blogs created to prevent or detect a crime http://www.opsi.gov.uk/acts/acts1997/ukpga_19970040_en_1

This blog is brougt to you consistent with subsection 3 of the Protection from Harassment Act - i.e. blogs created to prevent or detect a crime http://www.opsi.gov.uk/acts/acts1997/ukpga_19970040_en_1



Friday, 6 July 2012

Neil Carlin (Paxil) promotes ECT - see FIDDAMAN blog

http://1boringoldman.com/index.php/2012/02/06/wisdom-in-his-pages/


" ....Breggin needs to understand that severe emotional suffering cannot always be fixed with empathetic talk therapy.


It is about properly informed choice. ....."




most popular post - FIDDAMAN confirms his day off from cold turkey to go to rock concert !

Your argument about me attending a concert during my cold

turkey period was pretty lame - do you not think being stuck in a one-bedroom
flat dealing with Zaps, sweats, anger etc warrants a day off?









Thursday, 5 July 2012

named GSK whistleblowers to get £ millions - patients as usual get nothing, see FIDDAMAN blog


Glaxo whistleblowers could get millions thanks to Civil War law

Four men will get share of record £1.9bn fine levied on GSK for mis-promotion of drugs in the US

LAST UPDATED AT 10:15 ON Wed 4 Jul 2012

FOUR GlaxoSmithKline whistleblowers whose testimony allowed US authorities to secure a record settlement with the drug company are set to share up to £159m thanks to a law dating back to the Civil War.



Earlier this week the UK pharmaceuticals giant was fined £1.9bn after admitting its US arm mis-promoted two drugs for unauthorised uses, including the treatment of children, and held back safety information on a third drug from America's Food and Drug Administration.



Now the whistleblowers at the centre of the largest healthcare fraud settlement in US history - Greg Thorpe, Thomas Gerahty, Blair Hamrick, and Matthew Burke – are set to cash in.



Under the Federal False Claims Act, a US law dating back to 1863 which was originally designed to stop war profiteering after the Civil War, the men are entitled to a share of the settlement. While the Department of Justice is yet to determine the exact percentage of the fine they will receive, The Telegraph reports that the total sum to be shared will be a minimum of £96m, and could be as high £159m.



For the whistleblowers, it is the reward for a fight that stretches back almost a decade and brought serious financial hardships.



Greg Thorpe, the father of four who has racked up close to $1m in debt since starting the legal action against his old employers in 2003, said the case had taken its toll. "I cannot be certain, if I knew beforehand what was coming after filing this case, that I could do it again."



Blair Hamrick, a Glaxo salesman from Colorado, started his legal action after the company allegedly ignored his concerns over mis-promotion of drugs. Hamrick lost his house after the case begun and said the saga had been "a dark cloud hanging over our heads".



The lawyer for the other two whistleblowers suggested the windfall on its way was deserved: "It was an historic settlement for the US taxpayers and it's important to note that this settlement would not have happened without these men." ·



.



Read more: http://www.theweek.co.uk/business/47779/glaxo-whistleblowers-could-get-millions-thanks-civil-war-law#ixzz1zmuAfTRx

Antidepressant lawyers will sue for anything - generics being less effective - like FIDDAMAN

Generic-Antidepressant Must Pay Settlement for Being Less Effective



http://www.jdjournal.com/2012/07/04/generic-antidepressant-must-pay-settlement-for-being-less-effective/

Generics of Wellbutrin have been judged inferior to the name-brand and thus will pay a national settlement. The popular antidepressants alternatives use the same active drug, Bupropion hydrochloride, but uses an inferior release technology, releasing the drug into the system in one quick dump rathar than the more effectively slow chemical release of brand name Wellbtrin. The total number of class members may be as many as 2.24 million people.


$3.2 million have been awarded in attorney fees, $1.3 million in class counsel costs, amidst other fees. The defendants, Teva Pharmaceuticals and Impax Laboratories, were both targeted in the suit. Said the plaintiffs:

“The representative plaintiffs all took defendants’ products to treat their depression but their symptoms instead worsened. Had they known that the differences in defendants’ products rendered them useless as antidepressants, plaintiffs would not have purchased defendants’ medication. Defendants failed to disclose important information to consumers, in violation of California consumer protection laws.

Whether this met the stipulation of Federal rule of Civil Procedure 23(b), so that individual class members would also receive compensation, and not just attorneys, was a “close” call according to the judge. He said the request for statutory damages would not count under Rule 23 (b) because the statutory damages “avoid an individualized calculation of damages. Plaintiffs also proposed a complicated mechanism whereby restitution damages could be calculated for the entire class.”







There have been some complaints against this that only lawyers would have benefited from the settlement.





Wednesday, 4 July 2012

GSK GlaxoSmithKline - whistleblowers to share between 15-30 per cent of $1bn - nice work if u can get it FIDDAMAN


If past practice is followed, Mr Thorpe himself and three other whistleblowers will now be eligible to share between 15-30 per cent of $1bn, part of the final settlement.



But as he said in a statement: “To those who would want to be whistleblowers and try and better society to ‘right a wrong,’ you need to be forewarned it can be a long and difficult road … I cannot be certain, if I knew beforehand what was coming after filing this case, that I could do it again.”






GSK failed to act on illegal drug marketing













http://www.ft.com/cms/s/0/336820de-c52b-11e1-b6fd-00144feabdc0.html#axzz1zell30UT


Senior GlaxoSmithKline executives failed to act on repeated warnings from employees over illegal marketing of its drugs, according to testimony from a whistleblower whose alerts triggered the company’s record $3bn settlement with US regulators this week.



Complaints raised from 2001 by Greg Thorpe, a sales representative worried about the lavish promotion to doctors of drugs beyond their authorised use, sparked investigations within the pharmaceuticals group. But the investigations triggered his dismissal rather than any internal reforms.






