Pharmaceuticals Anonymous

Showing posts with label fraud. Show all posts
Showing posts with label fraud. Show all posts

Sunday, May 29, 2011

Another Doctor on Big Pharma’s Payroll



When Dr. Victor Tapson, a Duke University researcher, wrote the Food and Drug Administration urging that the agency delay the approval of a generic blood thinner, it was a recommendation that carried some clout. Tapson, after all, was writing on behalf of the American College of Chest Physicians. But now it seems Tapson has some explaining to do. A Senate Finance Committee report released last week found that Tapson was on the payroll of a pharmaceutical company that was trying to protect its profits by blocking the release of a generic rival. POGO Investigator Paul Thacker explains how Tapson was part of a major lobbying push by drugmaker Sanofi-Aventis. Link

Friday, July 30, 2010

Mental health experts ask: Will anyone be normal?

The APA started the DSM as a fundraiser. Now look where it's got us.


Mental health experts ask: Will anyone be normal?

By Kate Kelland

LONDON | Tue Jul 27, 2010 5:23pm EDT

LONDON (Reuters) - An updated edition of a mental health bible for doctors may include diagnoses for "disorders" such as toddler tantrums and binge eating, experts say, and could mean that soon no-one will be classed as normal.

Leading mental health experts gave a briefing on Tuesday to warn that a new edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM), which is being revised now for publication in 2013, could devalue the seriousness of mental illness and label almost everyone as having some kind of disorder.

Citing examples of new additions like "mild anxiety depression," "psychosis risk syndrome," and "temper dysregulation disorder," they said many people previously seen as perfectly healthy could in future be told they are ill.

"It's leaking into normality. It is shrinking the pool of what is normal to a puddle," said Til Wykes of the Institute of Psychiatry at Kings College London.

The criteria are designed to provide clear definitions for professionals who treat patients with mental disorders, and for researchers and pharmaceutical drug companies seeking to develop new ways of treating them.

Wykes and colleagues Felicity Callard, also of Kings' Institute of Psychiatry, and Nick Craddock of Cardiff University's department of psychological medicine and neurology, said many in the psychiatric community are worried that the further the guidelines are expanded, the more likely it will become that nobody will be classed as normal any more.

"Technically, with the classification of so many new disorders, we will all have disorders," they said in a joint statement. "This may lead to the belief that many more of us 'need' drugs to treat our 'conditions' -- (and) many of these drugs will have unpleasant or dangerous side effects."

The scientists said "psychosis risk syndrome" diagnosis was particularly worrying, since it could falsely label young people who may only have a small risk of developing an illness.

"It's a bit like telling 10 people with a common cold that they are "at risk for pneumonia syndrome" when only one is likely to get the disorder," Wykes told the briefing.

The American Psychiatric Association did not immediately respond to a request for comment.

The scientists gave examples from the previous revision to the DSM, which was called DSM 4 and included broader diagnoses and categories for attention deficit hyperactivity disorder (ADHD), autism and childhood bipolar disorders.

This, they said, had "contributed to three false epidemics" of these conditions, particularly in the United States.

"During the last decade, how many doctors were harangued by worried parents into giving drugs like Ritalin to children who didn't really need it?," their statement asked.

Millions of people across the world, many of them children, take ADHD drugs including Novartis' Ritalin, which is known generically as methylphenidate, and similar drugs such as Shire Plc's Adderall and Vyvanse. In the United States alone, sales of these drugs was about $4.8 billion in 2008.

Wykes and Callard published a comment in The Journal of Mental Health expressing their concern about the upcoming DSM revision and highlighting another 10 or more papers in the same journal from other scientists who were also worried. DSM 5 is due to be published in May 2013.

Sunday, June 27, 2010

Video: The Beautiful Truth


The cancer societies tell us that no diet has ever been devised that can cure cancer. Is that true?
Link

Monday, June 21, 2010

Medicating Children: A “Whistleblower’s” Lawsuit Raises a Novel Legal Question

calvinhobbesritalinjpg


From Robert Whitaker's Blog, MAD IN AMERICA, at Psychology Today

"In the past few years, a number of pharmaceutical companies have admitted to federal charges that they illegally
marketed psychiatric medications for non-approved uses, with the companies paying large sums to settle the cases.
Now, a legal complaint filed by the Law Project for Psychiatric Rightsin an Alaskan federal court is raising a
related question. When healthcare providers bill Medicaid for prescriptions of psychiatric drugs to children for non-
approved uses, are they committing Medicaid fraud?
The case, United States ex-rel Law Project for Psychiatric Rights v. Matsutani, was unsealed earlier this year, and
legal papers were recently filed that have brought this novel question -- which obviously has profound implications
for the prescribing of psychiatric medications to poor children and adolescents -- into sharp focus.
The Law Project for Psychiatric Rights (PsychRights) , which is headed by Alaskan attorney James Gottstein, filed its
whistleblower complaint in April 2009. Known as a qui tam lawsuit, PsychRights sued on behalf of the federal
government under the False Claims Act, which allows private individuals to pursue legal complaints against
individuals or companies that are allegedly defrauding the government. In December, the federal government
declined to join PsychRights in the case.
PsychRights named Alaskan state officials, hospitals, mental health agencies, psychiatrists, and pharmacies as
defendants. In its complaint, PsychRights argues that the federal government has agreed to provide Medicaid
reimbursement only for those outpatient drugs that are prescribed for an FDA-approved use or for a use supported
by a medical compendium (such as the DRUGDEX Information System.) PsychRights maintains that the defendants
defrauded the federal government when they billed Medicaid (or the federal Children's Health Insurance Program)
for outpatient drugs that didn't meet this standard.
As part of its complaint, PsychRights identified 16 commonly prescribed psychiatric medications that have no
"medically accepted indication" for youth under 18 years old, and it also identified the limited number of "medically
accepted indications" that exist for 32 other psychiatric drugs. PsychRights compiled this list of "approved" uses by
methodically going through the drug compendiums, and it serves as the evidential heart of the complaint, for it
reveals that psychiatric medications are regularly prescribed to poor children for non-approved uses. PsychRights is asking the federal court to stop this practice (which it argues is harmful), and to pay hefty financial penalties for the fraudulent claims made to date."


Riveting! Thank you, Robert Whitaker.

