| The CDC's Wisdom
After
reading this you can just imagine how surprised I was when I found at the
CDC’s website devoted to the influenza vaccine, a recommendation for the
vaccine in the second trimester of
pregnancy. Click on pregnancy and read
this very reveling article by Dawn Richardson. This link below will take you to the
CDC's actual recommendations. When you have time go read it. It is 63 pages!
http://www.cdc.gov/mmwr/pdf/rr/rr5004.pdf
This vaccine contains 25
micrograms of ethyl Mercury in one dose. The CDC has studied 2000 pregnant
women and no adverse fetal effects were found. They state additional
studies are ongoing as data is limited with regard to the effects of low
dose or intermittent exposures. They also explain federal guidelines were
not designed for intermittent or bolus exposures. The CDC believes that the
average 110-pound woman is allowed to have 5 micrograms per day without
adverse reactions. If she were to get a flu shot and have a tuna fish
sandwich for lunch she would have just received 42 micrograms of Mercury,
eight times the safe level. The package inserts published by the flu
vaccine manufacturers state that "Animal reproduction studies have not been
conducted with
influenza
virus vaccine.” It is also not known whether influenza virus vaccine can
cause fetal harm when administered to a
pregnant
woman. If you look at the
MSDS
for Thimerosal, it says, "Exposure to
mercury in utero and in children can cause mild to severe mental
retardation and mild to severe motor coordination impairment." Eli
Lilly MSDS June 13, 1991.
Eli Lilly
is the
manufacturer of thimerosal. There have been no
safety studies done on
thimerosal since 1929 and that study was done by K.C.Smithburn on patients
dying from meningitis! Rhogam shots are another way
the fetus is subjected to mercury. In 2002 this shot was
"encouraged" for
6--23 month old children and continues to be encouraged. Vaccination of
children aged 6 months and older who have certain medical conditions also
continues to be strongly recommended. Maybe this isn't such a good idea..
Read here for some articles that might make you think twice before doing so.
Flu shots and
children. Children with chronic conditions such as cystic
fibrosis are often given the flu shot in hopes they will not come down
with the flu. In a recent
Cochrane study, the reviewers'
conclusions were as follows: There is currently no evidence from
randomized studies that influenza vaccine given to patients with CF is of
benefit to them.
Here is
a few excepts from an excellent article you shouldn't miss reading. It
explains how damaging mercury can be in the developing fetus.
This is the web
address for the complete article.
:
http://www.ewg.org/reports/bodyburden2
Don't miss it!
In a decades-long mercury poisoning disaster in Minamata,
Japan that began in the 1950s, some babies born to women who ate
mercury-polluted seafood died within days of birth, while their mothers were
free of symptoms. Autopsies revealed that in adults, mercury induced lesions
that were concentrated in a few areas of the brain. In the fetus, however,
mercury spawned lesions over nearly the entire brain cortex. In the decades following Minamata, scientists have developed
a much fuller understanding of children's vulnerability to chemicals,
discovering links between a host of health problems — including asthma,
childhood cancer, and brain damage — and such common contaminants as solvents,
pesticides, PCBs, and lead (Trasande and Landrigan, 2004). A recent National
Academy of Sciences study suggests that environmental factors contribute to at
least 28 percent of childhood developmental disabilities (NAS 2000a).
The latest research investigates not only relationships
between disease and exposures, but the root causes of chemically-induced disease
with in utero origins. This research pinpoints traits of a fetus that
contribute to vulnerability: low levels of some chemical-binding proteins in the
blood, immature excretion pathways, and an immature blood brain barrier, for
instance, which combine to increase the transfer of chemicals from the blood to
the aptly named "target organs" that may ultimately bear the harm. In the
article I found some really good reasons not to get a flu shot while pregnant:
 | An immature, porous blood-brain barrier allows greater chemical exposures
to the developing brain.
