Drug-Target Interactions and Drug Repositioning

Plandemic II: Indoctornation

Modern Medicine is a Disease

Drug Side-Effect Prediction Via Heterogeneous Drug Network

Are Your Medications Safe?

Overdosed America: The Broken Promise of American Medicine

Johns Hopkins study suggests medical errors are third-leading cause of death in US

Abraham Flexner on staff at the Carnegie Foundation, and funded by the Rockefeller Foundation, 'sourced' the American 'medical' reformation following US Congressional acceptance of the "Flexner Report."

This infamous treatise exclusively benefited the IG Farben/Rockefeller petrochemical pharmaceutical alliance that vilified every form of natural healing, replacing nutrition with petrochemicals to monopolize healthcare.

In her 1993 book The Molecular Vision of Life, Dr. Lily E. Kay, whom a 2001 MIT News Office obituary referred to as "one of the outstanding historians of biology of her generation," argued that the "new biology" was largely forged by the Rockefeller Foundation and its subsidiary program at the California Institute of Technology (Caltech) through a consensus between a scientific elite and a business elite whose broader aims centered on eugenics and the need to create a mechanism of social control and human engineering:

"The new science did not just evolve by natural selection of randomly distributed disciplinary variants, nor did it ascend solely through the compelling power of its ideas and its leaders. Rather, the rise of the new biology was an expression of the systematic cooperative efforts of America's scientific establishment - scientists and their patrons - to direct the study of animate phenomena along selected paths toward a shared vision of science and society." - Dr. Lily E. Kay

chemical compounds

Clinical Trials

Merck' Alzheimer' Drug Fails in Phase III

American Medical Association urges ban on TV drug ads

Rockefeller wiped out natural cures to create big pharma

Ders mensch als industriepalast

Practioners of alternative healing methods consider the application of chemical toxins and surgeries to be 'allopathic medicine'.

"The Allopathic approach to healing is a far cry from Hippocratic method of healing which attempted to use natural methods to balance 'humors.'

"The term "allopathy" was invented by German doctor Samuel Hahnemann.

He conjoined allos "opposite" and pathos "suffering" as a referent to harsh medical practices of his era which included bleeding, purging, vomiting and the administration of highly toxic drugs.

These practices were based on the ancient Greek humoral theory which attributed disease to an imbalance of four humors (i.e., blood, phlegm, and black and yellow bile) and four bodily conditions (i.e, hot, cold, wet and dry) that corresponded to four elements (earth, air, fire, and water).

Physicians following the Hippocratic tradition attempted to balance the humors by treating symptoms with "opposites." - William Jarvis

Reliance on toxic chemical drugs is based upon the philosophy of Santorio Santorio, also known as Sanctorius.

Santorio argued throughout his career that the fundamental properties of human health were mathematical ones, such as number, position, and form - breaking from describing the body and its functions in terms of Aristotelian (and Galenic) elements and qualities.

This radical break with traditional medical theory and natural philosophy proposed that the human body was a clockwork machine the workings of which were determined by the shapes and positions of its interlocking parts.

This, therefore, could be broken down into constituent molecules.

Beginning from a fundamentally unsound foundation Santorio made 'phenomenal' properties, seen from a mechanistic Newtonian viewpoint, central to his worldview of nature and medicine.

While the central metaphor of Aristotelian natural philosophy and Galenic medicine was organic, Santorio made it mechanical: the clock (more generally, the machine) became the metaphor for nature opening up a window for biochemistry and, later, molecular biology.

While his 'trail and error' experiments were replicated and augmented by his followers and finally surpassed by those of Antoine Lavoisier he is still regarded by many as the father of experimental physiology.

"The pen is mightier than the sword.

Mightier than pen or sword is the pill."

Aldous Huxley

united nations drug crimes incite youth

Pill Peddlers

If Drug Companies Were Honest

"How does a doctor subscribing to "first do no harm" find himself or herself prescribing either drugs that are inherently harmful or drugs at hazardous levels? Follow the money". - Tom Pula

"When patients ask for a drug, they tend to get the drug regardless of whether it is appropriate for them." - Joel Weissman, health policy expert

"The reason for encouraging independent studies of clinical trials is that doing so can offer clues to risks and dangerous side effects that begin to show up in significant numbers only after the drug is on the market." - Ricardo Alonso-Zaldivar

"According to the 2005 Partnership Attitude Tracking Study, 40% believe that prescription medicines are "much safer" to use than illegal drugs.

These controlled substances are not just highly dangerous, but they can prove lethal." - Joseph T. Rannazzisi, May 16, 2007

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Nonpsychotropic Medication-Induced Psychosis

1990   Americans spend $40 billion on prescription medications.

1998   JAMA study estimates 106,000 prescription medications deaths.

2004   Americans spend $190 billion on prescribed medications.

2006   Americans spend $280 billion on prescription medication.

2009   Pharmaceutical manufacturers gain FDA approval to distribute medical journal articles describing unapproved off-label uses of drugs.

2011   Record 4 billion prescriptions in US

2015   Americans spend $413 billion on prescribed drugs.

Over 1000% increase in twenty five years.

80% of the active pharmaceutical ingredients used to make drugs sold in America are imported and 40% of finished drugs are made in foreign countries - much of both from China.

When designing a chemical, the manufacturer must first decide what degree of chemical purity is needed based on the intended use.

