Over 6.8 million Americans have received the Johnson & Johnson C****-** v*****e, which is now facing renewed scrutiny after six of those recipients developed a rare, severe type of blood clot that has caused the FDA and Centers for Disease Control and Prevention (CDC) to recommend a pause in the rollout. But for those millions who have already received the one-shot v*****e, what does that mean?

According to the FDA, all six cases involved women between the ages of 18 and 48, and the symptoms occurred six to 13 days post-v******tion. The blood clot, called cerebral venous sinus thrombosis, which was seen in combination with low levels of blood platelets, is treated differently than other clots.

As such, the agency now recommends that people who have received the Johnson & Johnson v*****e and develop severe headache, abdominal pain, leg pain, or shortness of breath within three weeks after inoculation contact their health care provider.

Health care providers are also being asked to report such a*****e e***ts to the V*****e A*****e E***t Reporting System. The agency said the pause is also meant to inform the health care community so that they can better prepare for the potential occurrence of these clots, and "plan for proper recognition and management due to the unique treatment required."

https://www.foxnews.com/health/johnson-johnson-c****-**-v*****e-what-to-do
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In my opinion, if you develop severe headache, abdominal pain, leg pain, or shortness of breath within any time frame of receiving this v*****e - or any of them - you should contact your doctor.....blood clots are very dangerous.

IBM Deutschland Press Release

Fresh off the heels of its most recent scandal, J&J’s Public Relations Department acknowledged intentionally lacing its baby powder with deadly asbestos and assured the public its experimental v*****e would not contain asbestos as an active ingredient.

Today, in a carefully crafted statement, J&J acknowledged inducing malignant mesothelioma in mothers and children had negatively impacted its marketing budget.The public should know, J&J is committed to proactively resolving all future inadvertent disclosures. J&J’s CEO also admitted, getting caught manufacturing carcinogenic baby powder was a nuisance and offered his sincere apology to his Board of Directors for the distraction.

According to the FDA, J&J’s marketing statement more than compensates the the millions of children and their parents who were injured or k**led by J&J’s deadly Baby Powder product.

In response, J&J contributed $100 to the FDA’s Good Corporate Citizen’s Fund and thanked its embedded employees at the Agency for understanding how difficult it was for J&J to agree on the wording of its statement. J&J emphasized that without total indemnity for their crimes against humanity, J&J’s Board would never have admitted its failure to contain a rogue whistleblower had become a distraction.

With J&J’s mass murder behind us, the FDA is assured J&J’s non peer reviewed “v*****e” safety studies can be completed by 2034.

According to IBM Reichsstaffelfuhrer Dr Bill Gates and Holy Roman Emperor Klaus Schwab, J&J’s recombinant DNA adenov***s, in combination with AstraZeneca’s modified Chimpanzee feces, are now definitively poised, after 75 years, to deliver the fatherland its “final solution.”

Over 6.8 million Americans have received the Johnson & Johnson C****-** v*****e, which is now facing renewed scrutiny after six of those recipients developed a rare, severe type of blood clot that has caused the FDA and Centers for Disease Control and Prevention (CDC) to recommend a pause in the rollout. But for those millions who have already received the one-shot v*****e, what does that mean?

According to the FDA, all six cases involved women between the ages of 18 and 48, and the symptoms occurred six to 13 days post-v******tion. The blood clot, called cerebral venous sinus thrombosis, which was seen in combination with low levels of blood platelets, is treated differently than other clots.

As such, the agency now recommends that people who have received the Johnson & Johnson v*****e and develop severe headache, abdominal pain, leg pain, or shortness of breath within three weeks after inoculation contact their health care provider. Don't lose sight of the fact that none of these so-called '"v*****es" have been approved by FDA.

Health care providers are also being asked to report such a*****e e***ts to the V*****e A*****e E***t Reporting System. The agency said the pause is also meant to inform the health care community so that they can better prepare for the potential occurrence of these clots, and "plan for proper recognition and management due to the unique treatment required."

https://www.foxnews.com/health/johnson-johnson-c****-**-v*****e-what-to-do
*************

In my opinion, if you develop severe headache, abdominal pain, leg pain, or shortness of breath within any time frame of receiving this v*****e - or any of them - you should contact your doctor.....blood clots are very dangerous.

You do have to wonder. How many people died because the Democrat/C*******t Party demonized Hydroxychloroquine, and now Ivermectin. Both drugs have been around for decades are INEXPENSIVE, safe and have proven effective, (not only as a treatment, but as a prophylactic,) and this comes from doctors who actually treated c****-** patients, and had to fight to do so in many cases thanks to the Democrat/C*******t Party. Last year when it was determined that it was a C****av***s we were dealing with, (and before it was politicized,) I heard a doctor on the radio who in response to the question of "what's the best thing to do?" replied, start by taking large amounts of vitamin D3, vitamin C and zinc. Turns out he was right all along. So, you have to wonder why these doctors were vilified, and why inexpensive therapeutics were demonized, and still are.

Over 6.8 million Americans have received the Johnson & Johnson C****-** v*****e, which is now facing renewed scrutiny after six of those recipients developed a rare, severe type of blood clot that has caused the FDA and Centers for Disease Control and Prevention (CDC) to recommend a pause in the rollout. But for those millions who have already received the one-shot v*****e, what does that mean?

According to the FDA, all six cases involved women between the ages of 18 and 48, and the symptoms occurred six to 13 days post-v******tion. The blood clot, called cerebral venous sinus thrombosis, which was seen in combination with low levels of blood platelets, is treated differently than other clots.

As such, the agency now recommends that people who have received the Johnson & Johnson v*****e and develop severe headache, abdominal pain, leg pain, or shortness of breath within three weeks after inoculation contact their health care provider.

Health care providers are also being asked to report such a*****e e***ts to the V*****e A*****e E***t Reporting System. The agency said the pause is also meant to inform the health care community so that they can better prepare for the potential occurrence of these clots, and "plan for proper recognition and management due to the unique treatment required."

https://www.foxnews.com/health/johnson-johnson-c****-**-v*****e-what-to-do
*************

In my opinion, if you develop severe headache, abdominal pain, leg pain, or shortness of breath within any time frame of receiving this v*****e - or any of them - you should contact your doctor.....blood clots are very dangerous.