Apotex - contamination     www.apotexholocaust.com            www.pharmaholocaust.com
I live like a walking death in twilight zone / some where in between death and a life being deprived of all Human Rights and Constitutional / Law 
protection by habitual offenders. I was assessed by three (3) independent psychiatrists to eliminate offender's speculations about my insanity 
prompting "delusions" etc. All psychiatrists stated clearly, that I am sane /I do NOT have/had any mental illness. No family history of any.
WSiB Ontario - a criminal/ terror Agency

Dear Sir/Madam,
WSiB Ontario - a criminal/ terror Agency!
WORNING TO ALL THOSE WHO ARE THERE TO SUPPORT CLAIMS OF INJURED WORKERS. 
DOCTORS, HEALTH CARE PRACTITIONERS TERRORIZED BY WSiB WITH LEGISLATED 
CONSEQUENCES FOR SUPPORTING INJURED WORKERS.
WSiB HAS THE POWER TO RE- INTERPRET/ QUESTOION DOCTORS AND HEALTH PROVIDERS 
DIAGNOSIS AND OCUSE ANY ONE OF Fraud and non-compliance. No wonder 99% of my 
Doctors refused to generate any records of my injuries or sabotaged them or 
strait forward falsified them.
"Fraud and non-compliance: definitions, penalties, and reporting.
What can I do if I suspect that a patient, an employer, a supplier, or 
another health care practitioner is not dealing honestly with the WSIB?
You can use our toll-free action line or e-mail address to report suspected 
cases of non-compliance and fraud.
In 1997 the WSIB announced a Zero Tolerance Strategy to ensure compliance 
and combat fraud. The Strategy included increased resources, a "tips "Action 
Line, and the authority to conduct surveillance. The WSIB will identify 
non-compliance, fraud and irregularities by workers, employers, providers 
and suppliers and take appropriate action. This may result in charges under 
Sec.149 (4) (submitting false or misleading statements) of the Workplace 
Safety and Insurance Act, or Sec.380 (fraud) of the Criminal Code.
"When reporting fraud or non-compliant behaviour you are not required to 
provide your name, address, or any other information that may identify you".
What constitutes an offence in dealing with WSIB?
It is an offence when a health care provider or supplier intentionally does 
any of the following.
What is the penalty for submitting false or misleading statements?
Conviction can result in the following penalties:
For an individual: A fine not to exceed $25,000 and/or a jail term of up to 
six months.
For a corporation: A fine not to exceed $100,000.
(Sec.158 (1) of the Act)
The court may also order restitution of the full amount of money obtained by 
commission of the offence (Sec.149 (5) of the Act).
Would a conviction under the Workplace Safety Insurance Act or the Criminal 
Code affect my licence to practice?
In cases where a health care practitioner is convicted, the WSIB notifies 
the appropriate regulatory body and provides a factual summary. The
regulatory body will take whatever action it deems necessary.
Want to get involved in preventing fraud in Canada's healthcare system?
The Canadian Health Care Anti-Fraud Association acts on behalf of public and 
private sector healthcare organizations interested in preventing fraud in 
the Canadian healthcare environment."
In Ontario WSiB commits crimes against INJURED WORKERS!
Despite fact, that Government Agencies (and politicians ) were aware of the 
situation for many years did not do any thing to rehabilitate the system 
(provided cover up for those activities).
People in position of power are promoting (become accessory) to Domestic 
terrorism by WSiB!!!.
Government Agencies refused to report crimes by WSiB and other Agencies 
against General Public to Police.
Many key Government Agencies are dysfunctional and criminal.
"Who does Not Know the Truth, is simply a Fool.
Yet who Knows the Truth and Calls it a Lie, is a Criminal."
WSiB by its incompetence, luck of education / professionalism / expertise 
and criminal orientation as a Policy, totally ignores / is oblivious about 
side effects of treatments and medications they forcibly subject injured 
workers to undergo, additionally deteriorates injured workers condition and 
it is imposed on "victims" in criminally sadistic manner etc. A number of 
medications intended to treat psychiatric disorders are themselves capable 
of causing psychiatric adverse effects. Unfortunately,
these medication-induced adverse effects can be mistaken for a lack of 
therapeutic efficacy, leading to increased dose prescribing, leading to even 
more adverse effects. In addition, a number of medications not intended to 
treat psychiatric disorders are capable of causing psychiatric adverse 
effects..
