Vaksin Unapproved !

Dari situs resmi CDC yang menyatakan bahwa vaksin2 mrna yang belum di approve bisa diijinkan krn situasi Emergency :

An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives.

CDC adalah :

https://www.fda.gov/vaccines-blood-biologics/vaccines/emergency-use-authorization-vaccines-explained

Karena vaksin mrna buatan Amerika/Eropa ini baru ditemukan dan baru dicoba pada manusia dlm situasi sangat Emergency sehingga efek jangka panjang 5 tahun keatas belum diketahui khususnya pada saraf manusia, meskipun hal ini dibantah oleh produsen yg belum memiliki data jangka panjang dan dengan entengnya setiap kasus2 effek seriuss spt kematin sesudah vaksin selalu dibantah dan sulit dibuktikan. Padahal ilmu kedokteran dan farmasi itu selalu berkembang dan butuh perbaikan2 dan disempurnakan agar aman, bukan main bantah saja.

Pfizer Vaccine Confirmed to Cause Neurodegenerative Diseases :

In a shocking new report on the COVID-19 vaccines, it has been discovered that the Pfizer coronavirus vaccine may have long term health effects not previously disclosed, including “ALS, Alzheimer’s, and other neurological degenerative diseases.”

“The current RNA based SARSCoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing,” the report declares.

“In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients.” Prion-based diseases are, according to the CDC, a form of neurodegenerative diseases, meaning that the Pfizer vaccine is potentially likely to cause long term damage and negative health effects with regards to the brain.

This is especially concerning since the Pfizer vaccine is an mRNA vaccine, an untested type of vaccine which creates new proteins and can actually integrate into the human genome, according to a report from the National Library of Medicine. In other words, degenerative brain conditions may appear at any time in your life after receiving the vaccine.

“The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations,” explains the report. TDP-43 is a protein known to cause dementia, ALS and even Alzheimer’s, according to Alzpedia. Similarly, the FUS protein is known to cause ALS and Hereditary Essential Tremors, according to the Human Genome Database.

The experiment done for the report was to determine whether or not these two harmful proteins embed themselves into our DNA, as an mRNA vaccine is expected to do. The report determined that “the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations,” meaning that both proteins have the potential to embed themselves into our DNA and cause harmful neurological diseases.

The report’s abstract summary concludes that

“The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.” The report itself ends with this warning: “

The vaccine could be a bioweapon and even more dangerous than the original infection.”

National File actually reached out to the CDC to inquire as to why the Pfizer vaccine is still being distributed despite these credible allegations. No response was received prior to publication.

Dikutip dari situs FDA diatas : These studies provide additional safety information on common short-term side effects and risks"

FDA hanya memantau efek jangka pendek pada relawan2 ujicoba dan efek 5 thn keatas pada saraf motorik manusia belum diketahui krn vaksin ini statusnya Emergency dan Unapproved.

Quoted from FDA ;
An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives.

Bahan2 vaksin :
How are vaccines developed?)&gclid=EAIaIQobChMIiJ6C1L_n8AIVyZ1LBR3z2QxPEAAYASAAEgLmnPD_BwE

Di zona MEE tercatat 316 kasus blood clotting sesudah vaksinasi AstraZenecca