Subject: more swedish nurse vaccine deaths
From: Keith R
Date: Sun, October 25, 2009
Hi Ken,
I read this a.m. that Germany is in an uproar on a preferred safer
vaccine being administered to health care workers and top government officials
called Celvapan.The German Chancellor Angella Merkel expects to see one third of the
German population receive the GSK version of the vaccine known as Pandemrix.
Google
"Dying Swedish nurses, swine flu vaccine " to discover 4 have died in the last several days and 190 are
very sick, many with severe reactions hours after the shot.
Merkel claims she will
receive the Pandemrix version to show the public it is safe after all. How nice it
would be to provide the assistance. Interesting how these figureheads think we are so
naive to believe a word that comes out of their mouth. A common belief worldwide is
growing - more and more people are learning about this insanity. Uniting together to
resist this effort to poison and kill is gaining momentum.
Links for articles pertaining to these comments can be found at
FOURTH PERSON DIES IN SWEDEN FROM SWINE FLU JAB: NO END IN SIGHT
Saturday, 24 October 2009 11:30
News - Highlighted News
The news that a fourth person has died after taking the "swine flu" jab in Sweden is focussing attention on the failure of the Swedish Medical Products Agency (MPA) to halt the "swine flu" programme even as reports of serious side effects flood in.
The Swedish drug regulator has allowed the "swine flu" jab campaign to be launched even though there is no safety or efficacy data on the vaccine. GlaxoSmithKline's Pandemrix with mercury and squalene has been given approval under new and lax European Union regulations formulated by the European Medicines Agency, (EMEA) for a "pandemic emergency" that do not require safety or efficacy data.
The EMEA derives three-quarters of its funding from pharmaceutical companies.
The "swine flu" jab has been authorised for use only on condition that governments and companies implement "post-authorisation" studies to check it is safe and effective. However, the MPA in Sweden appears to have limited its role in collecting data on death and damage to spontaneous reports from doctors and patients.
In addition, there appears to be no accurate data available on how many people have been given the "swine flu" jab in Sweden.
The MPA has said it has no such data and the SMI has said that its system for collecting data on vaccines is flawed.
EU's own guidelines on "post authorisation" studies highlight the need to collect accurate data on "vaccine exposure".
Quote:
two people have dropped dead in sweden after taking the „swine flu“ vaccine, the swedish newspaper aftonbladet reported yesterday.
Gunillla sjolin-forsberg from Sweden’s medical product’s agency (Läkemedelsverket) said that a man in his fifties died 12 hours after receiving the pandemrix „swine flu“ shot, which is made by glaxosmithkline.
A 65-year-old women died two days after receiving the „swine flu“ jab, according to aftonbladet.
The deaths were reported within days of the launch of the country’s mass „swine flu“ vaccination programme.
Glaxosmithkline’s pandemrix vaccine, which contains the adjuvant squalene, is classified as bioweapon by eu and us regulators according to a biopharma databas.
According to the Swedish newspaper Expressen, 190 nurses reported suffering serious side effects after receiving the „swine flu“ shot. Side effects reported include extreme pain in the arm at the point of injection, an inability to sleep after injection; profuse and continuous nausea and vomiting; falling blood pressure, severe headaches, fainting, fevers, muscle aches.
A swedish nurse who took the shot wednesday a week ago told Expressen:. "my whole body was shaking. It was so bad I couldn’t even hold a glass of water in my hand.”
Another nurse, Jennaly, could hardly walk five meters after being sick following the “swine flu” vaccination. She was completely healthy before taking the shot but the following day she had a fever of 39 degrees [celcius].
“I could hardly go five meters to the bathroom,” she said.
The fever lasted three days. Many of her colleagues who took the jab suffered from similar side effects.
“I know of at least ten who got fever. We are 80 people where I work.”
Rebecka Andersson, the first person in Sweden to be vaccinated, said she got a fever and felt sick.
"I lost all my strength,“ she said. "I am never sick so it was the vaccine in my case."
Her classmates were vaccinated at the same time. Five of the 19 became sick through the „swine flu“ jab.
Sjolin-forsberg said in a phone interview with theflucase.com today, Friday, that the agency had officially received only100 reports from doctors and another 100 from patients so far about side effects, but she admitted that the agency’s data on side effects were not up to date and collected on a weekly basis and that the agency relied on „spontaneous“ reports.
Six of these reports were classified by the agency as serious, she said. Among this group were people who were hospitalised as a result of allergic reactions to the jab.
She indicated that the "swine flu" jab was not responsible for the death of the man in his fifties but that heart disease was.
However, the jab was targetted at sick people on the grounds that it is supposed to help people not kill them.
There is no clinical data on the impact of the jab on pregnant women and children even though these are also target groups.
It is not clear how many people in Sweden have received the swine flu jab so far.
Sjolin-forsberg said that 500,000 doses of the vaccine had been delivered, but that the agency had no data on how many "swine flu" shots had actually been administered.
The Swedish Infectious Disease Control Agency, SMI, responsible for collecting the data of vaccinations said that their system for tracking vaccinations, Svelak, covered only some hospitals, and there was, therefore, no system in place for collecting comprehensive data.
The SMI press spokesperson Aase Sten could not be reached by phone at the time of writing this report.
Pandemrix, like all other swine flu jabs, has been given approval by the EMEA under special emergency pandemic regulations that do not require the drug to be tested for "safety and efficacy“ before it is administered as long as studies are carried out after it is administered.
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