Click to enlargeDocuments included in the Department of Justice probe eventually launched with Mr Thorpe’s support highlight a corporate culture that appeared to focus more on commercial returns than ethics or patient safety.



His examples formed part of a larger case that ranged across a series of GSK’s drugs, and which US prosecutors argued both risked patient harm – including increased risk of suicidal feelings among adolescents taking the company’s antidepressants – and unjustifiable costs for the healthcare system.



In October 2001, Mr Thorpe was initially issued a warning by his manager, ostensibly for criticising the company’s incentive compensation programmes and making “negative comments” towards managers and team members.



He pursued his concerns internally, inspired by an initiative launched by David Stout, then US head of the company, called “Taking the high road” to make the company a leader in ethics and compliance in sales and marketing.



In a January 2002 report, he described the “indifference and pompous attitude” of senior managers. He cited the illegal promotion of the antidepressant Wellbutrin for ADHD; paying nurses for promoting a GSK migraine treatment; and a ski trip for doctors to Colorado that, he believed, was “buying the business through bribery”.



He described a call from a doctor’s assistant requesting a deep tissue massage, cleansing facial, foot reflexology and pedicure, following a lunch and presentation from a doctor promoting Wellbutrin, illegally, for weight loss. “Can you imagine if the Wall Street Journal got a copy of this invitation,” he wrote.



After querying entertainment for doctors that would cost $350 per person, beyond GSK’s limit of $75-$125, he was apparently told by his manager that it had been approved because it would be paid nominally by an outside vendor, so “it should not be noticed on our expenses”.



An email in February 2002 from Arjun Rajaratnam, then GSK’s global head of compliance, to a colleague referred to Mr Thorpe’s concerns over doctors selling books on the “off label” use of Wellbutrin at company-sponsored events. “Can you help me find a way to show GSK’s due diligence,” he asks.



In November 2002, Mr Thorpe raised his concerns in a letter copied to Mr Stout, Bob Ingram, GSK’s chief operating officer, and Mr Rajaratnam.



Mr Thorpe was forced out of GSK, and says in DoJ filings that he was never given the full benefits negotiated in his departure package – a matter that remains subject to litigation between him and the company. He says that he was unable to find fresh employment, unable to speak about his case and left more than $700,000 in debt.



Regulators probed his claims over a decade. They alleged falsification of documents by a lawyer over internal presentations provided to doctors for use in promotion of the company’s medicines. But the case was dropped on the grounds that seizure of the documents involved breaching attorney-client privilege.



GSK has since changed most of its top US management, and installed a range of new procedures including tight limits on entertainment and a ban on bonuses linked to prescription volumes for sales reps.



Mr Stout is now a non-executive director of Shire. Mr Ingram is chairman of Elan. Mr Rajaratnam is chief compliance officer at Smith & Nephew. None responded to requests for comment on Tuesday.



If past practice is followed, Mr Thorpe himself and three other whistleblowers will now be eligible to share between 15-30 per cent of $1bn, part of the final settlement.




But as he said in a statement: “To those who would want to be whistleblowers and try and better society to ‘right a wrong,’ you need to be forewarned it can be a long and difficult road … I cannot be certain, if I knew beforehand what was coming after filing this case, that I could do it again.”

Glaxo Agrees to Pay $3 Billion - can be rationalized as the cost of doing business - FIDDAMAN blog

Despite the large amount, $3 billion represents only a portion of what Glaxo made on the drugs. Avandia, for example, racked up $10.4 billion in sales, Paxil brought in $11.6 billion, and Wellbutrin sales were $5.9 billion during the years covered by the settlement, according to IMS Health, a data group that consults for drugmakers.





“So a $3 billion settlement for half a dozen drugs over 10 years can be rationalized as the cost of doing business,” Mr. Burns said.




http://www.nytimes.com/2012/07/03/business/glaxosmithkline-agrees-to-pay-3-billion-in-fraud-settlement.html?_r=2&pagewanted=all




Glaxo Agrees to Pay $3 Billion in Fraud SettlementBy KATIE THOMAS and MICHAEL S. SCHMIDT
















In the largest settlement involving a pharmaceutical company, the British drugmaker GlaxoSmithKline agreed to plead guilty to criminal charges and pay $3 billion in fines for promoting its best-selling antidepressants for unapproved uses and failing to report safety data about a top diabetes drug, federal prosecutors announced Monday. The agreement also includes civil penalties for improper marketing of a half-dozen other drugs.






The fine against GlaxoSmithKline over Paxil, Wellbutrin, Avandia and the other drugs makes this year a record for money recovered by the federal government under its so-called whistle-blower law, according to a group that tracks such numbers.




In May, Abbott Laboratories settled for $1.6 billion over its marketing of the antipsychotic drug Depakote. And an agreement with Johnson & Johnson that could result in a fine of as much as $2 billion is said to be imminent over its off-label promotion of another antipsychotic drug, Risperdal.



No individuals have been charged in any of the cases. Even so, the Justice Department contends the prosecutions are well worth the effort — reaping more than $15 in recoveries for every $1 it spends, by one estimate.



But critics argue that even large fines are not enough to deter drug companies from unlawful behavior. Only when prosecutors single out individual executives for punishment, they say, will practices begin to change.



“What we’re learning is that money doesn’t deter corporate malfeasance,” said Eliot Spitzer, who, as New York’s attorney general, sued GlaxoSmithKline in 2004 over similar accusations involving Paxil. “The only thing that will work in my view is C.E.O.’s and officials being forced to resign and individual culpability being enforced.”



The federal whistle-blower law, officially the False Claims Act, dates to 1863 and was originally envisioned as a check on war profiteering after the Civil War.



Whistle-blowers get a share of any money recovered by the federal government. So far, according to Patrick Burns, spokesman for the whistle-blower advocacy group Taxpayers Against Fraud, at least $10 billion has been agreed to in settlements this fiscal year, which ends in September.



