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On the morning of 2 October 2009, one of us (Joan)
joined an audience of mostly health professionals and
listened as Dr. Diane Harper, the leading international
developer of the HPV vaccines, gave a sales pitch for
Gardasil. Gardasil, as you may know, is the new vaccine
that is supposed to confer protection against four
strains of the sexually transmitted Human Papillomavirus
(HPV). Dr. Harper came to the 4th International Public
Conference on Vaccination to prove to us the real
benefits of Gardasil. Sadly, her own presentation left
me (Joan) and others filled with doubts. By her own
admission, Gardasil has the doctors surrounding me
glaring at a poor promise of efficacy as a vaccine
married to a high risk of life-threatening side effects.
Gardasil, Dr. Harper explained, is promoted by Merck,
the pharmaceutical manufacturer, as a “safe and
effective” prevention measure against cervical cancer.
The theory behind the vaccine is that, as HPV may cause
cervical cancer, conferring a greater immunity of some
strains of HPV might reduce the incidence of this form
of cancer. In pursuit of this goal, tens of millions of
American girls have been vaccinated to date.
As I sat scribbling down Merck’s claims, I wondered
why such mass vaccination campaigns were necessary.
After all, as Dr. Harper explained, 70% of HPV
infections resolve themselves without treatment in one
year. After two years, this rate climbs to 90%. Of the
remaining 10% of HPV infections, only half coincide with
the development of cervical cancer.
Dr. Harper further undercut the case for mass
vaccination campaigns in the U.S. when she pointed out
that “4 out of 5 women with cervical cancer are in
developing countries.” (Harper serves as a consultant to
the World Health Organization (WHO) for HPV vaccination
in the developing world.) Indeed, she surprised her
audience by stating that the incidence of cervical
cancer in the U.S. is so low that “if we get the vaccine
and continue PAP screening, we will not lower the rate
of cervical cancer in the US.”
If this is the case, I thought, then why vaccinate at
all? From the murmurs of the doctors in the audience,
it was apparent that the same thought had occurred to
them.
In the U.S. the cervical cancer rate is 8 per 100,000
women.1
Moreover, it is one of the most treatable forms of
cancer. The current death rate from cervical cancer is
between 1.6 to 3.7 deaths per 100,000 cases of the
disease.2
The American Cancer Society (ACS) notes that “between
1955 and 1992, the cervical cancer death rate declined
by 74%” and adds that “the death rate from cervical
cancer continues to decline by nearly 4% each year.”3
At this point, I began to wriggle around in my seat,
uncomfortably wondering, is the vaccine really
effective? Using data from trials funded by Merck, Dr.
Harper cheerfully continued to demolish the case for the
vaccine that she was ostensibly there to promote. She
informed us that “with the use of Gardasil, there will
be no decrease in cervical cancer until at least 70% of
the population is vaccinated, and in that case, the
decrease will be very minimal. The highest amount of
minimal decrease will appear in 60 years.”
It is hard to imagine a less compelling case for
Gardasil. First of all, it is highly unlikely that 70%
or more of the female population will continue to get
routine Gardasil shots and boosters, along with annual
PAP smears. And even if it did, according to Dr.
Harper, “after 60 years, the vaccination will [only]
have prevented 70% of incidences” of cervical cancer.
But rates of death from cervical cancer are already
declining. Let’s do the math. If the 4% annual decline
in cervical cancer death continues, in 60 years there
will have been a 91.4% decline in cervical cancer death
just from current cancer monitoring and treatment.
Comparing this rate of decline to Gardasil’s projected
“very minimal” reduction in the rate of cervical cancer
of only 70 % of incidences in 60 years, it is hard to
resist the conclusion that Gardasil does almost nothing
for the health of American women.
Despite these dismal projections, Gardasil continues
to be widely and aggressively promoted among pre-teen
girls. The CDC reports that, by 1 June 2009, over 26
million doses of Gardasil have been distributed in the
U.S.4
With hopes of soon tapping the adolescent male
demographic, Merck, the pharmaceutical manufacturer of
the vaccine, and certain Merck-funded U.S. medical
organizations are targeting girls between the ages of 9
and 13.5
As CBS news reports, “Gardasil, launched in 2006 for
girls and young women, quickly became one of Merck's
top-selling vaccines, thanks to aggressive marketing and
attempts to get states to require girls to get the
vaccine as a requirement for school attendance.”6
Just as I began, in my own mind, to question ethics
of mass vaccinations of prepubescent girls, Dr. Harper
dropped another bombshell. “There have been no efficacy
trials in girls under 15 years,” she told us.
Merck did study a small group of girls under 16 who
had been vaccinated, but did not follow them long enough
to conclude sufficient presence of effective HPV
antibodies.
