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Thread: OSHA: Employers may be liable for 'adverse reaction' from mandated coronavirus shots

  1. #1

    OSHA: Employers may be liable for 'adverse reaction' from mandated coronavirus shots


    Employers may be liable for 'any adverse reaction' from mandated coronavirus shots: OSHA
    It's also possible that employers requiring the injections may be held legally liable for violating federal law.
    Mon May 10, 2021 - 7:43 pm EST
    Employers may be liable for 'any adverse reaction' from mandated coronavirus shots: OSHA | News | LifeSite

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    WASHINGTON, D.C., May 10, 2021 (LifeSiteNews) — The federal Occupational Safety and Health Administration (OSHA) has put employers on notice that should they attempt to require employees to receive injections of experimental COVID-19 gene-therapy vaccines a resulting adverse reaction will be considered "work-related" for which the employer may be held liable.

    OSHA released its new guidance on April 20 under a "Frequently Asked Questions" section of its website having to do with COVID-19 safety compliance.

    The question asks whether an employer who mandates employees receive these experimental COVID-19 shots is required to record any adverse events as a result of these injections. Such recording requirements of serious work-related injuries and illness may not only leave an employer vulnerable to worker's compensation claims, but such incidents could also impact the employer's safety record.


    The question and answer in full:

    If I require my employees to take the COVID-19 vaccine as a condition of their employment, are adverse reactions to the vaccine recordable?

    If you require your employees to be vaccinated as a condition of employment (i.e., for work-related reasons), then any adverse reaction to the COVID-19 vaccine is work-related. The adverse reaction is recordable if it is a new case under 29 CFR 1904.6 and meets one or more of the general recording criteria in 29 CFR 1904.7.


    This clarification comes as an increasing number of employers seek to mandate the experimental injections despite possible illegality. The Wall Street Journal (WSJ) reported this beginning trend in varieties of fields, including machine operators, office workers, restaurant waiters, and medical staff.

    "The Houston Methodist Hospital network is mandating vaccines for both existing employees and new hires, barring an exemption," Chip Cutter of the WSJ wrote. "Those who fail to comply will at first be suspended without pay, and later terminated."

    Under the new OSHA clarification, such employers may be held liable for injuries due to these requirements.

    For example, 39-year-old nurse aide Janet More died last New Year's Eve within 48 hours of receiving one of these injections. According to her brother, she at least had the impression "it was a mandatory vaccine that she had to take for her job."

    A similar case involves the sad death of 28-year-old Sara Stickles, a nutritional specialist at Swedish American hospital in Rockford, Illinois who died just five days after her second shot of one of the mRNA gene-therapy vaccines. She too had the clear impression that these injections were required by her employer.

    While the National Childhood Vaccine Injury Act of 1986 shields pharmaceutical manufacturers from any liability due to injuries or death caused by their products (which many Americans have said is significantly problematic in itself), scenarios such as these could still leave employers who mandate these injections liable for significant damages.

    And adverse events with regard to these shots are not uncommon. Data released from the Centers for Disease Control and Prevention (CDC) last Friday reveal that between December 14, 2020 and April 30 a total of 157,277 adverse events were passively reported to the U.S. government's primary reporting system (VAERS), including 3,837 deaths and 16,014 serious injuries.

    While causation is not explicitly confirmed through the VAERS reporting system, neither can it be presumed that all such adverse events are reported. Indeed, one study in 2010 found that "fewer than 1 percent of vaccine injuries" are reported to VAERS, suggesting the actual numbers of deaths and injuries due to these experimental substances are significantly higher.

    Furthermore, it's also possible employers requiring these injections may be held legally liable for violating federal law. According to America's Frontline Doctors (AFLDS), products approved for emergency use only "are prohibited from being mandated by federal law." The U.S. Food and Drug Administration's emergency use authorization (EUA) specifically states that individuals must have the free "option to accept or refuse" these vaccines. Many argue the prospect of being terminated from one's job by refusing such vaccines certainly undermines such necessary freedom.

    Therefore, attorneys Mary Holland, president of Children's Health Defense, and Greg Glaser warned last January that employers and universities who seek to defy the EUA law and attempt to require such injections of employees and students "are likely to lose if challenged in court."

    In order to assist individuals who wish to challenge their employers, schools, or universities that are requiring experimental COVID-19 vaccine injections, AFLDS has provided a template letter that can be sent to these entities and persons putting them on notice of their legal vulnerability.

    "The law is clear. An experimental vaccine cannot be mandated," the introduction reads. And the text, drafted in the second person to the mandating authority, states, "Any employer, public school, or any other entity or person who mandates experimental vaccines on any human being is not protected from liability for any resulting harm. While vaccine manufacturers may be shielded from liability, your institution is not protected, and neither are you."

