November 21

ADD Manufactured Disorders

Another treasured piece of research, done by an Anonymous. Enjoy.

Adderall Age 0-6 0-17

information aquired during: “Live Research Ananlysis Open Sourced Learning Exerimental Documentary Series / Test #1.0  text file created on [Friday, ‎November ‎09, ‎2018, ‏‎3:53:02 PM]”     the information was recorded for educational and learning purposes, it documents how information that was unknown to the researcher is obtained and the screen recording is a visual backing up the sources used, how the information is gathered and transfered, to have factual source data to analyze,  as stated above this is for a larger research project, these documentaries are exactly what they say they are, live documentation of research, understanding in attempts to “based off information available” to “determine” how to “answer questions”, and how to “find the answer using data”, “desktop recording software”, “the internet”, as many “web browsers” and tabs as you can keep track of, a calculator and also “notepad” or text document, the session was not done while taking adderall, those taking adderall, might enjoy watching for it is sped up over 400%, the music added is a audio mix titled concentration programing music, it is its own mix, the 4.3 hour live recording, was edited to create the timelapse, the video was pre edited to condense the original time of 04:18:11, to the documentary ver. for a mainstream viewer to grasp,time of 01:05:26

Desktop Screen Record Time:
start record/stop record
Friday, ‎November ‎09, ‎2018, ‏‎7:03:58 PM
Friday, ‎November ‎09, ‎2018, ‏‎11:22:10 PM

all other video edits where made after the initial timelapse compression, that consisted of finding the most important items in the recording, and keeping them close to realtime, the rest of the video is between 300-500% faster than original, the added screenshots you see in the intro are the key values obtained overall, so you see by watching the video how the information was obtained and calculated and with what data and where the data came from.

further test will be performed live,ADD

this time using information aquired during the initial test. This is a learning tool, in editing the original video in order to present it on the open platform, calculation errors have been made, the next video will start from scratch and will use this file and its already used source links to further the research, it will be classified as “Test #2.0”, analysis of the findings for the test #1.0 experiment, will help further the efficiency when “Test #2.0” is performed.  this intro paragraph you are reading right now is typed at 11:28 am 11/14/2018 – this is an experiment test, a documentary series, open source learning, the data from Test # 1.0 will be used to question from, new findings in between this time, and the live recording of Test # 2.0 including errors of past work will be presented in the start of Test # 2.0,   it will be interesting to see what new questions and understandings come to those that watch this documentary series, a whole new list has developed including specifics that still need muliple sourcing verification, maybe start doing the same thing, recording your desktop, to provide yourself another layer of proof of work, as stated above, that is your tool for analysis of your work, thus helps to further your work, including frees up the mind for the memeory is recorded live, so you can go back and watch what you learned, and for those that are already Master with research, the more you do this and incorporate into your work, the deeper it will sink into those that follow your work, turn the key finding into a text to speech script, and put the “research live documentary of sources” on top of it, quite the challenge!

video documentary tile?

~ Diet Pill Drug Dealers Test #1.0 ~
hyperkinetic reaction of childhood?


“The Formula ADDictive”

source links, see video and end of article!

Stanton made an oral tender offer of $11​1⁄2 per share for the company to buy back Buffett’s shares. Buffett agreed to the deal. A few weeks later, Warren Buffett received the tender offer in writing, but the tender offer was for only $11​3⁄8. Buffett later admitted that this lower, undercutting offer made him angry.[13] Instead of selling at the slightly lower price, Buffett decided to buy more of the stock to take control of the company and fire Stanton (which he did). However, this put Buffett in a situation where he was now majority owner of a textile business that was failing.

Berkshire’s class A shares sold for $327,260.00 as of September 25, 2018, making them the highest-priced shares on the New York Stock Exchange, in part because they have never had a stock split and have only paid a dividend once since Warren Buffett took over, retaining corporate earnings on its balance sheet in a manner that is impermissible for mutual funds.

In 2008, Berkshire invested in preferred stock of Goldman Sachs as part of a recapitalization of the investment bank.  As of July 13, 2016, Buffett owned 31.7% aggregate voting power of Berkshire’s shares outstanding and 18.0% of the economic value of those shares.[22] Berkshire’s vice-chairman, Charlie Munger, also holds a stake big enough to make him a billionaire, and early investments in Berkshire by David Gottesman and Franklin Otis Booth, Jr. resulted in their becoming billionaires as well. Bill Gates’ Cascade Investment LLC is the second largest shareholder of Berkshire and owns more than 5% of class B shares. Berkshire’s insurance businesses provide insurance and reinsurance of property and casualty risks primarily in the United States. In addition, as a result of the General Re acquisition in December 1998, Berkshire’s insurance businesses also includes life, accident, and health reinsurers, as well as internationally based property and casualty reinsurers. Berkshire’s insurance companies maintain capital strength at exceptionally high levels.

approximately 70 domestic and foreign-based insurance companies.

Berkshire Hathaway Assurance – Berkshire created a government bond insurance company to insure municipal and state bonds. These type bonds are issued by local governments to finance public works projects such as schools, hospitals, roads, and sewer systems.[44] Few companies are capable of competing in this area.

On June 8, 2017, it was announced that Berkshire Hathaway had settled with California’s insurance regulator, allowing its Applied Underwriters unit to sell a revised version of its “controversial” compensation insurance policies for workers in the state.

so sell insurance to gov workers,?

Berkshire currently holds 89.8% of Berkshire Hathaway,  A major subsidiary of Berkshire Hathaway Energy is Northern Powergrid, which operates in the UK.  Berkshire Hathaway (BRK.A/BRK.B) a No. 1 or No. 2 holder for each of the Big 4 US airlines.

Climate Change is Forcing the Insurance Industry to Recalculate
Insurers are at the vanguard of a movement to put a value today on the unpredictable future of a warming planet

“price of climate”

well there is weather modification systems there are predictive quantum simulation systems, how is insurance ahead of the game to turn the coin to make the money, do they say they predict this, and create a rush for insurance, do they use scenerios to profit from, do they have access to the ability to have insider trading knowledge from governmental operations, that are then used in advanced to maintain the leading spot thus maximizing profits…

do these companies fight political battles to ensure dominance when it comes to revenue, profits and market control. American multinational conglomerate holding company. Buffett has spoken frankly about Berkshire’s need to find new places to invest its large pile of cash, which stood at $111 billion at midyear. Bloomberg reported that Berkshire Hathaway (NYSE:BRK-A)(NYSE:BRK-B) proposed making a convertible loan to Uber in an amount “well above $3 billion.”  is this not just for the media, so people dismiss that they probably talked about all kinds of other stuff as well.

uber and warrent buffet directly met in june
work deals for monopolization?
‘I’m a great admirer of Dara’

KSAsb invest into uber billions in sept..

some of the repeatable elite business practice – plus then be direct access to insider information, If the borrower (Uber) succeeds, and its stock appreciates, the lender (Berkshire) can take part in the upside by converting the debt into equity. You can think of it as a loan that has the potential to generate a stock-like return, while offering many of the protections of being a creditor rather than an owner.

