Vaccine News – Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013

An interview with Robert Kennedy Jr. on vaccines
By Helen Branswell
In the early days of 2017, proponents of vaccination were deeply concerned. Donald Trump, who has long espoused a debunked link between vaccines and autism, was set to enter the White House. He met with environmental activist Robert Kennedy Jr., who has for years argued that vaccines can cause a range of developmental and other health conditions. Kennedy emerged to report he’d been asked to chair a commission into vaccine safety.
But seven months later, no such commission has been appointed and the crisis-mired White House has declined to say whether the plan has been shelved.
STAT contacted Kennedy to see where plans stood. He would only speak on condition that STAT publish the interview in a Q&A format. He argued that his assertions — which are disputed as a misreading of the scientific literature by many mainstream scientists — have been misquoted and misrepresented in the media.
Here is STAT’s conversation with Kennedy. It has been lightly edited, for length and readability.
The question I want to ask you relates to the vaccine safety commission that you had announced in January that you were going to head, after you met with then President-elect Trump. It’s been a number of months now, and there hasn’t been any further public announcement. And so we’ve been wondering: Where does this stand?
I’ve had no discussions specifically about the vaccine safety commission, probably since February. I’ve spoken to the White House about other issues of vaccine safety and had a number of follow-up meetings.

Study – The putative role of environmental aluminium in the development of chronic neuropathology in adults and children. How strong is the evidence and what could be the mechanisms involved?
Abstract
The conceptualisation of autistic spectrum disorder and Alzheimer’s disease has undergone something of a paradigm shift in recent years and rather than being viewed as single illnesses with a unitary pathogenesis and pathophysiology they are increasingly considered to be heterogeneous syndromes with a complex multifactorial aetiopathogenesis, involving a highly complex and diverse combination of genetic, epigenetic and environmental factors. One such environmental factor implicated as a potential cause in both syndromes is aluminium, as an element or as part of a salt, received, for example, in oral form or as an adjuvant. Such administration has the potential to induce pathology via several routes such as provoking dysfunction and/or activation of glial cells which play an indispensable role in the regulation of central nervous system homeostasis and neurodevelopment. Other routes include the generation of oxidative stress, depletion of reduced glutathione, direct and indirect reductions in mitochondrial performance and integrity, and increasing the production of proinflammatory cytokines in both the brain and peripherally. The mechanisms whereby environmental aluminium could contribute to the development of the highly specific pattern of neuropathology seen in Alzheimer’s disease are described. Also detailed are several mechanisms whereby significant quantities of aluminium introduced via immunisation could produce chronic neuropathology in genetically susceptible children. Accordingly, it is recommended that the use of aluminium salts in immunisations should be discontinued and that adults should take steps to minimise their exposure to environmental aluminium.

Australia Bans Truth-Telling Mother From Country For Three Years…And It Backfired
The date was August 8th and the Vaxxed team had just wrapped up a two-week tour of Australia, where the communities of parents received their info with great interest. It was time for the team, consisting of a medical doctor, a scientist, a videographer, and a mother of a vaccine-injured son to pass through Australia’s Department of Immigration within the airport on the way to their flight to New Zealand. Three passed through unhassled, one didn’t. Vaxxed team member Polly Tommey describes what happened to her:
“I get taken to one side and that’s when two immigration police take me into a room and tell me that I’ve been detained and ask for my phone…and then they told me that I was in violation of my Visa and they took my phone and went right through everything in my phone. They typed in ‘Australia’ they went through every contact and every email that there had been with myself and the team. They took my phone away and photographed everything.”
In an instant Tommey was a persecuted individual who moments later would find out she was officially banned from Australia for three years. Next, it came time for airport security immigration officers to address one of the reasons Tommey was being harassed:
“Then they asked me about Vaxxed. Did I have a copy of it? Endless questions about Vaxxed being a very dangerous film with lies…I’m a mother recording stories from parents. And parents come to me to tell their stories. I didn’t seek them out, they come to me. And that is more of a threat than anything else?”
How did we get to the point where a mother can be banned from a western country for simply offering a voice to families?

