[t]he objective … was to determine the tissue distribution of mRNA-1647,” as opposed to mRNA-1273 used in Moderna’s COVID vaccine.

In one appendix to the study, a “clarification” was issued in the toxicokinetic report regarding the half-life of mRNA injected into the rats, noting:The average value of terminal half-life for the muscle (i.e. injection site) in Sections 4.2 and 5 of the toxicokinetic report should be read 14.9 [hours] instead of 8.39 [hours] based on the results of the toxicokinetic evaluation.”

The study further notes that the wording of the conclusion was modified to read, “The half-life … of mRNA-1647 was reliably estimated in muscle (site of injection), proximal popliteal and axillary distal lymph nodes, and spleen with average values for all construct t½ [half-life] of 14.9 8.39, 34.8, 31.1 and 63.0 hours, respectively.” [Emphasis in original]

Another appendix, titled “Summary Mean (±SE) mRNA-1647 Pharmacokinetic Parameters in Sprague-Dawley Rat in Plasma and Tissues Following 100μg Intramuscular Injection Administration of mRNA-1647 on Day 1,” reveals that, in addition to distributing to the muscle site, lymph nodes and spleen, the mRNA particles also distributed to the bone marrow, brain, eyes, heart, liver, lungs, stomach and testes.

A separate study indicates that the mRNA-1647 particles injected into rats were “observed in muscle (i.e. site of injection), followed by proximal (popliteal) lymph nodes, axillary lymph nodes and spleen, suggesting the mRNA-1647 distribution to the circulation by lymph flow.” (The mRNA was delivered via “lipid nanoparticle dispersion.”)

“These previously hidden records about the COVID-19 vaccine safety and efficacy studies raise a number of disturbing questions,” said Judicial Watch President Tom Fitton. “The fact that it has taken a federal lawsuit to get access to this material is yet another scandal.”

Sources :

FAUCI EMAILS

80X More Deaths Following COVID-19 Shots than Influenza Vaccines 2020 through 2022

December 18, 2022

80X More Deaths Following COVID-19 Shots than Influenza Vaccines 2020 through 2022

by Brian Shilhavy
Editor, Health Impact News

An examination of the U.S. Government’s Vaccine Adverse Events Reporting System(VAERS) reveals that since the Fall of 2020 through today, people injected with COVID-19 shots die 80 times more frequently following those shots, than people who die after being injected with the flu shots.

Also, people receiving a COVID-19 shot suffer side effects 40 times more frequently than people who are injected with flu shots.

Here are the current stats in VAERS for people receiving a COVID-19 shot since they were issued an emergency use authorization in December of 2020. (Source.)

Here are the stats for the flu shots since September of 2020 (beginning of the “Flu season”.) (Source.)

To determine the rate of side effects and deaths suffered from these shots, we need the number of doses distributed for these time periods, and we find those numbers on the CDC website.

Total doses of COVID-19 shots distributed to date are 931,341,585. (Source.)

Total doses of flu shots distributed from September 2020 through December 10, 2022 are 527,610,000. Number of doses for the 2020-2021 and 2021-2022 flu seasons are found here, and total doses for the current 2022-2023 flu season through December 10, 2022 are found here.

Based on these numbers supplied by the U.S. Government, one person dies for every 2,284,026 flu shots, while one person dies for every 28,370 COVID-19 shots, which is a rate 80 times higher than the flu shots.

One person is suffering a side effect for every 25,217 flu shots, while one person is suffering a side effect for every 629 COVID-19 shots, which is a rate 40 times higher than the flu shots.

What is interesting about the CDC’s report on doses of COVID-19 shots distributed, is that even though 931,341,585 doses have been distributed, only 660,400,812 doses have been administered. So only 70% of the COVID-19 “vaccines” the U.S. Government has purchased have actually been injected into people. The other 30% presumably were discarded, or will be discarded after they reach their expiration date.

That of course makes the rate of people dying and suffering injuries following injections of COVID-19 shots even higher!

  • 1 death per 20,117 shots
  • 1 side effect per 446 shots

I do not know if statistics exist for the ratio of shots distributed to shots administered for the flu shots, which is why for comparison purposes we need to use the “shots distributed” statistics.

Governor DeSantis, Dr. Ladapo, and Other Florida Doctors are LYING About the Safety of Childhood Vaccines!

How about other vaccines that are approved by the FDA and part of the CDC childhood vaccination schedule?

At a recent event in Florida with Governor Ron DeSantis and his Surgeon General Joseph Ladapo, several other doctors sat a round table to discuss how COVID-19 shots were harmful and should NOT be recommended for children. See:

Why Hasn’t Governor DeSantis Stopped the COVID Vaccines in Florida When He Admits They are Killing People?

However, some of these doctors that sat at the table told parents to not stop injecting their children with other vaccines, and told them that these vaccines were “safe and effective.” One doctor, Dr. Joseph Friaman, even emphatically stated that other childhood vaccines had nearly no side effects. He said that they were rare, “1 in a million.”

Listen to their own words:

Let’s “fact check” this.

The U.S. National Vaccine Injury Compensation Program keeps stats on the number of doses distributed for all FDA-approved vaccines that are on the CDC childhood vaccination schedule. You can view those stats covering the time period of 01/01/2006 through 12/31/2021 at the U.S. Government website here.

During those years, there were over 4 billion doses of vaccines distributed (4,093,221,119).

Next, we can do a search in VAERS to see how many deaths and side effects were recorded from these vaccines during that same time period. The results are here.

During these years, there were 553,216 injuries and deaths recorded in VAERS from all non-COVID vaccines. That means a side effect from these vaccines was recorded in VAERS for about every 7,400 shots distributed.

