PHARMACEUTICAL

The biggest Scam in the history of the U.S.

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Only two countries in the world allow pharmaceuticals to advertise directly to the masses

Now look what has happened! A Trillion dollar fake pandemic, changing children's gender; making them life long dependents on pharmaceuticals, mandatory multiple vaccinations for children, natural remedies being declared illegal (while the people at the FDA that did so, retire serving on some high-paying 'consultant' job with a pharmaceutical) and adding all sorts of things to our food supply. Sick people will buy more drugs!
Pharmaceuticals are some 40% of the income for national media, they will never say anything against them, e.g. they no longer publish the drugs found in the blood of shooters.

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Toilet paper... water... food... medications. People hoarded these items in 2020 as the world locked down in fear off COVID-19.

Next, the FDA demonized and blocked life-saving medications like Ivermectin – causing an untold amount of death and paving the way for the even deadlier COVID-19 mRNA vaccine.

An election year is here and it’s happening again.

It’s starting to feel like the perfect storm:

1. Remove reliable OTC medications and supplements from the shelves
2. Use wars and new China pandemics to enact severe shortages in prescription pharmaceuticals
3. Force lockdowns to push mail-in ballot voting, and as a bonus…
4. …fill Big Pharma’s wallet by mandating a deadly experimental “vaccine.”

After decades on the market, the FDA declared that the active ingredient in popular cold medicines like Dayquil, Mucinex, Sudafed, and Theraflu is ineffective. CVS and other pharmacies are pulling the products from store shelves.

Antidepressants are being prescribed for more than just depression and the consequences include an increased risk of suicide.

“She said she was in a lot of pain all the time,” said Mr. Niggemann, 57, who was at Ms. Stern’s side as she struggled with the adverse effects of an antidepressant—and painful withdrawal symptoms each time she tried to wean off them.

“She suffered from migraine headaches, tremors, burning pain sensations in her nerves, and dark thoughts about demons and hell.“ Mr. Niggemann said Maggie knew she had everything to live for, but the pain, caused by the effects of the medication, was too intense. ”Her teeth were grinding down, her toes were curled. That is what these antidepressants do.”

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Big Pharma’s big push to get patients to take their meds

Drug companies around the globe are spending big to push patients to take their pills. (a subscription based newsletter)

The pharma industry loses tens of billions in worldwide sales each year when patients don’t fill, or refill, their prescriptions.

So drug makers from London to Tokyo to Cambridge, Mass., are pouring money into programs aimed at cajoling — or nagging — patients to take every last pill their doctors prescribe. The companies are investing in smart pills that will send alerts when they haven’t been swallowed at the prescribed time. They’re subsidizing gift cards to thank patients who…

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Deadly Medicines and Organized Crime: How Big Pharma Has Corrupted Healthcare

Book, by Peter Gotzsch

PRESCRIPTION DRUGS ARE THE THIRD LEADING CAUSE OF DEATH AFTER HEART DISEASE AND CANCER. In his latest ground-breaking book, Peter C Gotzsche exposes the pharmaceutical industries and their charade of fraudulent behaviour, both in research and marketing where the morally repugnant disregard for human lives is the norm. He convincingly draws close comparisons with the tobacco conglomerates, revealing the extraordinary truth behind efforts to confuse and distract the public and their politicians.

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The War on Ivermectin

December 29, 2023 Dr. Pierre Kory, Highwire and Science Direct

Dr. Pierre Kory, MD, MPA, a critical care doctor, wrote the book, The War on Ivermectin, about the anti-parasitic drug that won the Nobel Prize. Ivermectin is described in a new 12-minute mini-documentary as being safe, effective and cheap. Ivermectin was slandered during the COVID pandemic because COVID vaccines would not have received the emergency use authorization (EUA) if ivermectin was recognized as being effective.