The Wild Doc – What Officials Can Do To End Unnecessary Drug Overdoses/ Vaccine Awareness Month Brings New Confirmation That Vaccines Are Causing SIDS.

Relevant to the back-end profits (and back-end injuries) industry is generating from the autism epidemic. Abilify is in the class of second generation antipsychotics frequently pushed on individuals with autism by mainstream doctors as part of the $5 billion (and rising) “autism drug” market.

Dr.Russell Blaylock Exposes The Gardasil, HPV Vaccine Fraud
A shocking interview by Mike Adams (The health ranger) with Dr. Russell Blaylock who exposes to total criminal fraud of HPV vaccines and the vaccine industry.

Hear Why He Calls The HPV Vaccine a Crime Against Kids!
The HPV vaccine continues to be a hotly debated issue. Robert Scott Bell, popular radio host and homeopathic practitioner, discusses the theory behind the HPV vaccine and whether or not he thinks it’s safe.
http://www.ihealthtube.com

The Health Ranger – Gardasil HPV Vaccine Hoax Exposed
This video exposes the truth about Gardasil and HPV vaccinations: They don’t work and may actually be dangerous to women. The FDA knew HPV did not cause cervical cancer in 2003.

HPV Gardasil Vaccine Proves Lethal – 236 Girls have now Died
236 Girls have now died in America – http://sanevax.org/
Irish Times 8.1.2012-Schoolgirl vaccine uptake of 82% beats target figures http://j.mp/zuYds8
236 girls have now died in America and the rest of the World, But the Irish Times keeps this quite, Irish Dr Kevin Kelleher, assistant national director of health protection at the HSE, welcomed the high uptake on Gardisil Vaccinations, he fails to give the facts also, says its excellent!
The 82 per cent uptake was “excellent” and was equal to or greater than those achieved in the first year of programmes in other countries such as the United Kingdom and Australia. He said the figures were great credit to the vaccination teams.

MMR gave our boy organ failure and then loss of legs #vaxxed #truth #science #Praybig

Why My Wife and I Decided Not To Vaccinate Our Daughter
Author: Jason Christoff
When my wife was pregnant we knew the vaccine issue was coming our way and we put it off as long as possible. As the day fast approached, I started to investigate and compile some information for my wife because she trusted that I would make sure she understood what the main issues were regarding vaccination. We had heard vaccinations were potentially dangerous but we didn’t know if that applied to all children or just some. We weren’t aware if vaccination was beneficial for some babies and maybe not for others. We were new to being parents and we didn’t want to make any mistakes. We certainly didn’t want our baby getting sick if we could do something about it proactively. We wanted our baby to have the most comfortable journey through life possible and if that meant giving our new born vaccines, so she could avoid disease now and in the future, then that’s what we were going to do. After researching for a couple of days, we were more than shocked at what we were uncovering.

Study – Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden.
RESULTS:
Excess risks among vaccinated compared with unvaccinated people were of low magnitude for Bell’s palsy (hazard ratio 1.25, 95% confidence interval 1.06 to 1.48) and paraesthesia (1.11, 1.00 to 1.23) after adjustment for age, sex, socioeconomic status, and healthcare utilisation. Risks for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, and rheumatoid arthritis remained unchanged. The risks of paraesthesia and inflammatory bowel disease among those vaccinated in the early phase (within 45 days from 1 October 2009) of the vaccination campaign were significantly increased; the risk being increased within the first six weeks after vaccination. Those vaccinated in the early phase were at a slightly reduced risk of death than those who were unvaccinated (0.94, 0.91 to 0.98), whereas those vaccinated in the late phase had an overall reduced mortality (0.68, 0.64 to 0.71). These associations could be real or explained, partly or entirely, by residual confounding.
CONCLUSIONS:
Results for the safety of Pandemrix over 8-10 months of follow-up were reassuring -notably, no change in the risk for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, or rheumatoid arthritis. Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign. Small numbers of children and adolescents with narcolepsy precluded any meaningful conclusions.