    The Informed Consent Action Network's legal team is also offering help to individuals in this difficult position.

    More information can be found here. Forced to Get the COVID Vaccine? ICAN May Be Able to Help. • Children's Health Defense









    This I say therefore, and testify in the Lord, that ye henceforth walk not as other Gentiles walk, in the vanity (futility) of their mind, having the understanding darkened...
    (Ephesians 4:17-18)

    Blessed is the man that walketh not in the counsel of the ungodly...
    (Psalm 1)

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  3. #2
    Administrator fuego's Avatar
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    Well that for sure would stop them from requiring it. You'll find out just how much they really believe in the vaccine or or just virtue signaling.

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  5. #3
    My job (at a state university) is requiring it. The question of liability has come up, especially since other state workers are not required to, in fact, other state workers are being paid $100 to get the vaccine. We (who are also state workers) are not eligible for the $100 since we don't have a choice. Considering that we had doctors (and lawyers) on the committee that made the recommendation, I would really be curious about how they addressed those issues.

  6. #4
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    Quote Originally Posted by Susan View Post
    My job (at a state university) is requiring it. The question of liability has come up, especially since other state workers are not required to, in fact, other state workers are being paid $100 to get the vaccine. We (who are also state workers) are not eligible for the $100 since we don't have a choice. Considering that we had doctors (and lawyers) on the committee that made the recommendation, I would really be curious about how they addressed those issues.
    I couldn't care less whether a person gets the vaccine or not. But when it starts being mandated by companies, sports arenas. Govt. employers, etc, that does tend to rile me somewhat.

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  8. #5
    UPDATE:


    OSHA says employers who mandate the COVID vaccine won't have to report its adverse effects
    Agency wants to avoid "discouraging workers" from receiving shot.
    OSHA says employers who mandate the COVID vaccine won't have to report its adverse effects | Just The News

    The Occupational Safety and Health Administration has relaxed its rules for reporting work-related adverse events involving the COVID-19 vaccine, releasing employers from an earlier requirement that they report any incidents suffered by their employees due to a mandated vaccine.

    In April, OSHA said on its website that any businesses that require the COVID-19 vaccine as a condition of employment are required to report adverse reactions that arise from an employee's taking the vaccine.

    "If you require your employees to be vaccinated as a condition of employment (i.e., for work-related reasons), then any adverse reaction to the COVID-19 vaccine is work-related," the agency said, directing employers to follow standard reporting protocol in such cases.

    Yet by this month, OSHA had reversed that determination
    , updating the guidance on its website to clarify that employers no longer have to make an entry in the business's "OSHA recordkeeping log" if an employee experiences a medical event due to the vaccine.

    "[The Department of Labor] and OSHA, as well as other federal agencies, are working diligently to encourage COVID-19 vaccinations," the new guidance states. "OSHA does not wish to have any appearance of discouraging workers from receiving COVID-19 vaccination, and also does not wish to disincentivize employers' vaccination efforts."

    "As a result, OSHA will not enforce 29 CFR 1904's recording requirements to require any employers to record worker side effects from COVID-19 vaccination through May 2022. We will reevaluate the agency's position at that time to determine the best course of action moving forward."

    The U.S. Centers for Disease Control and Prevention, meanwhile, has listed numerous potentially fatal adverse events associated with the COVID-19 vaccine, though all of them appear to be rare relative to the tens of millions of shots administered so far.

    Among those alleged adverse events is "thrombosis with thrombocytopenia syndrome," a condition which involves blood clots, as well as anaphylaxis, a condition which, in the rare instances it has been reported, "almost always occurs within 30 minutes after vaccination."

    The CDC, via its Vaccine Adverse Event Reporting System, says that several thousand deaths have occurred following the administration of the COVID-19 vaccine, though "a review of available clinical information, including death certificates, autopsy, and medical records has not established a causal link to COVID-19 vaccines."

    "Over 285 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through May 24, 2021," the agency reported on its website."During this time, VAERS received 4,863 reports of death (0.0017%) among people who received a COVID-19 vaccine."
















    This I say therefore, and testify in the Lord, that ye henceforth walk not as other Gentiles walk, in the vanity (futility) of their mind, having the understanding darkened...
    (Ephesians 4:17-18)

    Blessed is the man that walketh not in the counsel of the ungodly...
    (Psalm 1)

  9. #6
    Senior Member Smitty's Avatar
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    Our Company has not mandated or forced us as of yet to take the vaccine or "else."
    But I did print out the letter to present to them if they take any future measures to "force" us to take the "jab" or face termination.
    If you put God First, you have Him at Last.