WSiB forcibly (by many means of coercions/ CRIMINAL MEANS etc.) forces 
injured workers to undergo unnecessary medical treatments (surgical 
proceedings, pharmacological treatments etc.) which often tremendously 
deteriorate injured workers conditions -often causing additional and 
irreversible damage. WSiB a criminal / terror Agency tormenting injured 
workers of Ontario and does it in legalized manner.
How come WSiB ( "INSURANCE AGENCY" ) MANAGED TO LEGISLATE CRIMINAL IMMUNITY 
AND MANY OTHER FAR REACHEING LEGISLATIVES ALLOWING AGENCY TO DO SURVELIANCE, 
TO INPOSE RULES ON INDIVIDUALS AND BUSINESSES, TO FORCE INJURED WORKERS TO 
BE SUBJECTED TO UNNECESSARY MEDICAL / PHARMACOLOGICAL TREATMENTS etc.
ORGANIZED AND LEGALIZED CRIME!!!!!!!!!
1. "We're often your doctor's biggest source of information."
It's comforting to imagine your physician sitting behind his desk after 
hours, carefully perusing reports on the latest drugs. While some still do 
their research the old-fashioned way, many doctors today get the bulk of 
their information from drug reps who are pushing specific medicines. To make 
sure physicians are paying attention, pharmaceutical companies spend more 
than $50 billion a year on promotional activities, according to a 2008 
report, the most recent available.
Typically, says Allen F. Shaughnessy, doctor of pharmacology and professor 
of family medicine at Tufts University, a drug rep gives a 90-second spiel 
that hits three or four salient points, followed by the classic sales pitch. 
And often doctors will bite. Reps "are very effective in changing physician 
behavior," says Shaughnessy. That interaction is necessary says a spokesman 
for the Pharmaceutical Research and Manufacturers of America (PhRMA), an 
industry group, because the companies have the most knowledge about the 
treatments that took them years to develop.
To gauge how seriously your physician relies on drug reps, Shaughnessy 
suggests that you press for details: "Ask why you are taking the drug he is 
prescribing, and make sure you understand what they explain." This approach 
will either get you the information you need, "or else you'll see a 
physician who blusters and carries on about why you are questioning him," 
says Shaughnessy. The latter scenario "will show you that they don't have a 
clue."
2. "Hype is our favorite medicine."
Choosing a medication shouldn't be like choosing Pepsi over Coke. But that's 
very much what's happening, thanks to the drug companies and their ad 
agencies. With famous faces like Sally Field, NBA star Alonzo Mourning and 
Lance Armstrong all playing spokesperson for various brands of medication, 
the companies marketing prescription drugs have learned to harness celebrity 
star power to help boost their brands.
Blame it on the Food and Drug Administration. In the late 1990s, the agency's 
decision to liberalize drug advertising allowed direct-to-consumer, or DTC, 
campaigns, and pharmaceutical ad budgets skyrocketed. From 1996 to 2005, 
spending on DTC campaigns increased 330 percent, according to a 2007 study 
by The New England Journal of Medicine, the most recent study available.
"It's horrendous," says Brian L. Strom, M.D., chairman of biostatistics and 
epidemiology at the University of Pennsylvania. "It's directly in conflict 
with proper therapeutics. But the manufacturers use patients as arms of 
their marketing departments." It can be dangerous, too. When Olympian 
Dorothy Hamill appeared promoting Vioxx for her arthritis pain, 
prescriptions were filled before the drug's heart risks became known. Strom 
says the drugs advertised are exactly the ones patients should not use. "If 
you needed them, I would have given them to you already," he says.
3. "There's no such thing as a free sample."
Patients love getting free trial-size medications from their doctors, 
doctors like giving them away, and drug companies rely on samples to filter 
new treatments into the pharmaceutical mainstream. In pushing free samples, 
drug companies hope that physicians will continue to prescribe the new-and 
often pricier-medication long after the honeymoon period is over. If the 
sample drug works and is tolerated, the physician will often continue to 
prescribe it instead of alternatives. The small outlay for free samples will 
eventually be compensated by large profits when physicians start prescribing 
the drug at full price, says Allan S. Brett, a professor of medicine and 
director of the Division of General Internal Medicine at the University of 
South Carolina.