The settlement, which requires court approval, stems from claims made by four employees of GlaxoSmithKline, including a former senior marketing development manager for the company and a regional vice president, who tipped off the government about a range of improper practices from the late 1990s to the mid-2000s.



Prosecutors said the company had tried to win over doctors by paying for trips to Jamaica and Bermuda, as well as spa treatments and hunting excursions. In the case of Paxil, prosecutors claim GlaxoSmithKline employed several tactics aimed at promoting the use of the drug in children, including helping to publish a medical journal article that misreported data from a clinical trial.



A warning was later added to the drug that Paxil, like other antidepressants, might increase the risk of suicidal thoughts in teenagers. Prosecutors said the company had marketed Wellbutrin for conditions like weight loss and sexual dysfunction when it was approved only to treat major depressive disorder.



They said that in the case of Avandia, whose use was severely restricted in 2010 after it was linked to heart risks, the company had failed to report data from studies detailing the safety risks to the F.D.A.



“Today’s multibillion-dollar settlement is unprecedented in both size and scope,” said James M. Cole, the deputy attorney general. “It underscores the administration’s firm commitment to protecting the American people and holding accountable those who commit health care fraud.”



The initial terms of the settlement were announced in November, and Glaxo had already set aside cash for the settlement. In a statement Monday, the company said it has since changed many of its policies, including no longer rewarding sales representatives for the number of drug prescriptions sold.



Andrew Witty, the chief executive, sought to portray the illegal actions as part of the company’s past.



“Whilst these originate in a different era for the company, they cannot and will not be ignored,” he said in the statement. “On behalf of GSK, I want to express our regret and reiterate that we have learned from the mistakes that were made.”



The three criminal charges involved Paxil, Wellbutrin and Avandia and included a criminal fine of $1 billion. The remaining $2 billion involves fines in connection with a civil settlement over the sales and marketing practices of the blockbuster asthma drug Advair and several other drugs.



Part of the civil settlement also includes claims that the company overcharged the government for drugs. Glaxo did not admit any wrongdoing in the civil settlement.



Despite the large amount, $3 billion represents only a portion of what Glaxo made on the drugs. Avandia, for example, racked up $10.4 billion in sales, Paxil brought in $11.6 billion, and Wellbutrin sales were $5.9 billion during the years covered by the settlement, according to IMS Health, a data group that consults for drugmakers.






“So a $3 billion settlement for half a dozen drugs over 10 years can be rationalized as the cost of doing business,” Mr. Burns said.



Mr. Burns and others have said that to institute real change, executives must be prosecuted criminally or barred from participating in the Medicare and Medicaid programs, an action known as “exclusion.”



This has occurred in only a handful of cases, and rarely in a case involving a major pharmaceutical company. In 2011, four executives of the medical device company Synthes were sentenced to less than a year in prison for conducting clinical trials that were not authorized by the Food and Drug Administration.



That same year, the former chief executive of K.V. Pharmaceutical was sentenced to 30 days in jail and fined $1 million for selling misbranded morphine tablets. The previous year, the Department of Health and Human Services excluded him from doing business with the federal government.



Those in the pharmaceutical industry have stressed that the activities revealed in the recent settlements occurred many years ago, and practices have changed radically since then. The Glaxo settlement includes an agreement by the company to withdraw bonuses from top executives if they engaged in or supervised illegal behavior, believed to be a first.



“That creates pressure and it creates an element of responsibility,” said Erika Kelton, who represented two of the four whistle-blowers in the Glaxo case. “I think it’s a good step in the right direction.”

Tuesday, 3 July 2012

GSK GlaxoSmithKline put aside more than £2bn to pay for the settlement in 2011 - FIDDAMAN blog

"The settlement ends a seven-year investigation into Glaxo's mis-promotion of medicines in the US, which is the company's largest research centre after Britain and home to almost a fifth of its 100,000 employees. Glaxo warned shareholders last November that it had put aside more than £2bn to pay for the settlement. "






http://www.telegraph.co.uk/finance/newsbysector/pharmaceuticalsandchemicals/9371404/US-fines-Glaxo-record-3bn-for-mis-promoting-drugs.html







US fines Glaxo record $3bn for mis-promoting drugs


GlaxoSmithKline paid for American psychiatrists to enjoy luxury weekends in Hawaii as it illegally sought to persuade them to prescribe an anti-depressant drug for children, US authorities alleged, as they handed the UK drugs company fines totalling a record $3bn (£1.9bn).



In 2000 and 2001, Glaxo's sales staff regularly held forums to discuss Paxil in destinations including Hawaii and Puerto Rico, where the psychiatrists attending were treated to golf, deep-sea fishing and balloon rides, according to the Department of Justice. Photo: Getty By Richard Blackden, US business editor

8:54PM BST 02 Jul 2012

The historic penalty came as Britain's biggest drugmaker admitted to mis-promoting two medicines, Paxil and Wellbutrin, in the US between 1998 and 2003. The settlement also saw Glaxo admit that it failed properly to report all the necessary safety data to US regulators concerning Avandia, a diabetes drug, between 2001 and 2007.



The settlement ends a seven-year investigation into Glaxo's mis-promotion of medicines in the US, which is the company's largest research centre after Britain and home to almost a fifth of its 100,000 employees. Glaxo warned shareholders last November that it had put aside more than £2bn to pay for the settlement.




"We are determined to stop practices that jeopardise patients' health, harm taxpayers and violate public law," said James Cole, US deputy attorney general.



Glaxo admitted promoting Paxil, an anti-depressant, to patients under 18 even though it did not have permission from the Food and Drug Administration (FDA) to do so.