|
 | A baby's organs and systems are rapidly developing, and thus are often
more vulnerable to damage from chemical exposure.
|
 |
In the third trimester the mother's body dissolves
stored, maternal fat, shunting it to the baby through the blood, but with
this fat the child also receives the persistent pollutants clinging to it,
like PCB's, flame retardants, and dioxins.
|
 |
Some chemicals are directly toxic to an exposed child —
lead and mercury, for example, which harm a developing brain — while other
chemicals induce a chain of events that may culminate in a diagnosed
health problem later in life.
|
 |
Methylmercury exposure in the womb causes measurable
declines in brain function in children exposed to levels corresponding to
58 parts per billion in maternal blood (NAS 2000b). Researchers in the
Netherlands found a doubling in the risk of heart attacks and death from
coronary heart disease at methylmercury hair levels of 2 mg/kg, which
corresponds to about one fifth the assumed safe maternal blood level (Salonen,
et al. 1995). Increased diastolic and systolic blood pressure and
decreased heart rate variability in developmentally exposed children have
also been observed at doses below what the EPA considers a safe maternal
blood level (NAS 2000b, Sorensen et al. 1999).
|
 |
Methylmercury is toxic to the developing fetal brain,
and exposure in the womb can cause learning deficiencies and can delay
mental development in children. The U.S. Centers for Disease Control (CDC)
recently reported data showing that one of every six American women of
childbearing age already has mercury in her blood at levels that the
National Academy of Sciences considers potentially unsafe for the
developing fetus. Most women are exposed to methylmercury through seafood,
which accumulates the metal, much of which is released to the environment
from the burning of coal at coal fired power plants. High dose
methylmercury poisoning during development causes severe neurotoxicity,
including mental retardation in humans (NAS 2000b). Methylmercury also
causes developmental malformations and altered immune, reproductive,
cardiovascular and kidney function (NAS 2000b).
|
 | (Remember a flu shot has 25 micrograms of mercury) |
Here is an excerpt from an email on how thimerosal is disposed of....."A
large portion of these vaccines contain a chemical called "Thymerasol," a
mercury based preservative, as an ingredient. Because of this mercury
content, the returned material must be disposed of as hazardous waste. The
current method of disposal consists of throwing the individual vials of
vaccine, container and all, into 55-gallon drums which are in turn taken
off-site by a haz. waste disposal firm (this waste stream totalled 9,600
gallons in 1996, at a cost of $600/55-gallon drum)." The rest of the
letter is here....disposal
It
is interesting how the CDC personnel attempt to predict which viruses will
infect people in the United States. They decide based on a large amount of
guesswork, which influenza viruses are distributed to vaccine manufacturers
early in the year for influenza vaccine production for administration that
autumn. Flu shot history is replete with examples of poor matches between
influenza viruses in the vaccine and those actually infecting people.
Results for the 1989-1990 season were described as, "mixed at best" with
"Medicare payments significantly higher for those who had been vaccinated,"
according to Kidder and Schmitz in the 1993 report Options for the Control
of Influenza II. Read this article for next years shot info.
Flu Vaccine 2006-2007 Strains To Be Determined By Advisory Cmte. Feb. 17
(Today is Jan 26, 2006)
Influenza virus strains to be included in the vaccine for the 2006-2007 flu
season will be discussed by FDA’s Vaccines & Related Biological Products
Advisory Committee Feb. 17. During last February’s deliberations for
the 2005-2006 flu season, the committee recommended retaining the previous
flu season’s A/New Caledonia/20/99 (H1N1)-like strain and switching to an
A/California/7/2004 (H3N2)-like strain from the previous A/Fujian/411/2002-like
strain.
The committee also recommended keeping the same influenza B strain, the
Yamagata lineage B/Shanghai/361/2002-like strain. The committee also
suggested the development of a bivalent B strain vaccine for pediatric
patients, who do not get cross protection from a single B strain. Since last
year’s advisory committee meeting, two companies have entered the U.S.
influenza vaccine market.