While some believe that free samples are an important source of medication 
for uninsured patients who can't afford to pay, studies have shown that most 
free samples are actually given to insured, says Brett. A bigger issue is 
safety, says Joel Lexchin, an emergency medicine doctor and professor at the 
School of Health Policy and Management at York University in Toronto. "What 
is being sampled is usually the newest product that has less known about its 
overall safety profile," says Lexchin.
In a recent statement about free samples, PhRMA said: "Clearly, the most 
important components of a prescribing decision are the physician's clinical 
knowledge and the patient's unique situation. Free samples can provide a 
useful tool in the prescribing decision."
4. "Your doctor is our bounty hunter."
Facing mounting pressure to bring new medicines to market, drug companies 
often pay doctors who refer patients for their studies. And depending on the 
drug being tested, the payments will often be in thousands of dollars per 
patient. It should be noted, these aren't payments for referring a patient. 
The physician is receiving payment to enroll a patient in a study, but he or 
she is involved in the research as well, says Daniel Carlat, a psychiatrist 
in Newburyport, Mass., who writes about the pharmaceutical industry on his 
blog.
"Because there are such large financial incentives to enroll patients in 
studies, there's the possibility that the patient might be enrolled 
inappropriately," says Carlat. The problem is that patients who might be 
better served by getting standard medical treatment might instead be 
enrolled in a trial - and end up getting a placebo or another medication 
that they shouldn't.
The American Medical Association says it provides guidelines for physicians 
to manage potential conflicts of interest, and advises doctors to "be 
mindful of the conflicting roles of investigator and clinician and of the 
financial conflicts of interest that arise from incentives to conduct trials 
and to recruit subjects."
5. "You'll find out about side effects the hard way."
The arthritis painkiller Vioxx, a blockbuster drug after it was introduced 
in 1999, was taken off the market in 2004 when a study linked the drug to an 
increased risk of stroke and heart attack. Bextra, another painkiller, was 
also removed from the market in 2005 after it was found to pose heart risks.
The problem is that after a drug is approved, there's not a real systematic 
way for identifying side effects, and making sure those are captured and 
detected in a reliable way, says James G. Stevenson, associate dean for 
clinical sciences at the University of Michigan Health System's College of 
Pharmacy. There is a post-marketing surveillance process in the U.S., but it's 
voluntary. It relies on physicians and health-care providers to report 
possible problems with a drug to the FDA or the manufacturer. "It's their 
choice to do something with the information," Stevenson says.
Critics point to the drug industry's funding of the FDA through so-called 
user fees - in the range of hundreds of millions of dollars a year. A 
company pays user fees when it submits the research that the FDA reviews 
before deciding to approve a reject a new drug. (These fees were legislated 
in 1992, under the Prescription Drug User Fee Act, with the aim of helping 
drugs get FDA review quicker.) Groups like Public Citizen, a consumer 
advocacy organization, say there's an inherent conflict of interest. An 
agency cannot effectively regulate an industry that pays the salary of so 
many of its employees, says Dr. Sydney Wolfe, director of Public Citizen's 
Health Research Group.
Concerns about a conflict of interest are misplaced, according to the PhRMA, 
which says that the legislation has done much to advance public health and 
that safety is a big focus of the FDA drug review process.
6. "With all these complicated drug names, it's no wonder you're confused!"
The FDA reviews over 500 proprietary (or "brand") name drugs a year, through 
the Office of Surveillance and Epidemiology. Before a drug's final moniker 
is settled on, it has to pass an expert panel review, handwriting and verbal 
analyses, a computer analysis, and overall risk evaluation, collectively 
aimed at minimizing the risk of soundalike and look-a-like names. But 
problems persist: Medication errors result in more than 7,000 deaths a year, 
according to the Institute of Medicine. How to avoid getting the wrong 
medication? Check your pills against those represented in an up-to-date 
illustrated reference book, such as "The Pill Book" by Harold Silverman 
(14th edition is set for release in April).