In 2000 and 2001, Glaxo's sales staff regularly held forums to discuss Paxil in destinations including Hawaii and Puerto Rico, where the psychiatrists attending were treated to golf, deep-sea fishing and balloon rides, according to the Department of Justice.



Related Articles

GlaxoSmithKline to buy Cellzome for £61m

15 May 2012

Glaxo makes hostile bid for Human Genome

09 May 2012

Shareholder: GlaxoSmithKline offer is bitter pill

29 Apr 2012

GlaxoSmithKline sells OTC drugs for £164m

20 Apr 2012

Unlike drug companies, doctors are allowed to prescribe medicines for uses that do not have approval by the FDA. According to the US government's lawsuit, one psychiatrist said that "the style of conference would have been more suitable for a convention of sales reps; this is supposed to be a scientific meeting. To me, the music lights, videos and MCs are off-putting and a distraction (even demeaning)."



Glaxo said yesterday that it has changed the way its sales staff are paid by eliminating individual sales targets and aligning their compensation more closely to the quality of treatment a patient receives.



The settlement "brings to a resolution difficult, long-standing matters for GSK", Sir Andrew Witty, Glaxo's chief executive, said. "I want to express our regret and reiterate that we have learned from the mistakes we made."



Glaxo will pay a $1bn criminal fine, with the rest settling civil liabilities. A portion will also go to whistleblowers who originally warned of the mis-promotion

Monday, 2 July 2012

Jon Jureidini - PAXIL Seroxat study paid for by Scientology linked lawyers Baum Hedlund - see FIDDAMAN blog

Jon Jureidini


MBBS, FRANZCP, PhD

Title: Clinical Professor

Position: Head, Department of Psychological Medicine, Women's & Children's Hospital: Senior Research Fellow, Department of Philosophy, Flinders University of South Australia

http://health.adelaide.edu.au/psychiatry/staff/clstaff/jureidini_jon.html

Professional Affiliations:

Healthy Skepticism (www.healthyskepticism.org)

Women's and Children's Hospital Patient Care Ethics Group



Teaching Interests:

Clinical Appraisal, child development, psychiatric diagnosis



Clinical Interests:

Consultation-Liaison Psychiatry, Medicine and the pharmaceutical industry



Research Interests:

Suicide and antidepressants; language and communication in medicine



Key Publications:

Jureidini, J. (2009) How do we safely treat depression in children, adolescents and young adults? Drug Safety 32(4): 275-282.



Jureidini, J. (2008). Mind magic. In Rethinking ADHD: International Perspectives. timimi, S., Leo J (Eds). London: Palgrave Macmillan.



Jureidini, J., McHenry, L., Mansfield, P. (2008) Clinical Trials and Drug Promotion : Selective Reporting of Study 329. International Journal of Risk and Safety in Medicine 20: 73-81



Mares S & Jrueidini J, 2004. Psychiatric assessment of children and families in immigration detention? Clinical, administrative and ethical issues. Australian Journal of Public Health 28:520-6.



Donald T & Jureidini J, 2004. Parenting Capacity , 13:5-17



National and International Collaborations:

Canadian Womens' Health Network. SSRI use in pregnancy.



Declaration of Financial Interest:


In the last 5 years, Jon Jureidini has accepted no fees or other remuneration from drug companies, nor does he hold any shares. He was engaged by Baum Hedlund to provide an independent analysis of the data of GSKs Study 329 of paroxetine.




Contact Details:

Telephone: +61 8 8161 7226

Facsimile: +61 8 8161 7032

Email: jon.jureidini@health.sa.gov.au





Sunday, 1 July 2012

Safety warning over Britain’s most common antidepressant ....and it's not Seroxat as FIDDAMAN would like you to think

Safety warning over Britain’s most common antidepressant


A warning has been sounded over antidepressant drugs taken by more than a million patients in Britain.

http://www.telegraph.co.uk/health/9367001/Safety-warning-over-Britains-most-common-antidepressant.html

A study for medical regulators found that the drugs increase the risk of heart problems which can cause sudden death.



Doctors have been told to lower the maximum dose of the UK’s most widely prescribed antidepressant, Citalopram, for all patients.



However, regulators have admitted that it is not clear whether the lower dose is safe — as this was not tested.



Although GPs were informed of the health risk when it emerged last autumn, and may have explained the matter to patients, no public warning was issued.



Last night, experts criticised the Medicines and Healthcare products Regulatory Agency (MHRA), the prescriptions watchdog, for failing to make a public announcement — as it has done over other alerts, such as the PIP breast implant scandal.



Related Articles

Prozac affects cancer cures

12 Jan 2005

Anti-depressants 'can make men infertile'

24 Oct 2006

Depression treatment pinpointed

09 Oct 2006

Citalopram is used to treat depression, anxiety and obsessive compulsive disorders. More than 13 million prescriptions were issued in England and Wales last year — more than twice as many as those for Prozac-style antidepressants.



In the study, carried out for the European Medicines Agency (EMA), it was found to be three times more likely to cause cardiac abnormalities than other types of antidepressants.



The study of healthy volunteers found that the likelihood of electrical defects in the heart rose dramatically as the dose was increased. The abnormalities — known as QT prolongation — makes people vulnerable to heart arrhythmias and to Torsade de Pointes, a rare speeding of the heart rhythm which can be fatal.



The research found the risk of Torsade de Pointes also rose threefold with the drug, when compared with the antidepressants fluoxetine (better known as Prozac), paroxetine (Seroxat) and sertraline (Lustral).



A second study found that a variant of Citalopram known as escitalopram, often sold as Cipralex, for which a million prescriptions were issued last year, also increased risks to the heart.



Prescriptions for antidepressants are normally issued for one to two months, meaning that between one million and two million patients are affected by the safety warnings.



Peter Walsh, from Action Against Medical Accidents, a patient safety charity, criticised the failure by regulators to alert the public.