Read the rest at
http://www.psychologytoday.com/blog/mad-in-america/

Some of our previous posts on Robert Whitaker's views and anti-psych meds articles -

http://www.thestreetspirit.org.
This site is owned by The American Friends Service Committee (AFSC),
a Quaker organization that includes people of various faiths who are committed to social justice and peace.

http://www.thestreetspirit.org/August2005/mad.htm

http://www.thestreetspirit.org/August2005/madinterview.htm

http://www.thestreetspirit.org/August2005/leonards.htm

http://www.thestreetspirit.org/August2005/zyprexa.htm

http://web.archive.org/web/20071119112008/http://www.namiscc.org/newsletters/February02/JohnNashDrugFreeRecovery.htm

http://pharmaceuticalsanonymous.blogspot.com/2009/12/us-kids-represent-psychiatric-goldmine.html

http://pharmaceuticalsanonymous.blogspot.com/2008/05/royal-recovery-from-schizophrenia.html

Saturday, March 27, 2010

Wachovia Bank - Money Laundering, Plea Bargain

This is a bit off our usual path, but Wachovia handles NAMI's money. Links:
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Money Laundering, Plea Bargain

WACHOVIA ENTERS INTO DEFERRED PROSECUTION AGREEMENT
March 17, 2010
FOR IMMEDIATE RELEASE

Bank Agrees to Pay $160 Million

Wachovia Bank, N.A. (“Wachovia”), one of the largest banks in the United States, has entered into a deferred prosecution agreement with the U.S. Attorney’s Office in the Southern District of Florida and the Asset Forfeiture and Money Laundering Section of the Criminal Division of the Department of Justice to resolve charges that it willfully failed to establish an anti-money laundering program. Today’s agreement is the result of an investigation into Wachovia’s transactions with Mexican currency exchange houses, commonly known as “casas de cambio” (“CDCs”), announced Jeffrey H. Sloman, United States Attorney for the Southern District of Florida, Lanny A. Breuer, Assistant Attorney General for the Criminal Division of the Department of Justice, Mark R. Trouville, Special Agent in Charge, Drug Enforcement Administration (DEA), Miami Field Division, Daniel W. Auer, Special Agent in Charge, Internal Revenue Service, Criminal Investigation Division (“IRS-CID”), John C. Dugan, Comptroller of the Currency, Office of the Comptroller of the Currency (OCC), and James H. Freis, Jr., Director, Financial Crimes Enforcement Network (FinCEN). The agreement also resolves Wachovia’s admitted failure to identify, detect, and report suspicious transactions in third-party payment processor accounts.

A criminal information, filed March 12, 2010 and unsealed today, charges Wachovia with willfully failing to maintain an anti-money laundering program from May 2003 through June 2008, in violation of the Bank Secrecy Act (“BSA”). According to the information and other documents filed with the court today, including a detailed Factual Statement and a Deferred Prosecution Agreement (“the Agreement”), Wachovia failed to effectively monitor for potential money laundering activity more than $420 billion in financial transactions with the CDCs.

As part of the Agreement filed today, Wachovia has agreed to forfeit $110 million to the United States, which represents proceeds of illegal narcotics sales that were laundered through Wachovia. FinCEN also assessed a $110 million Civil Money Penalty that is deemed satisfied by the forfeiture to the U.S. government, for serious and systemic BSA violations. Moreover, pursuant to the terms of the Agreement and the OCC’s separate Cease and Desist and Civil Money Penalty Orders, Wachovia has agreed to pay an additional $50 million fine to the U.S. Treasury. The total sum of $160 million is due within five days from the date of the Agreement.

In light of Wachovia’s willingness to acknowledge responsibility for its actions and omissions, its cooperation and remedial actions to date, and its promised continued cooperation and remedial actions in the future, the government has agreed to defer prosecution of the criminal charge in the information for 12 months. If Wachovia fully complies with its obligations under the Agreement, the U.S. agrees to dismiss the criminal information at the end of the 12 months. Earlier today, the Agreement was accepted in federal court in Miami by U.S. District Judge Joan A. Lenard.

According to the documents filed with the court, Wachovia was aware, as early as 1996 and through 2004, of the high risk that drug money was being of laundered through the CDCs. Wachovia was also aware that other U.S. banks had stopped doing business with the CDCs because of these concerns. Wachovia, however, continued to expand its business with the CDCs. Indeed, from at least May 2004 through December 2007, Wachovia provided correspondent banking services to various Mexican CDCs, including wire transfer, bulk cash, and pouch and remote deposit capture services, among others.

According to the documents, Wachovia allowed CDCs to wire transfer funds through accounts at Wachovia to recipients throughout the world. Wachovia also offered a “bulk cash” service to CDCs, through which the CDCs collected large sums of dollars that would be physically transported to the United States for deposit. In addition, Wachovia offered a “pouch” deposit service and later, a “remote deposit capture” (“RDC”) service, which allowed the CDCs to deposit at Wachovia items drawn on U.S. banks, including checks and traveler's checks, presented by their Mexican customers. According to the documents filed today, Wachovia did not have an effective anti-money laundering policy or procedure to monitor these transactions to detect and report potential money laundering activity, as required by the BSA. As a result, from May 1, 2004 through May 31, 2007, at least $373 billion in wire transfers were made from the CDCs to Wachovia accounts; more than $4 billion in bulk cash was transported from the CDCs in Mexico to accounts at Wachovia; and approximately $47 billion was deposited at Wachovia accounts through the RDC service. These monies included millions of dollars that were subsequently used to purchase airplanes for narcotics trafficking operations. Ultimately, more than 20,000 kilograms of cocaine were seized from these airplanes.

According to court documents, Wachovia also maintained account relationships with certain third-party payment processors for the telemarketing industry from 2003 to 2008. These processors deposited more than $418 million using remotely-created checks into Wachovia accounts on behalf of the telemarketers. Remotely-created checks are created when the holder of a checking account authorizes a payee to draw a check on that account but does not actually sign the check. In place of the account-holder’s signature, the remotely-created check generally bears a statement that the customer authorized the check. These checks were often returned as “unauthorized” resulting in return rates that, in some cases, exceeded 40 percent of the deposited checks. Wachovia admitted that it failed to identify, detect, and report the suspicious transactions in the third-party payment processor accounts, as required by the BSA, due to deficiencies in its anti-money laundering program. Specifically, Wachovia failed to conduct appropriate customer due diligence by delegating most of this responsibility to business units instead of compliance personnel. Wachovia also failed to monitor high return rates for remotely-created checks and report suspicious wire transfer activity from the processors’ accounts.

U.S. Attorney Jeffrey H. Sloman stated, “On the heels of the UBS international banking case, in which we held accountable the largest bank in Switzerland, today we announce the deferred prosecution of Wachovia, one of the largest banks in the United States. Wachovia’s blatant disregard for our banking laws gave international cocaine cartels a virtual carte blanche to finance their operations by laundering at least $110 million in drug proceeds. Corporate citizens, no matter how big or powerful, must be held accountable for their actions. Today’s historic agreement makes it clear that such conduct will not be tolerated and imposes the largest penalty in any BSA case prosecuted to date.”

“As this case demonstrates, financial institutions - no matter how large - will be held accountable when they allow dirty money to pollute the U.S. banking system,” said Assistant Attorney General Lanny A. Breuer of the Criminal Division. “With billions of dollars flowing through our financial institutions each day, it is imperative that banks maintain robust anti-money laundering controls to identify possible illegal activity.”

“A narcotics investigation always involves two things: drugs and money,” said Mark R. Trouville, Special Agent in Charge, Drug Enforcement Administration, Miami Field Division. “DEA Agents and our law enforcement partners investigating a multi-national drug trafficking organization were able to seize drugs and identify the associated financial trail. Diligent investigative work exposed how this organization capitalized on weak anti-money laundering practices at Wachovia to further their drug trafficking abilities.”