With so many drug names floating around, it's not surprising that there are 
mix-ups. Each drug has a brand name and most have a generic name. Names can 
potentially look or sound similar. "There are only have so many letters in 
the alphabet," says Stevenson of the University of Michigan. PhRMA says it 
has worked with and continues to work with the FDA and other groups to 
prevent medication errors.
7. "Don't trust anything you read about our drugs online . . ."
If you're searching the Internet for information on, say, arthritis, what 
better place than a site like Arthritis.com, right? Not necessarily. While 
you will certainly get information there, it will come from Pfizer, maker of 
arthritis drug Celebrex - not exactly an unbiased source. Similarly, if you're 
looking to read up on depression, you'll find the site Depression.com is run 
by GlaxoSmithKline, maker of antidepressants Wellbutrin and Paxil. The 
problem with these drug-sponsored medical-information sites is that they can 
easily be mistaken for noncommercial information sources.
Even when such affiliations are made clear, the fine line between editorial 
and advertorial-which can be as subtle as the exclusion of seemingly minor 
details-becomes even finer when viewed on a computer screen. Nevertheless, 
Robert Rosa, professor of medicine and dean of regulatory affairs at 
Northwestern University's Feinberg School of Medicine, doesn't think it is 
an issue for most readers of these sites. They are sophisticated enough to 
realize that the company is sponsoring the information, he says.
The most egregious misinformation online comes from companies peddling 
non-FDA-regulated products such as vitamins, minerals, and supplements, 
according to Brooks Edwards, M.D., the founding medical editor-in-chief of 
MayoClinic.com. "The most important thing in evaluating information is 
knowing where it's coming from," Edwards says. "Sometimes you can tell on 
the Internet, and sometimes you can't."
8. ". . . and be extra careful when ordering meds over the Internet."
Given that Americans spent more than $300 billion on prescription drugs in 
2009, the temptation to shop around online for the cheapest prices can be 
alluring, especially for those who value privacy. But like with most things 
in life, cheaper doesn't necessarily mean better. In fact, when it comes to 
buying prescription drugs over the Internet, big discounts might mean 
counterfeit capsules.
The World Health Organization says counterfeit medicines pose huge health 
risks and that the growth in international trade of pharmaceutical 
ingredients and medicines adds further complexity to the issue. In over 50% 
of cases, drugs purchased online from illegal sites that conceal their 
physical address have been found to be counterfeit, according to the WHO.
Since web site content is unregulated, the FDA's only recourse is to issue 
warnings to the public about unreliable online purveyors of pharmaceuticals. 
It recommends that when buying medication online, you do so only from 
licensed pharmacies located in the United States; also, make sure the site 
requires a prescription and has a pharmacist available to answer questions 
by phone. You can find a list of state-licensed pharmacies on the National 
Association of Boards of Pharmacy web site.
9. "We know your medication history-because we bought it."
When a prescription is billed to a third party - any HMO or pharmacy 
benefits-management company - that third party can sell the data back to the 
drug manufacturer. This allows drug companies to know - in a particular zip 
code, for example - which medications are being prescribed and in what 
amounts, says Stevenson. And manufacturers can use that information to 
better target their sales efforts. "It's like market research," Stevenson 
says.
In 2006 the American Medical Association made it an option for doctors to 
keep their prescribing information inaccessible to reps. As of 2010, about 
25,000 had opted out (out of more than 700,000 patient-care physicians).
Such information is extremely valuable to pharmaceutical companies, which 
use it to gauge the degree to which individual doctors are prescribing one 
medication over another in the same class. Then, in order to stimulate 
sales, drug companies offer a range of perks to groups of physicians plucked 
from the drugstores' sales info. Their swag arsenal includes everything from 
dinners out to trips for medical conferences-all of which ultimately 
contribute to the rocketing costs of medication. "Doctors think of 
themselves as totally rational," says Tufts' Allen Shaughnessy."They get 
offended when I tell them that they are human and cannot be wined and dined 
without being influenced." PhRMA says prescription data help companies 
properly educate doctors about drugs in a targeted manner. And in the event 
of a drug shortage, a suspected drug counterfeiting or drug recall, "the 
federal system relies on the manufacturer to communicate directly and 
promptly with prescribing physicians," a PhRMA spokesman said in a 
statement.
