American Pharmaceutical Companies Accused of Carrying Out Clinical Trials With Chinese Military

A bipartisan House committee has revealed that American pharmaceutical companies carried out drug trials in conjunction with the Chinese military for more than 10 years.

The revelation came in a letter penned by Republican and Democratic leaders on the House Select Committee on the Chinese Communist Party (CCP) to the commissioner of the Food and Drug Administration (FDA), Robert Califf. In the letter, they pressed him to supply information about these clinical trials for new medications.

In their letter, they explained: “These collaborative research activities raise serious concerns that critical Intellectual Property is at risk of being transferred to the [Chinese military] or being co-opted under the People’s Republic of China’s National Security Law.”

They also expressed reservations about how much the results of clinical trials produced by China can be trusted.

The letter states that hundreds of clinical trials for drugs have been carried out at medical centers and hospitals in China that are affiliated with the People’s Liberation Army (PLA) at sites such as the PLA’s Air Force Medical University and the PLA’s General Hospital and Medical School.

One of the institutions is operated by the PLA’s Academy of Military Medical Sciences, an institution which the Department of Commerce has banned businesses in the United States from sharing technology with due to national security concerns.

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Pharmacide; Killing Us Softly

To many, scientific lingo is as indecipherable as hieroglyphics, not to mention all the confusing opinions of experts, drug salesmen, supplement salesmen and a corrupted phalanx of government “protective” agencies/protecting the bottom lines of the healthcare monopoly.

Who could trust anything after evil Golem Fauci’s weaponized flu and fraudulent vaxxxines killed millions. He has been shaking down congress every few years for decades just to fund phony drug solutions for “pandemics” like swine flu, AIDS, MPOX and Zika to enrich corporate cronies and complicit colleagues.   But that’s only the tip of the iceberg; crooked medicine has been crippling and killing millions each year for at least a century!!!

If anyone can sift truth from the coercive douchebaggery of government trolled/controlled mass media, please get in touch.

The Rockefeller business model depended on eliminating all competition and establishing itself as the foremost authority in medicine.  In the early 20th century they managed to disparage and have legally banned many electronic therapies including the Rife Machine, some of which surface today in conventional circles to address mental problems.  Ditto ultraviolet blood irradiation and HBOT/hyperbaric oxygen therapy. They tried to destroy Chiropractic and Naturopathy  as well as many nutritional and herbal medicines.  Their darkest “success” came when they kneecapped Linus Pauling and disparaged Vitamin C to keep the public from learning of its value.  They also suppressed many cancer cures along with chelation therapy thereby keeping a steady stream of uninformed chronic disease sufferers packing medical offices in search of a drug solution.

While the profession made great strides in trauma-care and acute interventions, they buried actual prevention and safe natural treatments leading to suffering and death for millions.

They “overlooked” nutrition, but not before floating malicious lies recommending health-wrecking polyunsaturated fats and oils with cholesterol/heart disease mythology,… when saturated fats like butter and lard are wise scientifically verified choices.  They birthed the shady idea of sun avoidance and the use of carcinogenic chemical sunscreens. They promoted ineffective side-effect riddled vaxxxines for generally non-life threatening diseases.  They bolstered their “god status” with Latinesque word-salads meant to be unintelligible to the “congregation.”

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Prescription Drugs Are the Leading Cause of Death

Overtreatment with drugs kills many people, and the death rate is increasing. It is, therefore, strange that we have allowed this long-lasting drug pandemic to continue, and even more so because most of the drug deaths are easily preventable.

In 2013, I estimated that our prescription drugs are the third leading cause of death after heart disease and cancer,1 and in 2015, that psychiatric drugs alone are also the third leading cause of death.2 However, in USA, it is commonly stated that our drugs are “only” the fourth leading cause of death.3,4 This estimate was derived from a 1998 meta-analysis of 39 US studies where monitors recorded all adverse drug reactions that occurred while the patients were in hospital, or which were the reason for hospital admission.5

This methodology clearly underestimates drug deaths. Most people who are killed by their drugs die outside hospitals, and the time people spent in hospitals was only 11 days on average in the meta-analysis.5 Moreover, the meta-analysis only included patients who died from drugs that were properly prescribed, not those who died as a result of errors in drug administration, noncompliance, overdose, or drug abuse, and not deaths where the adverse drug reaction was only possible.5