Berkshire Hathaway ultimately made billions of dollars for shareholders by linking similar deals with Goldman Sachs and Bank of America during the financial crisis of 2008 and European debt crisis of 2010. In each deal, Berkshire received a high return on preferred stock, and received warrants that would allow Berkshire to profit if shares of the banks recovered. (They did.)

Howard Graham Buffett

******************** ******************** ******************** ***** ********************

What happened

Shares of Teva Pharmaceutical Industries (NYSE:TEVA), the world’s largest producer of generic drugs, rose 28.3% in the first half of 2018, according to data from S&P Global Market Intelligence. A key investor signaled confidence in the company’s ability to remain strongly profitable, and investment bank analysts followed suit.

Here’s How Teva Pharmaceuticals Pulled Off a 28.3% Gain in the First Half of 2018
Demand for generic drugs is on the rise, and investors are convinced the trend will keep this profitable company moving in the right direction.

In the first quarter of the year, Berkshire Hathaway (NYSE:BRK-A)(NYSE:BRK-B) doubled its stake in Teva Pharmaceuticals.

Generic adderall “Teva”

diagnosed with Adult ADHD:

“My insurance recently stopped paying for my name brand Adderall prescription. I talked to the pharmacist & they assured me that the generic was not only exactly the same medication as the name brand but also made by the same company.

“faced the reality of my ADD diagnosis. After a full month on Adderall (generic), my confidence was creeping up and i was feeling very productive. I was even early to meetings a few times! The next month was rocky. I filled the same kind of rx, but the generic manufacturer was different. I started to experience depression and frustration. I was literally moments away from an “F You” at work. I went back to the doctor and he looked at the medication. He said that not all generics are created equally and he had many patients that have experienced the same thing.”

“My daughter started on generic adderall for ADD and was convinced that it was placebo. She got no focus at all from it
it made me wonder about generic drugs”

in fact, society is so far gone, the initial targetted generation, that has now had its own children just see it as a normality…  they do not even question the Diagnosis is not a real problem, it is the human condition coping with the stress and life of modern living, depending on environment,

Generic of Adderall® Tablets [CII]

these chemicals, its deceptive false diagnosis,

I was just talking with my doctor about that this morning (I FINALLY got a chance to go in for a physical). He said, and I quote, “All those kids are on speed. I had a kid in here just yesterday who said he needed Adderall or he couldn’t work his sixteen-hour days. You know, I hate doing it; it’s like giving narcotics to junkies. But I’m just one guy; what am I gonna do about it?”

The long term side affects of psychostimulants, i.e. Adderall, Vyvanse, Retilin, etc., have no current studies to date since they are a relatively new pharmological drug being prescribed (being less than 15 years).

The study, published Monday in the journal Pediatrics, looked at all calls to US poison control centers for unintentional or intentional exposure to ADHD medications between 2000 and 2014 among children and adolescents. The researchers found that the number of calls increased from 7,018 in 2000 to 11,486 in 2014 — a 64% increase.

“During the early 2000s, there were a number of FDA warnings that came out” describing the potential adverse effects of these medications. Attention deficit hyperactivity disorder is a neurobehavioral condition characterized by an ongoing pattern of inattention, hyperactivity and/or impulsivity that interferes with functioning or development, according to the National Institute of Mental Health. National Institute of Mental Health and FDA how is this the deciding factor?

Adderall causes emotional and cognitive effects such as euphoria, change in desire for sex, increased wakefulness, and improved cognitive control. At these doses, it induces physical effects such as a faster reaction time, fatigue resistance, and increased muscle strength. In contrast, much larger doses of Adderall can impair cognitive control, cause rapid muscle breakdown, or induce a psychosis (e.g., delusions and paranoia)

quote, wiki,
The risk of developing an addiction is insignificant when Adderall is used as prescribed at fairly low daily doses, such as those used for treating ADHD; however, the routine use of Adderall in larger daily doses poses a significant risk of addiction due to the pronounced reinforcing effects that are present at higher doses.

the child prescriptions that started this whole pandemic of addiction, is based on a current 18-20 person that was forced the prescription, at least for 10 years and below the age of 13-14, no child at that age below 13 can have this undocumented and not proveable disorder and claim medical condition, insurance, pharmaceutical manufacturers, government regulatory agencies, taxations, policy makers, lobbyist, all play major roles in the rush integration of this drug, so the current 18 year old is not able to function as a normal human being and this is a firm understanding that, you do not have ADHD or ADD, you never did,
no you have had this pumping in your blood while your body is in its most crucial development stages, your reliance upon this harmful substance is an attack that came on you as a child, your innocense is what was targeted, your guardians ignorance and disinformation opened your body up for an a dangerous cocktail, now you are addicted, and not by your choice, you never needed a drug to do school work,  but is unlikely to arise from typical long-term medical use at therapeutic doses.[19][20][21] Drug tolerance develops rapidly in amphetamine abuse (i.e., a recreational amphetamine overdose), so periods of extended use require increasingly larger doses of the drug in order to achieve the same effect