The just-passed health-care reform also has a provision requiring drug and 
device companies, starting in 2013, to publicly report payments and gifts 
made to doctors. Some companies already do disclose such payments. However, 
there's nothing in the provision that actually prevents doctors from giving 
these paid speeches, notes Allan Coukell, director of the Pew Prescription 
Project, a drug safety initiative of the Pew Charitable Trusts.
10. "We're in cahoots with your insurer."
Stephen Fried was in the midst of writing "Bitter Pills," an exposé of the 
pharmaceutical industry, when a doctor suddenly switched his uncle from 
Procardia XL to a similar high-blood pressure drug called Norvasc. Fried 
says he found out that "drug companies offer substantial discounts [to 
health care managers] if they put all their [appropriate] patients on a 
particular drug." Insurers, of course, are trying to cut costs amid a 
continued rise in health care expenditures, and doctors typically do what 
the HMO requests. The problem? "You can have seizures, heart problems, 
dementia," Fried says. "The only reason to switch drugs should be to enhance 
your health. But most drug switches are made for dollars and cents."
A drug company providing financial incentive to a pharmacy benefits manager 
to switch a patient from one drug to another without good reason is 
obviously problematic, says Carlat, the Newburyport, Mass., psychiatrist. 
Even when drugs are in the same class and are designed to treat the same 
symptoms, they are not necessarily identical. One drug may not work as well 
as the other, and could have a different set of side effects, he says.
AND GOVERNMENT OF ONTERIO IS SILENT / SLIPING ( MAYBE DOES NOT CARE?) SO 
FAR!!!!!!!!!!!!!!!!!!!
What needs to be done to make Government acting according to its Policies 
/promises and LAW ???
Injured workers of Ontario await Government's support / action!!!!!
ELECTIONS ARE COMING. IT IS TIME FOR INJURED WORKERS AND ONTARIANS AS WHOLE 
TO MAKE ELECTIONS ISSUE OUT OF THAT CRIMINAL WSiB!!!!!!!!!!!!!!WSiB 
Ontario - a criminal/ terror Agency!
Criminal Corporations have substantial influence over WSiB's 
activities/processing of claims.
WSiB acts from position of power (criminal immunity) and further victimizes 
already suffering people.
Through out duration of processing it does infringe on criminal and sadistic 
tendencies.
It is paradoxical, that diagnoses /conclusions are being made by some of 
WSiB's personnel with out any medical / investigative knowledge /skills. 
Victim's evidence submissions, Reports of WSiB's qualified and professional 
investigators are not enough to adjudicate obvious cases.
This is very serious systemic problem and needs to be addressed immediately.
Injured workers are always forced by WSiB TO BE WITH THEIR PANTS DOWN AND 
PREDATORY WSiB does suffering workers right from the behind where it hearts 
the most!
Sadists , deviants , psychopaths, criminals do at their will injured workers 
due to criminal immunity and many other far reaching Legislatives granting 
criminal Agency power / rights to RAPE suffering people!!!
Agency established to assist General Public and protect / assist it in time
of desperation /suffer and misfortune, become criminal/ terror, profit 
oriented identity
placing well being of victims on back burner of its activity / objectives.
Through out duration of processing it does infringe on criminal and sadistic
tendencies.
WORKER ADVISER- A TWIN WITH WSiB CRIMINAL AGENCY FINANCED BY WSiB ( from 
WSiB'S budget)!
Worker Adviser communicated to me - " WE ARE RETAINED TO REPRESENT YOU ON 
ESTABILISHED / APROVED BY WSiB YOUR MEDICAL CONDITIONS , NOT TO REPRESENT 
YOUR BEST INTEREWST". SCANDAL, CRIME, DECIVE!!!!!!!!!!!!! FAIR PRACTICES 
COMMISSION ALSO IS FINANCED BY WSiB and plays WSiB's tune, not working for 
injured workers
ALL THOSE AGENCIES ARE SUSTAINED BY WORKERS OF ONTARIO! AL THOSE 
ADJUDICATORS, "ADVISERS", REPRESENTATIVES ARE BEING PAIED BY WORKERS OF 
ONTARIO AND ALL OF THEM ARE ENEMIES OF WORKERS OF ONTARIO. PARASITES AND 
CRIMINALS!!!!!!!!!!!!!!!!
