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FDA to add blood clot warnings on J&J coronavirus vaccines


Food and Drug Administration (FDA) said the Johnson & Johnson Wuhan coronavirus (COVID-19) vaccine will now include a warning about blood clotting risks. Its announcement came after the
Centers for Disease Control and Prevention (CDC) lifted the suspension of the single-dose COVID-19 vaccine. The two government agencies previously recommended a halt on the J&J vaccine amid reports of blood clots with low platelet count in some patients.
According to the CDC’s Mortality and Morbidity Weekly Report for April 30, the FDA has added a warning for patients 18 to 49 years old regarding “clotting events … reported among vaccine recipients.” It emphasized the importance of the warning “to ensure that women aged [below] 50 years old are aware of the increased risk [of the clots] … and that other COVID-19 vaccines are available.” The report recommended that updated fact sheets for the vaccine should be provided to both recipients and their caregivers before inoculatio ....

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Denmark PERMANENTLY BANS Johnson & Johnson coronavirus vaccine over blood clot deaths


https://www.afinalwarning.com/516522.html
(Natural News)
Denmark announced that it will no longer use the Johnson & Johnson Wuhan coronavirus (COVID-19) vaccine after more reports linking it to blood clots. The Scandinavian country previously dropped the AstraZeneca vaccine because of blood clots in some vaccinated citizens. Denmark’s decision contrasted that of U.S. health authorities who lifted the suspension on the J&J vaccine.
The
Danish Health Authority (SST) announced the suspension in a May 3 statement. It said that “the benefits of using the [J&J] COVID-19 vaccine do not outweigh the risk of causing the possible adverse effect [of blood clots.] Therefore, the [SST] will continue the Danish mass vaccination program without the COVID-19 vaccine from Johnson & Johnson.” ....

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Vax deaths continue to mount up as Oregon woman dies from blood clot after getting J&J vaccine


https://www.afinalwarning.com/513904.html
(Natural News)
A 50-year-old woman in Oregon died of a blood clot about two weeks after she got the single-dose Johnson & Johnson Wuhan coronavirus vaccine. State officials confirmed her death on April 22, becoming the 10th person to suffer from the said adverse reaction. The report of the woman’s death came a day before advisers to the
Centers for Disease Control and Prevention (CDC) would meet regarding the vaccine’s suspension.
Oregon Health Authority (OHA), it received word of the adverse reaction on April 20. Two days earlier, on April 18, the CDC was notified of the incident. The statement noted that the woman received the one-dose vaccine before authorities recommended halting its use temporarily. ....

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J&J coronavirus vaccine shipments halted due to ingredient MIX-UP during production


https://www.afinalwarning.com/508309.html
(Natural News)
Fifteen million doses of the Johnson & Johnson Wuhan coronavirus vaccine were ruined as a result of the wrong ingredient being added during production. The incident occurred in a factory in west Baltimore which federal authorities flagged for multiple violations. Because of the mishap, delays have been anticipated in the federal government’s vaccine rollout.
A government official said the
Department of Health and Human Services (HHS) discovered that Emergent BioSolutions ruined the 15 million doses by adding the wrong ingredient. The company’s Bayview facility in Baltimore is also producing AstraZeneca vaccines. Unfortunately, workers at Emergent accidentally included an ingredient meant for the AstraZeneca jabs in a batch of J&J vaccines. ....

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Company that helps Johnson & Johnson produce coronavirus vaccines has a string of citations for quality control problems


Food and Drug Administration (FDA) for quality control problems in the past.
Johnson & Johnson announced Wednesday, March 31, that a batch of its COVID-19 vaccine could not be used because it did not meet quality standards. Specifically, a vaccine ingredient made by Emergent BioSolutions at its Baltimore factory failed to meet quality standards. Johnson & Johnson said the factory, known as Bayview, had not yet been approved by the FDA to make part of the vaccine.
It was unclear how many doses had been discarded and how the problem would affect future deliveries of Johnson & Johnson’s vaccine. But it was clear from the start that Emergent is a disaster waiting to happen for Johnson & Johnson. (Related: Johnson & Johnson threw out 15 MILLION DOSES of its coronavirus vaccine after sloppy worker mixed in the WRONG ingredient.) ....

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