New Study Proves the FDA Is Actively Suppressing Information About the Harmful Effects of Gardasil

by Lance D Johnson (NaturalNews.com )

Young, healthy women who experience amenorrhea, ovarian failure, and infertility have likely been damaged by Merck’s HPV vaccine. A new study published in the Journal of Toxicology and Environmental Health analyzed data on pregnancy outcomes, comparing women who received an HPV vaccine with those who did not. The data analysis is titled, “A lowered probability of pregnancy in females in the USA aged 25 who received a human papillomavirus vaccine injection.”

The study, uninfluenced by pharmaceutical money, analyzed data on 8 million women aged 25-29 living in the U.S. from 2007 and 2014. According to the analysis, conception rates would have fallen by 2 million if 100 percent of the females in the study would have received the HPV vaccine. The study warns that the HPV vaccine has a negative influence on fertility and more research is “warranted.”

Despite mounting evidence of harm, Merck seeks to fast-track Gardasil on new age group

Despite these grave concerns, the Food and Drug Administration (FDA) is currently fast tracking the process by which the Gardasil-9 is approved for use in women and men ages 27 to 45. Merck’s application for approval has been granted priority review, and is scheduled for an approval date of October 6, 2018. So, much important information about Gardasil’s risks will be suppressed as the FDA moves quickly on behalf of Merck’s business interests.

When Gardasil was initially licensed, many post-marketing reports poured in, claiming that vaccine recipients endured primary ovarian failure after vaccination. The cases of Gardasil vaccine damage that have been identified and reported to the U.S. Vaccine Adverse Events Reporting System (VAERS) are in excess of 58,000. Many cases have resulted in emergency room visits, seizures, and the diagnosis of autoimmune conditions. Additionally, approximately 11,000 cases have been filed, documenting “serious” disability and sudden death. Women should no longer be subjected to Merck’s deadly experimentations. Gardasil is an experimentation because the risks are concealed and the vaccine is fast-tracked for approval. (Related: Merck accused of fast tracking Gardasil for financial gain; judge orders the drug company to prove the effectiveness of this vaccine.)

One of the greatest dangers of vaccination, which is not studied by the drug companies or the FDA, are the prevalence of stealth viruses within the vaccines. While they do not impact the animal tissue in the vaccine or infect the animals used in the vaccine studies, these viruses can be dormant and revert to infectious form in humans. Watch “The criminalization of science whistleblowers: An interview with Judy Mikovitz, PhD.

Aluminum adjuvant: one of the most alarming issues of vaccine science

One of the biggest problems with the Gardasil vaccine is the use of aluminum as an adjuvant. The adjuvant is used to force the immune cells to respond to the antigen in the vaccine. Without the adjuvant, the immune response to the vaccine pathogen would be weak. The problem is that the aluminum is taken up into the immune-responsive cells and is carried throughout the body. This may cause the immune system to attack itself, as the aluminum persists as a threat in the body. This metal causes problems in the brain of humans. Studies show that brain tissue from autistic children contains high amounts of aluminum.

Aluminum is exponentially more dangerous through injection, than through ingestion. To suppress information on the harmful effects of vaccines, the drug companies base their vaccine safety on ingested aluminum amounts, not the impact of injected aluminum. There’s a big difference. Equally disturbing, GlaxoSmithKline and Merck spike their placebos with aluminum adjuvants to make the vaccine appear less dangerous. This shortcut helps the drug companies cut observation periods so they can conceal the risks of aluminum adjuvants in their HPV vaccines.

The devastating, traumatic failures of Gardasil are being suppressed and young women are suffering at the deceptive science of these devilish institutions. Despite the growing body of evidence of harm from Gardasil, Merck is seeking fast-track approval to unleash their vaccine on another vulnerable age group of the population. The FDA, ignoring the evidence of Gardasil’s harm to women’s ovaries and fertility, cannot be trusted to evaluate the drug company’s “science.” A moratorium should be issued on all HPV vaccines until there is sufficient evidence to prove the vaccine is no longer causing ovarian failure, autoimmune conditions, infertility, seizures, and death.

Read FDA.news for more headlines about the FDA’s dangerous junk science.

Sources include:

TandFOnline.com

GreenMedInfo.com

GreenMedInfo.com

Vaccines.News

GreenMedInfo.com

HippocraticPost.com

WorldMercuryProject.org

Vimeo.com





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AMA Says Take Your Meds While Doctors Take Your Guns

by JD Heyes


For some reason, the American Medical Association — which was founded to promote the American medical community — wants to wade into one of the premier political battles of our day: Gun control.