Many people die because of errors, e.g., simultaneous use of contraindicated drugs, and many possible drug deaths are real. Moreover, most of the included studies are very old, the median publication year being 1973, and drug deaths have increased dramatically in the last 50 years. As an example, 37,309 drug deaths were reported to the FDA in 2006 and 123,927 ten years later, which is 3.3 times as many.6

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Big Pharma Funds COVID Fact Checkers

FactCheck.org, the organization that flags “misleading” COVID-19 content for Facebook, is supported by the Robert Wood Johnson Foundation, a philanthropic organization funded by pharmaceutical giant and vaccine maker Johnson & Johnson (J&J), YouTube commentator Jimmy Dore reported.

Dore said his own shows have often been slapped with a “misleading” label when he covered issues related to COVID-19 or vaccines.

“These fact check organizations aren’t there to check facts,” Dore said. “They’re there to push a political point of view and an agenda and to discredit people.”

Dore said when the organization “fact-checked” his work in the past, its claims were always “bogus.” He said FactCheck.org never reached out to consult him about his content, it twisted his words and it never even pointed to any erroneous facts.

Instead, he said, “They didn’t like my headlines,” and they would say they were misleading.

Johnson & Johnson’s viral vector COVID-19 vaccine received emergency use authorization from the U.S. Food and Drug Administration in February 2021. After the shot was linked to dangerous blood clots, its use was suspended a couple of months later and it was eventually completely pulled from the market in May 2023.

The Robert Wood Johnson Foundation was established in 1952 by Robert Wood Johnson II, who ran J&J with a bequest of shares from the pharmaceutical giant. Today, although the foundation says it has diversified its holdings, it holds nearly $2 billion in J&J stock.

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Gardasil Fails to Protect Against Cervical Intraepithelial Neoplasia Over Time

The US Food and Drug Administration (FDA) approved the first human papilloma virus (HPV) vaccine in 2006 progressing to Gardasil 9, a 9-valent vaccine, for use in children as young as 9 years old in December 2014. The CDC recommends the HPV vaccine as part of the routine vaccination schedule for children ages 11–12, but it can be given as early as age 9. The vaccine is also recommended for adults up to age 26, and in 2018 the FDA expanded the age range to include adults up to age 45.

Adcock et al obtained data from January 1, 2007, to December 31, 2020, from the New Mexico HPV Pap Registry (NMHPVPR), the only comprehensive US statewide monitoring system for cervical cancer prevention. Over fourteen years through which the HPV vaccination should have had a population effect, the results are disappointing for the higher grades of cervical intraepithelial neoplasia 2 and 3, which are findings from a cervical biopsy that indicates abnormal cells on the cervix’s surface. It’s also known as high-grade or moderate dysplasia (CIN-2) and carcinoma in situ (CIN-3). CIN 2/3 is usually caused by infection with certain types of human papillomavirus (HPV).

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Clinical Trials of Childhood Vaccines: No Placebo-Controlled Long-Term Trials

Not a single routine childhood vaccine was licensed based on a long-term placebo-controlled trial. Not one. See the carefully created and fully referenced chart at https://icandecide.org/no-placebo which was compiled by our firm with funding from the Informed Consent Action Network (ICAN).

I will also be holding a Spaces event on Twitter this Tuesday at noon Eastern time to discuss this chart: https://twitter.com/i/spaces/1ynJODQVbDXxR. See you there!

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The mainstream media is helping Big Pharma promote high-profit weight loss injections

The mainstream media has long been used to advertise for and support the pharmaceutical industry, and anyone who has ever doubted this is the case was proven wrong by the way the media handled COVID-19 vaccines. Now, the “solution” they’re pushing on the masses is the weight loss drug Ozempic and others of its ilk, and much like the vaccines, they’re doing their best to gloss over the dangerous side effects.

Multiple mainstream media outlets have been doing segments on Ozempic, not only touting the injectable diabetes drug’s weight loss benefits but also pointing to other supposed benefits, like a clip on NBC that claimed it can reduce the risk of cancer.

What they’re not talking about nearly as much are the scary side effects of these so-called weight loss “miracles,” but that shouldn’t be surprising when you consider how heavily pharmaceutical companies advertise in the mainstream media. No one working for these outlets would want to write anything that risks upsetting the companies helping pay their salary.