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The Truth About the Drug Companies: How They Deceive Us and What to Do About It

Book by Marcia Angell

During her two decades at The New England Journal of Medicine, Dr. Marcia Angell had a front-row seat on the appalling spectacle of the pharmaceutical industry. She watched drug companies stray from their original mission of discovering and manufacturing useful drugs and instead become vast marketing machines with unprecedented control over their own fortunes. She saw them gain nearly limitless influence over medical research, education, and how doctors do their jobs. She sympathized as the American public, particularly the elderly, struggled and increasingly failed to meet spiraling prescription drug prices.

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Johnson & Johnson

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n 1886, with a “Safety First” motto, Robert Wood Johnson and his brothers bootstrapped a fledgling company based on a line of medicated plasters - sticky rubber strips that were loaded with mustard and other home remedies. When some customers complained the mustard and other herbs seemed to cause skin irritation, the brothers sent their customers free packets of powdered talc for relief.

Soon, mothers began applying the talc to infants’ diaper-chafed skin and began requesting more of the soothing po0wder. The Johnsons added fragrance that would become one of the most recognizable in the world and in 1893 began selling it as Johnson’s Baby Powder. It became their longest running product.

Fast forward 130 years and pharmaceutical giant Johnson and Johnson (J&J) is now frantically trying for the 3rd time to file bankruptcy to avoid paying out on Baby Powder lawsuits. This despite the company’s revenues for each of the last several years being close to $100 billion and the company now being valued at over 400 billion.

The current issue is that tens of thousands of people have filed lawsuits alleging that J&J baby powder (talcum powder) and a later version marketed too adults as shower to shower was the direct cause of them developing many different types of cancer, For decades when people applied J&J baby Powder some of it would aerosolized and be inhaled. In other instances it would be drawn through the mucus membranes near where it was applied on the body and absorbed into the bloodstream. The big problem was that it contains asbestos, a known carcinogen.

Apparently when in the ground, before being mined talc is essentially interwoven with naturally occurring asbestos. It is nearly impossible to completely separate them,. So J&J talcum powder products inevitably contain some amount of asbestos.

51,000 people have now alleged that J&J talc products have caused them cancers and have sued. In 2018 J&J was forced to pay $4.7 billion dollars to 22 women and their families. What came out in the course of the initial lawsuits was that J&J knew for decades that their asbestos-laced baby powder caused cancer.

In 1975 an internal memo revealed in court sated: “With respect to talc safety studies we will initiate new studies only as directed by confrontation... The principle advantage of this operating policy is that we minimize the risk of self-generation of scientific data which may be politically or scientifically embarrassing.” I.e. our own science can be used against us in court so we better not do any more studies on this product.

In 2020 J&J stopped selling talc based baby powder. Stating that that “demand for talc-based Johnson’s Baby Powder in North America has declined due to changes in consumer habits fueled by misinformation around the safety of the product and a constant barrage of litigation advertising.” (Seems like another instance where pharma tried to us the word misinformation to shape their preferred narrative by casting doubts on valid concerns.)

For perspective I’ll offer that lawsuits are nothing new for J&J. In 2013 they agreed to pay a 2.2 billion penalty in a drug marketing settlement where they acknowledged paying kickbacks to the prescribing doctors of the highly problematic anti-psychotic drug Resperdal. In 2019 during the closing statements of a law suit, the state of Oklahoma labeled J&J as an opioid ”kingpin.”

Which brings to 2023. In january7 an attempt by J&J to declare bankruptc7 to avoid pa7ying more Baby Powder settlements was dismissed when the judge said that the $400 billion dollar company “does not face imminent financial distress.” In July they tried again to declare bankruptcy in Texas called LTI. They then transferred all potential Baby Powder asbestos liability to the new corporate shell and kept all their monetary assets separate. LTL then filed for bankruptcy in North Carolina which if granted, as the potential to freeze the Baby Powder cases for years. But a second judge refused to buy their dancing act.

It certainty will be interesting to see how act 3 of J&J’s well orchestrated asset protection theater unfolds. I wonder if the current CEO and board of directors have any knowledge of the Johnson brothers’ original “Safety First” motto?

