American Medical Association will force people to take experimental Vaccines

Freedom of choice when it comes to injecting — or not — a poisonous vaccine may be a thing of the past if the AMA has its way.

By CHRISTINA ENGLAND | VACTRUTH | OCTOBER 26, 2012

The American Medical Association (AMA) recently published a paper proposing the introduction of a new law to force you and your children into experimental vaccine trials against your wishes. Your only way out of this directive would be to sign an ‘opt out form.’

In January, the AMA published a paper by Susanne Sheehy, BM BCh, MRCP, DTM&H, and Joel Meyer, BM BCh, MRCP on the ‘Virtual Mentor’ website, stating that there has been a steady decline in the numbers of healthy volunteers willing to participate in clinical trials. [1]

The AMA believes that more people should want to help in the development of new vaccinations.  They stated:

“Reasons for this decline are unclear but are likely to be multifaceted. One familiar problem is the payment of volunteers. To date, the relatively meager compensation that participants often receive could be seen to belittle and undervalue the contribution of these individuals to global health.”

VOLUNTEER PARTICIPATION TO BECOME A THING OF THE PAST

Because of the decline in willing volunteers, the AMA has decided that volunteer participation in vaccination trials should become a thing of the past. They said:

“If progression of promising vaccines from the lab to the clinic is to remain unaffected and financial inducement is an ethically unacceptable solution to the recruitment shortage, other strategies need to be considered. Compulsory involvement in vaccine studies is one alternative solution that is not as outlandish as it might seem on first consideration. Many societies already mandate that citizens undertake activities for the good of society; in several European countries registration for organ-donation has switched from “opt-in” (the current U.S. system) to “opt out” systems (in which those who do not specifically register as non-donors are presumed to consent to donation, and most societies expect citizens to undertake jury service when called upon.”

That’s right; according to the AMA we should all sign ‘opt out’ forms if we do not want to participate in vaccination trials. If, for some reason, we should forget to do this, then we should automatically be classified as giving passive consent!

In my opinion, agreeing to be a guinea pig for a vaccination trial is a little different from undertaking jury service, whether it is for the good of society or not. As for organ donation, there is one small fact the AMA appears to have forgotten; when our organs are taken, we are already dead!

I say this because a paper released fresh off the press makes abundantly clear just how catastrophic mistakes can be when vaccinations are fast-tracked onto the market.

PROOF OF WHAT WE ALREADY KNEW

The paper, written by Dr. Lucija Tomljenovic and Dr. Chistopher Shaw from the Department of Ophthalmology and Visual Sciences, University of British Columbia, states:

In the past several decades, there have been numerous studies and case reports documenting neurological and autoimmune adverse reactions (ADRs) following the use of various vaccines. Arthritis, vasculitis, systemic lupus erythematosus (SLE), encephalopathy, neuropathy, seizure disorders and autoimmune demyelinating disease syndromes are the most frequently reported serious adverse events.” [2]

The paper goes on to describe serious errors in the HPV vaccine Gardasil’s safety trials, which they say shows evidence of significant flaws in study design, data reporting and interpretation. They believe this has led to the death and injury of many young women.

Dr. Tomljenovic and Dr. Shaw have found the following alarming results after studying the brain samples of two young women who died shortly after they were administered with the Gardasil vaccination:

 “In both cases, the autopsy revealed no anatomical, microbiological nor toxicological findings that might have explained the death of the individuals. In contrast, our IHC analysis showed evidence of an autoimmune vasculitis potentially triggered by the cross-reactive HPV-16L1 antibodies binding to the wall of cerebral blood vessels in all examined brain samples. We also detected the presence of HPV-16L1 particles within the cerebral vasculature with some HPV-16L1 particles adhering to the blood vessel walls. HPV-18L1 antibodies did not bind to cerebral blood vessels nor any other neural tissues. IHC also showed increased T-cell signalling and marked activation of the classical antibody-dependent complement pathway in cerebral vascular tissues from both cases. This pattern of complement activation in the absence of an active brain infection indicates an abnormal triggering of the immune response in which the immune attack is directed towards self-tissue.”