That’s a lot more than 1 out of a million, as Dr. Friaman claimed! And of course the actual numbers are much HIGHER than this, because a report contracted out by the U.S. Government in 2011 found that less than 1% of all vaccine injuries are ever reported to VAERS. (Source.)

Here is the list of the vaccine manufacturers from VAERS that produced these vaccines that caused all these injuries and deaths, and each of these companies, especially the ones at the top of the list, have a criminal rap sheet where they have paid out $BILLIONS in criminal settlements.

So these doctors admit the COVID shots are bad, but they want you to trust them that all other vaccines, produced by the same corrupt companies, are somehow “safe”?

They can’t even prove these vaccines are effective! Dr. Bhattacharya mentioned the polio and MMR vaccines, and these are two of the biggest scams in the history of vaccines!

No child is dying in the U.S. today from measles, but many do die and are injured from the measles (MMR combo vaccine) vaccine.

All cases of polio today come from the vaccines. Please educate yourself on these non-COVID vaccines and the tremendous fraud surrounding them.

Here is an article I published earlier this year on the polio vaccine, and when you listen to Dr. Suzanne Humphries’ presentation on the history of the polio vaccine, you will see much of the same fraud we just observed with the COVID shots. The playbook doesn’t change much over the years.

The Polio Scam Makes a Comeback to Scare More Parents into Vaccinating Their Children – Vaccines NEVER Eradicated Polio: Vaccines CAUSE Polio

Also, the CDC has refused over the years to study the health of children who follow the CDC childhood vaccination schedule and are fully vaccinated versus parents who choose not to vaccinate their children, and for good reason, because unvaccinated children are clearly much healthier. See:

Unvaccinated Children are Healthier than Vaccinated Children – Most Censored Topic in the U.S.?

Source: https://healthimpactnews.com/

Pfizer and Clear Creek collaborate on SARS-CoV-2 PLpro inhibitors for COVID-19

Pfizer and Clear Creek collaborate on SARS-CoV-2 PLpro inhibitors for COVID-19

Microscope and coronavirus illustration
Microscope and coronavirus illustration

Dec. 7, 2022

Pfizer Inc. and Clear Creek Bio Inc. have entered into a research collaboration and exclusive license agreement to advance the discovery and development of potential inhibitors of the SARS-CoV-2 papain-like protease (PLpro) for the oral treatment of COVID-19. PLpro is an essential enzyme, which, along with the main protease (Mpro), plays an important role in viral replication. Under the agreement, the two companies will work together to identify a PLpro candidate to progress into the clinic, at which time Pfizer will be solely responsible for further development and commercialization activities. Clear Creek Bio will receive an undisclosed upfront payment and will be eligible to receive additional potential milestone payments plus royalties on future product sales (Pfizer News Release).

Source: https://www.bioworld.com/articles/692088-pfizer-and-clear-creek-collaborate-on-sars-cov-2-plpro-inhibitors-for-covid-19

Wake Up America. You’ve Been Conned. Only An Estimated 9,683 Covid-19 Only Deaths So Far In 2020, Not 180,000

About half-way down the screen page The Center for Health Statistics August 26, 2020 update on provisional death counts for Coronavirus Disease 2019 (COVID-19) states the following: “For 6% of the deaths, COVID-19 was the only cause mentioned.”

Oh.  You mean America is not undergoing a pandemic?  On average, abut 8000 people die per day from all causes in the United States.  In the first 8 months of 2020 there were only ~1200 excess deaths per month or 40 extra deaths per day exclusively due to COVID-19 coronavirus infections, with 80% of those among American age 65 and older.  By extrapolation, there were only ~8 excess COVID-19 only deaths per day among working-age adults and school-age children.

Translation: of the 161,392 accumulated COVID-19 RELATED deaths reported as of August 22, 2020 (80% being among Americans age 75 and older), only 6% or ~9683 accumulated deaths were classified as COVID-19 only. Among these COVID-19 only deaths, ~60% were age 75 and older; 80% were age 65 and older. So, there were only ~2000 COVID-only deaths in working age adults and school-age children.

Gilead Issues A Voluntary Nationwide Recall of Two Lots of Veklury® (Remdesivir) Due to Presence of Glass Particulates

COMPANY ANNOUNCEMENT

Gilead Issues A Voluntary Nationwide Recall of Two Lots of Veklury® (Remdesivir) Due to Presence of Glass Particulates

This recall has been completed and FDA has terminated this recall.

When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company.

Read Announcement

View Product Photos

Summary

Company Announcement

Date:December 03, 2021

FDA Publish Date:December 03, 2021

Product Type: Drugs

Reason for Announcement: Presence of glass particulates

Company Name: Gilead Sciences Inc.

Brand Name: Veklury

GileadProduct Description: Veklury® (remdesivir 100 mg for injection)


Company Announcement

Foster City, CA, Gilead Sciences Inc. (Nasdaq: GILD) today announced it is voluntarily recalling two lots of Veklury® (remdesivir 100 mg for injection) to the user level. Gilead Sciences Inc. received a customer complaint, confirmed by the firm’s investigation, of the presence of glass particulates.

Risk Statement: The administration of an injectable product that contains glass particulates may result in local irritation or swelling in response to the foreign material. If the glass particulate reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death. To date, Gilead Sciences Inc. has not received any reports of adverse events related to this recall.