Daniel W. Auer, Special Agent in Charge of the IRS-CID in Miami, stated, “The law requires all banks, including Wachovia, to notify the Department of Treasury when they detect suspicious activity. By failing to maintain an adequate anti-money laundering program, Wachovia disregarded numerous financial transactions that should have raised "red flags" and caused their bank to act a as conduit to launder money.”

“The practices targeted by today’s enforcement actions reflect a totally unacceptable breakdown in the standards expected of banks’ anti-money laundering systems and compliance. Today’s actions by the OCC and other agencies demonstrate our firm commitment to the highest standards of compliance in this arena and the success of continued coordinated efforts by the Department of Justice, OCC, and FinCEN to ensure compliance with the requirements of the Bank Secrecy Act,” said John C. Dugan, Comptroller of the Currency. “Financial institutions must maintain anti-money laundering compliance programs and policies that are adequate to identify, analyze and report suspicious activity and are commensurate with the risks being undertaken. With these actions, we are sending another strong message that we will not tolerate use of the U.S. financial system to launder illegal monies.”

“In the recent past, Wachovia was the fourth largest commercial bank in the United States, and held itself out as a global leader in correspondent banking,” said James H. Freis, Jr., FinCEN Director. “During FinCEN’s joint investigation with our law enforcement and regulatory agency partners, it became evident that, despite such a prominent role in the domestic and international banking sectors and accompanying resources, Wachovia did not institute systems, controls and other measures to manage risk commensurate with the scope and magnitude of its products, services and business lines, particularly foreign correspondent banking.”

Wachovia Bank will merge into Wells Fargo Bank later this month. The Agreement binds Wells Fargo, as Wachovia’s successor, to continue to implement remedial measures to fully bring Wachovia into BSA compliance.

The CDC-portion of this matter was investigated by the DEA’s Miami Field Division, IRS-CID’s Miami Office, FinCEN, and OCC. The case is being prosecuted by Assistant U.S. Attorneys Andrea G. Hoffman and Jared E. Dwyer of the U.S. Attorney’s Office for the Southern District of Florida. The investigation of the third-party payment processors was prosecuted by Trial Attorneys Constantine Lizas and Matthew Haslinger of the Criminal Division's Asset Forfeiture and Money Laundering Section. This portion of the case was investigated by the Internal Revenue Service Criminal Investigation, Philadelphia Field Office and the U.S. Postal Inspection Service, Philadelphia Division.

Attachments:
Information (PDF)
Agreement (PDF)
Statement (PDF)
A copy of this press release may be found on the website of the United States Attorney's Office for the Southern District of Florida at http://www.usdoj.gov/usao/fls. Related court documents and information may be found on the website of the District Court for the Southern District of Florida at http://www.flsd.uscourts.gov or on http://pacer.flsd.uscourts.gov.

Technical comments about this website can be e-mailed to the Webmaster. PLEASE NOTE: The United States Attorney's Office does not respond to non-technical inquiries made to this website. If you wish to make a request for information, you may contact our office at 305-961-9001, or you may send a written inquiry to the United States Attorney's Office, Southern District of Florida, 99 NE 4th Street, Miami, Fl. 33132.

...
Senator Charles Grassley is investigating NAMI's funding ties,
three-quarters of which may come from Pharma.
...

Now we look at this NAMI PDF on donations in a different light...

Sunday, February 14, 2010

CFS/ME - "Magical Medicine: How to Make a Disease Disappear"

PRESS RELEASE


Magical Medicine: How to make a disease disappear
-------------------------------------------------
12th February 2010

A formal complaint has been lodged by Professor Malcolm Hooper with
the Rt. Hon The Lord Drayson, Minister of State with responsibility
for the Medical Research Council (Science and Innovation) about the
'PACE' Clinical Trial of behavioural modification interventions for
people with Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome
(CFS).

PACE is the acronym for Pacing, Activity, and Cognitive behavioural
therapy, a randomised Evaluation, interventions that, according to
one of the Principal Investigators, are without theoretical foundation.

The MRC's PACE Trial seemingly inhabits a unique and unenviable
position in the history of medicine. It is believed to be the first
and only clinical trial that patients and the charities that support
them have tried to stop before a single patient could be recruited
and is the only clinical trial that the Department for Work and
Pensions (DWP) has ever funded.

Since 1993, the giant US permanent health insurance company
UNUMProvident has been advising the UK DWP about the most effective
ways of curtailing sickness benefit payments. The PACE Trial is run
by psychiatrists of the Wessely School, most of whom work for the
medical and permanent health insurance industry, including
UNUMProvident. These psychiatrists insist =96 in defiance of both the
World Health Organisation and the significant biomedical evidence
about the nature of it -- that 'CFS/ME' is a behavioural disorder,
into which they have subsumed ME, a classified neurological disorder
whose separate existence they deny. Their beliefs have been
repudiated in writing by the World Health Organisation.

In 1992, the Wessely School gave directions that in cases of ME/CFS,
the first duty of the doctor is to avoid legitimisation of symptoms;
in 1994, ME was described by Professor Simon Wessely as merely 'a
belief'; in 1996 recommendations were made that no investigations
should be performed to confirm the diagnosis and in 1999 patients
with ME/CFS were referred to as 'the undeserving sick'.

The complaint is supported by a 442 page Report which addresses areas
of major concern about the PACE Trial.

These include apparent coercion and exploitation of patients, flawed
methodology, apparent lack of scientific rigour, apparent failure to
adhere to the Declaration of Helsinki, the unusual personal financial
interest of the Chief Investigator, the vested financial interests of
the Principal Investigators and others involved with the trial and
the underlying non-clinical purpose of the trial.

The psychiatrists' unproven beliefs and assumptions are presented as
fact and trial therapists have been trained to provide participants
with misinformation; therapists have also been trained to advise
participants to ignore symptoms, a situation that may in some cases
result in death.

There are some extremely disquieting issues surrounding the MRC PACE
Trial and documents obtained under the Freedom of Information Act
allow the full story to be told for the first time.

People with ME/CFS do not seek any special consideration; they simply
wish to be treated equally to those who suffer from other classified
neurological disorders. As shown in the Report that accompanies the
complaint, the MRC PACE Trial clearly demonstrates that people with
ME/CFS are not treated equally to those with other chronic
neurological disorders.

The Report can be accessed at
http://www.meactionuk.org.uk/magical-medicine.pdf
File Size 6Mb
Adobe Acrobat format

CONTACT: Professor Malcolm Hooper 0191 =96 528 - 5536

- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -


Letter of complaint to the Rt Hon The Lord Drayson
--------------------------------------------------

Professor Malcolm Hooper Ph.D., B.Pharm., C.Chem., MRIC
Sunderland SR3


11th February 2010

The Rt Hon The Lord Drayson
Minister of State
(Science and Innovation)
1, Victoria Street
London
SW1H 0ET


Dear Minister

re: Complaint about the Medical Research Council

It is with deep concern that I lodge this formal complaint about the
Medical Research Council with you in your capacity as Minister with
responsibility for the MRC.