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FDA Issues Emergency-Use Authorization for Johnson and Johnson Covid-19 Injection

March 1, 2021

Dr. Meryl Nass, MD, an expert on the failures of the Johnson & Johnson anthrax vaccine that injured thousands of soldiers 20 years ago, says that, although there are some differences between this adenovirus injection and the other two RNA vaccines already approved, there are many similarities, such as the fact that this type of treatment has never been approved before, there never have been human trials that prove safety or effectiveness, there is no proof that it blocks infection and transmission, and there are numerous reasons to suspect it will cause extensive injuries and death.

The company says the product is 66% effective against moderate to severe disease in the trials, but merely having a headache and a cough was sufficient to place subjects in the “moderate to severe” category. That means many if not most of the so-called 66% effective results were people who would never have become seriously ill even without treatment of any kind. In other words, doing nothing might have produced better results that 66%. Full article.

• US Foster Care: Psych Drugs Are a $23 Billion Per Year Industry and Children Are Raped and Abused.
• Pfizer CEO, who said online “misinformation” is criminal, is found guilty of “misleading” vaccine statements
• Two Young Adults Die Following Johnson and Johnson Experimental Vaccinations (Summary & Story)
• 4-14-21 FDA Suspends Experimental Johnson and Johnson COVID Shot Linked to Fatal Blood Clots (Summary & Story)
• Johnson & Johnson COVID-19 vaccine said to cause the same autoimmune disease – Guillain-Barré Syndrome – that left me paralyzed when I was just 15 years old.
  The U.S. Food and Drug Administration (FDA) is will announce a new warning on Johnson & Johnson's (J&J) COVID vaccine saying the shot has been linked to Guillain–Barré syndrome (GBS), a “serious but rare” autoimmune disorder. The Washington Post attributed the news to “four individuals familiar with the situation.” Ninds.nih via (CHD) Guillain-Barré syndrome (GBS) is a rare and […]

Astra Zeneca

Marco Cavaleri, the chair of the vaccine evaluation team at the EMA, has said that there is a "clear link" between the AstraZeneca vaccine and deadly blood clots in the brain.

9 European Countries Halt Oxford/ AstraZeneca COVID Vaccine Due to Fears over Blood Clots and Deaths.

Another Italian Professor is Dead Following the AstraZeneca COVID Injection. Full article.

Denmark Ditches AstraZeneca's COVID-19 Shot. Health Minister Faints During Announcement. (Summary & Story)

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MODERNA

Moderna Hid 300K Vax Injuries

Covid vaccine maker Moderna received 300,000 reports of side effects after vaccinations over a three-month period following the launch of its shot, according to an internal report from a company that helps Moderna manage the reports.

That figure is far higher than the number of side effect reports about Moderna's vaccine publicly available in the federal system that tracks such adverse events.

Vaccine manufacturers like Moderna are legally required to forward all side effect reports they receive to the Vaccine Adverse Events Reporting System, where they are made public each week.

Inventor of mRNA Vaccine Says FDA Approved the Wrong Vaccine.

Dr. Robert Malone, the purported inventor of mRNA vaccines, stated in an interview with Steve Bannon that the mainstream media is lying about the Pfizer vaccine receiving FDA approval. He said the FDA issued two separate and distinct letters showing that the Pfizer shot is still under an emergency-use authorization and that the full FDA approval was given to a BioNtech product, ‘Comirnaty’, that is similar to the Pfizer gene therapy vaccine. This new shot, Comirnaty, has yet to be manufactured and won’t be available for several years because several cardio-toxicity studies have yet to be completed.

Run by the Centers for Disease Control and Food & Drug Administration, the VAERS system is crucial to tracking potential problems with vaccines. It helped scientists determine the Covid vaccines may cause heart problems in young adults.

NIH-Moderna Confidential Agreements

Updated MERS agreement -- the same day NIH and Moderna finalized the sequence for mRNA-1273. p. 85 "Jointly-owned by NIAID and Moderna" p. 105 https://www.documentcloud.org/documents/6935295-NIH-Moderna-Confidential-Agreements

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