The Root of Monkeypox? Internal Pfizer Document Reveals Vaccines Trigger ‘Autoimmune Skin Blistering’

As the World Health Organization began moving towards their global Pandemic Treaty, a new disease suddenly emerged. Mainstream media outlets diverted citizens from the WHO’s latest power grab with a blitzkrieg of foreboding monkeypox headlines. According to ‘experts’, the virus spread throughout Europe, Australia, and America in early May. Those afflicted develop protruding lesions. Symptoms include muscle pain, fever, headache, and chills. Medical professionals insist the zoonotic pathogen is due to human-animal exposure. However, some inquisitive researchers believe the mysterious outbreak could be linked to an unexpected source.

Inoculation-Induced Skin Blistering

Internal Pfizer documents present concerning findings regarding COVID-19 vaccines. During the clinical trials, laboratory technicians noticed test subjects experienced unusual side effects. According to a recently released dossier labeled 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021, recipients suffered from a host of inoculation-induced illnesses. One specific reaction listed is autoimmune blistering disease. The report reveals that 8,476 participants developed skin and subcutaneous tissue disorders. Immunized individuals developing similar ailments are also described in the federal VAERS database. Numerous entries state patients experienced epidermal abnormalities post-vaccination.

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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:

VALDECOXIB (BEXTRA)
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 (SELDANE)
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.

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