Bearing this knowledge in mind makes a mockery of the AMA’s belief that we should offer ourselves willingly as guinea pigs for vaccination experiments.

THE AMA WANTS YOU … FOR DEADLY DISEASES!

If all this is a little hard to believe, the AMA goes on to state:

“Society is unlikely to accept compulsory recruitment to a trial for a vaccine against the common cold if the vaccine causes severe complications in vaccinees. Increase the severity of the disease in question, however, and compulsory recruitment becomes a more palatable option.”

Unbelievable! The AMA is actually naïve enough to believe that society will be more willing to be used as guinea pigs in their vaccination trials, if the trials are for deadly diseases!

In my opinion, members of society are highly unlikely to be too keen to offer themselves up as human sacrifices in the pharmaceutical industry’s sick experiments, whether the experiments are for deadly diseases or not. I believe that society will more likely remember past vaccine trial disasters and turn around and run in the opposite direction as fast as they can.

WHAT THE AMA FORGOT TO INCLUDE IN THEIR PAPER

In the same month that the AMA proposed compulsory involvement in experimental vaccination trials, GlaxoSmithKline Argentina Laboratories Company was fined 400,000 pesos by Judge Marcelo Aguinsky following a report issued by the National Administration of Medicine, Food and Technology (ANMAT in Spanish) for irregularities during lab vaccine trials conducted between 2007 and 2008 that allegedly killed 14 babies. [3]

Hardly a glowing recommendation, is it? The deaths of these  innocent young babies represent only a small fraction of the adverse reactions and deadly mistakes suffered by children and adults around the world who have participated in experimental vaccine trials.

EVEN MORE VACCINE TRIAL BLUNDERS

In 1991, The Chicago Tribune reported that during vaccine trials for the AIDS vaccine in Paris, at least three people died from adverse reactions out of the 19 participants that took part. [4]

According to The Tribune, these deaths were not reported to any medical journals or to the French and American authorities that sanctioned the experiments. The Tribune said:

“When the French and American scientists collaborating in the experiment published an account of their research last year, they reported that there had been no deaths among the subjects. At the time the article appeared, two of the subjects had died.

The vaccine experiment continued despite the deaths. French government records show that, nearly three months after the first volunteer died, the study was expanded to include more subjects.” 

In 2008, The Telegraph reported that three Polish doctors and six nurses were facing criminal prosecution after a number of homeless people died following medical trials for a vaccine to combat the H5N1 bird-flu virus. [5] The Telegraph reported:

“The medical staff from the northern town of Grudziadz, are being investigated over medical trials on as many as 350 homeless and poor people last year, which prosecutors say involved an untried vaccine to the highly-contagious virus.

Authorities claim that the alleged victims received £1-2 to be tested with what they thought was a conventional flu vaccine but, according to investigators, was actually an anti bird-flu drug.”

In 2011, The Independent reported that pharmaceutical industries were exploiting the illiterate, the poor and the ill by signing them up to drug trials without their consent. [6] It was alleged that between 2007 and 2010 1,730 people died in India during such trials. These trials included:

  • The recruitment of hundreds of tribal girls without parental consent for an immunization study sponsored by the Bill and Melinda Gates Foundation on the nod of the warden of their government hostel. Several girls subsequently died. The study was later halted by the federal authorities.
  • The use by drug companies of survivors of the world’s worst poisonous gas disaster in Bhopal as “guinea pigs” in at least 11 trials without proper informed consent.
  • The completion by doctors at a government hospital in Indore, located in central India, of dozens of private trials that a police investigation found “violated the ethical guidelines.” The doctors who conducted the trials decided that not one of 81 cases in which a participant suffered an adverse effect was linked to the treatment. New trials were stopped while the state government investigated. A whistle-blower was fired.

ANOTHER (LIABILITY) FREE PASS FOR BIG PHARMA

Of course, it is unlikely that the pharmaceutical industries will ever be brought to justice for their crimes against society because on February 22, 2011, the U.S. Supreme Court shielded drug companies from all liability for harm caused by vaccines mandated by government when companies could have produced a safer vaccine. [7]

This basically means that any drug company selling vaccinations in America cannot be held accountable by a jury, in a court of law, if those vaccines give us brain damage but could have been made less toxic.  In other words, if you or your child becomes permanently disabled or autistic after receiving a vaccine mandated by the government you are on your own. [8]

CONCLUSION

It appears that pharmaceutical industries, medical professionals and government agencies have little regard for human life or indeed human suffering when it comes to vaccines. Their multi-billion dollar industry must go on at all costs. Whether it is the homeless, the poor or the vulnerable, they will exploit them and kill them without so much as a backwards glance.