biggest contradiction,

====*****==== ====*****==== ====*****==== ====

for one, there has not been enough time to say someone on adderall since a young child is not currently addicted?, *have you met college students*, talk to them about being on adderall since they were children, they are adults now above 18 and 21, them and others who have friends that have been the target, have major problems, cannot function without it, and many are the ones that seek and deal similar and other recreational pharmaceutical FDA drugs, people are addicted and to say they are not is a lie, extended use over a persons life will yeild negative results including complete dependency on it…  lets do a study on current users between the age of 18-24, that have been on adderall and similar medication prescriptions, since before they were age 13, and lets see how well they do when they do not have it, the drug. They must endure whatever comes there way [any withdrawls?], you must self document this also, have some studies in a controlled setting with the people at tables [1996?], then you got, say a VLOG challenge, go without the drug – video document your realtime experience and share it.  If you need medical attention and or psychiatric help, that can be provided, tell your Doctor and Insurance provider, see what will be provided.  they (You) would be the ones, this time around, that would “offer yourself up” to being studied, due to initial lack of studies and human testing for such[X] condition on such [y]{age group},~VLOGs~ free right, free speech to digital journal, express your personal experience with this diagnosed medication, including how you cope or what happens to you if you do not have it, or if you tried to go without and was unable to overcome? due in part to the chemical manipulation of the human will power, exploited using a controlled substance, a cut form of a deadly synthetic, put in play because it was an, already given “popular” treat, at triple dose then, renaming it and remarketing it through policies and business acquisitions for starters, who can explain as to the medical reasoning for any adjustments and generics to the chemical ratio content and how it relates to improving or curing the condition with the drug that is FDA approved, manufactured, and marketed as the only chemical means of treating the condition? Meaning, we changed it because, this way solves this medical problem and by changing the formula here is why? or we changed it to avoid ‘red tape’ hope no one notices, even if they do, tough to beat that much power and control of industry shareholders, to the policy writers and the ones that approve its “control, use, dealerships, partnerships, marketing and manufacturing INTERNATIONALLY”  for it is a fact, this formula that has been passed around [70+ years?], this is a locked in Pharmaceutical Manufactured Drug, industry facts alone show  a povable reason to maintain its proven status quo as the Norm for profitability, VS. its medical value and the provable reason for using this drug as medication, for a condition, that history records, as being adapted around the already known diet pill formula, so without proper documentation or evidence of medical only facts and test explaining why, or cause or the reason for ADHD, how can it be that this is the formula to medicate an unknown cause for condition?   this chemical formula of Adderall, and its licensed “generic counterparts” [the recent generics growth rates, further shows that not only U.S. negative medical condition growth rates, this same provable and repeatable process is now making its way in many other International Markets, many who did not have the “condition”, now they do? Using factual data, scientific analysis is now in effect, for the current market expansion known values worked in an equation, including manufacturing growth projections, projected population growth rates, including the previous slope of growth progression[hC], financially being positive gain, – numerical data can show the condition{a} is projected to be worse or a wider market value, stating the use or the reason for the manufacturing of a drug, for reason [x], is proven ineffective{y}, fraudulent[z], if the current projection of the future sales of this drug , or total net income revenue stream {$}, is higher than the population natural growth value{s}, including the previous positive slope of financial growth progression[hC], the conditions or manufacturing of the prescriptions unnatural growth can be seen {{AV}} – prescribing medication withoug knowing medically why it is diagnosed? without medical alone facts to back up the reason for substantial positive slope of progression rate [hC], in terms of Revenue stream and Net income, other than the negative stream of the condition growing and that is shown by the volume in sales for whom it is currently being Diagnosed, prescribed usage for, the age group of (2-5)?(6-13)(0-17)],

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As amphetamine-based diagnosis / medications / prescriptions grow, the “addiction condition” grows, thus maintaining this status quo or true agenda of reasoning behind the diagnosis.  Without that diagnosis one would not be able to get it distributed like it is, institutionalized, ran through insurance, government programs, time will tell, Test #2.0?
This drug overtime waters the mind/body down, to a “zombie like” state, actually raising the human tolerance for other controlled substances or narcotics, thus leaving the user craving more, opening the door, the gateway if you will, for other fun drugs like “molly”, now just where does that come from? and why is this generation compound of pharmaceutical addictions, mostly of American Children and teens, age (0?-17)?, after that age, culture is now finding its way to layer over even more deadly and mind/body destructive cocktails?

ADDictive chemical composition neural synthetic manipulation, the already known Variable in the equation being:

“to be able to generate a multilayered effect of: individual, business, corporate, and government, income revenue generated population and social control”

[[prescription of a controlled substance must be above age 18? why not? can medical show reason why not?why not leave (2-13) out?]]
~ you are the evidence, your experiences (realtime data for the equation) compounded can help save the ones that are starting this “cycle” for the first time, was it age (2-5)? or is it age (6)? (7-13)?, Humanity needs help with this, please, tell the world, the medical community, your family, your “drug dealer” and your government, with “live documentation” of what the prescription drugs, they approved, manufactured and have FED you since a young child, they have done this to you.  How has its usage affected you psychologically, physically and emotionally, are you angry that you never had a choice to not take it? does your life from then until now, its balance revolve around the medication?  Does thinking about not taking your prescription scare you, like you think you wont be able to make it?

Public financial records, business reports, do show how much profit has been obtained, showing a factual substantial Gains Margin{gM} year after year, without due cause of reason for sale, thus the (manner in which this business is being conducted[Z]) has been based on, or the (initial motive of opportunity of intent, to sell drugs to children and infants, untested then and now,{t})  pertaining to the using of this specific formula{p} or drug[b], for such [X] reason because of medical cause[Y], achieving diagnosis of {a}, yeilding a net income {$}:

over time [X]{a} has changed/adapted multiple times: [Y]=unknown={p}{a}”Disorder/Syndrome”{$}

[Y] = ({p}{a}={$})
[X] =  {t}[b]
[Z] = ({gM}=[Y]+[X])

(“these medications are highly effective” ~ at doing what exactly?)

“The etimology of ADHD/ADD is the FDA direct, approval, manufacturing, marketing and re-distribution of the amphetamine-based prescription medications”  ~anonymous~

“the cause of the condition is its solution”
– if the solutions foundation is fraudulent, then the condition its self, its pharmaceutical treatment are also fraudulent –

now we have more thoughts to question, just getting the basic numbers took some time,
“Live Test #2” will reapproach these ideas and understandings, further questioning the current status quo.

[10:18am-6:26pm final edit to notes][Test #1 completed {11/9/18 – 11/15/18}][riddle me this riddle me that]

——————————–   ——————— back to the live demonstration ————- ———– ————- —

Richwood Pharmaceuticals, which later merged with Shire plc, introduced the current Adderall brand in 1996 as an instant-release tablet.[167] In 2006, Shire agreed to sell rights to the Adderall name for the instant-release form of the medication to Duramed Pharmaceuticals.[168] DuraMed Pharmaceuticals was acquired by Teva Pharmaceuticals in 2008 during their acquisition of Barr Pharmaceuticals, including Barr’s Duramed division.[Chemically, Adderall is a mixture of four amphetamine salts; specifically, it is composed of equal parts (by mass) of amphetamine aspartate monohydrate, amphetamine sulfate, dextroamphetamine sulfate, and dextroamphetamine saccharate.

Shire Plc is a Jersey-registered, Irish-headquartered global specialty biopharmaceutical company. Originating in the United Kingdom with an operational base in the United States, its brands and products include Vyvanse, Lialda, and Adderall XR. Shire has its primary listing on the London Stock Exchange and is a constituent of the FTSE 100 Index. Shire has a secondary listing on NASDAQ.