ADVISE TO INJURED WORKERS:
The Burden of Proof in Personal Injury Claims
The Plaintiff (you) bears the burden of proving your case.
Most people have heard the term: "proof beyond a reasonable doubt". That is 
NOT the burden that applies in civil claims for compensation; it is the 
burden that applies to criminal prosecutions.
In a personal injury compensation claim you bear the burden of proof: "on 
the balance of probabilities". In other words, is more likely than not that 
the
Defendant was negligent and that the negligence caused your injuries.
The easiest way to think about this is to consider a pair of scales. All the 
evidence FOR your claim is placed on one side of the scale. All the evidence 
AGAINST your claim is placed on the other side of the scale.
As long as the scales tip to the side FOR your claim, even a little bit, 
then you have met the burden of proof on the balance of probabilities.
What Do I Have to Prove to Win my Case?
There are three things that you have to prove in order to win your accident 
compensation claim:
Breach of Standard of Care:
You will need to prove that the person that caused the accident did not meet 
the standard expected of a reasonably competent person. In other words, did 
they do something that they should not have done, or did they fail to do 
something that they should have done?
Causation:
If you can prove that the negligent person / Company breached the standard 
of care, you must also prove that the breach actually caused your injury (or 
made a pre-existing injury worse). For example, if you had chronic low back 
pain before the car accident, it may be difficult to prove that the car 
accident caused your back pain. But you may be able to prove that the 
accident made your pain worse.
Damages:
You have to prove what the consequences of the injury have been so that the 
court can award damages for pain and suffering, and any income loss and/or 
medical expenses as a result of your injury.
*** Severe Body & Brain Damaging Side-Effects of Antidepressants ***
The Neurotransmitter "Serotonin" & Serotonin Acting Anti-depressants
Since 1988 the pharmaceutical companies (starting with Eli Lilly, the 
manufacturer of "Prozac") have advertised to the people (direct to consumer) 
as well as to their family doctors, that if you suffer from depressive 
feelings, you must have a "biochemical imbalance" in your brain. The 
advertising finger was pointed at the neurotransmitter "serotonin", and it 
is used to explain nearly any emotional problem a person might have 
nowadays. Many other pharmaceutical companies came out with so many variants 
on the SSRI-antidepressant to try and capitalize on its popularity, by 
spreading this theory even further amongst the people. Theory? Yes, only a 
theory!
The Truth is that nobody in the medical field really knows if a "biochemical 
imbalance" is the cause of any mental disorder, and they do not know how 
even the hypothesized "biochemical imbalances" could produce the emotional, 
cognitive, and behavioural symptoms that characterize any mental disorder. 
Clever marketing tactics exercised on us by the pharmaceutical industry, 
prevailed above scientifical evidence and research. Greed, dis-respect and 
contempt of the population, prevailed above altruism, medical care and 
responsibility. It's the greatest shame of of this era. More information:
The Invention of the Biochemical Imbalance Myth
Organic conditions that are commonly misdiagnosed as mental disease
Can Psychiatry Be Retrieved From a Biological Approach?
Neuroscientist Elliot S. Valenstein Says No to Drugs
Primary care doctors prescribe SSRI-antidepressants to millions of adults, 
adolescents and children, certainly not only for treatment of depression 
anymore. SSRI's are prescribed for school phobias, bed wetting, eating 
disorders, sleep disturbances (insomnia), nail biting, hair pulling, 
headache, gambling addiction, alcohol addiction, back pain, stomach upset, 
premenstrual syndrome, etc., and even to "feel better then well". SSRI's 
have become all purpose "feel good pills", nowadays, in the year 2000. 
Unfortunately many doctors are unaware of the major consequences and some of 
them don't even seem to care. They argue that the positive effects of SSRI's 
far outweigh their negative effects. Nothing could be further from the 
truth.