If the AMA gets their way, then it will not be long before you or your child could be included into vaccination trials, if you have not signed an ‘opt out form.’ This means that if your child comes home with a form scrunched up at the bottom of their school bag and you do not find it, or if you forget to sign it, then the drug company will classify your absent-mindedness as passive consent and your child will be used as a pharmaceutical industry guinea pig.

References

  1. Virtual Mentor Susanne Sheehy, BM BCh, MRCP, DTM&H, and Joel Meyer, BM BCh, MRCP – Should Participation in Vaccine Clinical Trials be Mandated? http://virtualmentor.ama-assn.org/2012/01/pfor1-1201.html
  2. Lucija Tomljenovic and Christopher Shaw – Death After Quadrivalent Human Papillomavirus (HPV) Vaccination: Casual or Coincidental?  http://www.omicsgroup.org/journals/ArchivePROA/articleinpressPROA.php
  3. Buenos Aires Herald – GSK Fined Over Vaccine Trials; 14 Babies Reported Dead http://www.buenosairesherald.com/article/88922/gsk-lab-fined-$1m-over-tests-that-killed-14–babies
  4. Chicago Tribune – 3 Dead In Aids Vaccine Tests http://articles.chicagotribune.com/1991-04-14/news/9102030245_1_vaccine-experiment-vaccinia-disease-aids-vaccine-tests
  5. The Telegraph – Homeless People Die After Bird Flu Vaccine Trial in Poland http://www.telegraph.co.uk/news/worldnews/europe/poland/2235676/Homeless-people-die-after-bird-flu-vaccine-trial-in-Poland.html
  6. The Independent – Without Consent: How Drug Companies Exploit Indian ‘Guinea Pigs’ http://www.independent.co.uk/news/world/asia/without-consent-how-drugs-companies-exploit-indian-guinea-pigs-6261919.html
  7. Supreme Court of the United States. Russell Bruesewitz et al v. Wyeth et al No. 09-152. Argued October 12, 2010 – Decided February 22, 2011. http://www.supremecourt.gov/opinions/10pdf/09-152.pdf
  8. Natural Health Strategies – No Pharma Liability for Vaccine Damages:
    Supreme Court http://www.naturalhealthstrategies.com/pharma-liability.html

Trace from Gardasil vaccine found in brains of two dead girls who were injected

Researchers find that vaccine antigen HPV-16-L1 crossed brain barrier.

By NORMA ERICKSON | SANEVAX | OCTOBER 25, 2012

For the first time in history, a biologically plausible mechanism of action has been discovered linking a vaccine to a serious adverse event. Gardasil has left behind its genetic fingerprint in post-mortem central nervous system samples of two girls who took this vaccine.

Two teenage girls from opposite ends of the world – both dead before their time have two additional things in common. They both took Gardasil to try and prevent cervical cancer and fragments of the HPV-16-L1 antigen used in Gardasil have been found in blood vessels within their brains.

The HPV-16-L1 protein is one of the antigens used in both Gardasil and Cervarix. An antigen is a toxin or other foreign substance that induces an immune response in the body. Theoretically, these antigens are not supposed to cross the blood brain barrier. However, according to a recently concluded case study this may not be the case.

Using a new immunohistochemical (IHC) protocol they developed, Drs. Chris Shaw and Lucija Tomljenovic examined post-mortem samples taken from the cerebellum, hippocampus, choroid plexus and watershed cortex of a 19 year-old girl; as well as post-mortem samples of the cerebellum, hippocampus, choroid plexus, portions of the brainstem (medulla, midbrain, pons), right basal ganglia, right parietal and left frontal lobes of a 14 year-old girl. They tested for the presence of two of the specific antigens used in both Gardasil and Cervarix: HPV-16-L1 and HPV-18-L1.