Veklury is indicated for the treatment of adults and pediatric patients ≥ 12 years old and weighing ≥40 kg requiring hospitalization for COVID-19. The lyophilized form of Veklury (remdesivir 100 mg for injection) is distributed in single dose clear glass vials in powder form and reconstituted at the site of use. Veklury lots 2141001-1A and 2141002-1A were distributed nationwide in the United States, beginning October 2021. NDC, lot, expiration date and distribution dates can be found in the table below.Product DescriptionNDCLot #Expiration DateDistribution date to wholesalersVeklury® (remdesivir 100mg for injection) 61958-2901-022141001-1A
2141002-1A01/2024
01/202410/25/21-10/26/2021
10/26/21-11/02/2021

Gilead is notifying its distributors and customers via UPS next day air mail to hospital pharmacies and is facilitating the return of any remaining vials from the affected lots. Hospitals that have Veklury which is being recalled should stop using the affected lots and return the product vials per the instructions.

Consumers with questions regarding this recall can contact Gilead Medical Information at 1-866-633-4474 Monday to Friday 6am – 4pm PST or through their website at http://www.askgileadmedical.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

  • Complete and submit the report Online
  • Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.


Company Contact Information

Consumers: Gilead Medical Information 1-866-633-4474


Product Photos

REMDESIVIR
Brand name: Veklury “REMDESIVIR
  • Content current as of:12/03/2021
  • Regulated Product(s)
    • Drug
  • VEKLURY Brand Name for REMDESIVIR

INDICATION:
VEKLURY is indicated for the treatment of COVID-19 in adults and pediatric patients (≥28 days old and weighing ≥3 kg) with positive results of SARS-CoV-2 viral testing, who are:

  • Hospitalized, or
  • Not hospitalized, have mild-to-moderate COVID-19, and are at high risk for progression to severe COVID-19, including hospitalization or death.

CONTRAINDICATIONS:
VEKLURY is contraindicated in patients with a history of clinically significant hypersensitivity reactions to VEKLURY or any of its components

file://veklury_pi.pdf

HIGHLIGHTS OF PRESCRIBING INFORMATION
These highlights do not include all the information needed to use VEKLURY safely and effectively. See full prescribing information for VEKLURY.
VEKLURY® (remdesivir) for injection, for intravenous use VEKLURY® (remdesivir) injection, for intravenous use Initial U.S. Approval: 2020
—————————

RECENT MAJOR CHANGES————————–
Indications and Usage (1) 12/2022 Dosage and Administration
Dosage and Administration Overview (2.1) 04/2022 Recommended Dosage in Adults and Pediatric Patients 28
Days of Age and Older and Weighing at Least 3 kg (2.3) 04/2022 Dosage Preparation and Administration in Adults and Pediatric
• • • •
o For non-hospitalized patients diagnosed with mild-to-moderate COVID-19 who are at high risk for progression to severe COVID- 19, including hospitalization or death, the recommended total treatment duration is 3 days (2.3).
Renal impairment: VEKLURY is not recommended in patients with eGFR less than 30 mL/min. (2.4)
Administer VEKLURY via intravenous (IV) infusion over 30 to 120 minutes. (2.5, 2.6)
Dose preparation and administration: Refer to the full prescribing information for further details for both formulations. (2.5, 2.6) Storage of prepared dosages: VEKLURY contains no preservative. (2.7)
Patients Weighing At Least 40 kg (2.5)
Dosage Preparation and Administration in Pediatric Patients 28 Days of Age and Older and Weighing 3 kg to Less
Than 40 kg (2.6)
Warnings and Precautions, Hypersensitivity Including Infusion-related and Anaphylactic Reactions (5.1)
04/2022
04/2022 01/2022
———————-

DOSAGE FORMS AND STRENGTHS ———————-
• For injection: 100 mg of remdesivir as a lyophilized powder, in a single-dose vial. (3)
• Injection: 100 mg/20 mL (5 mg/mL) remdesivir, in a single-dose vial. (3)
——————————–

CONTRAINDICATIONS ——————————
VEKLURY is contraindicated in patients with a history of clinically significant hypersensitivity reactions to VEKLURY or any components of the product. (4)
—————————

WARNINGS AND PRECAUTIONS-—————-
Hypersensitivity including infusion-related and anaphylactic reactions: Hypersensitivity reactions have been observed during and following administration of VEKLURY. Slower infusion rates, with a maximum infusion time of up to 120 minutes, can be considered to potentially prevent signs and symptoms of hypersensitivity. Monitor patients during infusion and observe patients for at least one hour after infusion is complete for signs and symptoms of hypersensitivity as clinically appropriate. If signs and symptoms of a clinically significant hypersensitivity reaction occur, immediately discontinue administration of VEKLURY and initiate appropriate treatment. (5.1)
Increased risk of transaminase elevations: Transaminase elevations have been observed in healthy volunteers and have also been reported in patients with COVID-19 who received VEKLURY. Perform hepatic laboratory testing in all patients before starting VEKLURY and while receiving VEKLURY as clinically appropriate. Consider discontinuing VEKLURY if ALT levels increase to greater than 10 times the upper limit of normal. Discontinue VEKLURY if ALT elevation is accompanied by signs or symptoms of liver inflammation. (5.2)
Risk of reduced antiviral activity when coadministered with chloroquine phosphate or hydroxychloroquine sulfate: Coadministration of VEKLURY and chloroquine phosphate or hydroxychloroquine sulfate is not recommended based on data from cell culture experiments demonstrating a potential antagonistic effect of chloroquine on the intracellular metabolic activation and antiviral activity of VEKLURY. (5.3)
——————————–

ADVERSE REACTIONS
The most common adverse reactions (incidence greater than or equal to 5%, all grades) observed with treatment with VEKLURY are nausea, ALT increased, and AST increased. (6.1)

To report SUSPECTED ADVERSE REACTIONS, contact Gilead Sciences, Inc. at 1-800-GILEAD-5 or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch.


