Relief Therapeutics Holding AG (RLFTF)

[changes_iv]

Comparisons Between Pfizer’s EUA, Pfizer’s Cumulative Analysis of Post-Authorization Adverse Event Reports, and New Studies Raises Several New Questions

March 17, 2022 • by Zoe Wilson

There was a recent study that was published on January 25, 2022 with data compiled from December 2020 through August 2021.

https://jamanetwork.com/journals/jama/fullarticle/2788346

Individually, heart failure (HF) and Alzheimer Disease (AD) are severe threats to population health, and their potential coexistence is an alarming prospect. In addition to sharing analogous epidemiological and genetic profiles, biochemical characteristics, and common triggers, we recently recognized common molecular and pathological features between the 2 conditions. Whereas cognitive impairment has been linked to HF through perfusion defects, angiopathy, and inflammation, whether patients with AD present with myocardial dysfunction, and if the 2 conditions bear a common pathogenesis as neglected siblings is unknown.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5142757/

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by extracellular deposits of fibrillary ß-amyloid (Aß) plaques in the brain that initiate an inflammatory process resulting in neurodegeneration. The neuronal loss associated with AD results in gross atrophy of affected regions causing a progressive loss of cognitive ability and memory function, ultimately leading to dementia. Growing evidence suggests that vasoactive intestinal peptide (VIP) could be beneficial for various neurodegenerative diseases, including AD.

https://pubmed.ncbi.nlm.nih.gov/30498985/

“FIVE FREEDOMS” – NEWS FEED: 25-Year-Old Develops Myocarditis After Moderna Vaccine, Mother Says Doctors ‘Downplayed’ Connection

In an interview with The Defender, Deborah Brenner said some doctors “were totally against” connecting her son’s heart damage to the COVID vaccine when he suffered an adverse reaction just days after receiving his first dose of the Moderna vaccine. READ Megan Redshaw’s article in The Defender

https://dailyclout.io/?s=Myocarditis+


Op-ed: The Emergency Use Law Should Be Used for Emergencies—Like Now

By Dr. Jacobo Elgozy, DO | Jan 5, 2022
Imagine you have a loved one hospitalized in intensive care facing death from Covid-19. All approved therapeutics were tried. Time has run out and you have been told to prepare for the worst. Your doctor advises there is one last drug to try, a natural protein that has been safely used in early trials and shown signs of effectiveness in rescuing patients from ventilators when all else has failed. The National Institutes of Health is doing a global study to prove its effectiveness.

FDA/NIH let our amazing NEUROPEPTIDE (AVIPTADIL) go free to cure the people!!!

Unfortunately, the Food and Drug Administration will not give Emergency Use Authorization because the medicine showed only a 92 percent chance of being effective, rather than the “magic 95 percent” that is the traditional gold standard for approving drugs.

I was that patient. I contracted Covid while serving on the front lines of a hospital, caring for my own patients. My story has a happy ending only because my lifelong friend, an ICU doctor, moved heaven and earth to cut through the red tape and obtain the medicine for me with the FDA’s permission. I was especially lucky that the medicine was being tested at a nearby hospital and the pharmaceutical company immediately rushed an emergency dose to my bedside. I was as close to death as one can be, treated not only with a ventilator but also with extracorporeal membrane oxygenation (ECMO), which few survive. By the time I got the medicine and began to recover, the hospital was already preparing me for a lung transplant.

https://miamicourant.com/stories/617928153-op-ed-the-emergency-use-law-should-be-used-for-emergencies-like-now

REMEMBER THIS??

Wait what? FDA wants 55 years to process FOIA request over vaccine data

https://www.reuters.com/legal/government/wait-what-fda-wants-55-years-process-foia-request-over-vaccine-data-2021-11-18/

Elon Musk, hurry, free up Tweeter so that the people can propagate news on the adverse effects of COVID-19 vaccines while the promising NEUROPEPTIDE AVIPTADIL has been held back. Jon J, can you help?? Sure, that will be the day!!

https://www.standingforfreedom.com/2022/04/free-speech-absolutist-elon-musk-puts-censorship-on-notice-by-becoming-majority-shareholder-board-member-of-twitter/