They discovered the presence of HPV-16-L1 particles within the blood vessels in the brain (cerebral vasculature) with some of these particles adhering to the blood vessel walls. For the average medical consumer, this is the equivalent of a Gardasil fingerprint and it should not be in brain tissues.

Does the presence of HPV-16-L1 particles inside these girls’ cerebral vasculature provide evidence of a “Trojan Horse” mechanism by which these particles adsorbed to aluminum adjuvant gain access to human brain tissue? Remember, both Gardasil and Cervarix contain HPV-16-L1 virus-like particles (VLP’s) of the recombinant major capsid (L1) protein adsorbed onto aluminum adjuvants.

Tomljenovic and Shaw also discovered that the antibodies against HPV-16-L1, which were used to detect the presence of HPV-16-L1 particles, were also binding to the wall of cerebral blood vessels in the brain samples.

Their IHC analysis also showed increased T-cell signaling and marked activation of the classical antibody-dependent complement pathway in cerebral vascular tissues from both cases. This pattern of complement activation, in the absence of an active brain infection, indicates an abnormal triggering of the immune response in which the immune attack is directed towards the blood vessels of the brain, thus triggering an autoimmune cerebral vasculitis.

Cerebral vasculitis is a serious disease which typically results in fatal outcomes when undiagnosed and left untreated. The fact that many of the symptoms reported to the Vaccine Adverse Event Reporting System (VAERS) following HPV vaccination are indicative of cerebral vasculitis, but are unrecognized as such (i.e. intense persistent migraines, syncope, seizures, tremors and tingling, myalgia, locomotor abnormalities, psychotic symptoms and cognitive deficits) is a serious concern in light of Tomljenovic and Shaw’s findings.

Finally, there was clear evidence of brain hemorrhages in both cases which further demonstrated that a serious injury to the cerebral vasculature occurred.

For the average medical consumer, this evidence suggests that the antibodies produced in response to vaccination with the HPV-16-L1 may cause one’s immune system to attack its own blood vessels. HPV vaccines containing HPV-16-L1 antigens could therefore pose an inherent risk for triggering potentially fatal autoimmune vasculopathies.

There is little doubt that HPV vaccines are unsafe for some individuals. Who those individuals are and why they are more susceptible to serious adverse reactions than others remains unknown. More studies must be conducted to answer these questions.

The article by Drs. Chris Shaw and Lucija Tomljenovic entitled Death after qHPV vaccination: causal or coincidental, published in Pharmaceutical Regulatory Affairs today provides evidence of a biologically plausible mechanism of action linking a particular vaccine to serious adverse outcomes, perhaps for the first time in history. Although this study may not conclusively ‘prove’ causality, it seriously demonstrates the need for additional investigation. (Access entire article here.)

When reading this case study, one must understand the findings should be viewed with caution. This is a small sample size and there were no control samples available. However, the marked resemblance between the two cases strongly supports the present conclusions.

It is important to note that activation of the antibody-dependent complement pathway, as shown in Tomljenovic and Shaw’s analysis, typically occurs in neurodegenerative diseases which have an underlying immune trigger. This process is not a feature of a normal young brain.

Given that the autopsy in both cases revealed no major abnormality (anatomically, microbiologically or toxicologically) that might have been regarded as a potential cause of death; it appears plausible that the antigenic component of the HPV vaccine (HPV-16-L1) was indeed responsible for the fatal inflammation of the blood vessels.

Medical consumers need to know:

  • Vasculitis has long been recognized as a possible severe adverse reaction to vaccination.
  • Molecular mimicry (whereby the vaccine antigen resembles a host antigen) is generally accepted among medical professionals and scientists as a mechanism by which vaccines can trigger autoimmune diseases.
  • Tomljenovic & Shaw’s search of the VAERS database revealed numerous reports of post-HPV vaccination–associated vasculitis.
  • An analysis of these reports showed that post-HPV vaccination vasculitis-related symptoms most typically manifest within the first three to four months after vaccination, as was also reported in the two cases analyzed by Shaw and Tomljenovic.
  • Tomljenovic and Shaw also noted a striking similarity between the vasculitis-related symptoms reported to VAERS and those experienced by the two cases they examined.