You will doubtless be aware of the serious problems at the MRC that
were documented in the 2003 Report of the House of Commons Select
Committee on Science and Technology (HC 132) in which MPs issued a
damning judgment on the MRC, lambasting it for wasting funds and for
introducing misguided strategies for its research. MPs found
evidence of poor planning and of focusing on 'politically-driven'
projects that have diverted money away from top-quality proposals.
The unprecedented attack was the result of a detailed probe into the
workings of the MRC.
Sadly, very serious problems continue to exist at the MRC, with
disastrous results for patients with Myalgic Encephalomyelitis/
Chronic Fatigue Syndrome.

The attached 442 page Report addresses the background to the MRC
'PACE' Trial on 'CFS/ME', the biomedical evidence that disproves the
assumptions of the MRC trial Principal Investigators, the many
extremely disturbing issues surrounding the PACE Trial, and
illustrations from the Manuals used in the trial.

The unproven beliefs and assumptions of the MRC Investigators are
presented as fact; trial therapists have been trained to provide
participants with misinformation, and therapists have also been
trained to advise participants to ignore symptoms arising from the
interventions, a situation that may in some cases result in death.

Patients with ME/CFS do not seek any special consideration; they
simply wish to be treated equally to those with other classified
neurological disorders. As shown in the commissioned Report that
accompanies this complaint (a bound copy of which will follow), the
MRC Trial clearly demonstrates that people with ME/CFS are not
treated equally to those with other chronic neurological disorders.

Given the long-standing recognition that at least one of the
interventions used in the trial is contra-indicated for people with
ME/CFS, an intervention that is already known to have adverse effects
on 50% of those who have already undertaken it, there is
international concern about the MRC PACE Trial.

I urge you to read the attached Report and to respond to it with due
attention and alacrity. You may wish to know that the Report is
already on international academic websites.

Yours sincerely

Malcolm Hooper

Download report here


Kris Kristofferson, "In the News"

Friday, December 11, 2009

U.S. Sen. Grassley: Grassley works for disclosure of drug company payments to medical groups



Three Cheers for Senator Grassley!

12/8/2009

Link

WASHINGTON --- Senator Grassley has asked 33 medical groups for information about the financial backing they get from the pharmaceutical, medical device and insurance industries.

“These organizations have a lot of influence over public policy, and people rely on their leadership. There’s a strong case for disclosure and the accountability that results,” Grassley said.

Grassley said his inquiry follows a review of industry support for the National Alliance on Mental Illness, where he questioned the organization’s national office and state chapters. The Alliance subsequently adopted a new policy of publicly releasing industry support over $5,000. “It’d be good for the system if other organizations would follow NAMI’s lead in this area,” Grassley said.

For several years, Grassley has conducted extensive oversight and sought disclosure of financial ties with industry from research physicians, medical schools, medical journals, continuing medical education, and the patient advocacy community. He has worked to expose cases where there was vast disparity between drug-company payments received and reported by leading medical researchers. In response to Grassley’s work, the National Institutes of Health is working on new disclosure guidelines for federal grant recipients.

Grassley is also working for congressional passage of reform legislation he has sponsored with Senator Herb Kohl. Their bipartisan Physician Payments Sunshine Act would require annual public reporting by drug, device and biologic manufacturers of payments made to physicians nationwide.

“I’m interested in transparency,” Grassley said. “Letting the sun shine in and making information public is basic to building people’s confidence in medical research, education and the practice of medicine,” Grassley said.

This week, t he senator’s letters of inquiry were sent to the American Academy of Orthopaedic Surgeons, the Alzheimer’s Association, the American Academy of Allergy Asthma and Immunology, the American Academy of Dermatology, the American Academy of Family Physicians, the American College of Obstetricians and Gynecologists, the American College of Surgeons, the American Dental Association, the American Diabetes Association, the American Dietetic Association, the American Heart Association, the American Hospital Association Inc., the American Medical Association, the American Psychological Association, the American Society of Anesthesiologists, the American Society of Colon and Rectal Surgeons, the American Society of Consultant Pharmacists, the American Society of Health–System Pharmacists, the American Society of Hypertension, Inc., the American Society of Nephrology, the American Society of Plastic Surgeons, Children and Adults with Attention Deficit/Hyperactivity Disorder, Depression and Bipolar Support Alliance, the Heart Rhythm Society, Mental Health America, NARSAD, the National Association of Chain Drug Stores, the National Organization for Rare Disorders, the North American Spine Society, Screening for Mental Health Inc., the National Center for Mental Checkups at Columbia University (TeenScreen), The Leukemia and Lymphoma Society, and the American Cancer Society.

Here is the text of Grassley’s letter.

December 7, 2009

Dear _________________:

The United States Senate Committee on Finance (Committee) has jurisdiction over the Medicare and Medicaid programs and, accordingly, a responsibility to the more than 100 million Americans who receive health care coverage under these programs. As Ranking Member of the Committee, I have a duty to protect the health of Medicare and Medicaid beneficiaries and safeguard taxpayer dollars authorized by Congress for these programs.

For the last three years, the Committee has been looking into various aspects of the pharmaceutical industry, including consulting arrangements, and industry funding for Continuing Medical Education (CME). My inquiry was spurred, in part by press accounts documenting the lack of transparency in the relationships between the pharmaceutical industry and nonprofit organizations. For instance, in April 2008, The Wall Street Journal reported that industry representatives, including ten major drug companies, formed a coalition to promote looser restrictions on off-label marketing. [1] The coalition asked the National Alliance on Mental Illness (NAMI) to speak in favor of this issue.

On October 6th of this year, I sent letters to all fifty state chapters of NAMI asking them to disclose income from pharmaceutical companies. In that letter, I explained that NAMI National receives almost two-thirds of its funding from the drug industry. [2] I learned recently that a few days after I sent those letters, one of the founders of NAMI and member of the NAMI National Board of Directors emailed his resignation, stating that he was shocked at NAMI’s reliance on pharmaceutical industry funding. In particular he said: “This financial dependency presents a number of problems.”

In response to my concerns, NAMI began to disclose publicly on its website, any amount of funding exceeding $5,000 that it received from pharmaceutical companies and other foundations. This decision in favor of transparency by NAMI is encouraging.

In April of this year, the Institute of Medicine issued a report endorsing transparency and stating that protections against conflicts can be established without inhibiting productive relationships between medicine and industry to improve medical knowledge and care. I am hoping you can assist me in this effort by providing additional insights into these relationships as well as any changes in transparency that your organization may be planning for in the future. Operating with transparency sends a message that there is nothing to hide.

Accordingly, I would appreciate an accounting of industry funding that pharmaceutical, medical device companies, foundations established by these companies or the insurance industry have provided to the (Organization) (The term “industry funding” means any transfer of value, including but not limited to grants, donations, and sponsorship for meetings or programs, etc.) This request covers the period of January 2006 to the present.

