Pharm D Degree in 7 days!

Speaking of Certificates that do not mean anything, except you paid
for it….I found a place you can get a Doctor Degree in Pharmacy in
just 7 days. Looks like you can purchase the degree for less than our
pretend to be national organization NPTA charges for their “IV
Certificate.”

Why should NPTA be making all the money!

Joe Medina, CPhT

—————-

Here is some info on it:

“…Students seeking admission in our online Doctorate degree
program are required to have at least 8 years of work or life
experience relevant to their desired major.

If you want to get your PHD degree online on the basis of prior life
experience, the eligibility requirements for a Doctorate degree may be
satisfied in any of the following ways:

• Prior job experience in any field
• Previous educational achievements
• Employer-sponsored training and attendance of workshops
• Participation in organizations, both professional and non - professional
• Personal goals, lifestyle, hobbies, and travel
• Participation in volunteer activities and community service
• Independent reading, viewing, listening or writing

If you have the required work or life experience, click below to apply
for a work experience college degree in your desired major and get it
in just 7 days!…”

Yeast infection or Not?

Only one in every four women who seeks treatment for persistent yeast
infections actually has one, a new study suggests.

Women will frequently treat suspected yeast infections themselves with
over-the-counter (OTC) products, but the findings show that most of
the time this won’t help. In fact, using such medications repeatedly
may even cause harm, Dr. Susan Hoffstetter, the co-director of the
SLUCare Vulvar and Vaginal Disease Clinic at Saint Louis University,
told Reuters Health.

“We treat ourselves because we want our problems to go away quickly,”
Hoffstetter pointed out, adding that this isn’t only the fault of
patients. “We in medicine also do a lot of treating over the phone
just to keep women from having to come in.”

Hoffstetter and her colleagues looked at the medical records for 150
women visiting the clinic for the first time who reported persistent
yeast infections.

Lab tests showed that only 26 percent of the women were infected with
Candida — the fungus responsible for yeast infections. Other causes
of vaginal itching can include sexually transmitted infections, dry
skin, or inflammation, Hoffstetter noted, which won’t respond to OTC
antifungals and could even be aggravated by these products.

Overuse of OTC yeast infection remedies can alter the normal flora of
the vagina, which can lead to other health problems, the researcher
pointed out. And, she added, drug-resistant strains of Candida are
becoming increasingly common.

If a woman experiences pain during sex, burning sensations in the
vaginal area, a thick white discharge, and pain during urination, she
may indeed have a yeast infection, Hoffstetter said. And it’s probably
okay for women to self-treat if they experience these symptoms rarely,
and they get better with OTC medication, she added.

But women who think they are suffering from yeast infections that
never go away are likely to have some other problem, Hoffstetter said.
In such cases, she advised, it’s important for a woman to actually see
a doctor or nurse practitioner and have a pelvic exam and lab tests,
if necessary, rather than just getting medical advice over the phone.

Ample Supply of Flu Vaccine This Year - but is it the right one?

Come one, come all: After years of shortages and confusion, this fall
promises plenty of flu vaccine to go around — up to 132 million doses,
more than the nation has ever produced.

The ample supplies have the government urging vaccinations not just
for people at highest risk of dying from influenza, but for anyone who
wants to avoid a week of aching misery.

“Flu is a formidable foe,” Dr. Julie Gerberding, head of the Centers
for Disease Control and Prevention, said Wednesday. “It is not an
illness we should be complacent about.”

But new CDC data show only a fraction of people who need flu shots the
most get them, including just one in five babies and toddlers. And
there’s wide geographic variation, with Rhode Island reporting the
most high-risk adults vaccinated and Nevada the fewest.

Shots aren’t the only option. Wednesday, the government ruled that
it’s safe for younger kids than ever before to try a nasal-spray
vaccine called FluMist. Once only an option for people ages 5 to 49,
FluMist now can be used by children as young as 2.

Flu usually peaks in February, so a winter vaccination isn’t too late.
Still, Gerberding advised seeking vaccine early in case flu begins
striking before the usual November.

Indeed, there already are reports of sick schoolchildren in Hawaii,
although the geographic distance makes it impossible to predict if
that signals an unusually early flu season for the rest of the country.