Every vaccine carries some risk of adverse effects. Unlike most medications, vaccines are normally administered to healthy individuals. Therefore, it is all the more critical to identify those individuals who are at risk for serious adverse events after vaccines.

We consider ourselves a civilized society. The time has come to stop sacrificing the life and future of anyone for the greater good. The time has come to admit vaccine injuries occur, find out why and cure those already affected. Anything less is neither responsible, nor ethical.

Untested Toxicity Found in Gardasil Vaccine

HPV DNA bound to insoluble aluminum adjuvant.

By NORMA ERICKSON | SANEVAX | OCTOBER 19, 2012

Genetic modification of food has come under severe criticism from the scientific community as new health risks are being discovered. Do genetically modified vaccines carry any less risk? The study below outlines just a few of the unanswered questions about one of the genetically engineered vaccines currently in use, namely Gardasil®.

Dr. Sin Hang Lee of Milford Hospital recently published an article in The Journal of Inorganic Biochemistry entitled, Detection of human papillomavirus (HPV) L1 gene DNA possibly bound to particulate aluminum adjuvant in the HPV vaccine Gardasil®.

According to Dr. Lee’s research (sponsored by SaneVax Inc.), during the manufacture of Gardasil, Merck may have inadvertently created a new chemical compound composed of HPV L1 gene fragments chemically bound to the aluminum nanoparticles of the AAHS adjuvant used in the vaccine.

If this is true, the toxicity of this chemical has not been tested. No one knows what the potential health consequences the injection of this ‘ingredient’ may be.

Consider some key points extracted from the article by Dr. Lee:

A total of 16 samples of Gardasil® received from Australia, Bulgaria, France, India, New Zealand, Poland, Russia, Spain and the United States were found to contain fragments of HPV-18-L1 gene DNA which was readily detected in 15 of 16 samples tested, or HPV-11-L1 gene DNA, or a mixture of both. After submission of the manuscript, HPV-16-L1 gene fragments were also detected among these samples by a special protocol, Dr. Lee noted in his report.

Dr. Lee stated:

“Although the U.S. Food and Drug Administration recently announced that Gardasil® indeed does contain recombinant HPV L1-specific DNA fragments, the physical condition(s) of these HPV DNA fragments in the final vaccine product has not been characterized.”

Dr. Lee presented experimental evidence to assert that the binding mechanism between the HPV L1 gene DNA and the amorphous aluminum hydroxyphosphate sulfate (AAHS) nanoparticles in Gardasil® is of a chemical nature through ligand exchange of phosphate for hydroxyl, independent of the electrostatic forces. When aluminum (Al3+) and DNA interact, the binding site for Al3+ on the DNA chains is the phosphate groups on the DNA backbones.

For the average medical consumer, if the bond between the DNA and aluminum were electrostatic, it would be much like when you rub a balloon against your head until the static electricity builds up to the point where you can stick the balloon to a wall. As you may have noticed, given a short period of time, the balloon loses the static electric charge and falls off the wall. This is much the same as a vaccine in which the bond between the antigen and adjuvant is electrostatic. Once the vaccine is injected, the recipient’s normal pH level reduces the electrostatic attraction making the antigen and adjuvant separate from each other.

On the other hand, if the bond between the DNA and aluminum is chemical, it is more like taking a blob of super-glue and sticking the balloon to the wall. In this instance, no one knows how long the bond will remain intact.

In light of this substantial difference, Dr. Lee concluded:

“The short-term and long-term impact of the residual fragments of HPV L1 gene DNA, or plasmid DNA, if chemically bound to the mineral aluminum of AAHS nanoparticles is largely unknown and warrants further investigation.”

In Sept 2011, the SaneVax Team informed the FDA that HPV DNA fragments had been found firmly attached to the aluminum adjuvant in 100% of Gardasil samples tested by Dr. Sin Hang Lee of Milford Hospital.