If I wasn’t skeptical enough already, I really
started scratching my head when Dr. Harper explained,
“if you vaccinate a child, she won’t keep immunity in
puberty and you do nothing to prevent cervical cancer.”
But it turned out that she wasn’t arguing for postponing
Gardasil vaccination until later puberty, as I first
thought. Rather, Dr. Harper only emphasized to the
doctors in the audience the need for Gardasil booster
shots, because it is still unknown how long the vaccine
immunity lasts. More booster shots mean more money for
Merck, obviously.
I left Dr. Harper’s lecture convinced that Gardasil
did little to stop cervical cancer, and determined to
answer another question that she had largely ducked: Is
this vaccine safe?
Here’s what my research turned up. To date, 15,037
girls have officially reported adverse side effects from
Gardasil to the Vaccine Adverse Event Reporting System
(VAERS). These adverse effects include Guilliane Barre,
lupus, seizures, paralysis, blood clots, brain
inflammation and many others. The CDC acknowledges that
there have been 44 reported deaths.7
Dr. Harper, who seems to specialize in dropping
bombshells, dropped another in an interview with ABC
News when she admitted that “The rate of serious adverse
events is greater than the incidence rate of cervical
cancer.”8
This being the case, one might want to take one’s
chances with cancer, especially because the side effects
of the vaccine are immediate, while the possibility of
developing cancer is years in the future.
In the clinical studies alone, 23 girls died after
receiving either Gardasil or the Aluminum control
injection. 15 of the 13,686 girls who received Gardasil
died, while 8 died among the 11,004 who received the
Aluminum shot. There was only one death among the group
that had a saline placebo. What this means is that 1 out
of every 912 girls in the Gardasil clinical studies
died. (9,
see page 8.) The cervical cancer death rate is 1 out of
every 40,000 women per year.10
The numbers of deaths and adverse effects are
undoubtedly underestimates. Dr. Harper’s comments to
ABC News concur with the National Vaccine Information
Center’s claim that “though nearly 70 percent of all
Gardasil reaction reports were filed by Merck, a
whopping 89 percent of the reports Merck did file were
so incomplete there was not enough information for
health officials to do a proper follow-up and review.”11
On average, less than 10 percent—perhaps even less than
1 percent—of serious vaccine adverse events are ever
reported, according to the American Journal of Public
Health.12
Given the severity and frequency of Gardasil adverse
reactions, I definitely wasn’t the only one in Dr.
Harper’s audience who winced when she dismissed most
Gardasil side effects as “easily just needle phobia.”
Due to the young age of the trial participants and
the short duration of the studies, the effects of
Gardasil on female fecundity have not been studied. I
did discover, in my post-conference reading, that
Polysorbate 80, an ingredient in the vaccine (13,
see page 12), has been observed in a European clinical
study to cause infertility in rats.14
Is this an additional concern? Time will tell.
I do not wish to give the impression that Dr. Harper
presented, even inadvertently, a consistently negative
view of her own vaccine. She did tout certain “real
benefits,” chief among them that “the vaccine will
reduce the number of follow-up tests after abnormal PAP
smears,” and thereby reduce the “relationship tension,”
“stress and anxiety” of abnormal or false HPV positive
results.
To me, however, this seems a rather slim promise,
especially when weighed against the deaths and side
effects caused by the Gardasil campaign. Should
millions of girls in the United States, many as young as
9, be put at risk, so that sexually active adults can
have less “relationship tension” about false positive
Hepatitis results? Is the current rate of death,
sterility and serious immune dysfunction from Gardasil
worth the potential that in 60 years a minimal amount of
a cervical disease (that is already decreasing on its
own) may perhaps be reduced?
But what I really wanted to know is why Merck is so
eagerly marketing such a dangerous and ineffective
vaccine? Aren’t there other ways they could make a
profit? While Merck’s behavior is probably adequately
explained by the profit motive, what about those in the
Health and Human Services bureaucracy who apparently see
Gardasil as medicine’s gift to women? What motivates
them?
I (Steve) think that they see Gardasil as what one
might call a “wedge” drug. For them, the success of
this public vaccination campaign has less to do with
stopping cervical cancer, than it does with opening the
door to other vaccination campaigns for other sexually
transmitted diseases, and perhaps even including
pregnancy itself. For if they can overcome the
objections of parents and religious organizations to
vaccinating pre-pubescent—and not sexually active—girls
against one form of STD, then it will make it easier for
them to embark on similar programs in the future.
After all, the proponents of sexual liberation are
determined not to let mere disease—or even death—stand
in the way of their pleasures. They believe that there
must be technological solutions to the diseases that
have arisen from their relentless promotion of
promiscuity. After all, the alternative is too horrible
to contemplate: They might have to learn to control
their appetites. And they might have to teach
abstinence. |