Form for Employees Whose Employers Are Requiring CÖVÌD-19 Injections
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All over America, employees are facing a very tough decision right now. Although some wish to accept a CÖVÌD-19 injection, many do not. The problem is that a growing number of employers are trying to deny employees’ right to choose and their right to bodily integrity by requiring the ναccιnєs as a condition of employment. In the United States and other jurisdictions, that is a violation of the law. It is also a violation of fundamental human and religious rights.
In the U.S., the provisions of the 2005 Public Readiness and Emergency Preparedness (PREP) Act and a February 2020 declaration by the Secretary of the Department of Health and Human Services (HHS) mean that pharmaceutical companies cannot be held liable for injuries or deaths caused by the CÖVÌD-19 injections.1 However, other companies, institutions, and individuals can be held liable. This form is designed as a tool that employees can use to provide this critical information to employers, and to insist on a signature from the employer’s representative that holds the company liable if the employee should decide to accept the required experimental CÖVÌD-19 injection.
We are already seeing that health care providers are refusing service to individuals injured by the CÖVÌD-19 injections, and health and life insurance companies are declining coverage for ναccιnє-related injuries and deaths on the grounds that the injections are investigational ναccιnєs allowed under Food and Drug Administration (FDA) emergency use authorization (EUA) but not otherwise approved or licensed.2This denial of care and coverage poses a serious threat to the physical and financial well-being of employees presented with a requirement to get a CÖVÌD injection—perhaps even more so than the possibility of losing their job for not being ναccιnαted.
Reviewing this form with employers may open their eyes to the regulations in place and the liability they may face (that they may otherwise not be aware of). Everyone should consider reviewing the form with their employer as well as sharing it with co-workers. This could result in a positive impact for employees and could be a game-changer. Alternatively, if the employer representative refuses to sign the form, that may be an indicator of their concern about potential liability and should prompt an immediate discussion about how the employee can continue working for the company without being injected.
If you find yourself in a predicament with a company that refuses to hear you out, does not provide you with required information, or threatens termination of your employment, here are a few potential resources for contacting attorneys. America’s Frontline Doctors provides an intake form on their site that you can fill out and submit, and they will search for an attorney in your area who is taking on this type of case.3 There is a small fee for the search, and of course, attorneys have their own fees. The legal team of the Informed Consent Action Network (ICAN) is offering to assist employees/students who are being required by an employer/school to receive the CÖVÌD-19 injection.4 If you find yourself needing a ναccιnє injury case attorney, you might also try looking through this state list.5
This form was written by Corey Lynn of Corey’s Digs for The Solari Report.
NOTE TO EMPLOYEE: Be sure to docuмent the date and time you submit this form to your employer; also docuмent the date and time and their response if they refuse to sign it.
NOTE TO EMPLOYER: As your employee, I am requesting that you review this docuмent, provide the requisite information, and sign the form, in regards to your requirement that employees get a CÖVÌD-19 emergency use authorization (EUA) investigational ναccιnє.
1) If I agree to receive an EUA CÖVÌD-19 injection, does my employee health insurance plan provide complete coverage should I experience an adverse event, or even death?
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2) As an employee, does my life insurance policy provide any coverage in the event that I die from receiving an EUA CÖVÌD-19 injection?
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3) As an employee, will you be providing Workers’ Compensation, disability insurance, or other resources if I have an adverse event to an EUA CÖVÌD-19 injection and am unable to come to work for days, weeks, or months, or if I am disabled for life?
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4) The Food and Drug Administration (FDA) requires that EUA ναccιnє recipients be provided with certain ναccιnє-specific information to help them make an informed decision about vaccination.8 The EUA fact sheets that must be provided are specific to each authorized CÖVÌD-19 injection and are developed by the manufacturers of the injections (pfιzєr/BioNTech, mσdernα, Oxford/AstraZeneca, and the Johnson & Johnson subsidiary Janssen). The fact sheets must provide the most current and up-to-date information on the injections, and ναccιnє recipients must also receive information about adverse events. Have you read, understood, and provided me (and all other employees) with these fact sheets and with current information on adverse events so that I/we can make an educated decision?