GlaxoSmithKline
could launch two vaccines for the 2006-2007 season. FDA approved GSK’s flu
vaccine Fluarix in August. A month later, the firm announced plans to buy
Fluviral maker ID Biomedical; the company has said it hopes to have the
vaccine approved by the 2007 flu season.
Novartis also entered the flu vaccine market with its acquisition of
U.K.-based Chiron, which manufactures the flu vaccine Fluvirin. Fluvirin
manufacturing was halted in 2004 due to good manufacturing practice
deviations at its Liverpool facility. (Some nice words for sloppy
manufacturing) Chiron was cleared to recommence manufacture of the
vaccine in September. Other flu vaccines include Sanofi Pasteur’s Fluzone
and Medimmune’s intranasal FluMist.
To
give you an idea of how the flu virus is decided I will give you a little
background information. Virologists believe the whole thing starts with
birds. Waterfowl to be exact. They are what virologists call the "reservoir"
for influenza. They carry nearly all known types of influenza, with no ill
effects, and willingly share them with the rest of the animal kingdom
through their feces. All animals that get the flu, horses, ferrets, seals,
pigs, and human beings probably get it originally from birds. Viruses can
only infect and take over a cell if the proper "receptor" is present, and as
far as we know human beings do not have a receptor for avian or bird flu.
What's needed for human infection is another species that has both human and
avian flu receptors. In other words, the pig. Having both human and avian
receptors sets the pig up for all sorts of wonderful influenza
possibilities. The process can be as simple as a flu-contaminated duck
dropping feces into the dirt a pig is rolling around in, thus infecting the
pig who, in turn, passes the virus on to a farmer. It is possible for a pig
to be infected with one kind of flu, say a human flu, only to contract
another avian flu. Now the poor pig has two different types of flues
simultaneously. When it proceeds to re-infect a human being, it passes on a
pig-bird-human influenza.
Since the flu virus is
always mutating, necessitating a new vaccine each year, the World Health
Organization (WHO) has set up a vast international flu surveillance network.
Around the world, Technicians affiliated with the Centers for Disease
Control (CDC) collect influenza viruses from pigs and people in foreign
lands, e.g., China and take nose and throat cultures from patients suffering
from the flu. These samples are sent off to laboratories to be tested.
Suspect and interesting cases are forwarded to the Center for Disease
Control (CDC) or to the closest National Influenza Center for full analysis.
There are many such centers throughout the world. CDC personnel then attempt
to predict which viruses will infect people in the United States the
following year. Predicting which influenza viruses from China, for instance,
will infect people in Dayton, Ohio, a year later involves a great deal of
guesswork.
Analysis has shown that
there are three main families of the influenza virus; A, B, and C. Within
each of these families there are many viral strains. Both the A and B
families contain strains that cause illness, although the influenza A family
has more virulent strains than the B family. These families are further
categorized by the two types of proteins that make up the outer protective
coating of the virus. These proteins are known as hemagglutinin (h), and
neuraminidase (n). Viruses are named according to the type of proteins they
carry. Since there are at least fifteen varieties of h, and nine varieties
of n that can combine with each other in any way to create a different
strain, it is practically impossible for anyone to predict what might happen
with any kind of accuracy. Unless of course you are the CDC using your
crystal ball. Good explanation here by Jocelyn Kaiser in her article A
One-Size-Fits-All Flu Vaccine?
This is this years pick: 2002-2003
 |
A/Moscow/10/99(H3N2)-like
virus |
 |
A/New
Caledonia/20/99(H1N1)-like virus |
 |
B/Hongkong/330/01 |
Reading across starting with
the A. A stands for the virus in the A family Strain, the most virulent.
Moscow is the city or the name of the place where they were first isolated.