See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.
Revised: 12/2022

INDICATIONS AND USAGE

VEKLURY is a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleotide analog RNA polymerase inhibitor indicated for the treatment of coronavirus disease 2019 (COVID-19) in adults and pediatric patients (28 days of age and older and weighing at least 3 kg) who are:
• Hospitalized, or
• Not hospitalized and have mild-to-moderate COVID-19, and are at
high risk for progression to severe COVID-19, including hospitalization or death. (1)
————————

DOSAGE AND ADMINISTRATION
• The only approved dosage form of VEKLURY for pediatric patients weighing 3 kg to less than 40 kg is VEKLURY for injection (supplied as 100 mg lyophilized powder in vial). (2.1)
• Testing: In all patients, before starting VEKLURY and during treatment as clinically appropriate, perform renal and hepatic laboratory testing. Assess prothrombin time before starting VEKLURY and monitor as clinically appropriate. (2.2)

Recommended dosage:

*Adults and pediatric patients weighing at least 40 kg: a single loading dose of VEKLURY 200 mg on Day 1 followed by once- daily maintenance doses of VEKLURY 100 mg from Day 2 via intravenous infusion. (2.3)
*Pediatric patients 28 days of age and older and weighing 3 kg to less than 40 kg: a single loading dose of VEKLURY 5 mg/kg on Day 1 followed by once-daily maintenance doses of VEKLURY 2.5 mg/kg from Day 2 via intravenous infusion. (2.3)
Hospitalized patients: The treatment course of VEKLURY should be initiated as soon as possible after diagnosis of symptomatic COVID- 19 has been made. (2.3)
o For hospitalized patients requiring invasive mechanical ventilation and/or ECMO, the recommended total treatment duration is 10 days. (2.3)
*For hospitalized patients not requiring invasive mechanical ventilation and/or ECMO, the recommended treatment duration is 5 days. If a patient does not demonstrate clinical improvement, treatment may be extended for up to 5 additional days for a total treatment duration of up to 10 days. (2.3)
Non-hospitalized patients: The treatment course of VEKLURY should be initiated as soon as possible after diagnosis of symptomatic COVID-19 has been made and within 7 days of symptom onset. (2.3) 1

FULL PRESCRIBING INFORMATION: CONTENTS*
1 INDICATIONS AND USAGE
2 DOSAGE AND ADMINISTRATION
2.1 Dosage and Administration Overview
2.2 Testing Before Starting and During Treatment with VEKLURY
2.3 Recommended Dosage in Adults and Pediatric Patients 28
Days of Age and Older and Weighing at Least 3 kg
2.4 Renal Impairment
2.5 Dosage Preparation and Administration in Adults and Pediatric Patients Weighing at Least 40 kg
2.6 Dosage Preparation and Administration in Pediatric Patients 28 Days of Age and Older and Weighing 3 kg to Less Than 40 kg
2.7 Storage of Prepared Dosages
3 DOSAGE FORMS AND STRENGTHS 4 CONTRAINDICATIONS
5 WARNINGS AND PRECAUTIONS
5.1 Hypersensitivity Including Infusion-related and Anaphylactic Reactions
5.2 Increased Risk of Transaminase Elevations
5.3 Risk of Reduced Antiviral Activity When Coadministered with
Chloroquine Phosphate or Hydroxychloroquine Sulfate
6 ADVERSE REACTIONS
6.1 Clinical Trials Experience
7 DRUG INTERACTIONS
8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
8.2 Lactation
8.4 Pediatric Use
8.5 Geriatric Use
8.6 Renal Impairment
8.7 Hepatic Impairment
10 OVERDOSAGE
11 DESCRIPTION
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action 12.2 Pharmacodynamics 12.3 Pharmacokinetics 12.4 Microbiology
13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
13.2 Animal Toxicology and/or Pharmacology
14 CLINICAL STUDIES
14.1 Description of Clinical Trials
14.2 NIAID ACTT-1 Study in Hospitalized Subjects with
Mild/Moderate and Severe COVID-19
14.3 Study GS-US-540-5773 in Hospitalized Subjects with Severe
COVID-19
14.4 Study GS-US-540-5774 in Hospitalized Subjects with
Moderate COVID-19

14.5 Study GS-US-540-9012 in Non Hospitalized Subjects with Mild-to-Moderate COVID-19 and at High Risk for Progression to Severe Disease
14.6 Study GS-US-540-5823 in Hospitalized Pediatric Subjects
with COVID-19
16 HOW SUPPLIED/STORAGE AND HANDLING
17 PATIENT COUNSELING INFORMATION

  • Sections or subsections omitted from the full prescribing
    information are not listed.

FULL PRESCRIBING INFORMATION 1 INDICATIONS AND USAGE
VEKLURY is indicated for the treatment of coronavirus disease 2019 (COVID-19) in adults and pediatric patients (28 days of age and older and weighing at least 3 kg) who are [see Clinical Studies (14)]:
2 2.1 •
• •

2.2
Hospitalized, or
Not hospitalized and have mild-to-moderate COVID-19, and are at high risk for progression to severe COVID-19, including hospitalization or death.


DOSAGE AND ADMINISTRATION Dosage and Administration Overview
VEKLURY may only be administered in settings in which healthcare providers have immediate access to medications to treat a severe infusion or hypersensitivity reaction, such as anaphylaxis, and the ability to activate the emergency medical system (EMS), as necessary [see Dosage and Administration (2.5, 2.6),

Warnings and Precautions (5.1)].
Administer VEKLURY for the treatment of COVID-19 in adults and pediatric patients (28 days of age and older and weighing at least 3 kg) by intravenous infusion only. Do not administer by any other route.