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5) Have you reviewed the available databases of material adverse events reported to date for people who have received CÖVÌD-19 injections?9,10,11,12 Potential and reported adverse events include death, anaphylaxis, neurological disorders, autoimmune disorders, other long-term chronic diseases, blindness and deafness, infertility, fetal damage, miscarriage, and stillbirth.
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6) The FDA’s guidance13 on emergency use authorization of medical products requires the FDA to “ensure that recipients are informed to the extent practicable given the applicable circuмstances…[t]hat they have the option to accept or refuse the EUA product….” Are you aware of this statement? Have you informed all employees that they have the option to refuse?
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7) With respect to the emergency use of an unapproved product, the Federal Food, Drug and Cosmetic Act, Title 21 U.S.C. 360bbb-3(e)(1)(A)(ii)(I-III)14 reiterates that individuals be informed of “the option to accept or refuse administration of the product, [and] of the consequences, if any, of refusing administration of the product, and of the alternatives to the product that are available and of their benefits and risks.” If EUA CÖVÌD-19 investigational ναccιnєs are ever approved by the FDA, state legislation would be required to allow companies to mandate the CÖVÌD-19 injections. Are you aware of these facts?
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8) EUA products are unapproved, unlicensed, and experimental. Under the Nuremberg Code—the foundation of ethical medicine—no one may be coerced to participate in a medical experiment. The individual’s consent is absolutely essential. No court has ever upheld a mandate for an EUA ναccιnє. In Doe #1 v. Rumsfeld, 297 F. Supp. 2d 119 (2003)15, a federal court held that the U.S. military could not mandate EUA ναccιnєs for soldiers: “…[T]he United States cannot demand that members of the armed forces also serve as guinea pigs for experimental drugs” (Id. at 135). Are you aware of this?
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9) The United States Code of Federal Regulations16and the FDA require the informed consent of human subjects for medical research. The EUA CÖVÌD-19 injections are unapproved, unlicensed, investigational ναccιnєs that are still in their experimental stage. It is unlawful to conduct medical research on a human being, even in the event of an emergency, unless steps are taken to secure the informed consent of all participants. Are you aware of this?
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10) According to Federal Trade Commission (FTC) Guidelines17and the FTC’s “Truth In Advertising,”18 promotional material—and especially material involving health-related products—cannot mislead consumers, omit important information, or express claims. All of this falls under the rubric of “deceptive advertising” (whereby a company is providing or endorsing a product), whether presented in the form of an ad, on a website, through email, on a poster, or in the mail. For example, statements such as “all employees are required to get the CÖVÌD-19 ναccιnє to make the workspace safe” or “it’s safe and effective” leave out critical information. Critical information includes the facts that CÖVÌD-19 injections are unapproved EUA ναccιnєs that “may” or “may not” prevent CÖVÌD, won’t necessarily make the workspace safer, and could in fact cause harm. Not providing links or attachments of the manufacturers’ fact sheets and current information on adverse events is omitting safety information. Are you aware of this?
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11) Since the CÖVÌD lσcкdσωns began over one year ago, there have been over 178 reported breaches of unsecured protected health information (PHI), incidents investigated by the Office for Civil Rights (OCR). These breaches exposed millions of people’s personal health information. Although many of these incidents were attributed to hacking, some of the breaches to PHI fell directly under the 1996 Health Insurance Portability and Accountability Act (HIPAA), such as sharing a patient’s or person’s information with an unauthorized individual or incorrectly handling PHI.19 Can you please explain your obligations to me, under HIPAA law, and how you are going to protect my personal information – both with respect to your requirement that I receive this injection?
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12) Whereas pharmaceutical companies that manufacture EUA ναccιnєs have been protected from liability related to injuries or deaths caused by experimental agents since the PREP Act1was enacted in 2005, companies and all other institutions or individuals who mandate experimental ναccιnєs on any human being are not protected from liability. Are you aware that you do not enjoy such liability protection?