Perhaps of more concern, CDC is closely monitoring whether a new
strain that emerged near the end of Australia’s flu season will cause
illness here — a strain that this year’s vaccine doesn’t specifically
target.

Each year’s vaccine contains protection against three influenza
strains — two Type A strains, an H1N1 and an H3N2 version, plus a
milder Type B — that experts predict will cause the most illness. The
vaccine isn’t always a perfect match, and this year’s contains a
different H3N2 version than the newly emerging one, nicknamed
H3N2/Brisbane-like.

Get vaccinated anyway, Gerberding stressed. The other two strains in
the vaccine are causing illness around the world, and even if the
newer one travels here, too, the vaccine should provide some
cross-protection.

Every year, flu infects up to 20 percent of the population, causes the
hospitalization of 200,000 people and kills 36,000.

Who’s at highest risk? Anyone over 50 or under 5; people of any age
who have asthma, heart disease, weakened immune systems or other
chronic illnesses; and pregnant women.

Vaccine also is particularly recommended for relatives and caregivers
of those people, and health care workers — people who may be robust
enough to recover themselves, but could infect the more vulnerable
before they realize they’re ill.

“The day before you become sick, you’re already excreting the virus,”
warned Dr. William Schaffner of Vanderbilt University, vice president
of the National Foundation for Infectious Diseases.

That equals 218 million people who should be vaccinated each year.
Nowhere near that many seek vaccine. Last year, about 18 million of
the nearly 121 million doses produced weren’t used and had to be
thrown away.

But the CDC’s new estimates of how many high-risk patients get
vaccinated, gleaned from public-health surveys, shed new light on the
most troubling gaps.

People 65 and older are most likely to get vaccinated, 69 percent
during the 2005-2006 flu season, the latest count available.

But that’s still well under the national goal of vaccinating 90
percent of seniors — even though Medicare provides them flu shots for
free.

Just over a third of 50- to 64-year-olds are getting vaccinated, and
just 30 percent of high-risk younger adults, CDC found.

Flu vaccine is a little more complicated for young children, because
they need two doses a month apart the very first year they’re
inoculated. Just 21 percent of youngsters ages 6 months to 2 years
were fully vaccinated, and just over one in 10 who needed two doses
got both, CDC reported.

If a young child missed that necessary second dose last year, health
officials are recommending that he or she make it up this year with
two shots.

ADD medication gaining popularity as weight-loss drug

In a society where chronic obesity runs rampant, life is becoming
faster and faster-paced, and medication is the solution to almost
everything, Adderall is becoming a prevalent off-label diet pill for many.

Adderall contains four different types of amphetamines and is often
called amphetamine mixed salts. It is normally prescribed to those
diagnosed with attention deficit disorder - with or without
hyperactivity - and narcolepsy.

Adderall may help develop focus amd concentration, as well as decrease
fatigue, but the side effects include loss of appetite, weight loss
and insomnia.

“After six hours after taking the drug, I would feel slightly groggy,
the way I sometimes get in the early afternoon when my morning coffee
wears off. But when I’d lie down for an afternoon nap, I couldn’t (go
to) sleep,” said Joshua Foer, a freelance writer for Slate Magazine
who took Adderall as an experiment.

Although the purpose of a drug may be to help someone focus, people
are taking the medication to experience the side effects.

“Amphetamines classically reduce hunger,” said professor Dee
Shepherd-Look, who has been teaching psychology since 1970 and works
at the parent-child interaction program at CSUN in Monterey Hall.
“People notice that many drugs have desirable side effects and start
using them for reasons that are not intended. This is called off-label
use.”

At the children’s clinic where Shepherd-Look does her practice, the
number two drug prescribed is Adderall, one position shy from Ritalin.

Adderall is FDA-approved for children with attention-deficit
disorders. It has not, however, been clinically tested for the use of
weight loss. Still, some physicians across the nation do prescribe the
drug to, in part, assist with weight loss.

“In my personal view point, there is overuse of Adderall,”
Shepherd-Look said. “It is over-prescribed and overused. Sometimes you
use the drug to treat something that should be treated with
psychological methods and not simply medication.”

