The Food and Drug Administration suspends Johnson and Johnson experimental COVID shots due to severe side effects

by Brian Shelvey

The US Food and Drug Administration (FDA) announced today that it has recommended discontinuation of the Johnson and Johnson experimental COVID vaccine “out of great caution.”

From others Twitter account:

The U.S. Food and Drug Administration and CDCgov today released a statement regarding the Johnson & Johnson # COVID19 vaccine. We recommend that this vaccine be discontinued out of extreme caution.

As of 12/4, a 6.8m + dose of J&J vaccine has been administered in the US CDC and the FDA is reviewing data that includes 6 reported US cases of rare and severe type of blood clot in individuals after receiving the vaccine. For now, these negative events appear to be extremely rare

The treatment for this specific type of blood clot differs from the treatment that may usually be given.

The CDC will hold a meeting of the Advisory Committee on Immunization Practices (ACIP) on Wednesday to further review these cases and assess their potential significance. The Food and Drug Administration will review this analysis because it also investigates these cases.

For this process to be completed, we recommend this pausing. This is important to ensure that the healthcare provider community is aware of the potential for these adverse events and can plan due to the unique treatment required with this type of blood clot.

They later held a conference call about a J&J vaccine that was recorded on YouTube.

ZeroHedge News I posted some notes regarding the call:

Health officials who spoke on today’s call began repeating details about J&J’s halt decision that had been shared with the press earlier. Officials said they would share with doctors new vaccine “fact sheets” that outline some drugs that could be associated with a higher risk of blood clots.

After they said they only see symptoms in patients who received the JNJ vaccine, the first question from the press (posed by an FT reporter) was: What about AstraZeneca? In Europe, governments have imposed age restrictions on who can receive the AstraZeneca injection for similar reasons.

Officials responded by pushing aside a question from A to Z, before saying that they only hoped the halt would last for a few days. After pressing the cause of the clots, doctors said the extremely rare immune response triggers blood clots by sending signals in patients’ blood to clot. While they said they did not see complications with the other vaccines, Dr. Marks said the United States believes the problem with the JNJ and AZ vaccines is “related” to the adenovirus platform, although he did not provide many details.

At one point, Dr. Marx said: “The real thing observed here is not just the brain blood clusters … it happens together that creates a pattern, and this pattern is very similar to what was seen with another vaccine.”

A CNN reporter stated that they had been told this was something “being considered” earlier, and Schuchat explained that the CDC had first looked at how best to advise the healthcare community for treatment and response.

The FDA has left the door open to the possibility of drawing attention to new cases of blood clots. The Food and Drug Administration will actively research vaccines. The new guidelines to be released will help educate clinicians and other healthcare professionals about risk factors that could put patients at risk for an autoimmune reaction.

After providing examples of symptoms that might be on the list of possible warning signs, Dr. Marx was pressed to open more information about the symptoms after the doctor who was on the call asked him what specific symptoms these patients had noticed. The doctor noted that including “headache” in the list of suspected symptoms or “abdominal pain” could lead to further tests and doctor visits. At this time, Marx appears to be having trouble putting a number on the background rate for blood clots, and other questions about the prevalence of symptoms that can be seen on the FDA’s menu.

“This will translate into a lot more doctor visits for people like me,” the doctor said.

The press conference ended soon after. Of course, it’s not hard to understand why the FDA feels so uncomfortable. A wave of patients being asked to seek emergency care as a precaution could raise emergency occupancy rates once again. Suddenly, the numbers will tell us we’re back in the worst of the COVID pandemic.

Read the full article at ZeroHedge News.

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Dr. Merrill Nass, MD He commented on the decision to stop vaccinations today, raising questions about which lab actually made these batches that were distributed in the United States:

After closing several clinics in 4 states, due to a large number of adverse reactions to the J and J vaccines (which were not described but included many hospitalizations), the CDC and the US Food and Drug Administration discontinued the use of these vaccines. While it takes more time, see what happens. I heard this that a local person was hospitalized with a dangerous blood clot.

My question was, was this J and J vaccine really made by Janssen in the Netherlands, or was it perhaps an emergency vaccine made by BioSolutions that slipped through the back door before it was authorized, was packaged elsewhere and put into the vaccine made in Europe? Why are so many reactions suddenly?

I have been cautioning against using an EBS vaccine for more than 6 months. OTOH, vaccine design could be what’s causing the problems. Perhaps the adenovirus vector is the problem. Maybe a spike. Maybe something else. Please be careful! We are very close to herd immunity in most of the United States. We can treat this virus successfully.

When public health officials use the term “an abundance of caution,” you know what that means: “We’re broken up!”

Read the full blog post here.

Donald Trump is angry with the Food and Drug Administration – showing no concern for vaccine victims

Former President Donald Trump released a statement expressing his displeasure with the Food and Drug Administration for stopping the Johnson & Johnson footage. This was reportedly sent via email from the owner Save America Buck (Source):

The Biden administration has done terrible harm to people around the world by allowing the Food and Drug Administration and the CDC to stop using the Johnson & Johnson COVID-19 vaccine.

The results of this vaccine were extraordinary but now my reputation will be constantly challenged.

People who have already been vaccinated will be on alert, and it may have been all done for the sake of politics or maybe it was the FDA’s love for Pfizer.

The Food and Drug Administration needs to be controlled, especially with bureaucrats for so long within it.

They should not be able to cause such harm for possible political reasons, or perhaps because their friends at Pfizer suggested so.

They will do things like that to make themselves look important.

Remember, the FDA is working with Pfizer, which announced approval of the vaccine two days after the 2020 presidential election. They didn’t like me very much because I pushed them too hard. But if I don’t, you won’t have a vaccine for 3-5 years, or maybe not at all. It takes them years to work!

Test, clean up the registry, and quickly put Johnson & Johnson vaccine online.

The only way to defeat the China virus is with our great vaccines!

Read more at Health Impact News

What do you think?

Written by Joseph

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