Because reporting practices vary widely from one charitable organization to another, I would appreciate you also placing this income into a chart, detailing annual amounts of industry funding. For each year, please provide the following information for (Organization) :

1) Year;

2) Name of company;

3) Amount of funding; and

4) Reason(s) that the funding was provided.

In addition, please explain (Organization) policies for accepting industry funding and the disclosure requirements of your top executives and board members by answering the following questions. For each question, please respond by first repeating the enumerated question followed by the appropriate answer. Again, this request covers the period of January 2006 to the present:

1)

Please describe the policies for accepting industry funding and whether or not (Organization) allows companies to place restrictions or provide guidance on how funding will be spent.

2)

If (Organization) allows companies to place restrictions on industry funding, then please explain all restrictions and/or guidance for each transfer of value from industry. For every transfer of value with a restriction, please provide the following information: year of transfer, name of company, and restriction placed on funding.

3)

Please explain what policies, if any that(Organization) plans to adopt to ensure transparency of funding in order to provide a greater public trust in the independence of your organization.

4)

Please explain your policies on disclosure of outside income by your top executives and board members.

5)

Please provide the disclosures of outside income filed with your organizations by your top executives and board members.

In cooperating with the Committee’s review, no documents, records, data or information related to these matters shall be destroyed, modified, removed or otherwise made inaccessible to the Committee.

I look forward to hearing from you by no later than December 21, 2009.

Sincerely,

Charles E. Grassley United States Senator Ranking Member of the Committee on Finance

*****

The New York Times December 8, 2009

Grassley Seeks Details on Medical Financing by Gardiner Harris

A top Republican senator, Charles E. Grassley, has sent letters to the American Medical Association, the American Cancer Society and 31 other disease and medical advocacy organizations asking them to provide details about the amount of money that they and their directors receive from drug and device makers.

Such financing amounts are often considered proprietary by the organizations and their directors, but critics contend that the industry’s sway over such groups leads them to lobby on the industry’s behalf.

Mike Lynch, a spokesman for the A.M.A., said the organization had received the senator’s letter and would respond. Mr. Lynch said industry financing made up less than 2 percent of the organization’s budget.

Steve Weiss, a spokesman for the American Cancer Society, sent an e-mail message stating that the society “holds itself to the highest standards of transparency and public accountability, and we look forward to working with Senator Grassley to provide the information he requested.”

Kate Meyer, a spokeswoman for the Alzheimer’s Association, which also received a letter from the senator, said the organization “was going to answer all of his questions,” but she would not immediately say what share of the organization’s financing comes from drug or device makers.

The letter is part of Mr. Grassley’s long-running investigation into the influence of drug and device makers on the practice of medicine. Mr. Grassley, an Iowa Republican, has also long been interested in how charities get and spend their tax-deductible contributions.

“These organizations have a lot of influence over public policy, and people rely on their leadership,” he said. “There’s a strong case for disclosure and the accountability that results.” Earlier this year, Mr. Grassley sent a similar letter to the National Alliance on Mental Illness. The group told the senator that more than two-thirds of its donations came from the pharmaceutical industry. In response to the disclosure, Dr. H. Richard Lamb resigned from the group’s board.

Dr. Lamb joined the board of the organization in 2005, when he was “shocked to learn that approximately half of NAMI’s income comes from the large pharmaceutical companies,” he wrote in a resignation letter that Mr. Grassley made public. Alliance officials assured Dr. Lamb that the situation would change. “However,” Dr. Lamb wrote, “very little has changed, right up to the present day.” In an interview, Dr. Lamb said that NAMI’s dependence on the drug industry made some actions impossible. For instance, Dr. Lamb said that NAMI should consider warning against the use of some mental health drugs with life-threatening side effects. But Dr. Lamb said the organization could not consider such a move because it could threaten much of its financing.

Michael J. Fitzpatrick, the organization’s executive director, promised that the industry’s share of the group’s fund-raising would drop significantly next year.

Mr. Grassley’s request that organizations provide details about the outside income of directors may cause some consternation. While a few large patient advocacy groups have provided general guidance about their reliance on industry, almost none have given such details about their leaders.

Senator Grassley is looking at Pharma funding of universities too.
Link
For Immediate Release
June 24, 2009

"Grassley seeks information about medical school policies for disclosure of financial ties

WASHINGTON --- Senator Chuck Grassley has asked 23 medical schools for information about their policies for conflicts of interest and requirements for disclosure of financial relationships between faculty members and the drug industry.

Grassley sent his request to the 23 educational institutions that did not respond to an earlier request made by the American Medical Student Association for the same information. In that case, the schools reportedly replied to a survey by answering either "no response" or "decline to submit policies." Of the 149 schools asked, 126 provided information to the student association.

"There's a lot of skepticism about financial relationships between doctors and drug companies," Grassley said. "Disclosure of those ties would help to build confidence that there's nothing to hide. Requiring disclosure is a common sense reform based on the public dollars and public trust at stake in medical training, medical research and the practice of medicine."

Grassley has been working to achieve uniform and universal disclosure of the money that pharmaceutical, medical device and biologic companies give to physicians. He has conducted extensive oversight of financial relationships, especially among doctors who conduct research with the $24 billion awarded annually in federal grants by the National Institutes of Health. Institutions receiving these federal dollars are required to track financial relationships, but Grassley has found enforcement of those requirements often to be either lax or in violation. Grassley also has sponsored reform legislation that would require payments from the drug industry to be publicly reported. Senator Herb Kohl is the cosponsor of the "Physician Payments Sunshine Act," S.301.

The 23 schools receiving Grassley's letter are: the Arizona College of Osteopathic Medicine, Edward Via Virginia College of Osteopathic Medicine, Medical College of Georgia School of Medicine, Northeastern Ohio University College of Medicine, Philadelphia College of Osteopathic Medicine, Rocky Vista University College of Osteopathic Medicine, Tulane University School of Medicine, University of Florida College of Medicine, University of Nevada School of Medicine, Albany Medical College, Chicago College of Osteopathic Medicine, Dartmouth Medical School, Howard University College of Medicine, Lake Erie College of Osteopathic Medicine, Louisiana State University School of Medicine - New Orleans, Meharry Medical College, Morehouse School of Medicine, New York College of Osteopathic Medicine of the New York Institute of Technology, Ponce School of Medicine, San Juan Bautista School Of Medicine, University at Buffalo School of Medicine, University of Medicine and Dentistry New Jersey - New Jersey Medical School, University of South Carolina School of Medicine. The text of the letter is below."

Sunday, December 6, 2009

Movie Trailer: The Idiot Cycle



Official trailer for "The Idiot Cycle" feature length documentary produced by Emmanuelle Schick Garcia and Laila Tahhar. To be released Fall 2009. www.theidiotcycle.com.