The AMA has shifted at least some of its attention recently away from pushing Big Pharma meds that kill more than 100,000 Americans a year to jumping on the gun confiscation bandwagon pushed by the Marxist Left.

As reported by TownHall,

the organization last week approved a wide-ranging list of “common sense” gun control demands that include banning the sale of “all assault-type weapons, bump stocks and related devices, high-capacity magazines, and armor piercing bullets.”

The list was okayed by the AMA’s House of Delegates, a pretend ‘legislative body’ that meets a couple times a year at overpriced venues to drink overpriced liquor and vote on medical and political ‘recommendations.

As TownHall noted further:

The lengthy list of gun policy changes also includes bans on the sale of firearms and ammunition to those under 21 years of age, prohibitions on the ownership and unsupervised use of firearms by those under 21, and the establishment of a national gun registry for all firearms and a gun licensing system for gun owners.
Also, the organization’s gun control proposals include a number of provisions ostensibly aimed at curbing domestic violence and abuse, including one recommendation for a new legal tool by which “family members, intimate partners, household members and law enforcement personnel” can go to court in order to have a person’s guns confiscated “when there is a high or imminent risk for violence.” 

No ‘risk’ of having that authority abused, right?

According to a blog post introducing the ‘common sense’ proposals, the AMA appears to ignore a well-established  constitutional  requirement — due process — which must be engaged before a person’s property or belongings can be confiscated by authorities. 

Were this proposal to be implemented, it would mean the accused would not have an opportunity to defend himself or herself in court. Also, the proposals contain nothing in terms of how “risk for violence” would actually be defined, which means that even people without criminal records or any previous history of violence or abuse could feasibly have their firearms taken from them.

Who gets to decide?

The lack of defining parameters also extends to the AMA’s call for confiscating “high-capacity magazines” and “armor-piercing bullets.” (Related: Prescription drugs far more dangerous to Americans than guns.)

Typically, “high-capacity” has meant those that can hold 10 or more bullets, though New York state defines the term as a magazine capable of holding only seven or more rounds. Lawmakers in that state, by the way, never really said how they determined what the “safe” or “appropriate” level of bullets was in order to ‘allow’ state residents the ‘right’ to defend themselves and family. For instance, no one really knows how they arrived at seven bullets rather than five, or 11, or eight or…well, you get the idea.

The AMA’s guidelines also do not provide any definition of “armor-piercing,” and while that may seem rather obvious, remember that these demands were written up by Leftist anti-gunners, so the term could mean something completely different.

And if the term is applied too broadly, then it could apply to any bullet capable of piercing Kevlar-based body armor, which would encompass nearly every rifle round above .22 caliber.

One thing to remember as well is that these proposals are not being made as a symbolic gesture. The Big Pharma-linked AMA is making them with the intent of presenting them to lawmakers all over the country and in Washington, D.C. and getting them implemented.

“People are dying of gun violence in our homes, churches, schools, on street corners and at public gatherings, and it’s important that lawmakers, policy leaders and advocates on all sides seek common ground to address this public health crisis,” said AMA Immediate Past President David Barb, MD. 

Yes, well, they’re dying more often in vehicles and from prescription drugs, but no one’s calling for them to be banned.

Read more about Big Pharma’s death toll at PharmaDeathClock.com.

J.D. Heyes is a senior writer for NaturalNews.com and NewsTarget.com, as well as editor of The National Sentinel.

Sources include:

TownHall.com

NaturalNews.com


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Mass Shootings and Psychiatric Drugs: The Connection

by Jon Rappoport of No More Fake News.


I’ve been tracking the connection since 1999, when I wrote a long white paper, for the Truth Seeker Foundation, on school shootings and psychiatric drugs. The paper was titled: “Why Do They Do It? School shootings Across America.”

The drugs aren’t the only causative factor, but they produce what I call the Johnny Appleseed effect throughout society. Sprinkle enough of the drugs among enough people and you get otherwise unexplainable violence popping up—in schools, in workplaces. The psychiatric plague eats out the country from the inside.

Here are excerpts from my 1999 report—

The massacre at Columbine High School took place on April 20, 1999. Astonishingly, for eight days after the tragedy, during thousands of hours of prime-time television coverage, virtually no one mentioned the word “drugs.” Then the issue was opened. Eric Harris, one of the shooters at Columbine, was on at least one drug.

The NY Times of April 29, 1999, and other papers reported that Harris was rejected from enlisting in the Marines for medical reasons. A friend of the family told the Times that Harris was being treated by a psychiatrist. And then several sources told the Washington Post that the drug prescribed as treatment was Luvox, manufactured by Solvay.

In two more days, the “drug-issue” was gone.