SSRI's may not be compared with regular medications, like insulin to treat 
diabetics. SSRI's are psychoactive, blood-brain barrier passing drugs and 
interact with the serotonergic system in the brain. Another example of drugs 
interacting with the serotonergic system are LSD and Ecstasy (MDMA). The 
serotonergic system is responsible for "how we perceive, experience and feel 
the inside and outside world". YOU and only YOU created the neuropaths of 
this serotonergic system through the years by learning new things over and 
over again. And so it represents YOUR serotonergic system with it's own 
unique structure, playing a big role in the composition of YOUR mind, YOUR 
consciousness, YOUR emotions, YOUR thoughts. When these serotonergic brain 
cells are artificially pushed (by SSRI's) to act beyond their capacity or 
boundaries, this can result in the most disastrous serious adverse 
reactions. People need to be informed about the risks especially when 
children are involved.
Serotonin Re-Uptake Inhibitor = Impairing Body Serotonin Metabolism
SSRI's are "Selective Serotonin Re-Uptake Inhibitors." Neuronal re-uptake of 
neurotransmitters is metabolism. What serotonin re-uptake inhibitor actually 
means is that the SSRI-antidepressant interferes with ones ability to 
metabolise serotonin, so that will build up. In other words, an 
SSRI-antidepressant impairs the ability of cells to metabolise serotonin, 
not only in the brain, but -since serotonin is widely distributed throughout 
the body- in the body as well! The greatest concentration of serotonin, 
around 90%, is not found in the brain, but is found in the gastrointestinal 
or digestive tract (human gut, intestines, bowels).
Originally, the neurotransmitter serotonin -thought to be secreted by the 
Pineal Gland- is called a neurohormone, because of it's specific regulatory 
effect on the activity of the Endocrine Glands in the human body. (1),(2) 
Affecting serotonin means affecting the Glandular Endocrine System. Next to 
it, serotonin affects the Cardiovascular System and the Respiratory System, 
under which, the lungs. Serotonin is also found in blood platelets and 
stimulates platelet aggregation (blood clotting). Furthermore, serotonin is 
known to affect contraction of smooth muscles (such as those of the gut) and 
blood vessel elasticity (vasoconstriction and expansion). More information:
Serotonin & the Pineal Gland
Fraudulent Clinical Trials and the FDA
Many primary care doctors and most people believe, that SSRI's have 
undergone independent tests controlled by the Food and Drug Administration 
(FDA) to insure safety. In fact the FDA does not "test" proposed new drugs. 
It relies almost exclusively on safety and efficacy data provided by the 
drug's sponsor. SSRI studies are constructed, financed, and supervised 
entirely by pharmaceutical companies themselves. The testing process is 
deeply flawed. The clinical tests of antidepressants (SSRI's) are remarkably 
short. Although the FDA's guidelines for large-scale clinical tests 
recommend they last at least 6 weeks, in some instances studies as short as 
4 weeks are accepted. Typically, the studies last 6 to 8 weeks!
And how about the US Food and Drug Administration (FDA)? Already in 1993, 
28,623 reports of adverse reactions to "Prozac" -the Eli Lilly SSRI, 
approved for the market since 1988- had been received by the FDA. These 
included effects such as delirium, hallucinations, convulsions, violent 
hostility, aggression, psychosis, 1,885 suicide attempts and 1,734 deaths - 
1,089 by suicide. However, this didn't seem to be enough to provoke the FDA 
to act against the SSRI manufacturer. As a major consequence from this lack 
of action, other pharmaceutical companies were permitted to follow Eli 
Lilly's example, resulting in more Prozac copy-cat SSRI's like Paxil, 
Zoloft, Celexa, etc., nowadays, and probably more to come in the near 
future. How many reports of adverse reactions to these SSRI's must the FDA 
receive to pull them from the market? Or has this already gone too far?
Personality Structure and Out of Character Behaviour
We now have legal psychoactive, blood-brain barrier passing drugs, acting on 
the serotonergic system (SSRI's), the dopaminergic system (SDRI's) and the 
nor-adrenergic system (SNRI's) in the brain. The neurotransmitters dopamine, 
epinephrine (adrenalin) and nor-epinephrine (nor-adrenalin) are called 
"catecholamines" and control the adrenergic systems in the central nervous 
system (CNS). They account for staying awake, mood, fight or flight 
response, etc.. Serotonin is the primary inhibitory neurotransmitter 
modulating the excitatory catecholamine systems in the CNS. Serotonin 
neurons control memory, mood, sex drive, etc.. Serotonin, dopamine and 
nor-epinephrine (nor-adrenalin) are the key-neurotransmitters involved with 
the construction of YOUR personality structure, as stated by doctor C. 