According to CSUN dietician Ellen Bauersfeld, at least 50 percent of
students come in to lose weight. Hundreds of students visit the Klotz
Student Health Center hoping to be prescribed drugs that can help shed
pounds.

“There are many that have done crash diets, nutritionally inadequate
and not feeling well,” Bauersfeld said. “There is so much nutrition
misinformation out there. … Students who try pills are driven for a
quick fix.”

She said that chronic dieters and patients who have a tendency to have
an eating disorder may resort to taking diet pills.

Shepherd-Look expressed concerns about a society that overuses drugs
for a quick fix.

“Whether hyperactive or overweight, people need to find out how to
cope with the issues without just popping a pill,” she said.

Amphetamines may initially help with weight loss, but data suggests
that when they are not taken anymore, the weight can come back, and
generally at a faster rate prior to the drug use.

Confused, advice?

I am back in the market for a Tech job since leaving Wal-Mart and
taking a scholarship for a semester. My license expired in May and I
did not renew it because here is what it says: (copied from website)

2007-2008 Pharmacy Technician Permit Renewal
IMPORTANT! - Unless you are currently employed in a licensed Oklahoma
pharmacy and under the immediate and direct supervision of a licensed
Oklahoma pharmacist, the Board will not renew your technician permit.
You may apply for reinstatement of your technician permit upon re-
employment in a licensed Oklahoma pharmacy

SO MY PROBELM IS THIS:

I was passed up for a job because my license was not “current” they
require you to already obtain a license. The catch is that I had a
license but let it lapse since I was not working as a tech. So, since
I am not under the immediate and direct supervision of a pharmacist,
how do I go about getting job that requires me to have a license?
Doesn’t make any sense to me. I tried explaining this to the hiring
supervisor and he didn’t catch on.

RX Fraud?

Hello everyone. I was wondering how much RX fraud you run into as a
tech? We have relief pharmacists that work once in awhile when my boss
is gone. It seems like everytime my boss is gone, the criminals come
in. Just last week, I recongized a lady that came in with a rx as one
we have to really watch. I alerted the pharmacist and she called the
doctor from a back phone. This lady altered the rx. There is another
lady that has tried everything. She will steal rx pads from the doctors
offices. She alters written rx’s. The last time she called in her own
rx pretending to be a nurse at the doctors office. This lady has worked
the whole area around where I live. She has been caught several times
and seems to always get out again. I have a memory for faces and names
of these people. I don’t forget. How do you handle rx fraud?

Pharmacist royal treatment

HI everyone,
I was just wondering if any other techs get the treatment that our
techs do concerning pharmacist. I know that pharmacist have gone to
school for years to receive their degree, but it seems as though the
techs do all of the work, without any recognition. Pharmacist get all
the praise and glory for filling a stat med or handling a problem that
the tech originally solved. To make things worse pharmacist get all
this responsibility for narcotics and signing of important documents
and they are the ones who make the mistakes of not correcting
discrepancies in the OMNICELL or narcotic log.(One pharmacist actually
lost a Morphine PCA, and still has a job). Let that had been a tech, we
would have lost our jobs and the DEA would have been on our backs.
My point being pharmacist get placed upon this pedestal as being
superior and without flaws, but in reality they are the ones making most
of the mistakes.
Just wanted to vent a little, does anyone else feel similar to this ?

OTC Erectile Drugs Come With Health Risks

Dr. Andrew Kramer recently looked over the medical history of one of
his patients who had been in the emergency department complaining of
chest pains.

Kramer was surprised by what he read: The patient had been taking
three to four dietary supplements for erectile dysfunction — every day.

“I would have never given him Viagra,” said Kramer, a urologist at the
University of Maryland Medical Center. “He was on the cardiac
transplant list.”

Heart patients are potentially at risk for a heart attack and an early
death when they combine erectile dysfunction drugs, such as Viagra,
with heart medications that contain nitrates, like nitroglycerine.

Both drugs lower blood pressure and together can lower it to deadly
levels.

Normally doctors won’t prescribe Viagra or Levitra to these men, but
they can look elsewhere — specifically, the Internet, where herbal
supplements of all sorts are available for sale.

