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Germany pauses AstraZeneca Vaxx after 31 reports of rate Blood Clots

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11 thoughts on “Germany pauses AstraZeneca Vaxx after 31 reports of rate Blood Clots”

  1. See European Medicines Agency(EMA) EudraVigilance Infographic!
    4576 DEAD and 199,213 “vaccine” INJURIES up to March 20th 2021.
    https://healthimpactnews.com/2021/4576-dead-199213-injuries-european-database-of-adverse-drug-reactions-for-covid-19-vaccines/
    Scroll down to end of the following article to where it says SEE ALSO, for the infographics for deaths and injuries in CANADA and U.K.
    6000% increase in Vaccine DEATHS in USA from 1/1/2020 to 31/3/2021 compared to the same period the previous year.
    https://medicalkidnap.com/2021/03/24/3964-dead-162610-injuries-european-database-of-adverse-drug-reactions-for-covid-19-vaccines/
    30 blood clot cases reported in U.K. following Astra Zeneca COVID injection
    https://www.rte.ie/news/world/2021/0402/1207578-britain-vaccine-clots/
    Rebuttal letter to European Medicines Agency from Doctors for Covid Ethics, April 1, 2021
    https://doctors4covidethics.medium.com/rebuttal-letter-to-european-medicines-agency-from-doctors-for-covid-ethics-april-1-2021-7d867f0121e
    PRESS RELEASE: Doctors and Scientists Accuse Medical Regulator of Downplaying COVID-19 Vaccine Dangers
    The European Medicines Agency is misleading citizens into medical experimentation, experts warn
    https://doctors4covidethics.medium.com/press-release-doctors-and-scientists-accuse-medical-regulator-of-downplaying-covid-19-vaccine-d2431d5abdab
    https://doctors4covidethics.medium.com/urgent-open-letter-from-doctors-and-scientists-to-the-european-medicines-agency-regarding-covid-19-f6e17c311595

  3. ‘The European Medicines Agency’s safety committee “has not yet reached a conclusion and the review is currently ongoing”, the Amsterdam-based EMA said in a statement.

    “We will communicate and hold a press briefing as soon as the review is finalised. This is currently expected tomorrow (Wednesday, 7 April) or on Thursday, 8 April,” it added.

    The statement came after the EMA’s head of vaccine strategy Marco Cavaleri was quoted in Italian media as saying that there was a “clear” connection and that the agency would announce it within hours.’

    ‘Marco Cavaleri said there were more cases of cerebral thrombosis among young people than expected’

    ‘….”In my opinion, we can say it now, it is clear there is a link with the vaccine. But we still do not know what causes this reaction,” Mr Cavaleri told Italy’s Il Messaggero newspaper in an interview.’

    ‘But it (the EMA) has said that a causal link between clots and the vaccine is possible and is expected to provide an updated assessment this week.

    “We are trying to get a precise picture of what is happening, to define in detail this syndrome due to the vaccine,” Mr Cavaleri said.

    He added: “Among the vaccinated, there are more cases of cerebral thrombosis … among young people than we would expect.”

    ‘Reports suggest that the Medicines and Healthcare products Regulatory Agency (MHRA) is considering proposals to restrict the use of the vaccine in younger people.’

    https://www.rte.ie/news/coronavirus/2021/0406/1208140-coronavirus-astrazeneca/

  5. ‘Meanwhile drug safety experts in the UK today said there “could be” a causal link between the vaccine and blood clots, but that the vaccination program should continue, “with risk mitigation for women under 55,” The Guardian reported.

    Saad Shakir, director of the drug safety research unit at Southampton University, told The Guardian the evidence accumulated in Europe and the UK “is consistent with causality.”

    AstraZeneca today halted the UK trial of its COVID vaccine in teenagers and children, citing “broader” concerns about blood clotting issues.’

    ‘….the Netherlands became the latest country to halt the use of AstraZeneca’s COVID vaccine. In an official statement April 2, the Netherlands Health Minister said he was suspending the vaccination for those under age 60 pending a further assessment by the EMA due to five cases of reported blood clots and the death of a woman who suffered a brain haemorrhage within 10 days of vaccination.

    Dutch Health Minister Hugo de Jonge said there should be no doubt whatsoever about the safety of vaccines.