From the site:
"It has now been scientifically demonstrated that there is indeed a link between chemical products and the appearance of diseases, such as cancers, infertility, degenerative diseases of the central nervous system and allergies."
CPME - Standing Committee of European Doctors, 2005
"There is little direct evidence of widespread ill health or ecosystem damage by the use of man-made chemicals."
Alan Perroy, Director General of the European Chemical Industry Council, in a 2001 letter to European Members of Parliament.

Once upon a time, a king accumulated most of the gold in his kingdom. His subjects were very poor, without land to grow food. When the subjects began to starve and watch their families perish, they realized they had nothing to lose.

They stormed the castle and found the king in a large room, cowering next to his mounds of gold, begging them not to steal his gold.

The subjects did not take the gold. But they left the room and locked the king inside.

Upon leaving they called out, "now you will be able to see the real worth of your gold."

The king, trapped in the room with no water, air or food, realized the gold was useless.

This story became the impetus for The Idiot Cycle - a film about cancer.

"Everyone should know that the 'war on cancer' is largely a fraud."
Dr. Linus Pauling, winner of the Nobel Peace Prize and the Nobel Prize in chemistry

Saturday, October 24, 2009

NAMI: Pharma Companies are its biggest donors

"Drug Makers Are Advocacy Group’s Biggest Donors

By GARDINER HARRIS
Published: October 21, 2009
WASHINGTON — A majority of the donations made to the National Alliance on Mental Illness, one of the nation’s most influential disease advocacy groups, have come from drug makers in recent years, according to Congressional investigators.

The alliance, known as NAMI, has long been criticized for coordinating some of its lobbying efforts with drug makers and for pushing legislation that also benefits industry.

Last spring, Senator Charles E. Grassley, Republican of Iowa, sent letters to the alliance and about a dozen other influential disease and patient advocacy organizations asking about their ties to drug and device makers. The request was part of his investigation into the drug industry’s influence on the practice of medicine.

The mental health alliance, which is hugely influential in many state capitols, has refused for years to disclose specifics of its fund-raising, saying the details were private.

But according to investigators in Mr. Grassley’s office and documents obtained by The New York Times, drug makers from 2006 to 2008 contributed nearly $23 million to the alliance, about three-quarters of its donations."

New York Times Link

Search for "grassley" to see our previous posts on this matter; here is one -
http://pharmaceuticalsanonymous.blogspot.com/2009/05/most-nami-money-is-from-psychiatric.html

Some day NAMI will have an interesting section at Little Sis.

Monday, September 21, 2009

Senator Grassley's Sleuth

"Grassley's Sleuth Gets Press In Nature
Most of you are aware of a long-running campaign by Sen. Charles Grassley (R-Iowa) to ferret out undisclosed pharma company funding of academic researchers who also wind up taking federal research money. Well, it ain't the Senator who does all the digging that leads to him going after the likes of Emory University psychiatrist Charles Nemeroff and Harvard University psych researchers. Instead, it is Paul Thacker, a former journalist and an investigator for the Senator, who is making researchers' lives hell--and appropriately so. I've known this for a long time but have kept my yapper shut when writing about Sen. Grassley.

Anyway, Nature has a nice article on Thacker and it includes Nemeroff himself basically apologizing for his mess and claiming he was in compliance with disclosure rules plus other researchers defending Nemeroff. Please. In a political world filled with scum and manure, it's good to see one good guy in the fray. And since I'm such a good guy, I'm making a copy of the article (usually requires a subscription) available to all of you. I encourage you to download it and read it."

From Philip Dawdy's wonderful Furious Seasons - PDF on Thacker - Senator Grassley's NAMI investigator

Philip is doing his seasonal fundraiser. Please donate here.... http://www.furiousseasons.com/

More tasty pharma scandals - involving Pfizer and NAMI - are here.

Wednesday, July 22, 2009

WSJ: Surgeon Didn't Disclose Company Ties


... a sweet news item ...
"UCLA Says Surgeon Didn't Disclose Company Ties


By DAVID ARMSTRONG

A top surgeon at the University of California at Los Angeles has lost his position as executive director of its spine center and faces an investigation by the school into his research after allegedly failing to disclose he was being paid by several companies whose products he was studying.

Between 2002 and 2008, Jeffrey Wang repeatedly failed to report on forms filed with the state and with the medical school that he was receiving consulting payments, stock options and royalties from five companies on whose products he was conducting research, according to the university. The failure to report these relationships "violated university guidelines," the school said.

"UCLA regrets that in the case of Dr. Jeffrey Wang, associate professor of orthopedic surgery, a pattern of non-disclosure could have persisted without our knowledge," the school said in a statement. "We are committed to examining our processes to determine how, as an institution, we will prevent similar problems in the future."

Dr. Wang didn't return a telephone call to his office seeking comment. He remains on the school faculty.

Dr. Wang was removed as co-executive director of the UCLA Comprehensive Spine Center. A university spokeswoman said the school is considering further sanctions against him.

The university also has appointed a committee to investigate Dr. Wang's work and determine whether the payments from companies affected his research and "if there are any mitigating actions needed to ensure the integrity of the research results." UCLA said it would make the results of that inquiry public, but that so far it has not found evidence of research misconduct. His research involved studying the products in both animals and humans.

UCLA alleges that Dr. Wang failed to disclose financial interests in connection with research projects sponsored by DePuy Spine Inc., a unit of Johnson & Johnson, which paid Dr. Wang $125,900 in royalty and consulting payments from 2002 through 2008; Facet Solutions Inc., a company in which Dr. Wang acquired options for 18,000 shares in 2004; Paradigm Spine LLC, an entity related to another company in which Dr. Wang received options for 20,000 shares; FzioMed Inc., which paid Dr. Wang $144,000 from 2002 through 2008; and medical-device maker Medtronic Inc., which paid Dr. Wang $275,000 in royalty and consulting payments from 2003 through 2008.

In the case of Medtronic, Dr. Wang did report some, but not all payments from the company, according to the school.

Dr. Wang published at least two favorable evaluations of Oxiplex, a product from FzioMed to prevent spinal adhesions. In 2004, he was the author of a study published in Neurosurgical Focus that found Oxiplex "easy to use and safe." That study noted FzioMed provided funding for the study, but didn't cite the payments to Dr. Wang.

A 2008 abstract published in the Spine Journal by Dr. Wang and a co-author found "consistent clinically significant improvement in outcomes resulting from the use of Oxiplex gel in lumbar spine surgery." While the abstract doesn't indicate Dr. Wang had a financial relationship with FzioMed, he is listed as a consultant to the company elsewhere in the journal.

A Food and Drug Administration advisory committee in July 2008 voted against approving Oxiplex for sale in the U.S. because it wasn't convinced the product was effective.

Most medical schools require doctors to report financial relationships and often have rules limiting how much they can receive from companies whose products are being studied. But medical schools often have difficulty verifying whether financial information filed by doctors is accurate.

A handful of states, including Massachusetts and Minnesota, have instituted public-reporting requirements in which drug and medical-device companies must disclose payments to physicians for many kinds of services, including consulting.

Two U.S. senators, Republican Charles Grassley of Iowa and Democrat Herb Kohl of Wisconsin, are pushing for a federal law that would require companies to report payments to doctors of more than $100."