Shire is a global biotechnology company focused on serving people with rare diseases and other highly specialized conditions. The company’s products are available in more than 100 countries

Teva Pharmaceutical Industries Ltd. (Hebrew: טבע תעשיות פרמצבטיות בע”מ‬) is an Israeli multinational pharmaceutical company headquartered in Petah Tikva, Israel.[1] It specializes primarily in generic drugs, but other business interests include active pharmaceutical ingredients and, to a lesser extent, proprietary pharmaceuticals. It is the largest generic drug manufacturer in the world[2] and one of the 15 largest pharmaceutical companies worldwide.[3]

Teva’s facilities are located in Israel, North America, Europe, and South America. Teva shares trade on both the New York Stock Exchange (via ADRs) and the Tel Aviv Stock Exchange. The company is a member of the Pharmaceutical Research and Manufacturers of America (PhRMA).  Pharmaceutical Research and Manufacturers of America (PhRMA, pronounced /ˈfɑrmə/), formerly known as the Pharmaceutical Manufacturers Association,[1] is a trade group representing companies in the pharmaceutical industry in the United States founded in 1958.[2] PhRMA’s stated mission is advocacy for public policies that encourage the discovery of new medicines for patients by companies engaged in pharmaceutical and biopharmaceutical research. Steve Ubl became PhRMA’s chairman in September 2015.[3] PhRMA is headquartered in Washington, DC

it is a refurbished diet pill from 1950-1960

Obetrol was the brand of amphetamine mixed salts based drugs indicated for treatment of exogenous obesity by the American pharmaceutical company Obetrol Pharmaceuticals. Obetrol was a popular diet pill in America in the 1950s and 1960s.[1]

A formulation of amphetamine mixed salts that included methamphetamine was approved by the U.S. Food and Drug Administration (FDA) on January 19, 1960 under the name Obetrol.[2] Between 1965 and 1973, this formula was offered in 10 mg and 20 mg strength through Obetrol Pharmaceuticals division of an American pharmaceutical company Rexar under the trade name Obetrol. Its indication was for exogenous obesity.

methamphetamine was approved by the U.S. Food and Drug Administration (FDA) on January 19, 1960 for a “diet pill”.
fast forwards to early 80s and developement of Aspertame, synthetic sugar, a replacement additive that is addictive, uses reverse marketing, creates thirst, used in carbonated beverages labels as a diet, drink since it is not real sugar, its calorie content is low, except you are reliant on the mild drug, it creates more thirst for more of the product, and it does have calories, the fda regulations only require above a certain amount so it can have above zero calories, and still have “Zero calories”, same generation that is been under adderall attack has been the target of that industry as well through the rebranding and development of diet products, discriminating and attacking obesity with skinny slogans and can change….

By the 1980s, the use of amphetamines—particularly methamphetamine—as an adjunct to diet and exercise in the treatment of exogenous obesity had become frowned upon by many in the medical community.[citation needed] As the decades evolved, so did the composition of Obetrol. By 1995, the year Shire Pharmaceuticals (then known as Shire-Richwood) acquired Rexar Pharmacal, Obetrol 10 mg. and 20 mg. tablets contained, (in equal proportions):

Dextroamphetamine sulfate
Dextroamphetamine saccharine
Amphetamine sulfate
Amphetamine aspartate

United Kingdom

its was a known proven mixture for abuse and addiction:

The ready availability of methamphetamine-based medications in the 1960s led to their use and abuse as recreational drugs.

Obetrol was the recreational drug of choice for artist Andy Warhol. Obetrolling or doubling was the process by which the character referred to tripping on Obetrol, because it increased his self-awareness and made him feel alive tripping on Obetrol,

Adderall gained FDA approval for the treatment of attention-deficit/hyperactivity disorder therapy on February 13, 1996. then 10mg now it is a 30 mg pill the triple dose.. from fda.

NDA 11-522/S-040
Page 5

is indicated for the treatment of Atten
tion Deficit Hyperactivity Disorder (ADHD) and Narcolepsy.

Attention Deficit Hyperactivity Disorder (ADHD)

A diagnosis of Attention Deficit Hyperactivity Disorder (ADHD; DSM-IV®) implies the presence of hyperactive-impulsive or nattentive symptoms that caused impairment and were present before age 7 years.  before age 7 years (this is a key component is making a valid drug for a child, all children have had difficulty adjusting to the modern society of visual programming, as the history of that is not of question the motive to rebrand obertrol, then later, sneak back in a “reason” to prescribe it to anyone especially children to get them hooked and be a junkie off it an not natural,,,

The symptoms must cause clinically significant impairment, e.g., in social, academic, or occupational functioning,  and be present in two or more settings, e.g., school (or work) and at home. The symptoms must not be better accounted for by another mental disorder. For the Inattentive Type, at least six of the following symptoms must have persisted for at least 6 months: lack of attention to details/careless mistakes; lack of sustained attention; poor listener; failure to follow through on tasks; poor organization; avoids tasks requiring sustained mental effort; loses things; easily distracted; forgetful. For the Hyperactive-Impulsive Type, at least six of the following symptoms must have persisted for at least 6 months: fidgeting/squirming; leaving seat; inappropriate running/climbing; difficulty with quiet activities; “on the go;” excessive talking; blurting answers; can’t wait turn; intrusive. The Combined Type requires both inattentive and hyperactive-impulsive criteria to be met. Specific etiology of this syndrome is unknown, and there is no single diagnostic test. Adequate diagnosis requires the use not only of medical but of special psychological, educational, and social resources.

etiology: the cause, set of causes, or manner of causation of a disease or condition

this syndrome can not be diagnose with medical evidence alone, yet the guiedlines of the condition, require the patient to have regular human tendencies, they group both extremes of the normal human condition, what people have and how they react is nothing new in civilization, neither are drugs, but with this it is the most obvious and easily provable corruptive schemes in big pharma including the current people who can testify for what it has done to them,,,   this happens when the testing is inclusive yet the product is still abused in recreation and in its diagnosis, last 10 years has become candy to the human mind, our collective generations is not stronger or smarter while using the dangerous drug, it is weaker and short lived,

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Long-Term Use:
The effectiveness of ADDERALL® for long-term use has not been systematically evaluated in controlled trials.
Therefore, the physician who elects to use ADDERALL® for extended periods should periodically re-evaluate
the long-term usefulness of the drug for the individual patient.

OK, well I do know and it is known by all other people that it is bad for the body, and plenty of collage students been on this drug for over a decade now, will not be happy once they truly absorb what has been done to them,  They know they have been a target, they do not know how to stop using it, to the degree of they feel they will die if they do not have it, nor can they function without it.