Injecting Aluminum Official Trailer
Watch Now on Vimeo On Demand: https://vimeo.com/ondemand/injectingaluminum
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IMDB: imdb.com/title/tt6749336/?ref_=fn_al_tt_1
In the early 90s, a mysterious muscular disease with symptoms that included severe muscle and joint pain began to surface among multiple patients in France. In 1993, a team of doctors in Paris discovered that these patients had developed a new disease called Macrophagic Myofascitis, or MMF, which occurs when the aluminum hydroxide adjuvant from a vaccine remains embedded in the muscle tissue and causes an immune reaction. Featuring interviews with patients, doctors, scientists, and influential politicians, Injecting Aluminum calls in to question the public health policies around aluminum in vaccines and examines aluminum’s devastating effects on the human body.

IMPFEN MUSS FREIWILLIG BLEIBEN!
In vielen Ländern Europas dürfen Eltern schon jetzt nicht mehr frei entscheiden, ob, wann und wogegen ihre Kinder geimpft werden. Auch in Deutschland werden die Daumenschrauben angezogen, aktuell wird diskutiert, man solle Eltern, die ihre Kinder nicht impfen, das Kindergeld entziehen!
Da Impfungen schwere Nebenwirkungen haben können, darf kein Staat und keine Institution Eltern vorschreiben dürfen, welche Pharma-Produkte ihren Kindern einverleibt werden!
Um den drohenden Impf-Zwang zu verhindern, rufen wir zur Teilnahme auf und bitten um Unterstützung:
Demonstration am 16.9.2017 in Berlin
FÜR EINE FREIE ZUKUNFT GESUNDER MENSCHEN!

Vaccination must be voluntary!
In many countries of Europe, parents are no longer allowed to decide whether, when and what their children are vaccinated. In Germany, too, the squeeze are being drawn up, and it is currently being discussed that parents who do not vaccinate their children should withdraw child benefit.
Since vaccination can have serious side effects, no state and no institution must be allowed to require parents to have the pharmaceutical products incorporated into their children.
In order to prevent the threat of vaccination, we call to participate and ask for support:
Demonstration on 16.9.2017 in Berlin
For a free future of healthy people!

Movie Vaxxed gets up QUEENSLAND Health Minister’s nose
By Brent Melville
QUEENSLAND Health Minister Cameron Dick was either seriously misinformed, ignorant, or flat out lying when, in response to the touring movie Vaxxed: From Coverup to Catastrophe, he said “there is no shred of credible scientific evidence to support claims that vaccinations are dangerous” (Gold Coast Bulletin, 15/7/17).
The same with Victorian Health Minister Jill Hennessy who stated on Seven News in February last year: “There are no risks in vaccinating your children – the science is really clear”.
Dr Hooker, who joined the Vaxxed tour, says there are in fact more than 100 studies on PubMed on autism, neurological developmental disorders (NDDs) and vaccination. But here’s a few specific studies our blind, deaf and dumb health ministers and their advisers refuse to look at.
1. Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden. https://www.ncbi.nlm.nih.gov/pubmed/21994316 Conclusion in part: “… Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign…”.
2. Autoimmune disorders (AIDs) after immunisation with Influenza A/H1N1 vaccines with and without adjuvant: EudraVigilance data and literature review. https://www.ncbi.nlm.nih.gov/pubmed/23022149 From abstract: “Of the 50,221 adverse reactions received in EudraVigilance for A/H1N1 vaccines (adjuvanted: 46,173, non-adjuvanted: 4048), 314 were AID (adjuvanted: 276, non-adjuvanted: 38). GBS was the AID with the highest number of reports (125, adjuvanted: 109, non-adjuvanted: 16).
3. Serious adverse events rarely reported after trivalent inactivated influenza vaccine (TIV) in children 6-23 months of age. https://www.ncbi.nlm.nih.gov/pubmed/19450636 From results: “During 1991-2001, VAERS received 128,717 reports…A total of 14.2% of all reports described serious adverse events, which by regulatory definition include death, life-threatening illness, hospitalization or prolongation of hospitalization, or permanent disability.”
4. “Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013.” https://www.ncbi.nlm.nih.gov/pubmed/25598306 Study results found: “VAERS received 29,747 reports after Hib vaccines; 5179 (17%) were serious, including 896 reports of deaths. Median age was 6 months (range 0-1022 months). Sudden infant death syndrome was the stated cause of death in 384 (51%) of 749 death reports with autopsy/death certificate records. The most common non-death serious AE categories were neurologic (80; 37%), other noninfectious (46; 22%) (comprising mainly constitutional signs and symptoms); and gastrointestinal (39; 18%) conditions.”