The following list describes the seven most common grades for chemicals and reagents, from highest to lowest grade/purity:

ACS grade meets or exceeds purity standards set by the American Chemical Society (ACS). This grade is acceptable for food, drug, or medicinal use and can be used for ACS applications or for general procedures that require stringent quality specifications and a purity of =95%.

Reagent grade is generally equal to ACS grade (=95%) and is acceptable for food, drug, or medicinal use and is suitable for use in many laboratory and analytical applications.

USP grade meets or exceeds requirements of the United States Pharmacopeia (USP). This grade is acceptable for food, drug, or medicinal use.

United States Pharmacopeia is acceptable for most laboratory purposes, but formulation should always be reviewed to ensure appropriate methodology.

NF grade meets or exceeds requirements of the National Formulary (NF).
The USP and the NF (USP– NF) jointly publish a book of public pharmacopeial standards for chemical and biological drug substances, dosage forms, excipients, compounded preparations, medical devices, and dietary supplements.

Laboratory grade is the most popular grade for use in educational applications, but its exact levels of impurities are unknown. While excellent for teaching and training, it is not pure enough to be offered for food, drug, or medicinal use.

Purified grade, also called pure or practical grade, meets no official standard; it is not pure enough to be offered for food, drug or medicinal use of any kind.

Technical grade is used for commercial and industrial purposes; it is not pure enough to be offered for food, drug or medicinal use of any kind.

Of critical importance here is the allowance of a huge amount of contaminants.

Purity of 95% with an allowance of 5% contaminants may not matter in a variety of applications but is critical in food, drug or medicinal use of any kind.

No manufacturer would dare to use a lower quality to increase profit !

No lab technicians would 'accidentally' use a lower quality grade!

Murder by fake drugs

"Apothecary, n. - The doctor accomplice,
undertaker benefactor and grave worm provider."

Ambrose Bierce

The US Chamber of Commerce and the Pharmaceutical Research and Manufacturers of America ("PHRMA") argue that exposing generic pharmaceutical manufacturers to state law tort liability will negatively impact the American healthcare system by denying doctors and patients in some states access to certain generic medications.

Under the Supremacy Clause of the US Constitution, federal laws represent the supreme law of the land and may preempt or override state laws.

1984   Hatch-Waxman Act allows generic drug makers to capture the market while bypass testing requirements by simply claiming their generic drug is equivalent to an approved brand-name drug and carries the same labeling.

1992   Prescription Drug User Fee Act (PDUFA) is marketed for its miraculous ability to reduce the time and cost of bringing "lifesaving drugs" to market in time to save substantial numbers of 'disease' victims.

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"Sick days are typically unplanned, which results in significant burdens to corporations ." - Rick Chaifetz, CEO of ComPysch

"People are being forced to chose between being a good employee or being a good family member" - Linda Meric, director of 9 to 5, National Association of Working Women

June 23, 2011 PLIVA, Inc. v. Mensing

Federal drug regulations applicable to generic drug manufacturers directly conflict with, and thus preempt, state-law tort claims alleging a failure to provide adequate warning labels.

Supreme Court holds "sameness" requirement of Hatch-Waxman Act preempts state imposition of stricter labeling requirements on generic drugs.

Supreme Court rules that federal law related to pharmaceutical regulations preempts a person's ability to sue in state courts and allege that a generic drug is poorly designed and manufactured.

Supreme Court rules that the FDA has authority over pharmaceuticals.

80% of all drugs consumed in the US are, from now on, exempt from liability for side effects, mislabeling and virtually any other adverse reactions.

Generic pharmaceutical manufatures become exempt from multi-million dollar court-imposed settlements and no longer have to worry about safety or side effects awarded to victims of their generic drugs.

"Today's court decision provides a disincentive for generic makers of drugs to monitor safety of their products and to make sure that they have a surveillance system in place to detect adverse events that pose a threat to patients." - Michael Carome, Public Citizen's Health Research Group

June 24, 2013 Mutual Pharmaceutical Co. v. Bartlett

Generic drug manufactures cannot be held liable under state law for not adequately labeling medication when federal law prohibits them from changing the label from the original brand name drug.

Commercial messages are ingrained by endlessly repetition.

Human aspire to be elevated into a position outside of nature.

But many commonly prescribed pharmaceuticals promote cancer !

Hormone replacement therapy is among the most controversial medications.

Industrially produced estrogen can promote uterine as well as breast cancer.

"Taking menopause hormones for five years doubles the risk for breast cancer." - Marilynn Marchione 12/13/08

Many pharmaceuticals warn of cancer causation.

Omeprazole (Prilosec©) causes abnormal cell growth and stomach tumors (carcinoids) in rats.

Spironolactone (Aldactazide©, Aldactone©) a blood pressure medicine, sometimes prescribed for hormonal imbalances and facial hair growth in women, causes tumors in rats.

Elidel© and Protopic©, are associated with lymphoma and skin cancer.

The rheumatoid arthritis injections Cimzia©, Enbrel©, Humira© and Remicade©, expensive bio-tech drugs have been associated with lymphoma.

"In the New England Journal of Medicine, Sept. 25, 2008, investigators noted a higher incidence of cancer in subjects taking Vytorin©." - Joe Graedon, pharmacologist & Teresa Graedon, nutrition expert

"Today's announcement that the ENHANCE study failed to find any positive benefit from the addition of Zetia® to a common, inexpensive, generic therapy raised concerns that attempts were made to mask the minimal value of this new drug."- Representative John Dingell, Committee on Energy and Commerce chairman 1/15/08

unique library index

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