  10. #7
    The question is, what was the reason for the death, was it the vaccine or something else.
    In the case of the second woman mentioned there was a autopsy and it showed that she died from a aneurysma in her brain.
    This is a sudden death always unexpected. You do not feel if you have a aneurysma. You are born with this condition. Over the years it grows, the walls of the vessel get thinner and thinner and suddently tear. The bleeding into the brain cause quickly big damage destroying the brain tissue. This is mostly ending with the tragic death of people.
    Now it has been told that with a different vaccine as the one she got there is clotting in blood vessel, the opposite to bleeding.
    From my work I know how this can be a huge shock, specially if it is a young person who is totally healthy, but the reason is a anormality by birth not a vaccination.

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    Administrator fuego's Avatar
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    Quote Originally Posted by tschau View Post
    The question is, what was the reason for the death, was it the vaccine or something else.
    In the case of the second woman mentioned there was a autopsy and it showed that she died from a aneurysma in her brain.
    This is a sudden death always unexpected. You do not feel if you have a aneurysma. You are born with this condition. Over the years it grows, the walls of the vessel get thinner and thinner and suddently tear. The bleeding into the brain cause quickly big damage destroying the brain tissue. This is mostly ending with the tragic death of people.
    Now it has been told that with a different vaccine as the one she got there is clotting in blood vessel, the opposite to bleeding.
    From my work I know how this can be a huge shock, specially if it is a young person who is totally healthy, but the reason is a anormality by birth not a vaccination.
    And therein lies the double standard/hypocrisy. When counting statistics for deaths from covid, there was hardly any discrimination at all on what actually killed them. It was listed as covid no matter what. Now that they won't have to report any ill affects, because we all know that maybe it wasn't the virus that killed them but a deeper problem and we don't want them held liable for that. They sure weren't worried about what really killed people when inflating their statistics concerning covid deaths. Hypocrisy.

  13. #9
    This I say therefore, and testify in the Lord, that ye henceforth walk not as other Gentiles walk, in the vanity (futility) of their mind, having the understanding darkened...
    (Ephesians 4:17-18)

    Blessed is the man that walketh not in the counsel of the ungodly...
    (Psalm 1)

  14. #10
    So if the Son sets you free, you will be free indeed. John's Avatar
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    You can download the database of Adverse reactions here:

    VAERS - Data

    252,524 adverse reactions reported.

    1336296,05/21/2021,NJ,,,,F,,"Hospitalized with a major surgery/ Some blood leakage in brain; Was in the hospital longer than than expected and has not received the second dose/ Missed second dose of Moderna-covid-19 vaccine; This spontaneous case was reported by a consumer and describes the occurrence of CEREBRAL HAEMORRHAGE (Hospitalized with a major surgery/ Some blood leakage in brain) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Brain operation in March 2021. On 15-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In March 2021, the patient experienced CEREBRAL HAEMORRHAGE (Hospitalized with a major surgery/ Some blood leakage in brain) (seriousness criteria hospitalization prolonged and medically significant). On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (Was in the hospital longer than than expected and has not received the second dose/ Missed second dose of Moderna-covid-19 vaccine). The patient was hospitalized on 01-Mar-2021 due to CEREBRAL HAEMORRHAGE. At the time of the report, CEREBRAL HAEMORRHAGE (Hospitalized with a major surgery/ Some blood leakage in brain) and PRODUCT DOSE OMISSION ISSUE (Was in the hospital longer than than expected and has not received the second dose/ Missed second dose of Moderna-covid-19 vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were provided. Patient had received the first dose of the Moderna Covid-19 vaccine and ended up being hospitalized in March with a major surgery that involved some blood leakage in brain. Patient had essentially missed the second Moderna Covid-19 dose scheduled in mid-March and at the time of reporting patient was about 90 days after receiving the first Moderna Covid-19 vaccine. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 11-May-2021: follow up received on 11-May-2021 Updated the Reporter, patient information and serious event added.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, Very limited information regarding these events has been provided at this time. Further information has been requested.",,,,,Y,,,,U,02/15/2021,03/01/2021,14,,UNK,,,,Medical History/Concurrent Conditions: Brain operation,,"USMODERNATX, INC.MOD20211",2,05/21/2021,,,,


    1336297,05/21/2021,PA,74.0,74,,M,,"Hallucination; This spontaneous case was reported by a consumer and describes the occurrence of HALLUCINATION (Hallucination) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. In April 2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Apr-2021, the patient experienced HALLUCINATION (Hallucination) (seriousness criterion medically significant). At the time of the report, HALLUCINATION (Hallucination) had not resolved. No concomitant medications were provided. No treatment drugs were reported. It was reported that patient refuses to see a doctor and says that everyone else is crazy. Company comment: Limited information regarding the second vaccination dose has been provided at this time and insufficient to assess the temporal association. No follow up is possible. A causal relationship cannot be excluded. Most recent FOLLOW-UP information incorporated above includes: On 09-May-2021: Follow up received on 09 May 2021 included no new information.; Sender's Comments: Limited information regarding the second vaccination dose has been provided at this time and insufficient to assess the temporal association. No follow up is possible. A causal relationship cannot be excluded.",,,,,,,,,N,04/01/2021,04/08/2021,7,,UNK,,,,,,"USMODERNATX, INC.MOD20211",2,05/21/2021,,,,