The FDA response included the following statement with no references to back it up:

“Recombinant technology has been used for many years to manufacture medicinal products. Gardasil does contain HPV L1-specific DNA fragments. This is expected, since DNA encoding the HPV L1 gene is used in the vaccine manufacturing process to produce the virus-like particles. The presence of these expected DNA fragments, which are inevitable in vaccine production, is not a risk to vaccine recipients, is not harmful, and this DNA is not a contaminant.”

As you can clearly see, there is no mention whatsoever is made about these fragments possibly being firmly attached to the aluminum adjuvant. The SaneVax Team as well as many eminent scientists and medical professionals around the world believe this ‘tiny’ detail should not be ignored.

If this ‘ingredient’ is indeed an ‘inevitable’ component of recombinant technology, medical consumers have a right to know when, for how long and under what circumstances it was tested for safety.

After an entire year of multiple communication attempts receiving no scientific documentation from the FDA that this ‘ingredient’ did not pose a health threat, the SaneVax Team sent another letter to the FDA Commissioner with one simple request.

This letter asked for copies of documents from the FDA showing:

1)    The date when the FDA and the manufacturer first knew small quantities of residual recombinant HPV L1-specific DNA fragments remain in the vaccine.

2)    The physical condition of the HPV- L1-specific DNA fragments in the Gardasil® vaccine.

To date, the FDA has made no effort to respond to this request. Do they have any documentation? If so, why do they not provide this critical information to medical consumers?

Surely, considering the fact that these fragments are an ‘inevitable’ component of recombinant technology, they have requested safety studies to determine any potential health impact. After all, they are responsible for the health and safety of medical consumers – aren’t they?

One more critical point:

Why did Merck not detect the residues of HPV-18-L1 gene DNA during the production of Gardasil®?

Dr. Lee offered the following explanation:

“…all HPV-18 isolates can be classified into 3 subtypes based on alignments of the DNA sequences of the variants, (i.e. the European, the Asian-American and the African subtypes). In Europe, it has been reported that all of the HPV-18 isolates from patients are found to be of the European or Asian-American variants. In the U.S., 91% of the HPV-18 isolates from white women are reported to be of the European and Asian-American variants, and 64% of the HPV isolates from African American women belong to the African variant.

Since the prevalence of the African variants of HPV-18 among European patients is negligible, the Dutch researchers who originally developed the HPV INNO-LIPA kit naturally selected an HPV-18 probe targeting a homologous sequence shared by all European and Asian-American HPV-18 variants for the testing.

However, the HPV-18 L1 protein-coding gene chosen by the manufacturer for Gardasil® closely related to an African subtype. Failure to detect a target sequence of an African variant HPV-18 DNA in the vaccine Gardasil® with a hybridization probe specifically designed for the European and Asian-American DNA variants may simply reflect the diversity of the L1 protein amino acid sequences within the genotype of HPV-18.”

For medical consumers, this brings additional questions. Has Gardasil® been tested for efficacy against all three HPV-18 variants?

Are families in the United States and Europe putting their children at risk of unknown health consequences resulting from the injection of a new chemical with untested toxicity in order to obtain ‘protection’ against only one type of oncogenic HPV?

The time has come for medical consumers to hold their national health ‘authorities’ accountable. These questions must be answered before any more children become ‘one less.’

(Note: Dr. Lee’s study was commissioned and sponsored by SaneVax Inc. for a future payment not to exceed one U.S. dollar.)

Merck Baldness Drugs cause Sexual Side Effects and Destroy Sperm

Labels changed for drugs for baldness, enlarged prostate. Proscar, Propecia effects continued after use was ended-FDA

REUTERS | APRIL 16, 2012

(Reuters) – Prescribing labels for Merck & Co’s drugs for baldness and enlarged prostate will add reports of sexual side effects that continued after use of the medicines was stopped, U.S. health regulators said.

Labels will be revised for Proscar, which treats symptoms of enlarged prostate, and hair-loss treatment Propecia, the Food and Drug Administration said. The active ingredient in both drugs is finasteride.

The Propecia label will now include notification of problems with libido, ejaculation and orgasms that continued after use of the drug was ended. Proscar’s label will include notification of decreased libido.

The labels of both drugs will also include a description of reports of male infertility and poor semen quality that normalized or improved after use of the drugs was stopped.