Study: Vaccine Induced Inflammation Cause of Obesity Epidemic – Not Diet
Childhood obesity is now a reason why the state could take away children from their parents. The rationale is that if a child is obese, it is the parents’ fault, because they failed to feed them properly. It is assumed that all childhood obesity is a result of diet.
However, most of us have probably seen first-hand just how different children are when it comes to food and putting on weight. Some children can eat junk food most of the time and never add weight, while some children can eat a healthy, organic diet and still add pounds.
Dr. J. Bart Classen has published a study claiming that the evidence for the overwhelming problem of childhood obesity is not diet, but “vaccine induced inflammation.”

Vaccines, not Diet, are Causing Epidemic of Obesity and Type 2 Diabetes According to New Paper from Classen Immunotherapies
MANCHESTER, Md., June 26, 2017 /PRNewswire/ — A newly published paper in June’s Journal of Endocrinology, Diabetes & Obesity, 5(3): 1107, by immunologist J. Bart Classen, MD of Classen Immunotherapies provides further proof of the dangers of vaccines. The paper reviews the growing evidence that many cases of obesity, type 2 diabetes and metabolic syndrome are inflammatory conditions and that vaccine induced inflammation is the cause of the epidemic of these diseases. Upon receiving a vaccine some individuals’ immune system becomes hyper active leading to autoimmune destruction of insulin secreting cells and the development of type 1 diabetes. Many other individuals produce increased cortisol and other immune suppressing molecules, to suppress the vaccine induced inflammation. This increased production leads to type 2 diabetes, obesity and metabolic syndrome. The new paper reviews evidence supporting vaccines, not diet, as a cause of the epidemics of obesity, type 2 diabetes and metabolic syndrome.

Study – Cause of the Obesity, Type 2 Diabetes and Metabolic Syndrome Epidemics, Vaccine Induced Immune Overload versus Nutrition Overload
Abstract
There is an epidemic of obesity, type 2 diabetes, metabolic syndrome and associated conditions. Patients with these conditions often have markers of
increased inflammation. Many researchers have published that nutrition overload caused the epidemic of obesity and the associated inflammation which
leads to type 2 diabetes and metabolic syndrome. A contrasting view has provided extensive evidence that vaccine induced immune overload has caused an
epidemic of inflammation and this inflammation caused epidemics of obesity, type 2 diabetes and metabolic syndrome. The data reviewed in these manuscripts
provides proof that immune overload, not nutrition overload has been the major contributing factor for the epidemics and inflammation associated with the
epidemics. Several lines of evidence are reviewed including evidence that inflammation precedes obesity in many patients, the lack of inflammation in many
obese patients, an epidemic of inflammation in thin patients, and an epidemic of obesity in children under 6 months of age. The failure to control the obesity
epidemic is blamed on the focus on nutrition and ignoring the root cause, vaccine induced immune overload. Once a patient has developed metabolic syndrome
with type 2 diabetes providers are too frequently subjecting their patients to further immune overload by administering yearly influenza vaccines and many
other vaccines. This action makes metabolic syndrome more difficult to reverse. The plan to reduce obesity must be focused on preventing immune overload
and not blaming patients for their diet. The epidemic of obesity can be reversed through discontinuation of vaccine practices that result in immune overload.