There are TWO different formulations of VEKLURY:
o VEKLURY for injection (supplied as 100 mg lyophilized powder in vial) must be reconstituted with Sterile Water for Injection prior to diluting with 0.9% sodium chloride injection.
The only approved dosage form of VEKLURY for pediatric patients weighing 3 kg to less than 40 kg is VEKLURY for injection (supplied as 100 mg lyophilized powder in vial).
o VEKLURY injection (supplied as 100 mg/20 mL [5 mg/mL] solution in vial) must be further diluted in 250 mL of 0.9% sodium chloride injection infusion bag.
There are differences in the way the two formulations are prepared. Carefully follow the product- specific preparation instructions below [see Dosage and Administration (2.5, 2.6)].

Testing Before Starting and During Treatment with VEKLURY


-Testing Before Starting and During Treatment with VEKLURY
Determine eGFR in all patients before starting VEKLURY and monitor while receiving VEKLURY as clinically appropriate [see Dosage and Administration (2.4) and Use in Specific Populations (8.4, 8.6)].
Perform hepatic laboratory testing in all patients before starting VEKLURY and while receiving VEKLURY as clinically appropriate [see Warnings and Precautions (5.2) and Use in Specific Populations (8.7)].
—-Determine prothrombin time in all patients before starting VEKLURY and monitor while receiving VEKLURY as clinically appropriate [see Adverse Reactions (6.1)].
3

2.3
• •
Recommended Dosage in Adults and Pediatric Patients 28 Days of Age and Older and Weighing at Least 3 kg
The recommended dosage for adults and pediatric patients weighing at least 40 kg is a single loading dose of VEKLURY 200 mg on Day 1 via intravenous infusion followed by once-daily maintenance doses of VEKLURY 100 mg from Day 2 via intravenous infusion.
The recommended dosage for pediatric patients 28 days of age and older and weighing 3 kg to less than 40 kg is a single loading dose of VEKLURY 5 mg/kg on Day 1 via intravenous infusion followed by once-daily maintenance doses of VEKLURY 2.5 mg/kg from Day 2 via intravenous infusion.
Hospitalized patients:
The treatment course of VEKLURY should be initiated as soon as possible after diagnosis of symptomatic COVID-19 has been made.
• The recommended total treatment duration for hospitalized patients requiring invasive mechanical ventilation and/or extracorporeal membrane oxygenation (ECMO) is 10 days.
The recommended treatment duration for hospitalized patients not requiring invasive mechanical ventilation and/or ECMO is 5 days. If a patient does not demonstrate clinical improvement, treatment may be extended for up to 5 additional days for a total treatment duration of up to 10 days.
Non-hospitalized patients:
The treatment course of VEKLURY should be initiated as soon as possible after diagnosis of symptomatic COVID-19 has been made and within 7 days of symptom onset.
The recommended total treatment duration for non-hospitalized patients diagnosed with mild-to- moderate COVID-19 who are at high risk for progression to severe COVID-19, including hospitalization or death, is 3 days.
VEKLURY must be diluted prior to intravenous infusion. Refer to Dosage and Administration (2.5, 2.6) for detailed preparation and administration instructions.
2.4 Renal Impairment
VEKLURY is not recommended in patients with eGFR less than 30 mL per minute [see Dosage and Administration (2.2) and Use in Specific Populations (8.4, 8.6)].
2.5 Dosage Preparation and Administration in Adults and Pediatric Patients Weighing at Least 40 kg
There are differences in the way the two formulations are prepared. Carefully follow the product-specific preparation instructions below.
4

VEKLURY for Injection (Supplied as 100 mg Lyophilized Powder in Vial)
Reconstitution Instructions
Remove the required number of single-dose vial(s) from storage. For each vial:
• Aseptically reconstitute VEKLURY lyophilized powder by adding 19 mL of Sterile Water for Injection using a suitably sized syringe and needle per vial.
• Only use Sterile Water for Injection to reconstitute VEKLURY lyophilized powder.
• Discard the vial if a vacuum does not pull the Sterile Water for Injection into the vial.
• Immediately shake the vial for 30 seconds.
• Allow the contents of the vial to settle for 2 to 3 minutes. A clear, colorless to yellow solution, free
of visible particles, should result.
• If the contents of the vial are not completely dissolved, shake the vial again for 30 seconds and
allow the contents to settle for 2 to 3 minutes. Repeat this procedure as necessary until the contents of the vial are completely dissolved. Discard the vial if the contents are not completely dissolved.
• Following reconstitution, each vial contains 100 mg/20 mL (5 mg/mL) of remdesivir solution.
• Use reconstituted product immediately to prepare the diluted drug product [see Dosage and
Administration (2.7)].
Dilution Instructions
Care should be taken during admixture to prevent inadvertent microbial contamination. As there is no preservative or bacteriostatic agent present in this product, aseptic technique must be used in preparation of the final parenteral solution. It is always recommended to administer intravenous medication immediately after preparation when possible.
Reconstituted VEKLURY for injection, containing 100 mg/20 mL remdesivir solution, must be further diluted in either a 100 mL or 250 mL 0.9% sodium chloride injection infusion bag. Refer to Table 1 for instructions.

Sudden death epidemic: Excess mortality among young, middle-aged Americans skyrockets

If these trends continue at this same rate, it’s an absolute disaster for our economy and society at large.