    1336298,05/21/2021,AZ,75.0,75,,M,,"Brain embolism; Missed second dose (51 days since first dose); Feeling a little weak; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of CEREBRAL ARTERY EMBOLISM (Brain embolism) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 003B21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history reported. On 20-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Apr-2021, the patient experienced CEREBRAL ARTERY EMBOLISM (Brain embolism) (seriousness criteria hospitalization, medically significant and life threatening). On 09-May-2021, the patient experienced ASTHENIA (Feeling a little weak). On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (Missed second dose (51 days since first dose)). The patient was hospitalized until 08-May-2021 due to CEREBRAL ARTERY EMBOLISM. On 08-May-2021, CEREBRAL ARTERY EMBOLISM (Brain embolism) had resolved. At the time of the report, ASTHENIA (Feeling a little weak) had not resolved and PRODUCT DOSE OMISSION ISSUE (Missed second dose (51 days since first dose)) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant products included cholesterol medication, high blood pressure medication, anxiety medication, allergies medication, and medication for brain embolism. Company comment:This case concerns a 51-year-old male who experienced cerebral artery embolism and asthenia and missed second dose (51 days since first dose) (missed dose). Based on the current available information and temporal association between the use of mRNA-1273 and the onset of the events of cerebral embolism and asthenia, a causal relationship cannot be excluded. The event of missed dose is assessed as not applicable.; Sender's Comments: This case concerns a 51-year-old male who experienced cerebral artery embolism and asthenia and missed second dose (51 days since first dose) (missed dose). Based on the current available information and temporal association between the use of mRNA-1273 and the onset of the events of cerebral embolism and asthenia, a causal relationship cannot be excluded. The event of missed dose is assessed as not applicable.",,,Y,,Y,,,,N,03/20/2021,04/17/2021,28,,UNK,,,,Comments: No medical history reported.,,"USMODERNATX, INC.MOD20211",2,05/21/2021,,,,


    1336299,05/21/2021,OH,37.0,37,,M,,"Bell's Palsy; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of BELL'S PALSY (Bell's Palsy) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 025B21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Apr-2021, the patient experienced BELL'S PALSY (Bell's Palsy) (seriousness criterion medically significant). On 07-May-2021, BELL'S PALSY (Bell's Palsy) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication were reported. Patient stated, he was given 2 medications of unknown names for treatment of bells palsy and symptoms gone way after a week of taking those meds. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Most recent FOLLOW-UP information incorporated above includes: On 10-May-2021: Event start date, stop date and outcome updated. Vaccine given date updated.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.",,,,,,,,,Y,04/13/2021,04/26/2021,13,,UNK,,,,,,"USMODERNATX, INC.MOD20211",2,05/21/2021,,,,


    1336300,05/21/2021,OH,,,,F,,"acute anaphylactic shock; A.fib; blurry vision; swollen lips; Numbing sensation in her hands and lips; tingling sensation in her hands and lips; This spontaneous case was reported by a consumer and describes the occurrence of ANAPHYLACTIC SHOCK (acute anaphylactic shock) and ATRIAL FIBRILLATION (A.fib) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 048B21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 11-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-May-2021, the patient experienced ANAPHYLACTIC SHOCK (acute anaphylactic shock) (seriousness criterion medically significant), ATRIAL FIBRILLATION (A.fib) (seriousness criterion medically significant), VISION BLURRED (blurry vision), LIP SWELLING (swollen lips), HYPOAESTHESIA (Numbing sensation in her hands and lips) and PARAESTHESIA (tingling sensation in her hands and lips). At the time of the report, ANAPHYLACTIC SHOCK (acute anaphylactic shock), ATRIAL FIBRILLATION (A.fib), VISION BLURRED (blurry vision), LIP SWELLING (swollen lips), HYPOAESTHESIA (Numbing sensation in her hands and lips) and PARAESTHESIA (tingling sensation in her hands and lips) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was withdrawn on an unknown date. Treatment for the events included diphenhydramine, metoclopramide, ketorolac, prochlorperazine and prednisone. The patient was advised not to receive the second dose of vaccine by her healthcare provider. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of these events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of these events, a causal relationship cannot be excluded.",,,,,,,,,U,05/11/2021,05/11/2021,0,,UNK,,,,,,"USMODERNATX, INC.MOD20211",2,05/21/2021,,,,
    I snipped out 5 reports. Tschau, when you get done analyzing these and ruling out the vaccine, I'll post a few hundred thousand more.

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