While some of these supplements may contain harmless ingredients, many
are indeed as potent as the real thing.

A recent Food and Drug Administration study showed that some of these
herbal remedies actually contained the active compound in prescription
brands as Viagra, Levitra and Cialis, making them potentially deadly
compounds.

The FDA issued a health advisory last week against these supplements.

“These products are promoted and sold on Web sites as ‘dietary
supplements’ for treating erectile dysfunction and enhancing sexual
performance, but they are in fact illegal drugs that contain
potentially harmful undeclared ingredients.”

“These companies are promoting medications that we would never give to
men with heart disease,” said Dr. Dragan Djordjevic, an internist
specializing in male sexual health at Rush University Medical Center
in Chicago.

The FDA specifically targeted the herbal supplements Zimaxx, Libidus,
Neophase, Nasutra, Vigor -25, Actra-Rx and 4EVERON, all of which do
not list the prescription ingredients on their labels.

For this reason, a patient may not realize the risks.

Erectile Dysfunction Common Among Older Men

“If they are not eligible for one of the classic drugs, they may go to
the supplements, and for this reason, it’s more poignant to let the
patient know that they can be harmful,” said Dr. Yair Lotan, an
assistant professor of urology at the University of Texas Southwestern
Medical Center in Dallas. “They may buy the supplement and not know
they are in danger.”

Doctors can’t estimate how many men have suffered from this drug
interaction because many patients don’t reveal that they are on
supplements.

In many cases, erectile dysfunction and heart disease are linked. Both
are caused by decreased blood flow due to buildup in the arteries.

“A person can come in with severely low blood pressure and die of a
heart attack, and not know they should have reported taking
supplements,” said Dr. Ira Sharlip, a clinical professor of urology at
the University of California at San Francisco and spokesman for the
American Urological Association.

Given that a large majority of Americans have erectile dysfunction,
however, doctors estimate that there are many who have taken or are
using these supplements.

It affects about 30 million U.S. men, including more than half of men
older than 40, according to Dr. Dominic Carbone, assistant professor
of surgery in urology at Wake Forest University Baptist Medical Center
in North Carolina.

May Help Some Men, However

Carbone estimates that he has at least six to 10 patients per month
ask him about supplements for erectile dysfunction.

They wonder whether the supplements are just as good as Viagra, he said.

He also recalls a patient coming in who had erectile dysfunction for
years without treatment and was taking eight to 10 supplements per day.

“The guy buying the supplements in a gas station is probably not
taking the recommended dose,” Carbone said.

Doctors say that some male patients feel forced to turn to the Internet.

Often they are still shy about bringing up the subject with their
doctors and prefer the anonymity of buying online.

Also, at about $10 a pill, Viagra can be too expensive for some men,
whereas supplements can go for a variety of prices, usually for less
than prescription drugs.

That isn’t always a bad thing, one doctor noted.

“The other side of the coin is we have made these drugs unavailable to
the poor. Medicaid does not cover Viagra. If something is off market
and is cheap, it may meet a need,” said Dr. Robert Davis, professor of
urology at the University of Rochester.

Many doctors agree, however, that the advisory is important to public
health.

“Not everyone on nitrates will see the sky fall when they take [these
supplements], but enough will to warrant an advisory,” Davis said.

FDA Warns Consumers about Counterfeit Drugs from Multiple Internet Sellers

The Food and Drug Administration (FDA) is cautioning U.S. consumers
about dangers associated with buying prescription drugs over the
Internet. This alert is being issued based on information the agency
received showing that 24 apparently related Web sites may be involved
in the distribution of counterfeit prescription drugs.

On three occasions during recent months, FDA received information that
counterfeit versions of Xenical 120 mg capsules, a drug manufactured
by Hoffmann-La Roche Inc. (Roche), were obtained by three consumers
from two different Web sites. Xenical is an FDA-approved drug used to
help obese individuals who meet certain weight and height requirements
lose weight and maintain weight loss.

