US calls for pause on Johnson & Johnson vaccine


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US calls for pause on Johnson & Johnson vaccine



The US Centers for Disease Control and Prevention and the US Food and Drug Administration are recommending that the United States pause the use of Johnson & Johnson’s Covid-19 vaccine over six reported US cases of a “rare and severe” type of blood clot. The six reported cases were among more than 6.8 million doses of the Johnson & Johnson vaccine administered in the United States. All six cases occurred among women ages of 18 and 48, and symptoms occurred 6 to 13 days after vaccination, according to a joint statement from the CDC and FDA. Dr. Carlos Del Rio and CNN’s Dr. Sanjay Gupta discuss the announcement.
#CNN #News

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17 Comments

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  1. 7 million people vaccinated with J J vaccine they say the place the vaccine was made was dirty and the staff were poorly trained good luck to whoever put this in their body. People look at this mess before you just put in arms. My God .

  2. Why did Israel say 12,000 people who were vaccinated (not Johnson) they had positive covid tests. But they have a cure now it is 97.5 and it's a nose spray. Why don't we have this cure in America?

  3. The challenge of change
    You have shift to new period requiring not only different skills but different ways of looking at things ? There is new continuity to change . It is no longer a matter of spasmodic shaking -up like spring clean-ing, but a progressive evolution . You need to view improvement in your knowledge and your work ways as a commonplace necessity. Tomorrow's manager must be able to move surely from policy to action in situations that will be different from anything any generations has experienced before .

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  5. Zyesami stops the replication of the COVID-19 virus and all variants (mutations) in the lungs.
    EUA coming soon!
    Relieve Therapeutics (RLFTF) owns the patent for Zyesami, and all rights worldwide.

    NeuruRX ran the FDA trials
    (BRPA, BRPAU) and has rights to sell Zyesami in America, Canada and Israel, (50% of revenue)

    NeuroRx Announces ZYESAMI™ (aviptadil, RLF-100) Met the Primary Endpoint of Its Phase 2b/3 Clinical Trial and Also Demonstrated a Meaningful Benefit in Survival from Critical COVID-19

    NeuroRx Announces ZYESAMI™ (aviptadil, RLF-100) Met the Primary Endpoint of Its Phase 2b/3 Clinical Trial and Al mm. Mom MLB c critically-ill patients with COVID-19, which is being developed in col laboration with Relief Therapeutics Holding AG (SIX:RLF, OTCQB:RLFTF).
    (PRNewsfoto/NeuroRx)
    (PRNewsfoto/NeuroRx)
    In addition to the robust overall significance across all 196 treated patients at all 10 clinical sites, the prespecified analysis of recovery from respiratory failure is clinically and statistically significant in the 127 patients treated by High Flow Nasal Cannula (HFNC) (P = .02), compared to those treated with mechanical or non-invasive ventilation at tertiary care hospitals. In this group, ZYESAMI™ patients had a 71% chance of successful recovery by day 28 vs. 48% in the placebo group (P = .017) and a 75% rate of successful recovery by day 60 vs. 55% in the placebo group.

  6. Zyesami stops the replication of the COVID-19 virus and all variants (mutations) in the lungs.
    EUA coming soon!
    Relieve Therapeutics (RLFTF) owns the patent for Zyesami, and all rights worldwide.

    NeuruRX ran the FDA trials
    (BRPA, BRPAU) and has rights to sell Zyesami in America, Canada and Israel, (50% of revenue)

    NeuroRx Announces ZYESAMI™ (aviptadil, RLF-100) Met the Primary Endpoint of Its Phase 2b/3 Clinical Trial and Also Demonstrated a Meaningful Benefit in Survival from Critical COVID-19

    NeuroRx Announces ZYESAMI™ (aviptadil, RLF-100) Met the Primary Endpoint of Its Phase 2b/3 Clinical Trial and Al mm. Mom MLB c critically-ill patients with COVID-19, which is being developed in col laboration with Relief Therapeutics Holding AG (SIX:RLF, OTCQB:RLFTF).
    (PRNewsfoto/NeuroRx)
    (PRNewsfoto/NeuroRx)
    In addition to the robust overall significance across all 196 treated patients at all 10 clinical sites, the prespecified analysis of recovery from respiratory failure is clinically and statistically significant in the 127 patients treated by High Flow Nasal Cannula (HFNC) (P = .02), compared to those treated with mechanical or non-invasive ventilation at tertiary care hospitals. In this group, ZYESAMI™ patients had a 71% chance of successful recovery by day 28 vs. 48% in the placebo group (P = .017) and a 75% rate of successful recovery by day 60 vs. 55% in the placebo group.

  7. Why anyone would trust J & J in the first place is beyond me. This is the company that put asbestos in their baby powder formula. Course CNN watchers don't care much for actual news.

  8. I took the J&J SHOT March 9th now I have luekema and had gotten my white blood count down to 20,000,00. After the shot I got a bad headach and it has not gone away. I went to my oncologist and my white blood count went up to 49,000.00. Check with your doctor before you take the shot if you have luekema!.

  9. The vaccine is the bioweapon. Specifically, the spike protein is the bioactive weapon, and it is designed to spread from person to person, being transmissible from the vaccinated in order to infect the unvaccinated.

    People who are injected with the mRNA vaccine are having their bodies turned into bioweapons factories, churning out spike protein particles which they shed through their mouths and skin, infecting everyone around them. The spike protein is biologically active and causes blood clots, leading to strokes, heart attacks, pulmonary embolism and infertility effects.

    We've finally figured out the exact mechanism of how this vaccine is designed to achieve global extermination. It's called a "self-replicating vaccine" because the vaccine spreads like a virus and infects everyone.

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