Robert Cloninger. Every drug that acts on the serotonergic system will 
affect (indirectly) the other neurotransmitter systems (dopaminergic, 
nor-adrenergic) in the brain (and visa-versa), thereby affecting YOUR 
personality structure, YOUR temperament, YOUR character.
This must be exactly what happened to the antidepressant influenced home, 
school- and workplace shooters/killers who have reached the attention of the 
media since 1988. It's striking how every time, when involvement of an SSRI 
comes to public attention, pharmaceutical companies defend their 
serotonergic drugs by telling us over and over again that the fact that a 
shooter was taking an SSRI, was purely a coincidence, that the shooter was 
treated with an SSRI for "mental illness" and that the SSRI had nothing to 
do with his/her violent behaviour, (remember that SSRI's are prescribed for 
almost anything, not only for "mental illness"). The pharmaceutical 
companies argue that there is no evidence that SSRI's cause suicide or 
violence. They refer to the "scientific rigorous battery of independent 
clinical trials" that the SSRI's have undergone under the auspices of the 
American FDA to insure their efficacy and safety. A recent study tells us a 
different story!
However, who needs "clinical trials" when there is so much and hard evidence 
of violence related to SSRI's in the media... Isn't it striking how many 
home, school- and workplace shooters have reached the attention of the media 
since 1988? The first SSRI-antidepressant named "Luvox" was approved for the 
market on 25 march 1987 and the SSRI "Prozac" on 29 December 1987! Do you 
see the connection already? We now have several SSRI's all acting on the 
same serotonergic system in the brain. Did these SSRI's help the shooters to 
become more happy? Oh yes, so happy that the natural boundaries of their 
personality structure were far exceeded! They lost their emotional 
connection with their conscience, they became disconnected, they were pushed 
over the edge, THEIR edge!!
Serious Adverse Reactions
After growing reports concerning withdrawal symptoms to 
SSRI-antidepressants, pharmaceutical companies renamed these phenomena 
"antidepressant discontinuation syndrome", avoiding the negative 
connotations of the word "withdrawal". This creates the illusion that one is 
familiar with the side-effects from SSRI's, that they are rarely reported 
and that their products are safe. Ofcourse they want the people and doctors 
to keep on believing that withdrawal only happens to a minority of people 
and that the symptoms are mild and short-lived.
In fact the side effects from SSRI-antidepressants are far more serious than 
just the addiction to it and withdrawal symptoms. Many individuals who took 
an SSRI-antidepressant or tried to get off an SSRI-antidepressant 
experienced the most horrible adverse reactions. Many individuals have 
suffered for years or are still suffering because they experienced an 
extremely negative reaction to one of these drugs!
What happened in the brains of these individuals? Scientists have recently 
discovered that Prozac induces muscle contractions in the worm suggesting 
that Prozac has other molecular targets in the brain. Researchers from 
Jefferson Medical College in Philadelphia have found changes in brain cells 
in rats treated with SSRI's. The brain cells shrivelled or took on abnormal 
corkscrew shapes. What happens to the serotonergic system in the brain? The 
same system that's stimulated by administration of LSD (Lysergic Acid 
Diethylamide), the system that's involved with our perception. Doctors 
reported LSD flashbacks in adolescents -with a history of use of LSD- after 
treatment with an SSRI-antidepressant.
We strongly suggest You think again before You decide to take any 
anti-depressant. If you are currently taking an SSRI, never stop cold turkey 
but slowly taper off. Don't go off medication without medical supervision. 
The best way to minimize withdrawal side effects is to wean off the 
medication, this process may take up to a year or longer.
all involved in sabotaging of my allegations must be INDICTED and convicted 
on multiple offences / crime (Criminal Code, Constitutional provisions, 
Bill - 45, Bill 107, Bill - 168 and other Law provisions ).
IN CANADA EVERY YEAR OVER 24000 PEOPLE UNNECESARY DIE DUE TO MEDICAL 
ERRORS!!!!!!!!!!!