None of the capsules ordered off the Web sites contained orlistat, the
active ingredient in authentic Xenical. In fact, laboratory analysis
conducted by Roche and submitted to the FDA confirmed that one capsule
contained sibutramine, which is the active ingredient in Meridia, an
FDA-approved prescription drug manufactured by Abbott Laboratories.

While this product is also used to help people lose weight and
maintain that loss, it should not be used in certain patient
populations and therefore is not a substitute for other weight loss
products. In addition the drug interactions profile is different
between Xenical and sibutramine, as is the dosing frequency;
sibutramine is administered once daily while Xenical is dosed three
times a day.

Other samples of drug product obtained from two of the Internet orders
were composed of only talc and starch. According to Roche, these two
samples displayed a valid Roche lot number of B2306 and were labeled
with an expiration date of April 2007. The correct expiration date for
this lot number is actually March 2005. Pictures of the counterfeit
Xenical capsules provided by Roche can be viewed at
http://www.fda.gov/bbs/topics/news/photos/xenical.html.

Roche identified the two Web sites involved in this incident as
brandpills.com and pillspharm.com. Further investigation by FDA
disclosed that these Web sites are two of 24 Web sites that appear on
the pharmacycall365.com home page under the “Our Websites” heading.
Four of these Web sites previously have been identified by FDA’s
Office of Criminal Investigations as being associated with the
distribution of counterfeit Tamiflu and counterfeit Cialis.

At this point, it appears that these Web sites are operated from
outside of the United States. Consumers should be wary, if there is no
way to contact the Web site pharmacy by phone, if prices are
dramatically lower than the competition, or if no prescription from
your doctor is required. As a result, FDA strongly cautions consumers
about purchasing drugs from any of these Web sites which may be
involved in the distribution of counterfeit drugs and reiterates
previous public warnings about buying prescription drugs online.

The Marketing of Drugs - Part III

WITH vast and profitable markets up for grabs, drug companies are
aggressively reaching beyond doctors and taking their marketing
messages directly to consumers.

Some of their promotional strategies have become hard to miss. Nightly
news broadcasts — a beloved habit for aging Americans — are brought
to you by the makers of prescription medications for high cholesterol,
arthritis, Alzheimer’s disease and erectile dysfunction; an Internet
search for a specific symptom, or a visit to any popular health site,
will bring up sponsored links and blinking ads for at least one
prescription medication used to treat that symptom; fans of NASCAR see
Viagra advertised every time No. 6 Mark Martin’s car rounds the track.
And women paging through a magazine for tips on reducing clutter can
scarcely avoid the faces and personal stories of actresses who are
managing their depression, osteoporosis or hot flashes with a
brand-name pill.

In 1997, the FDA loosened regulations governing the advertisement of
prescription medications directly to consumers. The change set off
explosive growth in marketing aimed at a general audience long on
interest and — compared with physicians — short on professional
skepticism. Today, drug makers spend roughly $5 billion a year to run
advertising campaigns that use many of the same appeals that marketers
use to sell breakfast cereal and toothpaste.

A study published in the Annals of Family Medicine’s January-February
issue analyzed the messages of 38 advertisements then running during
prime-time TV and found that 95% used emotional appeals to sell the
medication, often framing prescription-drug use as a means to regain
lost control over some aspect of life. None mentioned lifestyle change
as an alternative to product use, although roughly 1 in 5
advertisements suggested it might be a useful complement to the drug.
One in 4 described the causes of the disease the advertised drug
treats, who is at risk for it or how frequently the condition occurs
in the population. The study’s authors, led by UCLA researcher
Dominick L. Frosh, suggested that without such information, consumers
would have little reason to see prescription medication as a solution
that involves risks as well as possible benefits.

In all, 58% portrayed the advertised drug as a medical breakthrough –
a pharmaceutical twist on Madison Avenue’s “new and improved” message.

“It is time to ban direct-to-consumer advertising of prescription
drugs,” wrote Dr. Kurt Stange, editor of the Annals, in an
accompanying editorial. The advertisements consumers see “distort the
relationship between patients and clinicians. [They] manipulate a
patient’s agenda and steal precious time away from an evidence-based
primary care clinician agenda that is attempting to promote healthy
behavior, screen for early-stage treatable disease and address mental
health.”

