looked into it to this extent. The walls are slowly crumbling.
Unfortunately, they're crumbling so slowly that another "wall" is being
erected -- the promotion of antipsychotics like Geodon and Zyprexa for
everything from difficulty sleeping to PMS. There was a time not too long
ago that doctors knew that antipsychotic drugs were terrible drugs with
profoundly negative effects on a person. They even regretted prescribing
them for someone labeled as having 'schizophrenia'. But when these
pharmaceutical companies that make these drugs hired hundreds of extra sales
people to begin promoting these drugs, doctors fell under their spell and
obliged by prescribing them for just about anything. I believe that if
physicians have the license to prescribe drugs they should be able to see
through the sophisticated marketing shemes designed by Madison Ave.
advertising firms. Yes, these firms and the drug companies employ the best
and brightest industrial psychologists in the world. This is still no
excuse for physicians who must take complete responsibility for what they
prescribe. Their negligence is nothing short of criminal. --Catherine]
FYI
An investigative report in The Philadelphia Inquirer examined pharmaceutical
company ties to six, tax exempt organziations that identify themselves as
"patient advocacy" groups, "Each a leading advocate for patients in a
disease area."
The conflicts of interest are covert: the reporter notes that "although
patients seldom know it, many patient groups and drug companies maintain
close, multimillion-dollar relationships while disclosing limited or no
details about the ties....the groups rarely disclose such ties when
commenting or lobbying about donors' drugs. They also tend to be slower to
publicize treatment problems than breakthroughs. And few openly questioned
drug prices."
The following six organizations took in $29 million in drug company
donations last year: American Diabetes Association (ADA); National Alliance
on Mental Illness (NAMI); National Gaucher Foundation; Children & Adults
with Attention Deficit/Hyperactivity Disorder (CHADD); Arthritis Foundation
(AF); National Organization on Rare Diseases (NORD).
"For drug companies, patient groups carry credibility that the industry
sometimes lacks to target patients and "opinion leaders" who drive
prescriptions, and hence, sales." However, such coziness "raises questions
about the impartiality of groups that patients trust for unbiased
information."
The Inquirer describes some of the insidious ways that these groups work
covertly hand in glove with their pharmaceutical corporate benefactors:
"Merck explicitly wove the [Arthritis Foundation] into sales strategies. A
2001 internal memo, disclosed in product-liability trials, shows that Merck
sought to use the foundation's pain-management program to "demonstrate
additional benefits" of its products."
"Donations from Merck and Pfizer Inc. to the Arthritis Foundation more than
doubled, to at least $1.65 million combined, in 2000 as they launched Vioxx
and Celebrex." However when safety concerns emerged sales of these hazardous
drugs flattened, and the donations fell below $375,000 by 2004.
The National Gaucher Foundation, a supporter of people suffering from a
horrific rare disease, is reported to get "nearly all its revenue from one
drugmaker, Genzyme Corp." The foundation is criticized for promoting only
this company's product.
These covert financial ties bind these groups to pharmaceutical companies,
securing their help in promoting particular "diseases" to increase demand
for treatment-thereby expanding the market for their drugs. [1]
However, the most damning aspect about these collaborating "advocacy"
groups' is their withholding of vital safety information from their
membership: information about evidence of these drugs' hazardous-even
lethal-effects. Some would consider this a partnership in deception.
Surely, this is the ultimate betrayal of trust by organizations claiming
that their raison d'etre is to educate and advocate for the best interest of
their constituency--patients and families.
The Inquirer reports that The American Diabetes Association privately
enlisted an Eli Lilly & Co. executive to chart its growth strategy and write
its slogan. It received at least $2.5 million between 2003-2005. And the
Inquirer reports that "NAMI, did not disclose that Lilly marketing manager
Gerald Radke briefly ran its entire operation. Radke began in 1999 as a
Lilly-paid "management consultant," then left Lilly and served as NAMI's
paid "interim executive director" until mid-2001. The group acknowledged
this only after being shown Radke's resume listing the job."
Lilly donated at least $3 million to NAMI. For its part, NAMI promotes the
increased use of psychotropic drugs, lobbies against any cost-saving
restrictions on number of psychotropic drugs prescribed for one patient
under Medicaid, and even lobbies for laws allowing mental patients to be
forced to take antipsychotic drugs. The drugs most often prescribed for
involuntary patients-Janssen's Risperdal (risperidone) and Lilly's Zyprexa
(olanzapine)-cause debilitating, indeed, lethal effects. . NAMI's failure to
inform its constituents about the danger these drugs pose for patients, and
its continued aggressive promotion of these drugs despite the evidence, may
be viewed as confirmation that NAMI is an extension of Lilly's marketing
department.
The documented hazards:
1. During pre-marketing trials 2/3 of patients on Zyprexa dropped out and 1
in 145 died-some committed suicide.
http://www.ahrp.org/infomail/0702/12b.php]
2. In 2002, Duke University's analysis of FDA MedWatch reports identified
289 cases of treatment-emergent diabetes in patients who had been prescribed
Zyprexa for less than six months. In addition, the researchers found 100
cases of ketoacidosis (diabetic coma potentially, death) as a result of
Zyprexa use, 22 cases of Zyprexa-related pancreatitis, and twenty three
patients who died as a result of Zyprexa side effects.
http://www.ahrp.org/infomail/0702/12b.php
3. Dr. Arif Khan's independent analysis of FDA data found the suicide rate
in clinical trials to be 752 per 100,000 persons for those treated with an
atypical antipsychotics--risperidone, olanzapine, and quetiapine.
4. The government-sponsored, CATIE study findings: "Patients in the
olanzapine group gained more weight than patients in any other group, with
an average weight gain of 2 lb (0.9 kg) per month. A larger proportion of
patients in the olanzapine group than in the other groups gained 7 percent
or more of their baseline body weight. Olanzapine had effects consistent
with the potential development of the metabolic syndrome and was associated
with greater increases in glycosylated hemoglobin, total cholesterol, and
triglycerides after randomization than the other study drugs, even after
adjustment for the duration of treatment." See:
http://www.ahrp.org/infomail/05/09/20.php
5. Yale investigators reported earlier this month that 2/3 of the children /
adolescents in its speculative "schizophrenia prevention" experiment
conducted on healthy adolescents, dropped out. The investigators have yet
to report the adverse events suffered by the otherwise healthy youth during
the experiment.
Diabetes is by far the most prevalent serious risk linked to Zyprexa.
The fact that NAMI lobbies for laws facilitating involuntary
treatment-despite scientific evidence linking the drugs most often used on
involuntary patients-is a measure of this organization's duplicity and
betrayal of its mission.
The high incidence of diabetes among patients exposed to Lilly's
antipsychotic drug, Zyprexa, undoubtedly provides the company an opportunit |