Featured Image

tommaso79/Shutterstock

https://www.lifesitenews.com/author/dr-joseph-mercola/

STORY AT-A-GLANCE

  • In his new book, “Cause Unknown: The Epidemic of Sudden Deaths in 2021 and 2022,” former BlackRock fund manager Edward Dowd details data showing the COVID shots are a crime against humanity.
  • Insurance industry research in 2016 concluded that group life policyholders die at one-third the rate of the general U.S. population, so they’re the healthiest among us. Group life policyholders are those employed with Fortune 500 companies, who tend to be younger and well-educated.
  • In 2020, the general U.S. population had higher excess mortality than group life holders, but in 2021, that flipped. Ages 25 through 64 of the group life policyholders suddenly experienced 40 percent excess mortality, compared to 32 percent in the general population. In short, a far healthier subset of the population suddenly died at a higher rate than the general population.
  • American disability statistics are equally revealing. In the five years before COVID, the monthly disability rate was between 29 million and 30 million. After the COVID jabs, the disability trend changed dramatically. As of September 2022, there were 33.2 million disabled Americans ­– an extra 3.2 million to 4.2 million – a three standard deviation rate of change since May 2021.
  • Since May 2021, the overall U.S. population has experienced an 11 percent increase in disabilities, while the employed – which is about 98 million out of a total population of about 320 million – experienced 26 percent increased rate of disability. So, something was introduced into the workforce that caused working age people to die.

(Mercola) – In this video, I interview repeat guest Edward (Ed) Dowd, a former analyst and fund manager with BlackRock, the largest asset manager in the world. With more than $10 trillion in assets, BlackRock wields greater financial power than any country in the world with the exception of the U.S. and China.

Dowd has a knack for seeing trends, and was able to grow the assets he managed during his time at BlackRock from $2 billion to $14 billion. Ten years ago, he left BlackRock, moved to Maui, and became an entrepreneur. More recently, he’s come out as a whistleblower against the COVID shots and Big Pharma corruption.

In our last interview, we discussed the mathematical certainty of a financial collapse, and how COVID provided a convenient smoke screen to hide this reality.

Data reveal crimes against humanity

Dowd has now published a book, “Cause Unknown: The Epidemic of Sudden Deaths in 2021 and 2022,” in which he details the data showing the shots are a crime against humanity.

“When this product [the COVID shots] came to market, I was very suspicious because I know a lot about health care” Dowd says. “I was on Wall Street and I used to analyze health care stocks. I knew that normal vaccines took seven to 10 years to prove effectiveness and safety.”

He added:

This was an experimental vaccine, a non-traditional gene therapy that had never been tested on humans. I read the literature on the animal tests and they were an abomination. Then, this thing was approved in 28 days. They got rid of the control group. I knew it was Operation Warp Speed, so I was highly suspicious of this whole thing from the get-go.

Then in early 2021, I started hearing anecdotes that people were getting sick and/or injured, or died, from distant friends and relatives. I started reading about sudden athlete deaths, [and] suspected the vaccine right away. I didn’t have the data that I have now, but I said to myself, ‘You know, I’m going to look at insurance company results, funeral home results.’

That eventually led to excess mortality statistics… I’m known as ‘the excess mortality guy’ right now. What I’ve learned through my own personal experience is that Pharma is, on the whole, mostly fraudulent. Most drugs that have been approved by the FDA [U.S. Food and Drug Administration] aren’t really all that safe and effective.

They have to recall so many drugs every year. The FDA has been wholly captured by the pharma industry. 70 to 75 percent of the drug approval pharma arm of the FDA comes from pharma fees, directly from the companies, so this has been corrupted for a long time.

It’s now exposed primarily because [the COVID shot] is [injuring and killing] such a large amount of people. It’s hard to hide this one… This fraud is unveiled and out there for people to see, but it’s only in the echo chamber. Mainstream media is still beholden to Big Pharma because of all the ad spend and the government policymakers… [who] want this to go away.

There’s a giant cover-up going on as far as I’m concerned. The data that I’m going to talk about today is there for the global health authorities to see. They see what I see, and at this point it’s negligence, malfeasance, a cover-up and a crime.

That’s why I’m here, because I don’t believe anybody has a right to tell me what to do with my body, and I can’t believe this actually happened. The numbers I’m going to reveal to you are now a national security concern.

Group life insurance statistics tell a curious story

Dowd’s concerns are based on a variety of statistics, including but not limited to government mortality and disability data, as well as data from private insurance companies, such as group life insurance data. As explained by Dowd, group life policies are policies given to large Fortune 500 corporations and mid-sized companies.

Basically, when you start to work at one of these companies, you sign onto a policy from day one that includes a health care plan and life insurance plan (death benefit), which is typically one or two times your annual salary. The only way you can get a claim on these policies is if you die while employed. If you quit or get fired, you don’t get this claim.

There’s a “Died Suddenly” Epidemic…One Expert Went Through the Data and Reveals The “Coverup”

I don’t need to tell you that there’s a problem. You can see what’s happening with your own eyes. Over the past year or so, there has been a strangely large number of healthy, young people who are “dying suddenly.” These poor people are dropping like flies at an alarming rate. At first, stories of young, healthy people “dying suddenly” were peppered here and there, but now, there are so many of these stories, that I can’t keep up with them. And just imagine how many of these “sudden deaths” aren’t being talked about in the media.

Scary thought. 

Well, it’s gotten so bad, that people are now taking notice and talking about the “Died Suddenly” phenomenon. And one of those people is a former BlackRock fund manager who has poured through the data and what he found, is startling.

Lifestite reported that in his new book, “Cause Unknown: The Epidemic of Sudden Deaths in 2021 and 2022,” former BlackRock fund manager Edward Dowd details data showing the COVID shots are a crime against humanity.