 

Flu Vaccine is the most Dangerous Vaccine in the U. S. based on Settled Cases for Injuries

Flu Vaccine is the most Dangerous Vaccine in the U. S. based on Settled Cases for Injuries
Attorney Howard Gold of Gold Law Firm, who settled a case for GBS due to a flu vaccine in 2011, remarked:
Petitioners have three (3) years from the onset of the injury (or two years from date of death) to file a claim. Gold states that the “Program is not used as much as it could be because the American public is just not aware of it. I receive at least 5 calls a month from individuals who cannot obtain compensation because the deadline has passed. They just found out about it too late. We all need to do a better job in getting the word out to the public that the Program exists.” (Source.)
In November 2013, a healthy 19-year old young man died from a routine exam that included the flu vaccine. Chandler Webb received the flu shot on October 15th, and then died on November 19th, 28 days later. Since the flu shot is considered safe in the medical field, doctors waited too long to suspect that the flu shot was causing Chandler’s rapidly deteriorating medical condition, according to his mother. She believes that if they had investigated the adverse reaction to the flu shot immediately, he might still be alive today.

Just a quick cursory view of cases that are being compensated by this vaccine court shows that the most cases, by far, are cases for GBS and the flu vaccine.
The U.S Court of Federal Claims provides a referral list of attorneys that specialize in representing clients wanting to file claims for vaccine damages. The list is here, and contains 123 attorneys.
One of the law firms representing clients in the Vaccine Court is Maglio, Christopher, & Toale. This law firm has actually listed cases they have settled in the past couple of years here.
From what appears to be some point in 2010 through 2013, they have settled 132 cases

Preliminary Results: Surveillance for Guillain-Barré Syndrome After Receipt of Influenza A (H1N1) 2009 Monovalent Vaccine — United States, 2009–2010
GBS incidence was calculated and compared for the vaccinated and unvaccinated populations, which were estimated by age group, using data from CDC’s Behavioral Risk Factor Surveillance System (BRFSS) and National 2009 H1N1 Flu Survey (NHFS) telephone survey data for the counties in the EIP catchment areas, using methods published previously (4). The total person-time of follow-up was calculated by multiplying the population under surveillance by the number of days since the start of surveillance, October 1, 2009. Person-time at risk for GBS in the vaccinated population was calculated by multiplying the number of vaccinees by 42 days (or the number of days from vaccination to the end of the surveillance period if <42 days) (1). Children aged 6 months–9 years who received a second dose of 2009 H1N1 vaccine were presumed to have received it 28 days after the first dose, as recommended by the Advisory Committee on Immunization Practices,¶ giving them an additional 28 days of person-time at risk. To calculate the corresponding person-time in the unvaccinated population, the person time at risk for GBS was summed among the vaccinated population and then subtracted from the total person-time of follow-up under surveillance.
Incidence among the vaccinated population was calculated by dividing the number of GBS cases vaccinated within the risk window by the total amount of person-time at risk following vaccination. Incidence among the unvaccinated population was calculated by dividing the number of GBS cases unexposed to vaccine or exposed to vaccine outside the risk window by the total amount of person-time unexposed to 2009 H1N1 vaccine. Bootstrapping methods were used to estimate 95% confidence intervals (CIs) for the rate ratios that incorporated the variance of vaccine coverage estimates (5). A Poisson distribution was assumed for the occurrence of cases and a normal distribution for the vaccine coverage estimates; the Mantel-Haenszel method was used for age-adjusted CIs. A temporal scan statistic was used to assess for any significant clustering in the interval between vaccination and illness onset in vaccinated cases (6).
During October 1, 2009–May 10, 2010, a total of 529 reports of potential GBS were identified by EIP, of which 326 met the GBS case criteria. Of the 326 persons with GBS, 27 had documentation of 2009 H1N1 vaccination in the 42 days preceding illness onset, 274 did not receive vaccine, and the vaccine status of 25 was either unknown (six) or pending ascertainment (19) (Table 1). Sixteen of the 27 (59%) with documentation of 2009 H1N1 vaccination also reported antecedent illness symptoms in the 42 days before GBS onset; 78% of unvaccinated persons with GBS (215 of 274) reported antecedent symptoms (p=0.04). No clustering among vaccinated persons was observed in the period between vaccination and illness onset (p=0.54). Among the 27 GBS patients with 2009 H1N1 vaccination, four required ventilator support, and one remained hospitalized 30 days after GBS onset; among the 274 GBS patients who did not receive 2009 H1N1 vaccination, 37 (14%) required ventilator support, and 34 (12%) remained hospitalized after 30 days. Eight (2%) of the 326 GBS patients died (from any cause); none of the eight had received the 2009 H1N1 vaccine within 42 days of illness onset.
Among patients hospitalized through March 31, 2010, comparison of the incidence of GBS among those who received 2009 H1N1 vaccine and those who did not receive the vaccine revealed an age-adjusted rate ratio of 1.77 (CI = 1.12–2.56) (Table 2). If this preliminary rate ratio is confirmed in end-of-surveillance analyses, the attributable rate of GBS would be 0.71 per 100,000 person-years, corresponding to an attributable risk of 0.8 excess cases of GBS per 1 million vaccinations.**