In announcing the label changes, FDA cited events reported to the agency.

“The cases suggest a broader range of adverse effects than previously reported in patients taking these drugs,” FDA said in a notification posted on its website. But it also said no clear causal links between finasteride and sexual adverse events had been established.

FDA said sexual side effects were included in the labels of both drugs when they were approved in the 1990s. But in subsequent clinical trials, the side effects were resolved in patients who stopped using the drugs as well as in most patients who continued therapy, the agency said.

Last year, the labels of both drugs were revised to include erectile dysfunction that continued after patients stopped using the drugs, the FDA said.

Only a small percentage of men who use the drugs have experienced sexual side effects, the agency added. For example, it said, an analysis of clinical trials showed 3.8 percent of men taking Propecia reported one or more of the sexual side effects, compared with 2.1 percent of those who received a placebo.

FDA said it believes that finasteride remains safe and effective for its approved uses and that patients on Proscar and Propecia should contact their doctors if they have concerns.

In a statement, Merck said it believes both drugs are generally well tolerated and effective for their intended uses and that it supports efforts to ensure patient safety through monitoring of reported side effects.

The drugs are relatively modest-sized products for the U.S. drugmaker. Merck reported $447 million in Propecia sales last year, and $223 million for Proscar.

Merck shares were down 0.5 percent to $38.27 in afternoon trading on the New York Stock Exchange.

Murder of Blacks by the Pharmaceutical Industry, Vaccines and Cancer

By MIKE ADAMS | NATURALNEWS.COM | MARCH 26, 2012

No matter what you think about the Trayvon Martin shooting case, the degree of emotional and cultural outpouring in this case is impressive. But it seems to be taking place in a highly selective way. A shooting like what happened with Trayvon is tragic but rare, whereas at least a hundred African-Americans are killed by drug companies, vaccine pushers and cancer clinics every single day! And most of the drug companies are led by white men, so if there’s any justification for an outcry against white-on-black crime in America, it should be directed at the vaccine manufacturers, drug companies and cancer clinics, it would seem.

But no. The outcry is focused on one Hispanic man named Zimmerman who allegedly shot a young African-American man named Trayvon. Every life is precious, of course, but how is the life of one young man more precious than the lives of a hundred of other African-Americans who die each day at the hands of their doctors, oncologists and pharmacists? FDA-approved drugs kill 106,000 Americans a year according to the Journal of the American Medical Association. And cancer deaths disproportionately occur in blacks due to chronic vitamin D deficiency among those with dark skin color. If you’re curious to know why, watch my video explanation about sunlight and vitamin D. This video explains why the cancer industry refuses to tell black people the truth about why they need extra vitamin D to prevent cancer:
http://tv.naturalnews.com/v.asp?v=5A62FC73922FD51A88E62E42C5A0AD5E

Outrage is power, but such power must be focused at the right target

One thing I’ve always enjoyed about the black community in America is their sense of brotherhood; the sense that if you attack one of us, you attack all of us! Strength through community. We are more powerful when we act together than if we act in isolation. These are dignified philosophies for any community to follow, but they are all too easily misdirected if the people are not told the whole truth.

What am I saying, exactly? That the African-American community would be far more justified — and potentially save far more lives if they marched on Merck, Pfizer and AstraZeneca. You want to know who’s really killing your black babies? It’s the vaccine companies. The drug companies. The cancer clinics. In the cancer industry alone, it is widely known that people with dark skin color have chronic vitamin D deficiencies that accelerate cancer tumor growth. That’s why cancer tumors are far more aggressive in black men and women thanwhitemen and women.

The cancer industry views black people as business opportunities to be exploited for cash. It’s a form of medical enslavement, and it goes on day after day, year after year, with tens of thousands of victims each year in the USA alone, and not a single highly-visible black community leader has anything to say about it.

At least not that I’ve heard. Where is Jesse Jackson on the issue of black babies being made autistic by vaccines? Where is the leadership outcry against the cancer industry and its exploitation of black women for profit? Where are the rallies, the basketball team photo ops, and the church gatherings for all those African-American men, women and children who are sacrificed to the machine of white corporate profit that kills a hundred Trayvons a day across America?

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