The 10 stands for the sample number of flu isolated from the people
infected. And the 99 stands for the year the virus was isolated. The H3N2 is
the No. 3 hemagglutinin, No. 2 neuraminidase. The types of proteins that
make up the outer protective coating of the virus. So, to sum this up
quickly, the mucus from the throat of ten Moscow citizens in 1999 will make
up the vaccine that will save you in whatever city you might live in 2002
from the flu. I guess they had a lot left over from last year because only
the Hong Kong portion is new.
Flu package insert
From the FDA's Website:
Influenza Virus Vaccine 2003-2004
The trivalent influenza vaccine prepared for the 2003-2004 season will
include A/New Caledonia/20/99 (H1N1); A/Panama/2007/99 (H3N2), which is an
A/Moscow/10/99-like virus; and B/Hong Kong/330/2001-like virus. (The actual
influenza B virus being used in vaccines is either B/Hong Kong/330/2001 or
B/Hong Kong/1434/02.) These viruses are the same as the viruses used for
production of vaccine for the 2002-2003 season. Vaccine produced for the
2002-2003 season is now past its expiration date. It is recommended that
vaccine not be used beyond its labeled expiration date.
More than 95 million vaccine doses were available although more than 15
million were never used.
This just in from the CDC:
Experts are also concerned about antigenic drift.
According to a notice sent out on the CDC's Health Alert Network, about a
third of influenza A viruses isolated worldwide have changed
genetically from the current strain in the vaccine, although it is unclear
whether this will have a clinical impact. (Uh oh wrong strain)
Fujian Strain
It gets worse. I will
explain
how the vaccine is
made. It is grown in
chicken eggs.
(New: some manufacturers have started using
caterpillar cells
) This is done by injecting a
microscopic droplet of the flu virus scraped from the throats of infected
pigs, birds or humans, into the air sack above the embryo and the yolk. In
two to three days time the original droplet has become a tablespoon full.
The tops of the eggs are lopped off and the virus is suctioned out. The
largest vaccine makers may use up to one hundred fifty thousand eggs at once
from which they extract two hundred and fifty gallons of pure virus. This is
added to a huge vat that then must be kept free of bacteria. Mercury as well
as the other toxic ingredients I have already mentioned are added to keep
this witch's brew stable. To produce adequate supplies of the vaccine, the
drug companies growing the virus must repeat this process dozens of times,
using millions of eggs. All of this takes at least 6 months.
"Richard Compans, a virologist and chairman of the Department of
Microbiology and Immunology at Emory University School of Medicine, said the
current egg-based vaccine technology has been used at least since the 1950s.
"It involves inoculating large numbers of fertilized chicken eggs with a
virus preparation, and harvesting the fluid from these infected eggs and
putting the vaccine through a purification procedure," he said. "There is
potential for introducing contaminants, particularly at the stage of
inoculating eggs and harvesting material from the eggs."
Contents of the Flu Vaccine 2004-2005
Both the inactivated and live, attenuated vaccines
prepared for the 2004–05 season will include A/Fujian/411/2002
(H3N2)-like, A/New Caledonia/20/99 (H1N1)-like, and
B/Shanghai/361/2002-like antigens. For the A/Fujian/411/2002 (H3N2)-like
antigen, manufacturers may use the antigenically equivalent
A/Wyoming/3/2003 (H3N2) virus, and for the B/Shanghai/361/2002-like
antigen, manufacturers may use the antigenically equivalent B/Jilin/20/2003
virus or B/Jiangsu/10/2003 virus. Influenza viruses for both the
inactivated and live attenuated influenza vaccines are initially grown in
embryonated hens' eggs. Thus, both vaccines might contain limited amounts
of residual egg protein.