ADDERALL® is indicated as an integral part of a total treatment program for ADHD  that may include other measures (psychological, educational, social) for patients with this syndrome. Drug treatment may not be indicated for all children with this syndrome.

diagnose a sydrome without knowing the causes, or manner of causation of a disease or condition diagnosed mental disorder cause is unknown yet As of 2015 it is estimated to affect about 51.1 million people globally.   30–50% of people diagnosed in childhood continue to have symptoms into adulthood and between 2–5% of adults have the condition diagnosed in childhood

The medical literature has described symptoms similar to those of ADHD since the 19th century.[32] ADHD, its diagnosis, and its treatment have been considered controversial since the 1970s.[33] The controversies have involved clinicians, teachers, policymakers, parents, and the media. Topics include ADHD’s causes and the use of stimulant medications in its treatment.[34] Most healthcare providers accept ADHD as a genuine disorder in children and adults, and the debate in the scientific community mainly centers on how it is diagnosed and treated.[35][36][37] The condition was officially known as attention-deficit disorder (ADD) from 1980 to 1987, while before this it was known as hyperkinetic reaction of childhood. reaction of childhood.

the human condition changed when society and technology grew, its not hard to figure out actually, gen[x-Y] can attest to this better than anyone, for they are the experiment slightly ahead of and still involved in this exact problem, If you were born in 1988 then in 1998 you would have been 10 years old, so in 1994-1996 you would have been some of the first of this decadial attack on the generation of today, the future of the world in fact, once you get into those born between 1998-2004, you see the part of the generation that took the major hit, for the world technologically had been altered majorly at that point, cell phones, social media, were integrated into society, all had been around but at that time if you were already a highschool or junior high student in america at that time, consider yourself lucky, for looks like you experienced the last great time children and teenagers could have had, before the drug epidemic and the war on children. If born in 1998, you would be 20 years old currently and your opinion of what you feel from this drug are highly important, regardless what anyone or lack of “professional study” may say [longterm]… the ones who make it and approve it still have no studies on its long term effects…   from human intelligence gathering, its clear what happened, who did it, and that this pattern is getting ready to take another large pitfall once again, for now you have the compounded effect, next gen children just pushed through a fabricated reason, and they are products themselves so they do not question the condition itself, they just hope INSURANCE pays for it, even debate the various brands and effectiveness, well if it were a real medical condition and a useful drug, the drug would cure the condition for the drug was made knowing what causes the condition.

Shire Plc

Revenue    $15,160.6 million (2017)
Operating income
$2,455.2 million (2017)
Net income
$4,271.5 million (2017)
Vyvanse        $1,722M     Attention Deficit Hyperactivity Disorder (ADHD)
Adderall XR     $70.3M     Attention Deficit Hyperactivity Disorder (ADHD)     Imapx and Teva

attention-deficit/hyperactivity disorder

The pharmaceutical company Rexar reformulated their popular weight loss drug Obetrol following its mandatory withdrawal from the market in 1973 under the Kefauver Harris Amendment to the Federal Food, Drug, and Cosmetic Act due to the results of the Drug Efficacy Study Implementation (DESI) program (which indicated a lack of efficacy). The new formulation simply replaced the two methamphetamine components with dextroamphetamine and amphetamine components of the same weight (the other two original dextroamphetamine and amphetamine components were preserved), preserved the Obetrol branding, and despite it utterly lacking FDA approval, it still made it onto the market and was marketed and sold by Rexar for a number of years.

In 1994 Richwood Pharmaceuticals acquired Rexar and began promoting Obetrol as a treatment for ADHD (and later narcolepsy as well), now marketed under the new brand name of Adderall, a contraction of the phrase “A.D.D. for All” intended to convey that “it was meant to be kind of an inclusive thing” for marketing purposes.[178] The FDA cited the company for numerous significant CGMP violations related to Obetrol discovered during routine inspections following the acquisition (including issuing a formal warning letter for the violations), then later issued a second formal warning letter to Richwood Pharmaceuticals specifically due to violations of “the new drug and misbranding provisions of the FD&C Act”. Following extended discussions with Richwood Pharmaceuticals regarding the resolution of a large number of issues related to the company’s numerous violations of FDA regulations, the FDA formally approved the first Obetrol labeling/sNDA revisions in 1996, including a name change to Adderall and a restoration of its status as an approved drug product.[179][180] In 1997 Richwood Pharmaceuticals was acquired by Shire Pharmaceuticals in a $186 million transaction.

classified as a controlled substance – a class of drugs for which special controls are required for dispensing by pharmacists.

Most ADHD cases are of unknown causes. diagnoses begun after a teacher raises concerns (the world and enviroment for the child is counter productive to the human learning and creative process, the human mind is more advanced than, school systems of public educaiton can or offer, social distractions, peer pressure, visual stimulation rampart since the 90’s with computers then to socmint 2000 and beyond, then you get the children who had the ipad in hand before speech, my god people its not hard to figure out, if you are somewhat detached from this tech system atleast enought look at this objectively….

try to anyways..

ADHD is among the most common behavioral disorder among children or adolescents, according to Dr. Caleb Alexander, co-director of the Center for Drug Safety and Effectiveness at Johns Hopkins, who was not involved in the new study.

“It’s one of the most common disorders diagnosed in children, and the rates of diagnosis have increased a lot over the past two decades,” Alexander said.

“It’s been diagnosed more frequently in recent years than historically, but there are unlikely to be large baseline changes in the prevalence of this disorder. The changes in diagnosis are probably more from evolving thresholds for diagnosis than true changes in the population,” he added.

ADHD diagnoses among children in the United States more than doubled between 2005 and 2014, according to a 2017 study. Approximately 14% of all children in the US were diagnosed with the disorder in 2014, compared with 6.8% in 2005.

46% of the exposures were due to methylphenidate and 45% to amphetamine.

stimulants with overexposure symptoms
unclear why these medications are so effective in treating ADHD
increasing dopamine and norepinephrine in the prefrontal cortex of the brain, which is responsible for complex cognitive behaviors such as decision making and social control.

complex cognitive behaviors such as decision making and social control.
social control.

The researchers in the new study also compared exposure to ADHD medications among three age groups: 0 to 5 years, 6 to 12 years and 13 to 19 years.

“Students, for example, might take it to get through a final exam. But like other stimulants, they might also take it because it gives them a high.”

ADHD medications
disorder therapy

“We know that these medications are highly effective in the treatment of ADHD”

Children in North America appear to have a higher rate of ADHD than children in Africa and the Middle East; this is believed to be due to differing methods of diagnosis rather than a difference in underlying frequency.

wonder, maybe because of the access to endless visual stimulus, way more so than any other country..
diagnoses among children in the United States more than doubled between 2005 and 2014
behavioral disorder
before age 7 years
Specific cause of this syndrome is unknown, and there is no single diagnostic test.