WSJ -What s doctor did that was worth $1M

This is just a little gator - cleaning up the whole swamp will be a big job.

Saturday, July 18, 2009

The Swine Flu Fiasco

Read about Archie Kalokerinos's book on death through vaccination - EVERY SECOND CHILD here


Pigs fly Pictures, Images and Photos



THE SWINE FLU FIASCO

Archie Kalokerinos M.D.

"In 1976 I was working in the far north of Australia amongst Aborigines. I observed, in one community of only a few hundred people, when they were given the flu vaccine (probably the Victorian strain but this detail does not really matter because nobody outside a few selected individuals really knows what is in any particular batch), six men died suddenly soon afterwards. They were not all 'old’. One was in his early twenties. A few weeks later, in another community I found that individuals with heart or potential heart problems or diabetes were particularly likely to drop dead soon after being given the vaccine.

Obviously, there was a problem with some batches of the flu vaccine.

A few months later I was in America. President Ford had been told by his health advisers that there was going to be a huge epidemic of ‘swine flu’, that this could kill may thousands and the only way to prevent this catastrophe was to vaccinate the entire population of America – every man woman and child - with a specific vaccine.

So the vaccine was manufactured and the biggest vaccination campaign in history was begun. I was concerned because the vaccine could not be properly tested in a short period. None of the recipients would know anything about what they were being injected with and the chances were that many would die suddenly. Furthermore, it was extremely unlikely that an epidemic of swine flu would occur. So I spoke out. At first the newspapers got hold of what I said and headlined, ‘Australian Physician Call It Mass Murder’. Then I appeared on Kathy Crosby’s television program.

Watching that was a man in New York who did not like a gentleman named Gambino the Mafia boss. Gambino was about 70 years old and had a history of heart problems. It was a simple matter to get someone to persuade Gambino to have the flu shot and Gambino obliged by dropping dead. The newspapers got it right when they stated, ‘Mafia Flu Jab Conspiracy’.

People were dropping dead in the buildings where they received their shots. Others became paralyzed. The whole program ground to a halt.

President Ford decided to settle the matter quickly. In front of the whole world, on television, he rolled up his sleeve and ‘had his shot’. I claimed at the time that he was given a ‘dud’ shot and I am certain that this was actually done. Then President Ford invited all the news media men and women who were milling around to line up and have their shots. Only one man volunteered and he happened to be the White House press secretary. All the others refused the invitation.

There was not a single case of swine flu. There never was going to be an epidemic of swine flu. How was it that the world’s most powerful man with the world's greatest department of health got it all so wrong? No one really knows the answer but what ever it is it is certainly not clean and tidy."
Link


Something's definitely not right with Cherie Blair - perhaps political pork or a bad case of PR - but we doubt that the problem is Swine Flu.

Updates -
NEWS (AP) -US vaccine makers to be immune from lawsuits Link

UK - (Independent) Safety questions over swine flu jab - Link

Baxter vaccine patent oddities

CLG Pandemic News and Action Alerts

What is Guillain-Barré_syndrome?

The Swine flu vaccine's dirty little secret - Squalene



Monday, June 22, 2009

"Psychiatric diagnoses are less reliable than star signs"



'The psychologist Richard Bentall says that psychiatrists dish out drugs but ignore the value of good relationships

Ed Halliwell - The Times Online

Complain to your doctor about a mental health problem and you will probably leave the surgery with a prescription for drugs, despite increasing doubts about their effectiveness and fears about side-effects. The prevailing wisdom is that psychiatric disorders are genetically based brain diseases, biological abnormalities that can be controlled with medication. Every year, doctors in England dole out 31 million prescriptions for antidepressants alone.

It is a state of affairs that makes Richard Bentall furious. In 2004, Bentall, professor of clinical psychology at the University of Bangor, wrote Madness Explained, in which he argued that hearing voices, hallucinations and other symptoms of “severe” mental illness are just exaggerations of quirks experienced by us all. That won him the British Psychological Book Of The Year award. Now, in Doctoring The Mind: Why Psychiatric Treatments Fail, he criticises mental health services, and psychiatry in particular.

Doctoring the Mind paints a stark picture of a mental health system riddled with corruption and incompetence, in which shrinks live it up on pharmaceutical company cash while patients are disrespected, dehumanised and drugged to the eyeballs. Like the legendary “anti-psychiatrist” R.D. Laing before him, Bentall believes that people with mental health problems need understanding, support and respect. Unlike Laing, he offers evidence to back his claims, declaring himself a “rational anti-psychiatrist”.

“I am committed to the scientific world-view,” the 53-year-old says, his urgent voice rising above the rush-hour clatter of the station café in which we meet. “But the evidence doesn’t support the hardline biomedical view behind most psychiatric practice.” He takes a sip of coffee, then continues. “More alarmingly, the treatments based on it are not very effective. Outcomes for psychiatric disorders are no better than in the Victorian period.”'

Continues here.

Also see The Thud Experiment


The 29 medical causes of schizophrenia - infection, intoxication, deficiency or imbalance - are explained here.

Saturday, June 6, 2009

Video: Alison Bass, Journalist and Paxil Whistleblower, Gives a Talk


Visit Alison Bass at her site here.
Now comes news that Paxil is being touted to help cancer sufferers think more clearly. But chemo cancer therapy itself can cause brain fog, as we have seen, and if cancer is a fungus, this therapy is wrong.
What do YOU think?

Monday, March 2, 2009

AstraZeneca: "Lisa has done a great smoke-and-mirrors job"


AstraZeneca “buried” unfavorable studies of its $4.4 billion blockbuster psychiatric drug Seroquel, according to internal documents released Friday in a legal dispute between the company and lawyers for thousands of people who sued the company because they said the drug caused diabetes and weight gain.
In one of the documents, a 1997 e-mail message, Richard Lawrence, an AstraZeneca official, praised Lisa Arventis, the company’s Seroquel project physician at the time, for minimizing adverse findings in a “cursed” study. He wrote: “Lisa has done a great ‘smoke-and-mirrors job!’ ”
Lawyers suing AstraZeneca, a British drug maker whose United States headquarters are in Delaware, said the documents show it tried to hide the diabetes link for nearly a decade.
“AstraZeneca knew about the risk of weight gain and diabetes in 2000 and not only failed to warn physicians and patients but marketed in a way that represented there was no risk,” Edward F. Blizzard, a Houston-based lead lawyer on the cases, said in a conference call with reporters.

Read more about the Seroquel scandal at the New York Times. For the best investigative journalism anywhere on this, go see what Philip Dawdy has to say at Furious Seasons.

Friday, January 2, 2009

Evelyn Pringle: SSRI Pushers Under Fire

Brueghel: Blind leading the blind

"Throughout the 1990's, most doctors who attended conferences, medical seminars and other events were not aware that the so-called "key opinion leaders" encouraging them to prescribe the new generation of antidepressants for everything under the sun, including to children as young as infants, were nothing more than highly paid drug pushers for Big Pharma.