Luvox is of the same class as Prozac and Zoloft and Paxil. They are labeled SSRIs (selective serotonin reuptake inhibitors). They attempt to alleviate depression by changing brain-levels of the natural substance serotonin. Luvox has a slightly different chemical configuration from Prozac, Paxil, and Zoloft, and it was approved by the FDA for obsessive-compulsive disorder, although many doctors apparently prescribe it for depression.

Prozac is the wildly popular Eli Lilly antidepressant which has been linked to suicidal and homicidal actions. It is now given to young children. Again, its chemical composition is very close to Luvox, the drug that Harris took.

Dr. Peter Breggin, the eminent psychiatrist and author (Toxic Psychiatry, Talking Back to Prozac, Talking Back to Ritalin), told me, “With Luvox there is some evidence of a four-percent rate for mania in adolescents. Mania, for certain individuals, could be a component in grandiose plans to destroy large numbers of other people. Mania can go over the hill to psychosis.”

Dr. Joseph Tarantolo is a psychiatrist in private practice in Washington DC. He is the president of the Washington chapter of the American Society of Psychoanalytic Physicians. Tarantolo states that “all the SSRIs [including Prozac and Luvox] relieve the patient of feeling. He becomes less empathic, as in `I don’t care as much,’ which means `It’s easier for me to harm you.’ If a doctor treats someone who needs a great deal of strength just to think straight, and gives him one of these drugs, that could push him over the edge into violent behavior.”

In Arianna Huffington’s syndicated newspaper column of July 9, 1998, Dr. Breggin states, “I have no doubt that Prozac can cause or contribute to violence and suicide. I’ve seen many cases. In a recent clinical trial, 6 percent of the children became psychotic on Prozac. And manic psychosis can lead to violence.”

A study from the September 1989 Journal of Clinical Psychiatry, by Joseph Lipiniski, Jr., indicates that in five examined cases people on Prozac developed what is called akathesia. Symptoms include intense anxiety, inability to sleep, the “jerking of extremities,” and “bicycling in bed or just turning around and around.” Dr. Breggin comments that akathesia “may also contribute to the drug’s tendency to cause self-destructive or violent tendencies … Akathesia can become the equivalent of biochemical torture and could possibly tip someone over the edge into self-destructive or violent behavior … The June 1990 Health Newsletter, produced by the Public Citizen Research Group, reports, ‘Akathesia, or symptoms of restlessness, constant pacing, and purposeless movements of the feet and legs, may occur in 10-25 percent of patients on Prozac.’”

Other studies:

“Emergence of self-destructive phenomena in children and adolescents during fluoxetine [Prozac] treatment,” published in the Journal of the American Academy of Child and Adolescent Psychiatry (1991, vol.30), written by RA King, RA Riddle, et al. It reports self-destructive phenomena in 14% (6/42) of children and adolescents (10-17 years old) who had treatment with fluoxetine (Prozac) for obsessive-compulsive disorder.

July, 1991. Journal of Child and Adolescent Psychiatry. Hisako Koizumi, MD, describes a thirteen-year-old boy who was on Prozac: “full of energy,” “hyperactive,” “clown-like.” All this devolved into sudden violent actions which were “totally unlike him.”

September, 1991. The Journal of the American Academy of Child and Adolescent Psychiatry. Author Laurence Jerome reports the case of a ten-year old who moves with his family to a new location. Becoming depressed, the boy is put on Prozac by a doctor. The boy is then “hyperactive, agitated … irritable.” He makes a “somewhat grandiose assessment of his own abilities.” Then he calls a stranger on the phone and says he is going to kill him. The Prozac is stopped, and the symptoms disappear.

The well-known Goodman and Gilman’s The Pharmacological Basis of Therapeutics reveals a strange fact. It states that Ritalin [given for ADHD] is “structurally related to amphetamines … Its pharmacological properties are essentially the same as those of the amphetamines.” In other words, the only clear difference is legality. And the effects, in layman’s terms, are obvious. You take speed and, sooner or later, you start crashing. You become agitated, irritable, paranoid, delusional, aggressive.

In his book, Toxic Psychiatry, Dr. Breggin discusses the subject of drug combinations: “Combining antidepressants [e.g., Prozac, Luvox, Paxil] and psychostimulants [e.g., Ritalin] increases the risk of cardiovascular catastrophe, seizures, sedation, euphoria, and psychosis. Withdrawal from the combination can cause a severe reaction that includes confusion, emotional instability, agitation, and aggression.” Children are frequently medicated with this combination, and when we highlight such effects as aggression, psychosis, and emotional instability, it is obvious that the result is pointing toward the very real possibility of violence.