Dr. Guy Hatchard, a natural medicine advocate with a Ph.D. in Psychology, recently called out the corporate media for this practice, focusing on a lead article in The New Zealand Herald entitled “Wellington company director Finlay Thompson loses 30kg taking Ozempic, wants medication funded.”

Written by a young journalist, Ethan Manera, it discusses how the company director in question shed 66 pounds while participating in a U.S.-based trial of the drug and receiving it for free. As the trial period comes to a close, he is asking the government to fund the drug for himself and others who need to lose weight. In Thompson’s case, he simply can’t control his eating and has failed at multiple other attempts to lose weight.

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The Cult Of Vaccination

Vaccines are a pharmaceutical product. Yet they are treated like mana from God. To question a vaccine is blasphemy. There is so much faith in vaccines that pregnant women are now offered the flu, Tdap, COVID, and RSV, vaccines as a routine part of their prenatal care. Curiously the CDC started to call pregnant women, pregnant people and boldly claim that vaccines are safe for “pregnant people”. 

Every vaccine has this in section 8.1 of the manufacturer’s insert. Most pregnant women do not know about the pregnancy registry. What do we actually know about vaccines in pregnancy? Studies of pregnant woman given vaccines are done by the manufacturer, and those studies are heavily biased and insufficient. You can find all the vaccines on the market today on the FDA website. Also see testimony in New Hampshire by Attorney Aaron Siri about vaccine safety. Aaron Siri is a managing partner with Siri and Glimstad, they specialize in vaccine safety and injury. All licensed vaccines list their clinical trials. Aaron Siri goes into great detail on this. The vaccines on the market today lack proper safety clinical trials with true inert placebos. The Hepatitis B vaccine given to all newborn babies was studied for FIVE DAYS! See that for yourself HERE

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‘Fraud, Pure and Simple’: Merck Mumps Vaccine May Contain Up to 4 Times Approved Amount of Live Virus

Drug manufacturer Merck misrepresented the efficacy of its mumps vaccine for years, “overfilling” the vaccine with live mumps virus to meet efficacy targets despite the lack of safety testing — and the practice may be continuing today.

Merck appears to have concealed the practice from public health agencies, which have taken no action to stop it.

Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense, joined “The Defender In-Depth” this week to discuss the revelations, which stem from a lawsuit two Merck whistleblowers filed in 2010 under the False Claims Act.

The 3rd Circuit U.S. Court of Appeals in Philadelphia heard oral arguments in the case on July 9.

According to Hooker, the Merck measles, mumps rubella vaccine, MMR II — the only mumps vaccine licensed in the U.S. and listed on the childhood vaccine schedule for 12- to 18-month-olds — may contain up to 4 times the approved concentration of live mumps virus.

two-part deposition by Dr. David Kessler, former head of the U.S. Food and Drug Administration (FDA), also indicates that Merck, rather than informing regulators that it was “overfilling” its MMR vaccine, relied on passive surveillance — reports from parents regarding vaccine reactions in their children — to identify possible safety signals.

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U.S. Government ‘Saddled’ With COVID Vaccine Injury ‘Mess’ — While Vaccine Makers Avoid Liability

As early as January 2022, National Institutes of Health (NIH) researchers were aware of at least 850 peer-reviewed case reports and/or research articles about COVID-19 vaccine reactions, according to emails obtained by Children’s Health Defense (CHD).

In one email (name and agency redacted), NIH researchers were told the federal government was “saddled” with the “mess” of dealing with those injured by the COVID-19 vaccines, due to the liability shield enjoyed by vaccine manufacturers.

The emails, part of a 309-page batch of documents released to CHD on June 21, originated from a U.S. Food and Drug Administration (FDA) request to NIH researchers for input on a report highlighting several injuries common among people who received the vaccines.

CHD requested the documents via a Freedom of Information Act (FOIA) request to the NIH in November 2022. When the NIH hadn’t responded by April 2023, CHD sued the agency.

In an October 2023 settlement, the NIH agreed to produce up to 7,500 pages of documents at a rate of 300 pages per month.

The batch of documents released in June — which include emails to Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research — revealed that by fall 2021, key NIH researchers were aware of scientific studies on serious adverse events, including persistent neurological symptoms, following COVID-19 vaccines.

As with prior releases of the NIH documents, June’s tranche also included several emails from vaccine-injured individuals to NIH researchers, seeking help for their symptoms — with one person asking, “Why aren’t you studying vaccine injuries?”

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