    “The crucial question is still whether it concerns complaints after vaccination or due to vaccination,” he said in a statement, adding “it is wise to press the pause button now as a precaution.”…’

    ‘On April 5, Britain’s health regulator said it was considering a proposal to restrict the use of the AstraZeneca COVID vaccine in younger people over concerns about rare blood clots.’

    ‘…the MHRA has identified 30 cases of rare blood clot events and revealed seven people in the UK died from blood clots after getting the vaccine.’

    ‘As of March 31, the EMA had not yet identified any risk factors — such as age, sex or a previous history of blood clotting disorders — associated with AstraZeneca’s vaccine. The EMA issued a statement March 31 reiterating its previous conclusion that the vaccine’s benefits outweigh the risks, but cautioned that people should be aware of the “remote possibility” of rare blood clots and seek immediate medical attention in case of symptoms.’

    ‘Currently, Canada, Germany, France, Norway, Iceland, Denmark, Finland, Sweden and Switzerland have either suspended or placed use restrictions on AstraZeneca’s COVID vaccine.’
    6th April 2021
    https://childrenshealthdefense.org/defender/clear-link-astrazeneca-vaccine-blood-clots/

  6. The public health authorities and regulators keep saying that the benefits of the covid genetic “vaccines” outweigh the risks??!! Based exactly on what scientific data and analysis when the stages of the clinical trials have been fast tracked and accelerated to being experimented upon the mass population in general and when the cumulative and longterm risks are as yet unknown and/or public knowledge?! Some covid genetic “vaccine” clinical trials have administered various strains of a meningococcal vaccine in the control group! Is that gaming the system?!

    ‘The first cases of a rare blood clot associated with the AstraZeneca vaccine in Ireland is being investigated in a Dublin hospital.

    A 40-year-old woman is reportedly being treated in the Mater Hospital for cerebral venous sinus thrombosis (CVST), the blood clot on the brain which the European Medicines Agency has said is possibly linked to the AstraZeneca treatment.’

    ‘The patient’s sister said she was “horrendously sick” for a number of days after she received the shot.

    “After the two days she didn’t feel 100 per cent right,” she told the Irish Times.

    “On Saturday, Sunday, the 28th, 29th of March she started to develop these headaches and we were all putting it down to being a bit of stress, migraine, stuff like that but it just wouldn’t go away.

    “On Tuesday her face started to get puffy and swell up. She got an appointment with the doctor for Thursday morning and the doctor said I don’t like the look of you, and sent her straight to the Mater hospital, where she was admitted.”

    The patient will now be off work three months, won’t be able to drive for six weeks and will have to live with a relative for weeks, and possibly months, for observation reasons.’

    https://www.dublinlive.ie/news/health/astrazeneca-vaccine-blood-clot-materhospital-20347489

  9. ‘Blood thinners are needed but not heparin. Platelet transfusions aggravate the clots, so they are out. There is an urgent need to damp down the immune system, so it does not produce the PF4 antibodies. Intravenous immunoglobulin, in short supply, has been authorised by the NHS for all these cases. With appropriate treatment and earlier diagnosis as people have become aware of the symptoms, lives are being saved.’

    https://www.theguardian.com/society/2021/apr/13/how-uk-doctor-marie-scully-blood-clotting-link-astrazeneca-covid-jab-university-college-london-hospital

  10. AstraZeneca Changes Name of Vaccine to VAXZEVRIA

    The European Medicines Agency approved the change on March 25.

    ‘The British-Swedish pharmaceutical AstraZeneca announced that the COVID-19 vaccine, in conjunction with the British University of Oxford, has been renamed Vaxzevria.

    As reported in The Brussels Times, the name change was approved on March 25 following a request from the company and was announced on the website of the European Medicines Agency (EMA) and that of the Swedish National Medicines Agency (Läkemedelsverket).

    The new name does not imply a change in the formula of the vaccine, according to the Läkemedelsverket, but there will be a new labeling and packaging of the drug.

    For its part, the EMA recalled that the Vaxzevria vaccine is safe in people over 18 years of age, but that it has reduced its effectiveness from 79 to 76 percent.’

    March 31, 2021

    https://www.entrepreneur.com/article/368350

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