Mr Walsh said: “We need assurances that the necessary steps to protect patients from adverse effects of these drugs have actually been put in place. It is particularly disappointing that there has been so little transparency with patients and the public about this.”



In the study, electrocardiogram measurements showed that when volunteers were given a 60mg dose of Citalopram, it took twice as long for their hearts to recover from each beat, than when they were given a 20mg dose.



As a result, the EMA issued advice that the maximum dose for the drug must be lowered from 60mg to 40mg, and to 20mg for elderly people, who are vulnerable to toxic effects from drugs.



However, in documents seen by this newspaper, regulators admit that it is not clear whether a 40mg dose is safe, as the study did not examine such dosage.



Similar patterns were found with escitalopram, at a dose of 30mg. It already has a maximum dose of 20mg, which remains unchanged, except for patients over 65, where the safe level is 10mg.



Dr Amanda Varnava, a consultant cardiologist from Imperial College Healthcare trust, said: “I don’t think GPs should stop prescribing these drugs, but they do need to be more aware of the risks from upping the dosage.”



Data obtained by this newspaper discloses 6,386 reports of cardiac problems and seizures among patients who took Citalopram.



The reports, which were considered by the EMA, show 569 cardiac arrests and 112 sudden deaths among patients taking the pills. In 124 cases, patients suffered Torsade de Pointes.



Since Citalopram started being prescribed in the UK in 1995, 8,600 adverse reactions have been reported to the agency, including 155 deaths. In total, 223 cardiac disorders were recorded and 1,703 disorders of the nervous system.



An MHRA spokesman said its enforcement of the EMA’s recommended restrictions enabled health care professionals to give appropriate advice to their patients, and that the agency had ensured information leaflets were updated.

Saturday, 30 June 2012

Steve Green CCHR N Z presents award to Maria Bradshaw - both are co-founders of CASPER



CCHR NZ Event featuring special guest from CASPER - 23 June 2012 (4 photos)


Steve Green reads out the international Human Rights award that Maria Bradshaw received in Los Angeles in Feb 2012



http://www.facebook.com/pages/CCHR-NZ/102661973126426#!/photo.php?fbid=386308721428415&set=a.386308564761764.85865.102661973126426&type=1&theater






Maria Bradshaw bought by CCHR Scientology - just like FIDDAMAN

http://www.facebook.com/video/video.php?v=1970656203386

CCHR 2012 Human Rights Awards—Slide Show


.



CCHR International


Here's a slide show of our Human Rights Awards banquet featuring CCHR Commissioners, Actors Danny Masterson, Ethan Suplee, Jenna Elfman, Marisol Nichols and Nancy Cartwright, and this year's award winners, Detroit Mother Maryanne Godboldo, Psychology Instructor Lisa Cain, Child Advocate Maria Bradshaw and Chill EB. Click here to watch the Maryanne Godboldo human rights award video, presented by Ethan Suplee & Danny Masterson http://goo.gl/qY8xT

— with Marisol Nichols, Nancy Cartwright, Danny Masterson and JENNA ELFMAN at The Westin Bonaventure Hotel & Suites.



12:40.

Friday, 29 June 2012

@ GSK PAXIL SEROXAT withdrawal payout was $5600 = £3500 ...don't let FIDDAMAN fool you !


 ...they called me and just took my story over the phone. I hoped that it would make a difference, but figured I'd never hear from them again. I can't remember how much later it was, but I got a check in the mail for $5600!!! I suppose that I'm not suppose to talk about that, but I don't give a flying f who knows it. .....



https://www.paxilprogress.org/forums/showthread.php?t=44684

Wednesday, 27 June 2012

SSRI FIDDAMAN blog - Jury rejects insanity in Zoloft rape case; ex-cop will go to jail

A San Bernardino County jury Tuesday rejected a former Westminster police detective’s defense that he was legally insane due to antidepressant use when he kidnapped and brutally raped a waitress from the Ontario Mills Mall two years ago.


http://latimesblogs.latimes.com/lanow/2012/06/jury-rejects-insanity-in-zoloft-rape-case.html

The decision in the sanity phase of the trial means Anthony Orban will serve time in jail rather than receive treatment at a state mental hospital.



Deputy Dist. Atty. Debbie Ploghaus said Tuesday she was very happy with the verdict and considered the Zoloft defense to be a ruse concocted after Orban was arrested. "He's very dangerous. He's very manipulative," she said. "I truly believe in my heart that he had no intention of letting her go."



Orban testified that he had no memory of the lengthy attack and blamed a psychotic break induced by a powerful dose of the popular antidepressant Zoloft, which he also blamed for triggering hallucinations and suicidal and homicidal fantasies during the week of the abduction.



The same jury earlier this month found Orban guilty of kidnapping, rape and multiple counts of sexual assault, dismissing the defense’s claims that Zoloft had rendered Orban mentally “unconscious” and therefore not responsible for his actions.



Zoloft again was central to the defense in the sanity phase, when Orban’s attorney, James Blatt, tried to convince the jury that his client should be sent to a state mental hospital for treatment, not prison.



Defense witness Dr. Peter Breggin, a New York psychiatrist who has testified about the dangers of psychotropic drugs in trials across North America, told jurors that Orban was “zombie-like” in the days leading up to the attack. He said that Orban had stopped taking the prescribed antidepressant, then resumed it at full dose, provoking a psychotic break during which he was "delirious" and not fully aware of his actions.



The main witness for the prosecution, clinical psychologist Dr. Craig Rath of San Bernardino, on Thursday told the jury that Orban’s blackout was caused more by alcohol than by Zoloft. The day of the attack, Orban and a friend barhopped across Ontario, ordering eight margaritas and two pitchers of beer between them, according to evidence presented at the trial.



"He was not insane," said Roth, testifying about his court-ordered analysis of Orban’s mental state. "He understood the nature and quality of his acts and could distinguish between right and wrong."