Teva Pharmaceutical Industries
is an Israeli multinational pharmaceutical company headquartered in Petah Tikva, Israel.
Shares of Teva Pharmaceutical Industries (NYSE:TEVA), the world’s largest producer of generic drugs, rose 28.3% in the first half of 2018, according to data from S&P Global Market Intelligence. A key investor signaled confidence in the company’s ability to remain strongly profitable, and investment bank analysts followed suit.

In the first quarter of the year, Berkshire Hathaway (NYSE:BRK-A)(NYSE:BRK-B) doubled its stake in Teva Pharmaceuticals. When the company run by the world’s favorite investor makes a confident move like this, analysts start paying attention. In particular, David Maris, who downgraded Teva Pharmaceuticals in January, completely changed his tune and upgraded the stock a few weeks ago Teva Pharmaceutical Industries Berkshire Hathaway  doubled its stake generic drugs, rose 28.3%

2015 preliminary results:
Vyvanse     $1,722,000,000    Attention Deficit Hyperactivity Disorder (ADHD)
Adderall XR     $70,300,000            (ADHD)     Imapx and Teva

an increased focus on ADHD in younger children

William Henry Gates III Net worth  US$95.6 billion November 2018 board member of Microsoft.
Berkshire Hathaway (A shares) NYSE:BRK-A $328,020.00
Posted: February 22 1996 5:00 AM

Adderall (mixed salts of a single-entity amphetamine) is approved by FDA Feb. 13, the Florence, Kentucky specialty manufacturer and marketer announces. The drug will be available in 10 mg and 20 mg double-scored tablets in March, indicated for “treatment of narcolepsy, attention-deficit disorder with hyperactivity and exogenous obesity.”

treatment of exogenous obesity frowned upon by many in the medical community

Obetrol was the brand of amphetamine mixed salts based drugs indicated for treatment of exogenous obesity by the American pharmaceutical company Obetrol Pharmaceuticals. Obetrol was a popular diet pill in America in the 1950s and 1960s The company later became a division of Rexar Pharmacal Corporation. Rexar was acquired by Richwood Pharmaceuticals of Florence, Kentucky, which in 1995 merged with Shire Pharmaceuticals.

Rexar reformulated Obetrol to exclude methamphetamine and continued to sell this new formulation under the same Obetrol brand name. This new unapproved formulation was later rebranded and sold as Adderall by Richwood after it acquired Rexar resulting in FDA warning in 1994. Richwood submitted this formulation as NDA 11-522 and Adderall gained FDA approval for the treatment of attention-deficit/hyperactivity disorder therapy on February 13, 1996.  1980s, the use of amphetamines particularly methamphetamine as an adjunct to diet and exercise in the treatment of exogenous obesity had become frowned upon by many in the medical community. By 1995, the year Shire Pharmaceuticals (then known as Shire-Richwood) acquired Rexar Pharmacal, Obetrol 10 mg. and 20 mg. tablets contained, (in equal proportions):

Dextroamphetamine sulfate
Dextroamphetamine saccharine
Amphetamine sulfate
Amphetamine aspartate

Richwood acquired Rexar, the drug’s name was changed from Obetrol to Adderall, and the drug was marketed for use in the treatment of Attention Deficit Disorder (in both children and adults manufacture the drug for several years the drug Adderall was identical to the most recent formulation of Obetrol, except that the inscription on the pills was changed to “AD”
Obetrol was withdrawn from the market in 1973 under the DESI statute; Rexar reformulated the drug and continued marketing it without an approved sNDA. Richwood withdrew Adderall from the market following an FDA warning letter in October 1994 and submitted the drug as NDA 11-522…
Highest rates:

Kentucky:   14.8%
Arkansas:   14.6%
Louisiana:  13.3%
Indiana:    13.0%
Delaware and South Carolina: 11.7%
67.4%  (@ 6 of how many states? why?) 84% of world market is U.S. , or Kentucky is 21.95% of the 67.4%?

so Kentucky is 14.8% of the total world market? more of that math stuff percentages: will come back to this later [1:14pm 11/14/18]
*****how many age (2-5) for how long since 1996? particulary through insurance, and healthcare systems?*****

Some sociologists consider ADHD to be an example of the medicalization of deviant behavior, that is, the turning of the previously non-medical issue of school performance into a medical one.
ADHD is a genetic condition
use of stimulant medications in children

Shire closed the Rexar manufacturing facility and outsourced the manufacturing of “brand name” Adderall to a vendor in North Carolina. Other companies had begun manufacturing generic versions of Adderall, and the trade name was eventually sold to Barr Pharmaceuticals (acquired by Teva in 2008).  2008, Teva acquired Barr Pharmaceuticals for $7.5 billion, making Barr and Pliva (which Barr bought earlier) part of Teva Adderall (generic and branded)

The American Psychiatric Association states in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5, 2013) that 5% of children have ADHD 6.1% is more accurtate, the CDC says that 11 percent of American children, ages 4 to 17, had the attention disorder as of 2011. That’s an increase of 42 percent between 2003 and 2011.

In 2016:
Approximately 9.4% of children 2-17 years of age (6.1 million) had ever been diagnosed with ADHD
Ages 2-5: Approximately 388,000 children
Ages 6-11: Approximately 2.4 million children
Ages 12-17: Approximately 3.3 million children

The percent of children 4-17 years of age ever diagnosed with ADHD had previously increased, from 7.8% in 2003 to 9.5% in 2007 and to 11.0% in 2011-12.  The number of young children (ages 2-5) who had ADHD at the time of the survey increased by more than 50% from the 2007-2008 survey to the 2011-12 survey. The average age of ADHD diagnosis is 7 years old.
Symptoms of ADHD typically first appear between the ages of 3 and 6 its a bogus claim…  

Currently, 6.1 percent of American children are being treated for ADHD with medication.

Annual sales of Adderall XR® were approximately $1.5 billion in the United States for the twelve months that ended February 28, 2009, based on IMS sales data.

$1.5 billion in the United States
Adderall XR®

Shire sales 2017
VYVANSE        $1,917,300,000
ADDERALL XR      $327,000,000
MYDAYIS        $21,600,000

Neuroscience    $2,283.900,000 US     $380,200,000 INT    $2,664.100,00 Total sales
US total market 85.73%

Another Post You Might Enjoy:  Designer Diseases

Health News
June 20, 2017
Shire has won U.S. approval for a long-acting attention deficit drug aimed at adolescents and adults, boosting its stock of medicines for the cognitive condition that affects millions of children
The U.S. Food and Drug Administration (FDA) green light for Mydayis
Shares in Dublin-based Shire rose 1.5 percent by 0800 GMT in London on Wednesday following the overnight FDA news.
The new drug Mydayis, previously known as SHP465, contains the same active ingredient as Shire’s widely used attention deficit hyperactivity disorder (ADHD) treatment Adderall XR but is formulated to last up to 16 hours.