For years, the research that showed SSRI antidepressants (selective serotonin reuptake inhibitors) were dangerous and practically useless was kept hidden, while the studies published and presented to potential prescribers painted a glowing picture of success. These days, a person would be hard pressed to find someone who does not have a family member or friend labeled mentally ill and taking drugs like Prozac, Paxil, Zoloft, Lexapro and Celexa, or their chemical cousins Effexor, Cymbalta and Wellbutrin.

About once a year, a new round of headlines about all the money made by the SSRI pushers comes and goes; but nothing really ever seemed to stick, until now.

The Senate Finance Committee, with the ranking Republican, Senator Charles Grassley, leading the charge, is investigating GlaxoSmithKline regarding new revelations in a report filed in litigation showing that the company manipulated the numbers on adverse events related to suicidality in clinical trials back in 1989, to make it appear that Paxil did not increase the risk of patients experiencing suicidal behavior when, in fact, trial subjects on Paxil were eight times more likely to attempt or commit suicide than patients taking placebos.

Quite a few of the top pushers are also under investigation by the Committee due to revelations that millions of dollars has changed hands between the SSRI makers and the academics who signed off on some of the most fraudulently reported research in the history of modern medicine. A full list of names is easy to compile by scanning the literature on SSRI studies conducted on children. The same names appear repeatedly.

In alphabetical order, the Fortune 500 team of pushers, at a minimum, includes Drs Joseph Biederman, David Brent, Jeffrey Bridge, Daniel Casey, David Dunner, Graham Emslie, Daniel Geller, Robert Gibbons, Frederick Goodwin, Martin Keller, Andrew Leon, John Mann, John March, Charles Nemeroff, John Rush, Neal Ryan, David Shaffer, and Karen Wagner."

Article here

Friday, November 14, 2008

Smoked Out

The New York Times offers us a slideshow of the history of tobacco advertising in America, with babies, dentists, athletes and doctors - even Santa - urging us to smoke. Link

Saturday, March 29, 2008

"New" "Improved" Antipsychotics Hype

New Schizophrenia drugs no better than the old ones: Reuters
Here you can read about correct diagnosis
and, here, about mental health and vitamins.
isom ortho
Shown: Steven Carter and Abram Hoffer of the International Society of Orthomolecular Medicine

Thursday, March 6, 2008

The Pharmaceutical Drug Racket

thalidomide1
Image - Thalidomide deformities passed along to the next generation.

Substances that cause birth defects are called Teratogens.

Part 1

"One result of the vast over-consumption of drugs is the astronomical profits generated by the drug industry. Since the beginning of the sixties, drug industry profits (as a percentage of sales and company net worth) have surpassed all other manufacturing industries listed on the Stock Exchange. (20)

Another result is the inevitable deterioration of public health. According to the Food and Drug Administration (FDA), 1.5 million Americans were hospitalised in 1978 as a consequence of taking drugs and some 30 per cent of all hospitalised people are further damaged by their treatments. Every year, an estimated 140,000 Americans are killed because of drug taking (21) and one in seven hospital beds is taken up by patients suffering from adverse drug reactions. (22)

A report by the General Accounting Office in the United States revealed that 51.5 per cent of all drugs introduced between 1976 and 1985 had to be relabelled because of serious adverse reactions found after the marketing of these drugs. These included heart, liver and kidney failure, foetal toxicity and birth defects, severe blood disorders, respiratory arrest, seizures and blindness. The changes to the labelling either restricted a drug's use or added major warnings. (23)

HOW COMMON ARE DRUG ADVERSE REACTIONS?

According to the Adverse Drug Reactions Advisory Committee (ADRAC), the official federal government body responsible for monitoring the safety of drugs already in use: "There is a dearth [scarcity] of published information on the medical and economic importance of adverse drug reactions in Australia." (24) However, a recent study (1991), cited by the National Health Strategy report on drug use, claims that in 1987-88 there were between 30,000 and 40,000 hospital admissions in Australia because of drug taking and also that adverse drug reactions (ADRs) would have been a major factor for between 700 to 900 deaths a year. (25)

There are some who are highly critical of the official estimation of the extent of drug reactions within communities. Dr Julian Gold, head of the National Health Surveillance Unit of the Commonwealth Institute of Health, whose job as a medical epidemiologist is to collate information on the total health environment, estimates that up to 40 per cent of all patients in Australia may actually be victims of doctor induced (iatrogenic) illnesses. (26) A 40 per cent figure has also been estimated for the United Kingdom. (27) Generally of this amount, half are from drug reactions. (28)"

Part 2

"SOME FRAUDULENTLY TESTED DRUGS THAT INJURED AND KILLED

Paracetamol (painkiller) - 1,500 people had to be hospitalised in Great Britain in 1971.

Orabilex - caused kidney damages with fatal outcome.

MEL/29 (anti-hypertensive) - caused cataracts.

Methaqualone (hypnotic) - caused severe psychic disturbances leading to at least 366 deaths, mainly through murder or suicide.

Thalidomide (tranquilliser) - caused 10,000 malformed children.

Isoproterenol (asthma) - caused 3,500 deaths in the sixties.

Stilboestrol (prostate cancer) - caused cancer in young women.

Trilergan (anti-allergic) - caused viral hepatitis.

Flamamil (rheumatism) - caused loss of consciousness.

Eraldin (heart medication) - caused severe eye and digestive tract damage, and many deaths.

Phenformin (diabetes) - caused 1,000 deaths annually until withdrawn.

Atromid S (cholesterol) - caused deaths from cancer, liver, gall bladder and intestinal disease.

Valium (tranquilliser) - addictive in moderate doses.

Preludin & Maxiton (diet pills) - caused serious damage to the heart and the nervous system.

Nembutal (insomnia) - caused insomnia.

Pronap & Plaxin (tranquillisers) - killed many babies.

Phenacetin (painkiller) - caused severe damages to kidneys and red blood corpuscles.

Amydopyrine (pain killer) - caused blood disease.

Marzine (nausea) - damaged children.

Reserpine (anti-hypertensive) - increased risks of cancer of the brain, pancreas, uterus, ovaries, skin and women's breasts.

Methotrexate (leukaemia) - caused intestinal haemorrhage, severe anaemia and tumours.

Urethane (leukaemia) - caused cancer of liver, lungs and bone marrow.

Mitotane (leukaemia) - caused kidney damage.

Cyclophosphamide (cancer) - caused liver and lung damage.

Isoniazid (tuberculosis) - caused liver destruction.

Kanamycin (tuberculosis) - caused deafness and kidney destruction.

Chloromycetin (typhoid) - caused leukaemia, cardiovascular collapse and death.

Phenolphthalein (laxative) - caused kidney damage, delirium and death.

Clioquinol (diarrhoea) - caused blindness, paralysis and death.

DES (prevent miscarriage) - caused birth defects and cancer.

Debendox (nausea) - caused birth defects.

Accutane (acne) - caused birth defects.

Kanamycin (tuberculosis) - caused deafness and kidney destruction."