On October 5, 2004, CDC was notified by Chiron
Corporation that none of its influenza vaccine (Fluvirin®) would be
available for distribution in the United States for the 2004-05 influenza
season. The company indicated that the Medicines and Healthcare Products
Regulatory Agency (MHRA) in the United Kingdom, where Chiron's Fluvirin
vaccine is produced, has suspended the company's license to manufacture
Fluvirin vaccine in its Liverpool facility for 3 months. Guess why? The
vaccine supply was contaminated with a bacteria
serratia marcescens. Guess what else? It
is
not the first time. Why would our FDA contract with this company? Read
about this same company with a different name at the time here:
Medeva.
Take a look at this article. Seattle's Virginia
Mason Medical Center is insisting their doctors and nurses be injected
with the flu shot or else! They have until Jan. 1 to get the shot, or get
fired! Forced
vaccinations
UH OH! Wrong strain again!
http://www.sfgate.com/cgi-bin/article.cgi?file=/c/a/2004/10/24/FLU.TMP
San Francisco Chronicle
Scarce flu vaccine not designed for new strain
New Zealand variety worries officials
Sabin Russell, Chronicle Medical Writer
Sunday, October 24, 2004

To read the CDC's "Recipe" For Fostering Public
Interest and High Vaccine Demand", go to:
http://www.iom.edu/Object.File/Master/21/674/0.pdf
commentary on the
"Recipe" here
According to Hugh Fudenberg,
MD., the worlds leading immunogeneticist and 13th most quoted biologist of
our times (nearly 850 papers in peer review journals), if an individual has
had five consecutive flu shots between 1970 and 1980 (the years studied),
his/her chances of getting Alzheimer's Disease is ten times higher than if
they had one, two or no shots. (1) Dr. Fudenberg said that it was due to the
mercury that is in every flu shot (and many childhood shots). The gradual
mercury buildup in the brain causes cognitive dysfunction. Is that why
Alzheimer's
is
expected to quadruple? (2)
(1) Dr. Fudenberg at the NVIC International
Vaccine
Conference, Arlngton, VA September 1997.
(2) John's Hopkins Newsletter Nov. 1998.
On December 6, 2000 at the
Fourth National Immunization Conference in Halifax, Nova Scotia, Dr. Eleni
Galanis of Health Canada reported that almost 1000 Canadians have suffered
adverse reactions to the flu vaccine since October, 2000. That's nearly 80
times as many as for the same period last year. The side effects for the
flu vaccine include
 | Soreness, redness, or swelling where the shot was given |
 | Fever (low grade) |
 | Aches |
You should not get the flu vaccine if you have ever had a severe allergic
reaction to eggs or to a previous flu shot or have a history of
Guillain-Barré syndrome (GBS).
GBS may be triggered by an infection. The infection that most commonly
precedes GBS is caused by a bacterium called Campylobacter jejuni. Other
respiratory or intestinal illnesses and other triggers may also precede
an episode of GBS. In 1976, vaccination with the
swine flu vaccine was
associated with getting GBS. One
possible cause is that flu vaccine contains
Campylobacter, said
Dr. Chen CDC's immunisation
safety branch. He said that the vaccine is made in chicken eggs and that
40-50% of chickens are infected with Campylobacter, which is difficult to
eradicate.
Instead of being an
effective prevention, evidence indicates that flu shots are useless and
can be dangerous. Although endorsed and funded by federal and state
governments the shots seem only to benefit the companies that make them,
public health bureaucrats who promote them, and medical personnel who
administer them. The CDC feels the benefit of
the influenza vaccine outweighs the potential risks for Mercury exposure.
How would you like to be
forced to have a flu shot? Click on
'forced' and take a look at this hospital requirement for employment.
Since July of 1999, the FDA
has "encouraged" manufacturers to
remove thimerosal from vaccines. Some have
done it, others have not. Today, most vaccines that are being manufactured do
not contain thimerosal, or they only contain a "trace amount" 0.5
micrograms. Unfortunately we do not know how many of the old thimerosal
products are still on the shelf.
Take a look at this chart from the CDC. Does
it look like the flu or pneumonia vaccine is helping?