Jerusalem, Israel, April 2, 2009 – Teva Pharmaceutical Industries Ltd.
commenced commercial shipment of its generic version of Shire Pharmaceuticals’ Adderall XR®
Over 80 percent of Teva’s sales are in North America and Europe.
Under this agreement, Shire granted the Company the exclusive right to sell a generic version of Adderall XR®
First Generic Adderall XR® Capsules in the United States

Global  use  of  ADHD  medications  rose  threefold  from 1993 through 2003, whereas global spending (U.S. $2.4 billion in 2003) rose ninefold

In  1993,  thirty-one  countries  had  adopted the  use  of  ADHD  medications;  by  2003,  the number had grown to fifty-five.   countries  using  these medications at levels predicted by their per capita  GDP.  The  United  States  uses  them  at  a level  that  is   about  four  times  higher  than would be predicted by income alone, the  global  expenses  regarding ADHD  medications  were   U.S.$2.4  billion  by 2003, 2007 The  United  States dominates global spending on ADHD medications, making up approximately 92-95 % of the total expenditures, with a 22.6 % growth  rate  per  year.  Other  countries showed a slightly slower spending growth rate than the  United States about  21.0  percent per  year.

From1994to2003,U.S.sales volume increased 80 %, while prices increased 285 % in real dollars.  In contrast, in OECD countries sales volumes increased 322 %, while prices rose only 70 %.  322 percent   322

1993:  200,000,000
2003:  2,300,000,000     -80%
1994: 460,000,000
Ages 6-11:  69%

Among children with ADHD, 62% were taking ADHD medication.   Among children 2-17 years of age with current ADHD, about 77% were receiving treatment. percent of all children 2-17 years of age in the U.S. taking ADHD medication was 6.2%

getting tired now..   what is this saying to me right now..
total child population us millions
69.8 1969
63.5 1989
74.1 2009
73.8 2018
76   2029

73,800,000 – 6.2% = 4,526,000


14,580,000 2-5
24,400,000 6-11
25,000,000 12-17     **[[2019]]**

63,980,000 – 6.2 % = 3,966,760

******************** ********************

ERROR MADE – MARKED IN VIDEO OF, 800,000, ONE NUMBER OVER SIGHT, BY NOT USING COPY PASTE: WE ADJUST FIGURE AT [5:17-8:02pm 11/13/18] the number entered in the calculator, off live record, was entered incorrectly, 73,000,000, for total U.S. Population: age group (0-17) – 2018: meaning the amount of total Population of ADHD prescribed users, particularly age (2-5), w/b greater than the value you see in this live demonstration, by 49,600 total children.

73,800,000 – 6.2% = 4,575,600, or 0.0776% off balance,
[4,575,600 VS. 4,526,000] difference of 49,600 children, or initial mis calculation of, 0.0776%

go back and check if you like, its important to note, and make adjustments, question everything and check each others work.
800,000 now, also equates to 49,600, this video is an experimental project, unclassified, open sourced basic questions,
800,000 is 1.0840% of 73,800,000, the known total variable used from
49,600 is 6.2% of 800,000

The second calculation made, by default cancelled out the above err, was taking the 0-5 stat of 24,300,000 divided by 5 = 4,860,000 x 3 = 14,580,000 to get a more accurtate number of age 2-5 or by subtracting 40% of total age 0-5, this number is accurate, in this calculation model trying to find a basic number, that seems not to be anywhere.  for this was just an initial research trail, that revealed knowledge from facts that was buried in information, this has brought a clearer understanding on what other questions to asks, and where to find those answers, considering its not been tested under age 6? 20+ years of financial stats and demographics show is has been quite the go to for those having the need for a controlled substance at an age it is unapproved for?  this was the realization from the research, now thit is what must be sought out for answers, you were the experiment? and how do you feel?

the video edit has not been adjusted since noticing this, and fitting, the error takes place at “39:22” in the timelapse [4:18:11]

second error noticed, calculation between the age groups of (6-17) the stats used, were from the column 2019, not 2018 one colum over . 49,400,000 (2019) vs 49,500,000 (2018) difference of 100,000, or MORE children between age of 6-17 year [2018]

14,580,000 + 49,400,000 (2019) = 63,980,000 – 6.2% = 3,966,760
14,580,000 + 49,500,000 (2018) = 64,080,000 – 6.2% = 3,972,960
Mis calculation   =     6,200 = 0.1560% of 3,972,960 / [64,080,000 true value] = 6.2%   100,000 – 6.2% =6,200 = 0.1562% of 63,980,000= 0.0096   nV= 6.1903 adjV
6.36% are in the age group of age 2-5
252,680 year 2018                   *[5:56-7:22pm 11/14/2018]
*0.0099% error probability so far off the work done prior,394 off original number.[-16 tV] tough number to find? what do you think?

3,966,760 U.S. children age 2-17 being prescribed and taking ADHD medication 39% are in the age group of age 6-11: 1,626,371.6

6.36% are in the age group of age 2-5: 252286 year 2018

2008-2014 75% of claims received ADHD medication, and fewer than half received any form of psychological services. About 3 in 4 children ages 2-5 years with ADHD recorded in their health care claims from 2008-2014 received ADHD medication, and fewer than half received any form of psychological services. During 2008-2011, children ages 2-5 years covered by Medicaid were twice as likely to receive clinical care for ADHD compared with similar-aged children covered by commercial employer sponsored insurance.

price per 5mg  $6.80
price per 30mg $6.80

generic extended release
5 mg is around $438 for a supply of 100 capsules
price per 10mg  $4.60

But the students who sell Adderall at GW all have different stories – varying in their prescription status, income from selling and volume of sales. Unprescribed students, the clients for these dealers, said they’ve used these easily-accessible drugs to compensate for procrastinating school work and to meet approaching course deadlines.