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13) Are you aware that employees could file a civil suit against you should they suffer an adverse event, death, or termination from their place of employment?
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As the legally authorized officer of the employer/company, I have read all of the above information, have provided my employees with all of the information that the FDA requires be provided to recipients of the CÖVÌD-19 injections, and do hereby agree to assume 100% financial responsibility for covering any and all expenses from adverse events, including death, through insurance coverage or directly. In addition, I affirm that the employee will not be subjected to the loss of their job should they decline to receive a CÖVÌD-19 injection.
Endnotes:
Congressional Research Service. The PREP Act and CÖVÌD-19: Limiting Liability for Medical Countermeasures. Updated Mar. 19, 2021.
https://crsreports.congress.gov/product/pdf/LSB/LSB10443.
Del Bigtree interviews 3 medical professionals incapacitated by CÖVÌD injections. The Highwire, Apr. 29, 2021.
https://www.bitchute.com/video/A4d8FB2cIBTc/.
America’s Frontline Doctors. ναccιnєs & the law.
https://www.americasfrontlinedoctors.org/legal/ναccιnєs-the-law.
Layton, Catharine. Forced to get the CÖVÌD ναccιnє? ICAN may be able to help. The Defender, Jan. 29, 2021.
https://childrenshealthdefense.org/defender/forced-to-get-CÖVÌD-ναccιnє-ican-may-be-able-to-help/.
https://uscfc.uscourts.gov/sites/default/files/ναccιnє%20Attorneys.pdf.
The Solari Report. Family Financial Disclosure Form for CÖVÌD-19 injections. Mar. 1, 2021.
https://pandemic.solari.com/family-financial-disclosure-form-for-CÖVÌD-19-injections/.
The Solari Report. Form for Students Attending Colleges or Universities Requiring CÖVÌD-19 Injections. May 3, 2021.
https://pandemic.solari.com/form-for-students-attending-colleges-or-universities-requiring-CÖVÌD-19-injections/
Centers for Disease Control and Prevention. CÖVÌD-19 ναccιnє Emergency Use Authorization (EUA) Fact Sheets for Recipients and Caregivers.
https://www.cdc.gov/ναccιnєs/CÖVÌD-19/eua/index.html.
UK Medical Freedom Alliance. CÖVÌD-19 ναccιnє Info.
https://www.ukmedfreedom.org/resources/CÖVÌD-19-ναccιnє-info.
ναccιnє Adverse Event Reporting System.
https://vaers.hhs.gov.
CDC WONDER. About the ναccιnє Adverse Event Reporting System (VAERS).
https://wonder.cdc.gov/vaers.html.
National ναccιnє Information Center. Search the U.S. Government’s VAERS Data.
https://www.medalerts.org/.
U.S. Department of Health and Human Services. Emergency Use Authorization of Medical Products and Related Authorities: Guidance for Industry and Other Stakeholders. January 2017.
https://www.fda.gov/media/97321/download.
21 U.S. Code § 360bbb–3 – Authorization for medical products for use in emergencies.
https://www.law.cornell.edu/uscode/text/21/360bbb-3.
Doe #1 v. Rumsfeld, 297 F. Supp. 2d 119 (2003).
https://www.courtlistener.com/opinion/2326816/doe-v-rumsfeld/.
https://www.govregs.com/regulations/expand/title21_chapterI_part50_subpartB_section50.24#regulation_2.
Federal Trade Commission. Advertising FAQ’s: A Guide for Small Business.
https://www.ftc.gov/tips-advice/business-center/guidance/advertising-faqs-guide-small-business.
Federal Trade Commission. Truth in Advertising.
https://www.ftc.gov/news-events/media-resources/truth-advertising.
U.S. Department of Health and Human Services. Office for Civil Rights. Breach Portal: Notice to the Secretary of HHS Breach of Unsecured Protected Health Information.
https://ocrportal.hhs.gov/ocr/breach/breach_report.jsf;jsessionid=618E88DD94EE65D46D5785CB2A643553.
Topic: Form for Employees Whose Employers Are Requiring CÖVÌD-19 Injections (Read 589 times)