In 1986, The International Journal of the Addictions published a most important literature review by Richard Scarnati. It was titled, “An Outline of Hazardous Side Effects of Ritalin (Methylphenidate)” [v.21(7), pp. 837-841].

Scarnati listed over a hundred adverse affects of Ritalin and indexed published journal articles for each of these symptoms.

For every one of the following (selected and quoted verbatim) Ritalin effects then, there is at least one confirming source in the medical literature:

• Paranoid delusions
• Paranoid psychosis
• Hypomanic and manic symptoms, amphetamine-like psychosis
• Activation of psychotic symptoms
• Toxic psychosis
• Visual hallucinations
• Auditory hallucinations
• Can surpass LSD in producing bizarre experiences
• Effects pathological thought processes
• Extreme withdrawal
• Terrified affect
• Started screaming
• Aggressiveness
• Insomnia
• Since Ritalin is considered an amphetamine-type drug, expect amphatamine-like effects
• psychic dependence
• High-abuse potential DEA Schedule II Drug
• Decreased REM sleep
• When used with antidepressants one may see dangerous reactions including hypertension, seizures and hypothermia
• Convulsions
• Brain damage may be seen with amphetamine abuse.

Other ADHD medications, which also have a chemical profile similar to amphetamines, would be expected to produce some of the same effects listed above.

The ICSPP (International Center for the Study of Psychiatry and Psychology) News publishes the following warning in bold letters: “Do Not Try to Abruptly Stop Taking Psychiatric Drugs. When trying to withdraw from many psychiatric drugs, patients can develop serious and even life-threatening emotional and physical reactions…Therefore, withdrawal from psychiatric drugs should be done under clinical supervision…”

—end of excerpts from my 1999 white paper on school shootings and psychiatric drugs—

There is a problem. It is chilling. Pharmaceutical companies, which manufacture drug after drug for “mental disorders,” are doing everything they can to cover up the drugs’ connection to violence.

They use their lawyers and PR people—and their influence over the press—to scrub the connection.

And now, one typical, disturbing, official reaction to every new mass shooting is: build more community mental health facilities. Obama was prominent in this regard, after Sandy Hook in 2012. The implication? More drug prescriptions for more people; thus, more violent consequences.

’ll close with another excerpt from my 1999 report. It is the tragic account of Julie Marie Meade (one account of many you can find at ssristories.org (also here)):

Dr. Joseph Tarantolo has written about Julie Marie Meade. In a column for the ICSPP (International Center for the Study of Psychiatry and Psychology) News, “Children and Prozac: First Do No Harm,” Tarantolo describes how Julie Meade, in November of 1996, called 911, “begging the cops to come and shoot her. And if they didn’t do it quickly, she would do it to herself. There was also the threat that she would shoot them as well.”

The police came within a few minutes, “5 of them to be exact, pumping at least 10 bullets into her head and torso,” as she waved a gun around.

Tarantolo remarks that a friend of Julie said Julie “had plans to make the honor roll and go to college. He [the friend] had also observed her taking all those pills.” What pills? Tarantolo called the Baltimore medical examiner, and spoke with Dr. Martin Bullock, who was on a fellowship at that office. Bullock said, “She had been taking Prozac for four years.”

Tarantolo asked Bullock, “Did you know that Prozac has been implicated in impulsive de novo violence and suicidalness?” Bullock said he was not aware of this.  Tarantolo is careful to point out, “Violent and suicidal behavior have been observed both early (a few weeks) and late (many months) in treatment with Prozac.”

The November 23rd, 1996, Washington Post reported the Julie Meade death by police shooting. The paper mentioned nothing about Prozac. Therefore, readers were left in the dark. What could explain this girl’s bizarre and horrendous behavior?

The answer was there in plain sight. But the Post refused to make it known.



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Walgreen’s Pharmacy Leaves Something More To Be Desired

by Allen Williams


Observing operation at Walgreen’s pharmacy located at 78th and State Avenue in Kansas City, Kansas was a wonder to behold.  It is a modern drug dispensing facility with computer oversight, featuring a drive through, two service lines, an information window and a huge alphabetical prescription holding rack containing drugs for A to Z recipients, ready to dispense.

The first time I was there to have a prescription filled, the two service lines were six and seven persons deep and the drive through window processed a steady line of prescription orders.  (Eat your heart out McDonalds!) From what I could see there were a half dozen or so pharmacy techs of various nationalities scurrying about keeping the drive through window supplied and placing orders in the holding rack.  It was by far the most intensive activity in the entire store and undoubtedly responsible for Walgreen’s 2016 billion dollar profits.  It is for all practical purposes a highly successful retail network pharmacy.  But what about real healthcare?