The CDC says flu kills about 36,000 people every year in the United
States. But is this statement true? Read here for the facts.
The Flu Scare Game
. http://www.vaccinesafety.edu/thi-table.htm.
Here is what will be taking thimerosal's place.
2-Phenoxyethanol
Are preservatives like
thimerosal necessary in vaccines? The FDA regulations require preservatives
in multi-dose vials of most vaccines (with the exception of certain live
viral vaccines) to protect against inadvertent contamination from repeated
puncture of the seal. thimerosal does not prevent all bacterial
contamination, as evidenced by clusters of disease from group A
Streptococcus infections traced to multi-dose Diphtheria toxoid, Tetanus
toxoid, and Pertussis (DTP) vaccine vials that were contaminated after
opening.

"Straining to Find a Cure"
Financial Times (www.ft.com) (05/02/03) P. 14; Firn, David
Following analysis of the influenza virus in London, Melbourne, Tokyo,
Atlanta, Congo, and Madagascar, experts sent the most active and dangerous
strains to vaccine manufacturers in order to prepare for the next influenza
season. Fertilized hens eggs are used to create vaccines, which means
creating new mutations of the virus is a slow process. Researchers at
Solvay Healthcare in the United Kingdom are attempting to speed up the
process by using canine kidney cells grown in tissue culture to
produce the flu virus, which could cut production from six months to just
six weeks.

Scientists
are launching a research study to check the effectiveness of a new type
of flu vaccine that is made differently than the conventional vaccine,
which is grown in eggs. The experimental vaccine instead relies on a cell
line drawn from insects known as silk moths, which are better known for
their role as
pests attacking crops such as corn, cotton, barley and alfalfa. Producing
biological products in insect cell lines is common; the hepatitis B
vaccine, for instance, is produced by human cell lines, and scientists
from Rochester have developed an experimental vaccine against human
papilloma virus using an insect cell line.
To
read the whole article click on the Moth. I wonder what kinds of problems
will be associated with moth RNA and DNA injected into the human body.
Flu shots are also contraindicated when
you are taking certain other drugs. Check out this article to see the
drugs.
Interactions with flu shot
This just in...they have decided on next
years vaccine.
The 2005-06 trivalent vaccine virus strains
are A/California/7/2004 (H3N2)-like, A/New Caledonia/20/99
(H1N1)-like, and B/Shanghai/361/2002-like antigens.
For the A/California/7/2004 (H3N2)-like
antigen, manufacturers may use the antigenically equivalent A/New
York/55/2004 virus, and for the B/Shanghai/361/2002-like antigen,
manufacturers may use the antigenically equivalent B/Jilin/20/2003 virus or
B/Jiangsu/10/2003 virus.
Guess they called the physic hotline to get
the strains!
Here is what Dr Tom Jefferson had to say
about the vaccine: "The vaccine doesn't work very well at all," said study
author Dr. Tom Jefferson, an epidemiologist with the Cochrane Vaccines Field
in Rome. "Vaccines are being used as an ideological weapon. What you see
every year as the flu is caused by 200 or 300 different agents with a
vaccine against two of them. That is simply nonsense." The Cochrane
Review Group also found that the vaccine is only 28% effective when given to
people over 65.
http://www.wjla.com/news/stories/0905/262242.html
.."The findings are similar to those of a study done by U.S. National
Institutes of Health that found flu shots for the elderly in the United
States had not saved lives.
However, the World Health Organization and the U.S. Centers for Disease
Control and Prevention said the findings, published Thursday on the Web site
of the Lancet medical journal, do not change their recommendation that
elderly people get the shots."
HUH?
Here is the rest of the article:
Study
Sheds Doubt on Usefulness of Flu Vaccine
On this website the ingredients are listed:
http://medguides.medicines.org.uk/displaypage.aspx?t=medicine&i=53
|
Ingredients
|
|
If you are not able to take something that is listed
below for your form of Fluarix, or you have reacted badly to Fluarix
before, do not take Fluarix. Talk to your prescriber, pharmacist or
nurse at once and check that they still want you to have Fluarix.
