Murder in Virginia through Johnson’s evacuation trunk

This March, the United States will be alerted by the CDC (Centers for Control and Prevention of Diseases) and the FDA (United States Food and Drug Administration) revealing that there are 7 million doses available. of the Johnson & Johnson COVID vaccine, 6 people report suffering a preoperative secondary effect: the appearance of blood clots. For this reason, the application of this medicine is temporarily suspended, as has been researched into the cases.

The most preoccupying of all is that of the six individuals who received the dose of J&J presented serious adverse effects, one of them, a female of the state of Virginia wall.

Otra, from the state of Nebraska, finds himself in critical condition in a hospital, according to the New York Times.

The citation was aggregated that the woman failed to kill the Johnson & Johnson vaccine and that she was hospitalized, even though the other four remained, all were female sex patients, between 18 and 48 years old.

Death of a woman in Virginia after connecting the Johnson & Johnson vaccine to FDA investigationWe now know that the woman who died after receiving the vaccination was from Virginia.2021-04-13T22: 08: 50Z

FOX News has revealed that the health authorities are investigating the failure of the woman, who has not revealed her identity, as part of the larger investigation that she initiated to know more about the “adverse secondary effects” of the Johnson & Johnson evacuation reported to the moment,

FOX quoted Virginia State Vacation Coordinator Danny Avula as confirming that the death of the woman was mentioned in March, passed in March and is under investigation to establish whether or not it has any effects related to the Johnson & Johnson evacuation haber desencadenado su muerte.

The employee warned that when the decision of the woman was made, it was reported to the Notification Event of the Adverse Events in the CDC Vacancies.

“We are monitoring the actions of the federal governor to detain all of Johnson & Johnson’s vacancies while investing in a potentially extremely rare secondary effect. In Virginia, we will remove all Johnson & Johnson vehicles until this investigation is complete, ”the official said in a statement.

The death of a Virginia woman is part of the Johnson & Johnson investigationThe death of a woman in Virginia who received a Johnson & Johnson COVID-19 vaccine is part of the Centers for Disease Control & Prevention (CDC) investigating the side effects of the vaccine.2021-04-13T23: 22: 23Z

This break is a tranquilizer, which demonstrates that the systems that exist to monitor the safety of the vacancies are in operation. We are conducting an exhaustive overhaul on behalf of federal health officials. While we are doing this, we will continue the launch of the Virginia Vacancy at the moment with the other authorized vacancies, developed by Pfizer and Modern, ”he said. “The people who received the Johnson & Johnson vaccine and who developed intense cabbage pain, abdominal pain, pain in the pains or difficulty breathing during the last three weeks of the evacuation must communicate with their medical attention provider11 or the patient.” if it is a medical emergency ”.

About the woman who was found grave in the state of Nebraska, the Local Television Notice 6 News assured that a woman of 48 years had been taken “vacated by Johnson & Johnson Lot No. 1805020 on March 9 ”.

As for his condition, he was mentioned in the middle of the day: “he is currently hospitalized with deep hemorrhage and coagulation, suspected of having dysfibrinogenemia…. The information from the CDC, on the basis of the notification system for event notifications of vacancies known as VAERS, enumerates the condition of the woman as grave and “potentially mortal”.

To get acquainted with the situation with the evacuation of Johnson & Johnson, the Dr. Peter Marks, Director of the FDA’s Evaluation and Biological Investigation Center. Anne Schuchat, director of the CDC directorate and deputy head:

“People who have received the J&J vaccine and who develop severe cerebral palsy, abdominal pain, pain in the eyelids or failure to breathe during the last three weeks of the evacuation must communicate with their medical attention provider.”

Frenan evacuates Johnson & Johnson in EUA due to thrombosisThe Food and Drug Administration (FDA) also sought to free the application of the vaccine against # COVID19 from Johnson & Johnson by detecting possible cases of thrombosis in its females, 10 days after inoculation.2021-04-13T15: 14: 43Z

“Apply for medical attention providers to notify adverts of the vacancy notification system in https://vaers.hhs.gov/reportevent.html”, aggregate.

Agrarian officials: “At the moment, these adverse events are extremely rare. The safety of the COVID-19 vacancy is a maximum priority for the federal governor, and we will take very seriously all the information on posterior health problems in the COVID-19 vacancy ”.

The FDA and the @CDCgov issue a Johnson & Johnson vacancy statement to the # COVID-19. We recommend a break in the use of this vacancy for precaution. https://t.co/EOaNEScaRL

– US FDA and Español (@FDAenEspanol) 13 April 2021

Regarding the hallucinations in the six cases reported: “In these cases, a type of blood clot was observed called thrombosis of the cerebral venous vein (CVST) in combination with low levels of plaque in the blood (thrombocytopenia). The six cases will occur between women from 18 to 48 years, and the cases will be presented from 6 to 13 days after the evacuation. The treatment of this specific type of blood clot is different from the treatment normally administered. Generally, an anticoagulant drug called heparin is used to treat blood clots. In this context, the administration of heparin can be dangerous and it is necessary to administer alternative treatments ”.

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