For over a century the Food & Drug Administration has been a ruling authority on national health legislation. With an annual budget of $6.5 billion, the federal agency controls dietary supplements, vaccines, and pharmaceuticals. Many see the government organization as a benevolent force that only endorses products deemed safe for human consumption. However, history repeatedly proves the institution’s authorization is not always synonymous with safety. Throughout the decades, FDA-approved drugs have altered or ended countless lives. Electric shock therapy was used on children until 2020. Accutane resulted in more than 20,000 suicides. Zantac exposed millions to dangerous carcinogens and Vioxx caused 27,000 heart attacks. Ironically, the very same regulators vehemently opposed importing harmless baby formula during mass shortages.
These FDA-approved drugs have wreaked havoc on society:
Beginning in 2001, the NSAID was used to treat arthritis and menstrual pain. Only weeks later the inconspicuous pills were manifesting a plethora of afflictions. Bextra induced heart attacks, strokes, and gastrointestinal bleeding. Some contracted toxic epidermal necrolysis, a life-threatening skin condition. By 2009 Pfizer was criminally charged and ordered to pay $2.3 billion to victims.
Terfenadine is an antihistamine used for treating allergic reactions. Users worldwide suffered from severe adverse events including arrhythmias, palpitations, and cardiac arrest. Hundreds succumbed to heart issues triggered by the decongestant. Despite the rising fatalities, it remained on the market for 13 years.
Countless headlines emerged this week chronicling global outbreaks of a mysterious liver disease. Children worldwide are being hospitalized with severe symptoms including abdominal pain, respiratory complications, jaundice, diarrhea, and vomiting. Since April 21st there have been nearly 200 cases and several fatalities. Approximately 10% require a liver transplant. Strangely, patients tested negative for typical hepatitis strains including A, B, C, D, and E. World Health Organization representatives announced the surging illness is inexplicable. However, recently released court-ordered Pfizer documents provide further insight into the connection between COVID-19 inoculations and potential liver damage.
Vaccines Accumulate in the Liver
Last year pharmaceutical delegates repeatedly affirmed coronavirus vaccines did not leave the injection site. Yet it’s now clear these statements were not mere ignorance but blatant misinformation. Dossiers from January of 2021 detail concerning animal testing results. Scientists discovered immunizations migrate within 48 hours of administration. Ingredients quickly spread throughout recipients’ bodies. Areas affected include the adrenal glands, bladder, eyes, bone marrow, intestines, thymus, pancreas, salivary glands, lymph nodes, thyroid, testes, uterus, and pancreas. Significant acclimation of injection contents took place in the ovaries (.09%), spleen (1.03%), and liver (16.2%). Aggregation of synthetic materials inside organs can generate a host of physical ailments.
For more than a week the internet has been inundated with award show drama. During the 93rd Academy ceremony, comedian Chris Rock lightheartedly joked about Jaida Smith’s shaved head being reminiscent of G.I. Jane. Her husband Will angrily marched on stage and violently slapped the host. Viewers are torn on the authenticity of this televised episode. Some insist the assault was genuine while others believe it’s merely a staged performance to boost formerly plummeting ratings. However, what cannot be debated is the ensuing media frenzy. Seemingly overnight there is constant discussion and rampant news coverage of a particular autoimmune disease called alopecia areata. The headlining actress suffers from this condition which causes hair loss. In an interesting twist, Oscars-sponsor Pfizer just so happens to be finalizing a new drug that treats—you guessed it: alopecia.
Brought to You by Big Pharma
Hollywood has a dark track record filled with unbridled pedophilia, ritualistic abuse, and pushing an insidious agenda. Amid the pandemic-era celebrities have become Big Pharma’s most outspoken proponents. Pfizer and Eli Lilly representatives recently paid millions of dollars to broadcast the annual star-studded gala. Simultaneously, the multinational biotechnology company is completing Phase 3 clinical trials using a rheumatoid arthritis medication to treat alopecia. Baricitinib, a Janus kinase (JAK) inhibitor, is said to be effective in combating the disfiguring skin ailment. Soon these patented cytokine-restricting pills will be presented to the Federal Food & Drug Administration for additional review and approval. Cue the Oscars’ supposedly ‘random’ attention-grabbing incident. What better marketing campaign than bombarding potential consumers with information about the disorder your product claims to cure?
Seemingly overnight, the world is inundated by constant news coverage of Ukraine, imminent nuclear attacks, and World War III. Every passing hour delivers a broadcasting deluge focused on nefarious Russian forces. Naturally, the perfectly orchestrated diversion tactic is certainly no coincidence. With the population deliberately preoccupied, Pfizer quietly released court-ordered documents regarding COVID-19 vaccines. Revealed within this newly disclosed publication is a horrifying glimpse into the catastrophic effects of mRNA injections. Out of 42,000 recipients involved in the three-month study, 1,223 died. Given the staggering 3% fatality rate, one has to wonder: how did they plan on concealing such a significant spike in abrupt deaths?
Sudden Adult Death Syndrome
While drug manufacturers uncovered the mass scale of carnage induced by inoculations, bleak headlines began surfacing. Mainstream media outlets produced countless articles highlighting an emerging phenomenon dubbed Sudden Adult Death Syndrome. Also known as SADS, this condition refers to inexplicable mortalities amongst healthy young people. According to cited ‘experts’, robust individuals can sporadically pass away without any warning. Doctors claim these are merely cases of cardiac arrest. Curiously, this heart failure produces no apparent or detectible cause of death in autopsies. From the beginning, networks attempted to normalize formerly inconceivable events by utilizing a technique called predictive programming. Society was unknowingly being prepared for an insidious form of genocide.
Billions of people worldwide have been injected with the experimental coronavirus vaccine. Despite an alarming spike in overall deaths since its rollout, countless citizens are eagerly lining up for the latest booster. With each passing day, debilitating health complications continue to surmount. In 2021 alone the VAERS database collected more than 914,000 adverse reactions. Yet inoculated individuals are not the only ones suffering from jab-related consequences. Thousands of the unvaccinated experience side effects after being in close proximity to mRNA recipients. Some call the transfer of genetic substances ‘shedding’ while skeptics insist such claims are delusional conspiracy theories. However, Pfizer’s official medical papers define the phenomenon and issue a warning to staff members.
Pfizer’s Shedding Protocol
In November of 2020, a document was released titled “A PHASE 1/2/3, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLIND, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, IMMUNOGENICITY, AND EFFICACY OF SARS-COV-2 RNA VACCINE CANDIDATES AGAINST COVID-19 IN HEALTHY INDIVIDUALS”. Throughout the publication, there are sections concerning viral transmissions to unimmunized workers. Beginning on page 67, the pharmaceutical company details its strict occupational exposure protocol. Employees must alert an administrator of any associated secondary adverse events (SAE) within 24 hours. Here are some critical statements covered in the manual:
Contraction can result via skin contact or inhalation of molecular particles naturally expelled by the body.
Those at the greatest risk for ensuing side effects include healthcare providers, family members, and caretaker-type roles.
Breastfeeding women must file a report upon unplanned contact with clinical subjects irrespective of whether an SAE has occurred due to potential dangers to newborns.
If a recently pregnant female encounters a trial participant, she must immediately alert the safety department as messenger RNA can jeopardize the baby’s development or cause a miscarriage.