Only one pharmacist oversaw this circus of activity that I could detect with who knows how many unseen individuals behind the scene hastily filling little plastic pill bottles with various medicines.  It was Obamacare’s assembly line medicine in full operation, a boon to the fortunate few who hold exclusive distribution status.: “The Obama administration decided to make a deal with the PhRMA to get them to support the legislation,” he told Morning Consult. “PhRMA got a number of favorable provisions in the legislation.”

As you might expect, in any quasi chaotic operation born of special interest deals, things were bound to go wrong.  In the multicultural- multinational drug market, the ‘mission statement’ is more important than the reality of care. Walgreen’s president, Greg Wasson claims: “One of the most unifying forces behind Walgreens 113 years of success is our purpose: to help people get, stay and live well.”

Really? But shouldn’t that process commence by ensuring that patients obtain ALL their prescribed medicines and not someone elses? After arriving at Walgreen’s about a month ago, I had requested my prescription records be transferred to Walgreens from CVS.  You AREN’T ALLOWED to retrieve your own prescription from a pharmacy under Obamacare; it has to be requested by ANOTHER PHARMACY. 

On March 27th, I went to get my 2nd prescription filled that clearly indicated there were two remaining refills on the bottle.  However, I was told at the counter that they had NO prescription records for that medication.  I informed them you should have the records as I had requested them to be transferred from CVS the last time I was at Walgreens.  But I had to request the transfer of my 2nd prescription a second time and indicated that I would return on Wednesday of that week to pick it up.  

When I arrived at the counter on Wednesday a multicultural tech informed me that my pain killing medication was ready. I didn’t have a pain killing medication, I replied.  “Oh, then your Prednisone prescription is ready”, the tech said.  I don’t have a Prednisone prescription either; I wouldn’t take that stuff I replied.  Makes you wonder if diabetic customers are getting the correct medication and dosages, hmmm?  Nothing quite like being knowledgeable about whom you’re serving.

But regarding my 2nd prescription they said: “CVS didn’t send that prescription to us because you have no refills remaining.”  But that wasn’t true as the prescription vial I handed Walgreens clearly displayed TWO refills and it had not yet reached the 12-month expiration limit. 

The pharmacy didn’t seem to care about the administrative foul-up and refused to honor my request for a few emergency pills to hold me over until I could get the doctor to write a new prescription because as their pharmacist told me “.. it wasn’t legal.”  KMART did this regularly.  So was it legal to push off narcotic pain killers and prednisone on me because they mistook my identity?  It doesn’t invoke much confidence on my part in their professional capabilities.  Instead they had my third prescription ready (which I didn’t need) and tried to get me to take that in lieu of what I requested.  Starting to get the picture, yet?

Discussion with the pharmacist led to an agreement for Walgreen’s to contact my doctor and their automated system would then call me when my 2nd prescription was filled.  But, there was no call from Walgreen’s automated system and I had to call it myself (and my doctor) to find out that my prescription was ready to pick up nearly a week later.  It doesn’t matter what you arrange with Walgreens, you will only get what they decide you can have.  Is it just me?  Well read some of the 1220 Walgreen complaints and decide for yourself.

CVS and Walgreens are battling it out to control the market for prescription drugs so customer care is way down the line.  Patient care comes in number four right behind legal liabilities, HHS directives and company policy.  Emphasis is on pushing the distribution sales of prescription drugs to the dehumanizing level, everything else is secondary.

I arrived at Walgreens’ on April 3rd to pick up the 2nd prescription, the pharmacist waited on me directly.  I informed him that Walgreen’s automated system didn’t call me and that I had to call it instead.  He did the usual security check with my birth date and then asked me to type in the last four digits of my telephone number which the system didn’t take.  This suggests that I quite possibly could have left Walgreens with narcotics never prescribed for me because of their malfunctioning system.  He continued to try to get the system to accept my phone number and I finally had to tell the Pharmacist to ring up my charges  as he wasn’t responsible for the malfunction. It was the people who installed it.  They could play with their computer later; I just wanted to complete my business and leave.

My first hint that Walgreen’s was more a greed driven enterprise than a healthcare outlet occurred when I was forced into their system from the collapse of KMART’s pharmacy.  And mind you, not that KMART provided inferior products or service but it simply wasn’t as good as Walgreen’s in marketing their slice of the Obamacare drug cartel.  KMART’s final pharmacy closure sent my prescription records to CVS, the bottom of the birdcage in prescription medicine.

The reader is well advised to seek other drug store providers if at all possible.