Even after 23 major pharmaceutical companies agreed to a new slate of
voluntary guidelines limiting their advertising, Stange wasn’t buying
it. Self-monitoring, he wrote, “is not working . . . and cannot
realistically be expected to work.”

PhRMA, the drug manufacturers’ industry group, says direct-to-consumer
advertising empowers patients to take an active role in their
healthcare and spurs them to discuss symptoms, diseases and treatment
options with their doctors that might otherwise go unraised. The
industry group frequently cites a 2002 survey of consumers that found
that 43% were spurred by a prescription-drug ad to look for more
information about the drug or their health.

Although direct-to-consumer advertising has spurred the most political
and professional debate, it is only the most visible means of
prescription-drug marketing aimed at the consumer. To build markets
and encourage consumer loyalty to their products, drug makers have
invested heavily in a tactic known to public relations professionals
as “third-party marketing.” Through voices, groups and activities that
seem independent of them — but frequently are not — drug companies
have found another way to get their messages to consumers.

‘Third-party’ approach
ACCORDING to an article published in the British Medical Journal in
2003, the top five public relations firms specializing in healthcare
earned $300 million in 2002. These firms “are expert at ‘third-party
technique’ — helping the drug industry separate the message from what
could be seen as a self-interested messenger,” wrote authors Bob
Burton and Andy Rowell.

Last October, a commentary in the New England Journal of Medicine
detailed one little-noticed third-party marketing venture.
Underwritten by Eli Lilly, the campaign was designed to increase the
use in hospitals of a drug commercially known as Xigris, for the
treatment of sepsis, or blood poisoning. A preliminary study had
suggested some safety concerns with Xigris, and an FDA advisory panel
had urged more thorough study of the drug before its approval. But in
2001, the FDA approved its entry into the market. The controversy
appeared to sap first-year sales of Xigris, which fell short of
Lilly’s expectations.

Lilly’s response was to secure the services of a small public
relations firm, New York-based Belsito and Co. Belsito would begin
spreading the word to physicians and media outlets specializing in
medical news that Xigris was being rationed and that physicians were
being “systematically forced,” because of the drug’s high cost, to
decide which patients would live and which would die. A $1.8-million
educational grant from Lilly would fund the creation of a group of
physicians and bioethicists — named the “Values, Ethics and Rationing
of Care Task Force” — to study this rationing and its ethical
implications. And a Surviving Sepsis campaign was launched “in theory
to raise awareness of severe sepsis and generate momentum toward the
development of treatment guidelines,” wrote Dr. Peter Q. Eichacker and
two fellow investigators based at the National Institutes of Health,
in the NEJM.

Lilly’s financial inspiration of the campaign aimed at physicians,
patients groups and the media was not apparent to many of the
audiences reached. But its effect was quite clear, concluded a case
study of the campaign done by the Council of Public Relations Firms:
Sales of Xigris “have begun to trend upwards. Through the first
quarter of 2004, Xigris sales were up 36%.”

In such campaigns, public relations companies operate as off-site
extensions of a drug company’s marketing department. But sometimes,
the relationship of a drug company and a third-party voice is more
complex. The tie between patient-advocacy groups and drug companies is
a good example.

Drug makers richly support the nation’s proliferating patient-advocacy
groups, and only a handful of the charitable organizations refuse the
sponsorship of pharmaceutical firms, says Georgetown University’s Dr.
Adriane Fugh-Berman, who has studied these ties. That link presents
rich marketing opportunities for corporate sponsors with an interest
in reaching the patients the organizations advise and represent,
Fugh-Berman says. But it also raises real questions about the
independence of patients groups, she adds.

In marketing trade publications, the value of patients’ groups is
widely touted. As friends and allies to potential customers, groups
dedicated to patients who suffer from a specific condition can be
powerful marketing tools. Patients seek information and emotional
support from these groups, and trust them as an unbiased source of
advice. Groups that empower patients to seek treatment are eager to
foster awareness of their disease and, in the process, expand their
membership. When they are successful, patients groups have a natural
market-building effect.