Insurance industry research in 2016 concluded that group life policyholders die at one-third the rate of the general U.S. population, so they’re the healthiest among us. Group life policyholders are those employed with Fortune 500 companies, who tend to be younger and well-educated.

In 2020, the general U.S. population had higher excess mortality than group life holders, but in 2021, that flipped. Ages 25 through 64 of the group life policyholders suddenly experienced 40 percent excess mortality, compared to 32 percent in the general population. In short, a far healthier subset of the population suddenly died at a higher rate than the general population.
American disability statistics are equally revealing. In the five years before COVID, the monthly disability rate was between 29 million and 30 million. After the COVID jabs, the disability trend changed dramatically. As of September 2022, there were 33.2 million disabled Americans ­– an extra 3.2 million to 4.2 million – a three standard deviation rate of change since May 2021.

Since May 2021, the overall U.S. population has experienced an 11 percent increase in disabilities, while the employed – which is about 98 million out of a total population of about 320 million – experienced 26 percent increased rate of disability. So, something was introduced into the workforce that caused working age people to die.

Edward Dowd goes on to say:

This was an experimental vaccine, a non-traditional gene therapy that had never been tested on humans. I read the literature on the animal tests and they were an abomination. Then, this thing was approved in 28 days. They got rid of the control group. I knew it was Operation Warp Speed, so I was highly suspicious of this whole thing from the get-go.

Then in early 2021, I started hearing anecdotes that people were getting sick and/or injured, or died, from distant friends and relatives. I started reading about sudden athlete deaths, [and] suspected the vaccine right away. I didn’t have the data that I have now, but I said to myself, ‘You know, I’m going to look at insurance company results, funeral home results.’

That eventually led to excess mortality statistics… I’m known as ‘the excess mortality guy’ right now. What I’ve learned through my own personal experience is that Pharma is, on the whole, mostly fraudulent. Most drugs that have been approved by the FDA [U.S. Food and Drug Administration] aren’t really all that safe and effective.

They have to recall so many drugs every year. The FDA has been wholly captured by the pharma industry. 70 to 75 percent of the drug approval pharma arm of the FDA comes from pharma fees, directly from the companies, so this has been corrupted for a long time.

It’s now exposed primarily because [the COVID shot] is [injuring and killing] such a large amount of people. It’s hard to hide this one… This fraud is unveiled and out there for people to see, but it’s only in the echo chamber. Mainstream media is still beholden to Big Pharma because of all the ad spend and the government policymakers… [who] want this to go away.

There’s a giant cover-up going on as far as I’m concerned. The data that I’m going to talk about today is there for the global health authorities to see. They see what I see, and at this point it’s negligence, malfeasance, a cover-up and a crime.

I really encourage you to read the entire piece over at Lifesite. Click here.

DOCUMENTS REVEAL THE AUSTRALIAN GOVERNMENT HAS OPENLY PLANNED TO POISON ITS CITIZENS & CHILDREN

DOCUMENTS REVEAL THE AUSTRALIAN GOVERNMENT HAS OPENLY PLANNED TO POISON ITS CITIZENS & CHILDREN

Source : https://www.bitchute.com/channel/philosophers-stoneinfo/

Covid watchdog site says Alaskans died or suffered after hospitals denied treatment options By Joel Davidson Nov 22nd 2022

Covid watchdog site says Alaskans died or suffered after hospitals denied treatment options

   By  Joel Davidson    Nov 22nd 2022

By AlaskaWatchman.com

The COVID-19 Humanity Betrayal Memory Project

An ongoing nationwide project to document how Americans were treated during the Covid-19 outbreak includes several accounts of Alaskans who either died or were severely injured after receiving dangerous experimental drugs or being denied treatment options like ivermectin.

The COVID-19 Humanity Betrayal Memory Project now has nearly 350 documented case files. 

The COVID-19 Humanity Betrayal Memory Project is building an archive of what it calls “crimes against humanity committed during the COVID crisis.”

The goal is to establish a resource detailing the “individual victims of the FDA Death Protocol including remdesivir and the concerted effort to deny COVID victims safe and effective alternatives to expensive and often deadly Emergency Use Authorization drugs, victims of vaccine mandates, and others who have been harmed in the name of public health,” the website states.

The project includes hundreds of video interviews and specific data from survivors and family members of those who have died.

As of Nov. 22, the website contained 344 individual stories, including three from Alaska.

The overarching goal of the Covid19 Humanity Betrayal Memory Project is to provide information on how Americans can shed light on what happened to their friends and loved ones in order to ensure that this never occurs again.

“Everyday, we are hearing evidence of what we believe are crimes against humanity,” the website states. “We are archiving it, so that no one will ever be able to forget what was done in the name of public health … If you or someone you love has been harmed by the FDA Death Protocol including remdesivir, you can now sign up to join this amazing support group.”

Each person who contacts the group is called back for a detailed video interview, which recounts how they or their loved ones were treated by medical staff, doctors and administrators, including drugs and medical interventions.

The three Alaska stories all involve people who had not received Covid jabs. They each checked into the hospital for care and were given the experimental drug remdesivir, while being denied other treatments like ivermectin and hydroxychloroquine. The testimonials state that the patients were not told that remdesivir is an experimental drug, nor were they informed about its side effects. Two of the Alaskans died while in the hospital, while a third lived to personally tell his story.

ALASKA WATCHMAN DIRECT TO YOUR INBOX

The Alaska testimonies, like many of the others on the website, detail the confusion, anger and desperation which many families experienced as they watched loved ones suffer, and in many cases, die alone without effective advocates at their side.