During the trial, Ploghaus called the so-called Zoloft defense a "bunch of baloney," saying that Orban had "sex on his mind" shortly before the attack. The night before, he had an argument with his wife and, in the hours before the abduction, sent 45 text messages to a woman with whom he'd recently had an affair.



The victim, a 25-year-old waitress, testified earlier in the trial that Orban kidnapped her as she walked to her car in the Ontario Mills Mall parking lot, then forced her to drive north to Fontana. After they stopped at a self-storage lot, Orban brutally raped and tormented her, she said.



When Orban was distracted by an incoming cellphone call, the woman said, she jumped out of the car and ran to safety at a nearby liquor store. Police later recovered Orban's gun, with his name on it, from the victim's car

Japan introduction of PAXIL / Seroxat 1999 - linked to documented reduction of suicide - goodnews FIDDAMAN CASPER?

extract -


The number of suicides in Japan each year -- which hit a peak of 33,048 in 1999 -- declined 3.3% in 2000 and another 2.9% in 2001, the first full two years that SSRIs were available. However, the rate remains very high compared with earlier years, and many factors can contribute to suicide, so it's too early to tell whether the new drugs contributed to the reduction.






A newspaper ad by Japanese drug maker Shionogi & Co. promoting awareness of depression. It shows actress Nana Kinomi urging people to talk about the disease.







Japanese sales of GlaxoSmithKline's Paxil reached ¥12 billion ($96.5 million) in 2001, its first full year on the market, and the figure is on track to rise this year. By comparison, U.S. sales of the drug last year were $1.8 billion. Japanese sales of Luvox and Depromel -- the name under which the drug is sold by Meiji's marketing partner, Fujisawa -- totaled ¥14.5 billion last year. (In May Solvay removed Luvox from the U.S. market, where it had been approved to treat obsessive-compulsive disorder, after the Food and Drug Administration cited problems with documents filed by Solvay to the FDA. The company, which has been the drug's U.S. marketer, says Luvox is safe and expects it to be back on the market next year. The generic form of the drug, fluvoxamine, is still sold in the U.S.)



Other drug companies have also ramped up their efforts in Japan. Pfizer Inc. had started trials of its blockbuster Zoloft in Japan in the early '90s, but its crucial large-scale human trial failed to use strict enough standards when picking patients, says Kenneth Wolski, who oversaw the trial as head of development for Pfizer's Japan subsidiary until he left the company in 1996. The company's new-drug application, which has been pending with Japanese regulators since 1998, hasn't been approved. A Pfizer spokesman blamed the low awareness of depression in Japan at the time, and "different standards in clinical-trial design." Two months ago, Pfizer announced a new clinical trial of Zoloft at 20 sites across Japan.



And Prozac -- which had world-wide sales of $1.99 billion and U.S. sales of $1.53 billion last year -- is finally coming to Japan. Andrew Macarenas, head of Lilly's Japan operations, says it should be on the market by 2004 -- some 17 years after it first went on sale in the U.S. The company is preparing the way by paying for the activities of a committee of Japanese doctors that promotes awareness of depression. The committee holds seminars for doctors and operates a Web site. "A number of things are happening to take mental health out of the cupboard" in Japan, says Mr. Macarenas. "It's not a taboo anymore."



The message from drug companies has fit well with Japan's medical culture. Japanese doctors are accustomed to loading up patients with medication, and are permitted to sell drugs directly to patients, often at a significant profit. Meiji and Glaxo have conducted hundreds of seminars about depression for general practitioners and psychiatrists across Japan, and the companies say interest is strong.



Tuesday, 26 June 2012

Antidepressants Market Share by prescription 2008 - Paxil Seroxat became irrelevant like FIDDAMAN

GSK - in no great rush to release Paxil CR (Seroxat) Japan - more FIDDAMAN bullshit revealed

Dainippon Sum.Pharma : Anti-depressant Paxil CR Tablets newly launched


06/21/2012
10:52pm



June 22, 2012



Anti-depressant Paxil® CR Tablets newly launched



GlaxoSmithKline K.K. Dainippon Sumitomo Pharma Co., Ltd.



GlaxoSmithKline K.K. (President: Philippe Fauchet, Head Office: Shibuya-ku, Tokyo, hereinafter referred to as GSK) announces that it has launched its anti-depressant Paxil® CR Tablets 12.5mg and Paxil® CR Tablets 25mg (paroxetine hydrochloride hydrate, hereinafter referred to as Paxil® CR Tablets, CR stands for Controlled Release) in Japan on June 22, following its NHI price listing on the same day.



GSK and Dainippon Sumitomo Pharma Co., Ltd. (President: Masayo Tada, Head Office: Chuo-ku, Osaka, hereinafter referred to as DSP) have started co-promoting Paxil® CR Tablets from April 1, 2012.



Paxil® CR tablets is the controlled-release1 formulation of Paxil® tablets, an SSRI (selective serotonin reuptake inhibitor) anti-depressant. It received regulatory approval in Japan from MHLW on 18 January 2012 for the indication of depression and depressive state. Overseas, development of anti-depressants using new formulation technology are being conducted actively and with the approval of Paxil® CR Tablets, Japan too has entered the era of controlled-release formulations. Paxil® CR Tablets was approved in the US in 1999 and as of June 2011, has been approved and widely used in over 40 countries worldwide.