But drug makers have the deep pockets, and patients groups — until
they’re very large and well-established — are constantly scrambling
for money. As a result, according to those calling for reform, the
relationship is not always an alliance of equals.

“There’s an inherent conflict of interest,” says Merrill Goozner,
editor of Integrity in Science, a publication of the Washington-based
watchdog group the Center for Science in the Public Interest. “The
question becomes, ‘Are you doing the best for the patients you
represent, or are you doing the best for your sponsors?’ ”

Goozner says that patient-advocacy groups are especially vulnerable to
carrying drug companies’ messages, untempered by skepticism, directly
to their members. “They’re desperate” for a cure or treatment, he
says. “And no one likes to be told that this latest breakthrough is
not all it’s been cracked up to be,” especially when it’s being pushed
by a company that’s been generous with funding, he adds.

Last October, the magazine New Scientist published a survey gauging
the dependence of randomly selected U.S. patients’ groups on drug
manufacturers. Combing through the tax returns, annual reports and
voluntary disclosures of 29 nonprofit patient-advocacy groups, the
publication found that most accepted financial backing by companies
developing or producing drugs used to treat patients supported by the
group. In some groups, such as the American Heart Assn., the drug
makers’ financial backing was huge ($23 million in 2005) but
represented a small portion (4%) of revenue. For seven groups,
donations from interested drug companies represented more than
one-fifth of revenue. The Depression and Bipolar Support Alliance said
it received more than half of its 2005 funding from the drug industry,
and the Colorectal Cancer Coalition got 81% of its funding from drug
makers.

New Scientist’s probe found that some donations appeared directly tied
to marketing interests. In 2003 and 2004, when the drug giant Pfizer
was developing a drug to treat restless leg syndrome, it was a major
donor to the Restless Legs Syndrome Foundation. But in 2005, after
Pfizer announced it had abandoned development of the potential drug,
its donations to the patient group dried up.

Many of the best-known groups, including the Alzheimer’s Assn.,
American Cancer Society and American Diabetes Assn., typically have a
board of physicians who vet the scientific accuracy of the information
they provide to patients. And most solicit “unrestricted” grants that
allow them freedom to use the drug makers’ donations as they see fit.

But even large groups often provide a gateway to the products of
corporate sponsors, say those who have surveyed them. Many list
FDA-approved medicines available to treat the disorder that is their
focus and provide Web links that lead patients directly to marketing
sites. And many offer their corporate sponsors access to their
members, a potential gold mine of direct-marketing opportunity.

The corporate-donor pitch posted on the website of the national
infertility patient group, Resolve, is typical of many patient groups.
“Whether you become a site sponsor, a resource partner, or a sponsor
of Resolve’s chats, [the group’s website] is the ideal place for your
company to market its products and services to thousands of men and
women across the country,” the appeal states. Among the benefits the
group lists for becoming a member of the group’s “Corporate Council”
are access to data on utilization of the group’s programs and services
and “the opportunity to establish topics and sponsor special briefings
for patients, the medical community and public policy makers.” Serono
and Organon, both makers of prescription medication used to treat
infertility, are among the group’s corporate sponsors.

Patient groups also mobilize patients — sometimes armies of them –
to push for coverage of prescription drugs by insurance companies and
states’ Medicare and Medicaid agencies. To pharmaceutical companies,
this can make or break the market prospects for a new drug because 80
million Americans — among them, the heaviest prescription-drug users
– receive healthcare coverage through Medicare and Medicaid, and
roughly 155 million have prescription drug coverage through private
insurance companies.

Strength in numbers

WHEN insurers balk at reimbursing patients for new prescription
medications, these groups typically swing into action, rallying
sufferers to appear before public and consumer panels, contact
lawmakers, and provide media outlets a human face to attach to a
cause. Infertility patients mobilized by Resolve, for instance, have
been extremely effective in extending states’ insurance coverage of
infertility treatments. Groups such as the Depression and Bipolar
Support Alliance have fielded experts and patients who have done the
same for psychiatric conditions. And a wide range of patient groups,
most with substantial backing from the makers of erectile dysfunction
drugs, have mounted successful campaigns to get wary insurers to cover
drugs such as Levitra, Viagra and Cialis.

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