Nationally, families are now bringing wrongful-death lawsuit claims against hospitals for administering the controversial drug remdesivir to Covid positive patients without their informed consent. These suits claim that patients were given the toxic without being properly advised of the side effects, which include acute kidney failure, liver failure and multiple organ failure. At the same time, victims claim they or their loved ones were denied more established treatments like ivermectin.

ALASKA TESTIMONIES: Below are links to the three Alaska stories

— KEVIN HITE: A 62-year-old who check into Mat-Su Regional Hospital in September of 2021. He ultimately survived after enduring what his family described as horrific treatment. Click here to watch his video and learn the details of his testimony.

— FANNIE DOWNES: A 62-year-old woman who checked into Providence Hospital in Anchorage in August of 2021. Her husband said Fannie was given inferior medical care in the days leading up to her death. Her full story is documented here.

— EDWARD “DONNIE” WILSON: A 55-year-old man who checked into Mat-Su Regional Hospital in August of 2021. His daughter relayed an account of poor treatment and the shocking death of her father. The details of Wilson’s story are here.

Click here to support Alaska Watchman reporting.

Joel Davidson 

Joel is Editor-in-Chief of the Alaska Watchman. Joel is an award winning journalist and has been reporting for over 20 years, He is a proud father of 8 children, and lives in Palmer, Alaska. 


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7 Comments

  • Mongo Love CandyNovember 22, 2022 at 4:39 pmMurdering bastards!Reply
  • ClarkNovember 22, 2022 at 5:41 pmIvermectin never has been an ‘established treatment’ for Covid. Its been studied extensively and still hasn’t been proven effective. Hence why the CDC and WHO still say DON’T use it. Could be a real issue if hospitals didn’t inform patients about what treatments they were getting. But I find it highly doubtful patients weren’t told they were getting remdesivir. Unless they were on a ventilator in which case next of kin would be told/asked for consent. It had an EUA, so lawsuits arent going to accomplish much.Reply
  • @KGAK100November 22, 2022 at 6:48 pmI truly hope the details of these crimes come to light and those responsible are held to the fullest extent of the law possible its such a violation of every ethical principle this country stands for some how we have gotten to a place where i can give puberty blockers OFF LABEL mind you to teens simply with their consent but i cant give off label harmless drugs to a consenting adult to potentially save their life but instead these people were given an experimental drug without their consent and the staff in these hospitals stood there and watched them die a horrible gasping death there are no words in the english language the majority of the people no longer have any trust or confidence in hospitals they are soulless bastards i hope for justiceReply
  • Steve P PetersonNovember 22, 2022 at 6:52 pmThey want amnesty for what they have done. They might be forgiven (by some), but we will never forget what they did to our most vulnerable citizens… and got paid for each victim who succumbed to their malpractice.Reply
  • Kathy L.November 22, 2022 at 8:31 pmRemembering and honoring a saint. As I daily read “horror stories” of people I didn’t know who lived in other states, I had doubts. Little did I know and little was I prepared for all of this to hit so close to home. A dear Patriot, an older gent, was a member of our group. He was at all the rallies and was a worker of righteousness. One day, he grew ill enough with covid to go to hospital. He requested Ivermectin, Vit C & D and was denied by the hospital. He grew fearful that he might die and while he was still conscious, requested a dear friend to have power of atty. While this processed thru the court, he was put on a vent. The hospital took away his phone. No one was allowed to even see him. He was put on oxygen. It seemed he was slipping away and friends tried desperately to get him relocated to a different hospital that did treat with Ivermectin. One the day all was approved for his move, this sweet man left the earth and went to be with His Lord. Which is better! But it didn’t have to be that way, and somehow, we all feel the hospital was partly responsible. What if Ivermectin was immediately administered????Reply
  • Kathy L.November 22, 2022 at 8:47 pmHere’s another case where the right intervention would have saved a life.
    As I daily read “horror stories” of people I didn’t know who lived in other states, I had doubts. Little did I know and little was I prepared for all of this to hit so close to home. Friends of a friend down south. Her elderly mother (70) was admitted for covid. She went on fb asking for prayer. By then, everyone had heard of the success of Hydroxy and Ivermectin. The daughter told us she inquired about Hydroxy and was told by a doctor…”it doesn’t work!” In no short time, the woman was intubated, and given Remdesivir. By then, everyone had also heard how bad Rem was for people. The family was not allowed to see her in person nor were they allowed input. The doctor’s simply conveyed they were doing this, that or the other. Her condition grew worse each day. The family was only allowed to see her just before she passed. The doctors stated that her internal organs were in such bad shape (she had a collapsed lung) that if she had lived, it would have been a very long and very hard recovery. Gee…all issues caused by machines using too much force and a drug that’s really bad for you! Just like the symptoms noted in the article: acute kidney failure, liver failure and multiple organ failure. YUP…that’s what the doctor ordered. Again, this precious woman was a believer and is in heaven. But it needn’t have happened.Reply
  • CindyNovember 22, 2022 at 10:58 pmYour friend was not an aberration, nor was my husband, nor were the other two already on this website. Please everyone who lost a friend or a loved one go and document your nightmare. It is real, it happened and needs to be revealed. It is painful to remember and tell the facts but necessary for the truth to shed a light on this darkness. I know there are so many of you out there with hurt and anger this is a start to accountability for all those responsible for the deaths and harm they administered. Two other sites that I know are documenting are— Truth For Health Foundation go to Medical Legal Help and choose Sentinel Event and FLCCC Alliance go to Covid Resources and choose Testimonials. We will not shut up, comply and let our loved ones die!Reply

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