You can either take your Adderall as prescribed or earn some pocket … drug landscape of your own school to better place yourself in a position, is this not a contradiction to reasons for using it, or could this not be a major danger to people getting it as a recreational or study enhancement, Adderall XR may cause new or worsening psychosis (unusual thoughts or behavior), especially if you have a history of depression, mental illness, or bipolar disorder.
signs of psychosis–paranoia, aggression, new behavior problems, seeing or hearing things that are not real; signs of circulation problems

may not be able to use Adderall XR if you are allergic to any stimulant medicine. You may not be able to use this medicine if you have: severe anxiety, tension, or agitation (stimulant medicine can make these symptoms worse);  or a history of drug or alcohol addiction. Some medicines can interact with Adderall XR and cause a serious condition called serotonin syndrome. Be sure your doctor knows if you also take opioid medicine, herbal products, or medicine for depression, mental illness, Parkinson’s disease, migraine headaches, serious infections, or prevention of nausea and vomiting. Adderall XR is not approved for use by anyone younger than 6 years old.  Adderall XR has not been studied in children under 6 years of age.

The number of young children (ages 2-5) who had ADHD at the time of the survey increased by more than 50% from the 2007-2008 survey to the 2011-12 survey. About 3 in 4 children ages 2-5 years with ADHD recorded in their health care claims from 2008-2014 received ADHD medication.  6.36% are in the age group of age 2-5
252286 – 18% =  year 2018:  37842

69840 is 18% of 388,000 children that are of the age group of 2-5, this would be the estimated ADHD perscriptions given based on this data…

between 37,842 and 69,840 children age group of 2-5 estimated ADHD perscriptions, just in the year of 2017 / 18  were any prescribed Adderall XL?

there is a large population of U.S. children and adolescents who have been diagnosed with ADHD by a health care provider. Many, but not all, of these children received treatment that appears to be consistent with professional guidelines: diagnosed with ADHD by a health care provider, professional guidelines, approved by FDA manufactured by FDA approved facilities, generates Federal and State Tax Revenue…

Treatment for ADHD can include behavior therapy and medication. For children 6 years of age and older, the American Academy of Pediatrics (AAP) recommends both behavior therapy and medication as good options, preferably both together. For young children (under 6 years of age) with ADHD, behavior therapy is recommended as the first line of treatment, before medication is tried.

Shire plc
Vyvanse is used to treat attention deficit hyperactivity disorder (ADHD) in adults and in children who are at least 6 years old.
The   mode   of therapeutic   action   in   Attention-Deficit/Hyperactivity Disorder (ADHD) is not known. Amphetamines are thought  to  block  the  reuptake  of  norepinephrine and  dopamine into  the presynaptic  neuron  and  increase  the  release  of  these  monoamines into the extraneuronal space. The parent drug,lisdexamfetamine, does not bind to the sites responsible for the reuptake of norepinephrine and dopamine in vitro.

The safety and the efficacy of lisdexamfetamine dimesylate in children with ADHD three to five years old have not been established Lisdexamfetamine is a Class B/Schedule II substance in the United Kingdom and a Schedule II controlled substance in the United States (DEA number 1205)[9] and the aggregate production quota for 2016 in the United States is 29,750 kilograms of anhydrous acid or base.[10] Lisdexamfetamine is currently in Phase III trials in Japan for ADHD Trade names    Tyvense, Elvanse, Aduvanz, Venvanse, Vyvanse

US poison control centers receive 29 calls per day about children exposed to ADHD medications
Date: May 21, 2018
Source: Nationwide Children’s Hospital
The study found that there were more than 156,000 calls to US Poison Control Centers regarding exposures to attention-deficit hyperactivity disorder (ADHD) medications among children and adolescents 19 years of age and younger from January 2000 through December 2014, averaging 200 calls each week or 29 calls per day.

*1:55pm 11/14/2018*
19 years of age and younger
156,000 calls
January  2000 December 2014
total yr.  14
any age  (2-5)?

reminder: a child infant could be exploited by parent to get medicine to then take? probability overdiagnosis by professional on that account?

Teva in 2008

In 1982, Teva was granted approval by the U.S. Food and Drug Administration (FDA) for its Kfar Saba manufacturing plant, an essential milestone for marketing pharmaceuticals in the US
Kfar Saba
(FDA) approval
US pharmaceuticals

BHA had closed its first deal to insure $50 million in debt for a 2% fee a rating of AAA from S&P to clean, to calculated,
Decker is on the boards of directors of Berkshire Hathaway,[12] Intel Corporation,[Munger is critical of cryptocurrencies, referring to Bitcoin as “poison”.[13] In early 2018 he likened bitcoin to “harvested baby brains” in an interview with Yahoo Finance Munger uses the term “Lollapalooza effect” for multiple biases, tendencies or mental models acting at the same time in the same direction. With the Lollapalooza effect, itself a mental model, the result is often extreme, due to the confluence of the mental models, biases or tendencies acting together, greatly increasing the likelihood of acting irrationally.

Known for    Founding Virgin Group
Net worth    US$5.1 billion (April 2018)[3]
Criminal charge    Fraud of Excise duties and Purchase Tax
Criminal penalty    Probation and repayment restitution
Criminal status    Sentence completed

A series of disputes in the early 1990s caused tension between Virgin Atlantic and British Airways, which viewed Virgin as an emerging competitor. Virgin subsequently accused British Airways of poaching its passengers, hacking its computers, and leaking stories to the press that portrayed Virgin negatively. After the so-called campaign of “dirty tricks”, British Airways settled the case, giving £500,000 to Branson, a further £110,000 to his airline, and had to pay legal fees of up to £3 million. Branson distributed his compensation (the so-called “BA bonus”) among his staff.

Virgin Fuels, which was set up to respond to global warming and exploit the recent spike in fuel costs by offering a revolutionary, cheaper fuel for automobiles and, in the near future, aircraft. Branson has stated that he was formerly a global warming sceptic and was influenced in his decision by a breakfast meeting with Al Gore

In June 2006, a tip-off from Virgin Atlantic led both UK and US competition authorities to investigate price-fixing attempts between Virgin Atlantic and British Airways. In August 2007, British Airways was fined £271 million over the allegations. Virgin Atlantic was given immunity for tipping off the authorities and received no fine—a controversial decision the Office of Fair Trading defended as being in the public interest

 technological advancements for the good of mankind

suggested in the House of Commons that Branson’s criminal conviction for tax evasion might be felt by some as a good enough reason not to trust him with public money.

Branson’s Virgin Group sought to add Northern Rock Bank, to its empire after submitting an offer that would result in Branson personally owning 30% of the company and changing the company’s name from Northern Rock to Virgin Money.

In September 2014, Branson announced his investment in drone company 3D Robotics stating, “It’s amazing to see what a little flying object with a GoPro attached can do. Before they came along the alternative was an expensive helicopter and crew. I’m really excited about the potential 3D Robotics sees in drone

More here, here, here and here.

see video for more links!
tools of:
perspective analysis
intrusion analysis
objective analysis
projective analysis

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Posted 21/11/2018 by admin in category "Biological Kontrol