Sunday, 24 June 2012

GSK - SEROXAT Litigation massive payout - see Bob FIDDAMAN blog for details

A class action settlement has been reached in a class action lawsuit against GlaxoSmithKline LLC (“GSK” or “GlaxoSmithKline”) pending in the Superior Court for the State of California County of Los Angeles (styled Grair v. GlaxoSmithKline, Class Action Case No. BC 288536), alleging, among other things, that GlaxoSmithKline employed false and deceptive marketing by misrepresentations and failing to disclose material information to the class and healthcare providers that the prescription antidepressant medication Paxil, an FDA-approved prescription medication commonly used to treat depression, obsessive-compulsive disorder, generalized anxiety disorder, social anxiety disorder, and post-traumatic stress disorder, was habit forming or addictive and about Paxil’s risks and unique frequency and severity of symptoms on withdrawal or discontinuation of Paxil, according to the California Paxil Antidepressant class action settlement notice.


http://classactionlawsuitsinthenews.com/class-action-notices/paxil-antidepressant-class-action-settlement-of-class-action-lawsuit-against-glaxosmithkline-over-allegedly-false-deceptive-advertising/?utm_source=rss&utm_medium=rss&utm_campaign=paxil-antidepressant-class-action-settlement-of-class-action-lawsuit-against-glaxosmithkline-over-allegedly-false-deceptive-advertising&utm_source=Paxil+News&utm_medium=twitter

Class Members in the California Paxil Antidepressant settlement reportedly include the following persons, unless otherwise excluded:



All natural persons who: (1) commenced a Paxil prescription between January 14, 1999 and January 1, 2003; (2) were 18 years old or older at the time they commenced their prescription; and (3) were residents of the State of California at the time they commenced their prescription.



The Paxil Antidepressant settlement reportedly provides monetary compensation as follows:



GlaxoSmithKline shall pay up to a total of eight million five hundred thousand dollars ($8,500,000.00) to provide a full refund of the Out-of-Pocket Expenses of Settlement Class Members who timely submit a valid Proof of Purchase and a sworn statement verifying eligibility. In the event the total amount of valid claims submitted by Settlement Class Members with valid Proof of Purchase exceeds $8,500,000.00, then the payment to those Class Members will be reduced pro rata so that a total of not more than $8,500,000.00 will be paid to Settlement Class Members with valid Proof of Purchase. GlaxoSmithKline shall reimburse Out-of-Pocket Expenses incurred by Settlement Class Members who timely submit a sworn statement verifying eligibility but who do not have valid Proof of Purchase up to eighty dollars ($80.00) per claimant. In the event the total amount of valid claims submitted by Settlement Class Members who do not have valid Proof of Purchase exceeds five hundred thousand dollars ($500,000.00), then the payment to those Class Members will be reduced pro rata so that a total of not more than $500,000.00 will be paid to Settlement Class Members who do not have valid Proof of Purchase.



Under the California Paxil Antidepressant Class Action Settlement, only Out-of-Pocket Expenses, including copayments and deductibles, you incurred for Paxil from January 1, 1999 through January 1, 2003 will qualify.



The Paxil Antidepressant settlement also provides that GlaxoSmithKline shall include certain information about Paxil ® or Paxil CR® on its corporate website as long as Paxil® or Paxil CR® is listed as a GlaxoSmithKline product on that website and that should GlaxoSmithKline in the future market or sell Paxil® or Paxil CR® or generic paroxetine in the United States, then GlaxoSmithKline will not advertise the product as non-habit forming and will comply with all FDA requirements.



The Court will hold a Fairness Hearing at 9:00 a.m. on November 13, 2012 at Department 323 of the Superior Court for the State of California County of Los Angeles located at Central Civil West Courthouse, 600 S Commonwealth Ave., Los Angeles, CA 90005 to consider whether the Paxil Antidepressant settlement is fair, reasonable, and adequate and will decide whether to approve the settlement and the motion for attorneys’ fees, expenses, and awards to the Class Representatives.



For more information about the proposed Paxil Antidepressant class action settlement, visit the California Paxil Antidepressant settlement website:



www.capaxilclassaction.com



Saturday, 23 June 2012

Maria Bradshaw protests against Dr David Healy's favourite treatment ECT - thats some campaign your in FIDDAMAN !!




Margaret, Steve, Maria, Terata, Monte, Dana and Rita.




Recently the CCHR team visited Napier to attend the 6th National Electro Convulsive Therapy (ECT) Conference sponsored by drug company Eli Lilly.




In an unprecedented move, Steve managed to get CCHR into the conference due to the amount of work that CCHR had done working with victims of Electroshock.



Steve, Maria and Margaret sat in the front row of the conference, along with about 50 psychiatrists and other medical and psychiatric staff. Outside, the rest of the team approached the attendees in the break periods, handed out DVDs and conducted video interviews on those that were brave enough to take part and share their points of view.



The first speaker was the Ministry of Health (MoH) who explained that he had worked for the past decade with the Director of Mental Health and 8 of those years on two petitions against ECT from Patients Rights Advocacy Waikato (PRAW) and CCHR NZ!



A forensic consultant psychiatrist then spoke about the Lake Alice atrocities, including the psychiatrist in charge of the Child and Adolescent Unit, Selwyn Leeks. Again, this is CCHR's work, being the NGO that uncovered the abuses in the 1970s and assisted the child-victims through to present day! The presenter surmised that if the NZ Government

had investigated, apologised and paid out millions of dollars in compensation, that he believed the abuse did happen and that it is part of their (psychiatry's) history.



After going through a timeline of what happened at Lake Alice and some of the things overseas he told the audience that this is their history that they had to front up to it and even mentioned that psychiatry was an agent of social control. He came to the point in his slide that showed CCHR NZ's submission to the United Nations this year and asked if anyone had heard of them (to which Steve put his hand up announcing that he is from CCHR).





Margaret is an ECT survivor and had received the destructive treatment during her teenage years. Sadly her story is shared by many. CCHR NZ had acknowledged all the work she did a few years ago in bringing about awareness of ECT (including 3,000 petition signatures in 3 weeks). With extreme courage she asked the conference organiser if she could speak at the conference and then delivered a powerful 10 minute speech on why she thought the practice was barbaric and should be banned. This was in front of the key psychiatrists who administer ECT from around the country!



