In the marketing and licensure of the HPV vaccine, changes to cervical cells have been equated with death

In the marketing and licensure of the HPV vaccine, changes to cervical cells have been equated with death. This is called using a “surrogate marker” and in vaccine research, this is considered acceptable because we can’t otherwise prove a non-event is attributable to an intervention. There are leaps in logic and in science inherent in this practice, that render conclusions nothing more than false marketing.
In fact, none of the HPV vaccines have ever been proven to prevent a single case of cervical cancer. Don’t take my word for it, listen to what Diane Harper, one of the lead researchers for the vaccine, and a whistleblower, has to say

Around 2,000 reported side effects after using Gardasil cervical cancer vaccine have determined Japanese government officials to withdraw Gardasil from the market in 2013, despite the vaccine being highly promoted in the United States and now approved by the European Union.
“Japanese health officials have recorded nearly 2,000 adverse reactions – hundreds of them serious,” reported Judicial Watch, the Washington-based corruption watchdog that has been monitoring the effects – and health costs – of the drug’s use in the United States for years.
“The alarming reports have led Japan’s government to take action, suspending recommendation for the controversial vaccine which is billed as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV).”

Dr. Harper explained in her presentation that the cervical cancer risk in the U.S. is already extremely low, and that vaccinations are unlikely to have any effect upon the rate of cervical cancer in the United States

Dr. Harper explained in her presentation that the cervical cancer risk in the U.S. is already extremely low, and that vaccinations are unlikely to have any effect upon the rate of cervical cancer in the United States.  In fact, 70% of all HPV infections resolve themselves without treatment in a year, and the number rises to well over 90% in two years.  Harper also mentioned the safety angle.  All trials of the vaccines were done on children aged 15 and above, despite them currently being marketed for 9-year-olds.  So far, 15,037 girls have reported adverseside effects from Gardasil™ alone to the Vaccine Adverse Event Reporting System (VAERS), and this number only reflects parents who underwent the hurdles required for reporting adverse reactions.  At the time of writing, 44 girls are officially known to have died from these vaccines.  The reported side effects include Guillian Barré Syndrome (paralysis lasting for years, or permanently — sometimes eventually causing suffocation), lupus, seizures, blood clots, and brain inflammation.  Parents are usually not made aware of these risks.  Dr. Harper, the vaccine developer, claimed that she was speaking out, so that she might finally be able to sleep at night.  ’About eight in every ten women who have been sexually active will have HPV at some stage of their life,’ Harper says.  ’Normally there are nosymptoms, and in 98 per cent of cases it clears itself.  But in those cases where it doesn’t, and isn’t treated, it can lead to pre-cancerous cells which may develop into cervical cancer.’

Judges demand answers after children die in controversial cancer vaccine trial in India

Judges demand answers after children die in controversial cancer vaccine trial in India
Tribal girls were given shots of cervical cancer vaccines during trial
Children given Merck’s Gardasil and Cervarix vaccines
Petitioners also asked judges to investigate trials of new drug Gardasil 9
Drug has allegedly caused side-effects in children as young as nine
Investigation claims children were used as unwitting human guinea pigs
Supreme Court has given the government one month to provide answers

In 2009, tribal children from the Khammam district in Andhra Pradesh were administered with a Human Papilloma Virus (HPV) vaccine meant for cervical cancer. Around 16,000 girls between the age of 9-15 years were given three shots of vaccine, (manufactured by Merck) by the state health department. The girls were told that they were being given “well-being” shots. The incident started getting attention when some months later, several girls’ health deteriorated and the following year, five of them died. Two such similar cases of deaths were reported from Vadodara, Gujarat, where 14,000 tribal children were also vaccinated with the HPV vaccine Cervarix, made by Glaxo SmithKline.
Around the same time when these incidents were reported, young girls were hospitalised in northern Colombia with similar symptoms. Coincidentally, these girls had been given doses of vaccine too.
Skeletons started tumbling out when an NGO visited Andhra Pradesh. Health activists from the NGO Sama visited Khammam in March 2010 and found out that more than 100 girls were having epileptic seizures, stomach aches, headaches and mood swings. The girls also complained about early menstruation, heavy bleeding and menstrual cramps. Sama raised the issue that these students were made guinea pigs on the pretext of providing healthcare. The illiterate parents were kept in the dark about the real vaccine, and most of them gave their consent in the form of thumb prints.

What: A Phase V human papilloma virus (HPV) Phase V vaccine trial in Andhra Pradesh & Gujarat, India
PATH carried out a large  HPV Phase V vaccine trial in India. Phase V means using approved, not test, vaccines. Certain forms of HPV are associated with cervical cancer. The vaccines in question, Gardasil from Merck and Cervarix from GlaxoSmithKline, were granted marketing approval in India in 2008 while the PATH-sponsored trial began in 2009 as a joint project with the ICMR, using donated vaccines.
The purpose of the trial was to generate data to support the inclusion of the HPV vaccine in India’s Universal Immunization Programme (UIP).
Specifically recruiting from low-income rural, largely tribal, households, the trial was conducted on girls aged 10 to 14 using Gardasil in Khammam district of Andhra Pradesh (AP) state (n=13000), and using Cervarix in Vadodara in Gujarat state (n=10000).
The Problems
Public recognition of problems with this trial started with the reported death of 7 girls. This led to immediate suspension of the trial in 2010 even though it was supposed to run until 2011. Investigations showed these deaths weren’t directly connected to the vaccines (see table from the initial official investigation report, 1).
However, investigations triggered by these deaths instead uncovered serious violations of the process of informed consent (see official investigation reports below from 1, see also 2). Aged 10 to 15, girls in this trial were obviously below the age of  consent meaning their participation in the trial required the consent of  parents/guardians. In the course of Government of India (GOI)  investigations, the trial investigators ‘were asked to submit 100 consent forms, chosen randomly, for both AP and Gujarat for independent verification’ (1). These consent forms turned out to have several problems (see reports below from 1).