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Browsing Tag

Pregnancy and Birth-Control

FDA “Future Framework” Democide-Decision

How you know the world is run by evil reason — what number are we up to now? Unbelievable – the FDA could skip clinical trials in future to save the mRNA industry from the utter failures – where are the good guys… where?

FDA-Future-Framework

Dr Russell Blaylock

“The COVID-19 pandemic is one of the most manipulated infectious disease events in history, characterized by official lies in an unending stream led by government bureaucracies, medical associations, medical boards, the media, and international agencies.”

Dr Russell Blaylock, Retired Neurosurgeon, publishes ‘COVID UPDATE: What is the truth?‘ in Surgical Neurology International – 22 April 2022 – calling out all the COVID Lies & atrocities we’ve endured from the corporate media and government bodies and health regulators, including the lethal-Remdesivir & the so-called Vaccines, the censorship of early-treatments, as well as calling out Fauci, Gates, Daszak, CDC, WHO, the New World Order & The Great Reset.

COVID UPDATE_ What is the trut

QLD Senator: Truth Bombs “We won’t let you get away with it”

Queensland Senator Malcolm Roberts calls out the TGA, ATAGI, ABS, AHPRA, Liberal-Nationals, Labor, Greens, for running a protection-racket for the Pharmaceutical industry. He shares Pfizer and AstraZeneca’s criminal history & calls them out for fraud. He calls out the deliberate suppression of any health advice, because the vaccines are a gravy train. He brings up all the TGA FOI’s that highlight we have no honest or accurate safety data, and ends with a promise to not let them get away with it: “We are coming for you – we have the stamina to hound you down and we damn well will”.

SenMalcolmRoberts-truthbombs

Pfizer’s Own Trial Data: 1200+ Dead, 46.5% Required Hospitalization & 30% Unrecovered in the First 2 months & 12 days of Rollout

The Food and Drug Administration (“FDA”) has released Pfizer’s report on adverse events to its Covid injection for the first two-months and 12 days since post-emergency authorisation. Over this period Pfizer had received more than 42,000 reports, mostly from the United States. Almost 30,000 of these adverse event reports were from women and 26,000 related to nervous system disorders.

pfizer-trial-data-chart