Risk of Guillain-Barré Syndrome Following H1N1 Influenza Vaccination in Quebec
RESULTS
During the active surveillance period, 61 possible GBS cases were reported to public health authorities. Seventy-seven possible GBS cases were retrospectively identified in the MEDECHO hospital admission database. Thirty-seven cases were found in both sources, for a total of 101 cases. For all 101, medical charts were retrieved and analyzed. Eighteen possible cases were excluded: 12 cases with a final diagnosis other than GBS, 2 recurrent GBS cases, 2 cases with disease onset before October 13, 2009, and 2 other cases with onset after March 31, 2010. Thus, 83 cases were included in the analysis. The overall GBS incidence rate in the study population, representing 3 623 046 person-years of observation, was 2.3 per 100 000.
Of the 83 confirmed GBS cases included in the analysis, 42 had been immunized before disease onset (1-121 days after immunization) and all had received the ASO3 adjuvant H1N1 vaccine. For 25 cases, disease onset was 8 or fewer weeks after the vaccine was administered and they were considered exposed, whereas the 17 other cases were immunized more than 8 weeks before disease onset and were considered unexposed. Thus, for the cohort analysis, 25 GBS cases were considered exposed and 58 cases were considered unexposed.
The characteristics of GBS cases according to exposure status are shown in Table 1. Forty-nine cases were classified in the Brighton level 1 category, 22 cases in level 2, and 12 cases in level 4. The distribution of cases according to diagnostic category was similar in exposed and unexposed cases. The percentage of male patients was 69%. The median age was 49 years (range, 1-89 years). The percentage of elderly patients was higher in the exposed group than the unexposed group. The majority of patients (96%) were hospitalized; 25% developed severe paralysis of the lower limbs and were unable to walk at some point; and 17% developed respiratory distress syndrome and required intubation and/or assisted ventilation. Four patients died, all of whom were older than 60 years. Conditions occurring within 1 month before GBS onset as reported in medical records included a respiratory tract infection or influenzalike illness in 36% of cases, gastroenteritis in 18%, and trauma in 4%. A history of infection during the month prior to hospitalization was less frequent in exposed than in unexposed patients. The median interval between disease onset and hospitalization was 5 days (range, 1-34 days).
Of the 83 confirmed GBS cases identified during the 6-month study period, 56 (67% of total) occurred during a 12-week period from October 18, 2009 (2009 Centers for Disease Control and Prevention [CDC] week 42) to January 9, 2010 (2010 CDC week 1). The cluster was mostly explained by cases occurring in persons who were recently (≤8 weeks) immunized (22/56). Details on the distribution of cases are provided in eFigure 1.