Split influenza virus,
inactivated, each 0.5ml
dose containing antigens* equivalent
to
 | A/Fujian/411/2002 (H3 N2) - like strain: A/Wyoming/3/2003 X -147.
15 micrograms** |
 | A/New Caledonia/20/99 (H1N1) - like strain: A/New Caledonia/20/99
IVR-116. 15 micrograms** |
 | B/Shanghai/361/2002 - like strain: B/Jiangsu/10/2003. 15
micrograms** |
*propagated in eggs
**haemagglutinin
|
Good news about the flu
Read this article
for a good understanding of the live virus vaccines. This is an experiment
with the avian flu going on right now at John Hopkins.
New flumist
If you are still thinking
you want a flu shot watch this video!
The name to click on is "Eye on the flu"
The panel recommended that vaccines to be used in the
2006-2007 season in the U.S. contain the following:
 | an A/New Caledonia/20/99 (H1N1)-like virus; |
 | an A/Wisconsin/67/2005 (H3N2)-like virus
(
A/Hiroshima/52/2005strains); |
 | a B/Malaysia/2506/2004-like virus
(B/Ohio/1/2005 strains) |
®
®
,
Same ingredients as last year. Look at what the AMA
is telling doctors.....
Flu shots for everyone, all year, any time just use them
up! Think outside the box when referring to flu season,
don't let the calendar dictate the push to vaccinate.
http://www.ama-assn.org/amednews/2007/05/14/hlsb0514.htm
Abundance of flu shots may mean longer vaccine season
With 132 million doses of influenza vaccine possible
next season -- the most ever -- the challenge will be to
use it all.
By Susan J. Landers, AMNews staff. May 14, 2007.
Washington -- Broaden the flu vaccination season --
starting in September if possible -- and keep giving the
shots beyond Christmas, advised public health officials
and medical society representatives at a recent meeting.
With an abundant vaccine supply expected for the
upcoming flu season and additional manufacturers
to help stabilize the supply, physicians should
incorporate some new tactics to battle seasonal flu. The
calendar shouldn't run this show, concluded participants
at the 2007 National Influenza Vaccine Summit held last
month in Atlanta. The event, sponsored by the American
Medical Association and the Centers for Disease Control
and Prevention, occurs at least annually.

Go to this website and check this out...http://www.testmed.com/home/content/view/14/23/
This year's flu vaccine 2007 contains the following
3-strains: A/Solomon Islands/3/2006 (H1N1)-like (new for
this season), A/Wisconsin/67/2005 (H3N2)-like, and
B/Malaysia/2506/2004-like viruses.
The flu vaccine offers a 6 to 8 month window of
protection. Initial immunity is approximately 50% upon
receiving the vaccination, with full immunity within 2
weeks.
50%? Approximately? You have got to be kidding!
Watch this video
http://www.youtube.com/watch?v=3g5fxGu3Cxc&mode=related&search=
Here we go for next year. The date is March 4, 2008. The
predictions begins.
http://newsminer.com/news/2008/mar/04/feds-set-recipe-next-years-vaccine
CDC and international authorities expect Brisbane/10, a
version of the H3N2 flu, to still be around next year.
They predict a second new Type A strain, known as
H1N1/Brisbane/59, also will hit, along with a newer Type
B/Florida strain, prompting Thursday’s decision to put
all three in next year’s vaccine.
The panel recommended that vaccines to be used in the
2008-2009
influenza season in the U.S. contain the following:
* An A/Brisbane/59/2007 (H1N1)-like virus
* An A/Brisbane/10/2007 (H3N2)-like virus
* A B/Florida/4/2006-like virus
Are people waking up? Check this out...No
flu shot?
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