Relief Therapeutics Holding AG (RLFTF)

[changes_iv]

Dr. Naomi Wolf on Pfizer: “They hid. They concealed. They redacted.”

April 5, 2022 • by Bannon's War Room on Rumble

Dr. Naomi Wolf discusses the war on children and on Western values. Forcing children to wear masks is abusive because new studies show that this prevents them from developing normal facial recognition and the practice has a now-measurable effect on their IQ levels.

With all the new information surfacing from the WarRoom/DailyClout volunteers regarding the formerly secret Pfizer documents, and with attorney Stevan Looney’s new essay on the redacted documents in the secret Pfizer tranche now published on DailyClout.io, it is becoming clear that informed consent before receiving the vaccine was never even possible.

Bombshell: in order to process just the paperwork from the “large number of adverse events” — Pfizer’s own words — Pfizer had to hire 2,400 new, full-time employees and the company proudly informed the FDA of these thousands of new hires to grapple with the flood of adverse events they saw as early as February 28, 2021. Yet they did not disclose these adverse events to the public and neither did the FDA.

https://dailyclout.io/dr-naomi-wolf-on-pfizer-they-hid-they-concealed-they-redacted/

ZYESAMI/AVIPTADIL held back???

In a letter to NIAID Director Anthony Fauci and FDA Commissioner Robert Califf, Sen. Ron Johnson (R-Wis.) demanded to know why public health officials ignored three Emergency Use Authorization (EUA) requests from the drug manufacturer, NRx Pharmaceuticals, and refused to review data on ZYESAMI’s efficacy against COVID. The letter, co-authored by Sen. Ted Cruz (R-Texas) and Reps. Andy Biggs (R-Ariz.) and Chip Roy (R-Fla.), cited a physician who treated more than 20 patients who were suffering respiratory failure from COVID-19, and received ZYESAMI as authorized under Right to Try.

“It is our understanding the patients received ZYESAMI after prior administration of remdesivir did not improve the patients’ conditions. All the patients were at the very end stage of COVID and were not expected to recover,” the Republicans wrote.

‘Upon receiving ZYESAMI, no serious adverse events associated with use were reported and 16 of the 20 patients left the hospital. According to the physician, patients with ARDS normally have a 40 percent mortality rate. With ZYESAMI, the mortality rate decreased to roughly 10 percent.’

https://amgreatness.com/2022/03/09/in-letter-to-fda-and-niaid-ron-johnson-demands-to-know-why-promising-late-stage-covid-drug-was-never-approved/

VACCINE GOLD RUSH???

https://rumble.com/vxr1e3-vaccine-gold-rush-do-you-trust-gates.html

Blood clots

Like the drug regulatory authorities in other countries, the Danish Medicines Agency has received reports of blood clots in the time after vaccination.

At this time, the Danish Medicines Agency does not suspect the vaccine to cause side effects in the form of blood clots. Blood clots can be explained by several other factors such as the person’s health conditions, including other diseases and medication taken. In addition, the needle prick itself from the vaccine jab may – even when administered correctly – in rare cases cause blood clots. So, blood clots can occur in the time after vaccination without being related to the vaccine.

The reports of blood clots are monitored closely in a collaboration between the Danish Medicines Agency, the European Medicines Agency (EMA) and the other drug regulatory authorities in Europe. >>>