Amusingly too, the next item was a documentary on ECT (TV3 60 Minutes) and who should you see on the large screen but Margaret herself campaigning against ECT. We are very proud of you Margaret, well done!



On completion of the conference, Steve (kindly) offered all attendees an impactful 3 minute video on ECT and CCHR documentaries as a thank you for allowing CCHR NZ to attend the conference. The conference organiser announced this and each attendee (mostly psychiatrists) got copies of CCHR's "Making a Killing", "Marketing of Madness", and "Industry of Death" DVDs.



This has helped put CCHR NZ front and centre for victims of psychiatric abuse with the shock doctors and the MoH.



An amazingly productive effort by a team willing to get in there and help - THANK YOU!





Toran Henry death - manslaughter? ............what ever happened to that claim FIDDAMAN?

POLICE REVIEWING MANSLAUGHTER CHARGES FOLLOWING YOUTH SUICIDEPosted by: Clare Swinney ⋅ November 5, 2008 ⋅ Post a comment


Tags: Add new tag, Bradshaw, CCHR, Police, psychiatry Posted in: Health, News

From the Citizens Commission on Human Rights



http://uncensored.co.nz/2008/11/05/police-reviewing-manslaughter-charges-following-youth-suicide/

November 4th 2008



Auckland mother Maria Bradshaw revealed that the Police will be referring the case of the death of her son, Toran Henry, to Crown Law for possible manslaughter charges.








In a moving speech at the Citizens Commission on Human Rights exhibition opening at the ASB Showgrounds on the weekend, Ms Bradshaw said it was, “a small win in a hard battle to bring out the truth of Toran’s death.” Ms Bradshaw has fought with mental health officials since her 17-year-old son took his life while he was on antidepressants in March this year. Ms Bradshaw claims the level of care for her son was negligent and irresponsible and that he never should have been prescribed antidepressants at such a young age. She also claims the psychiatric doctor stated Toran would be able cease taking the drugs to drink alcohol on the weekends and resume taking them afterwards.





In her talk that was given at the opening of an exhibition displaying the horrors of psychiatric abuse she said her son had been upset at the break-up with his girlfriend and that he fell victim to the psychiatric system of drugging people for ordinary life problems. She claimed she was threatened to have her son taken off her if she did not go along with the antidepressant treatment, which she opposed.








The Police referral to have Crown Law examine the case for possible manslaughter charges comes on the heels of a damning yet-to-be-published external report into the mental health care surrounding Toran Henry’s death.





Citizens Commission on Human Rights director, Mr Steve Green cited another case where the United Kingdom Police levelled manslaughter charges against a psychiatrist, Dr Peter Fisher, the NZ psychiatrist who was involved in three deaths including the case where psychiatric patient, Mark Burton broke into his mother’s home and stabbed her to death the day after Fisher had discharged him. Dr Fisher moved to England, where he practiced illegally. UK police became involved due to negligence over the suicide of one of his patients who overdosed on painkillers.





“Serious adverse events from psychotropic drugs such as antidepressants are well known by doctors. International warnings have been published around suicide in under-18-year olds, including New Zealand’s own Medsafe,” Mr Green said.





Mr Green believes strong measures need to be taken to prevent future deaths by suicide by people on psychotropic medication. The United States has now recorded that half of their suicides are committed by people on antidepressants, a worrying trend he doesn’t want in New Zealand.







Background



Maria Bradshaw, mother of 17-year-old Toran Henry leant her weight behind the psychiatric labelling and drugging campaign, by travelling to Auckland especially to be a guest speaker. Amongst other things, she spoke out against the complete lack of objective medical tests in mental health, which ended with her son being prescribed an antidepressant and taking his own life earlier this year.





CCHR’s director, Mr Steve Green says the psychiatric abuse of human rights is worst when it is directed at kids, such as the Children of Lake Alice, which the Commission exposed in the mid 1970s. Current day psychiatric abuse of children are the powerful methamphetamine-based stimulants, anti-psychotics and anti-depressants administered for conditions such as Attention Deficit Hyperactivity Disorder (ADHD), which he says was literally voted into existence.





“In this country the use of anti-depressants for teenagers is very controversial with claims of how they cause suicidal behaviour,” he said. The Ministry of Health has issued advice to doctors and is requiring warnings on all antidepressants to indicate possible increased suicide risk and the need to closely monitor patients with depression, particularly young persons.









The Commission is now working on cases where young people have committed suicide while in mental health care and assisting families through the complaint processes. Suicide is a big issue; according to the Chief Coroner, 511 suicides were reported in the year ended in June, surpassing road deaths.





“One is too many, these are devastating events that are generally ignored, until it happens to your family or a close friend, when it is too late. This is why the Commission is now working on this level and holding public exhibitions, to help educate people – information empowers people and this is vital,” Mr Green said.





“The display highlights the absolute need to reform key areas of mental health treatment,” Green says and he cites the continued use of electric shock as well as the many abuses that have occurred within New Zealand psychiatry, like electric shocking children in the 1970s, the experimental use of deep sleep treatment and electro leucotomies on women in Nelson in the 1950s.





The 40-metre exhibition presents the often-brutal history of psychiatry in a series of panels and videos documenting over a century of human rights abuses around the world. Over 150 experts in medicine, law, psychiatry, education, etc were interviewed. The documentary comes with a warning however as no punches are pulled: it has an R-18 certificate.







CCHR was co-founded in 1969 by the Church of Scientology and Dr. Thomas Szasz, Professor of Psychiatry Emeritus from the State University of New York Health Science Center in Syracuse. As an international mental health watchdog they have successfully achieved hundreds of legislative protections against psychiatric abuse.



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Contact information:











Steve Green



Executive Director



Citizens Commission on Human Rights



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cchr@xtra.co.nz www.cchr.org.nz