Impfungen
Dr Elizabeth Wright Hubbard: It took considerable experience for me to be convinced that the chronic constitutional remedy is the best prophylactic.
Siehe: Papilomavirus für eine fundierte Meinung über eine bestimmte Impfung.
Effects of vaccination:
Apis: Sudden puffing up of whole body
Malan.: Dry rough skin remaining for years after vaccination.
Sil.: Abscesses or convulsions (also Thuja). Abscess in axilla, whole arm swollen, backache, nausea.
Mez.: Eczema and itching
Sars. Blood purifier after vaccination. Itching eruptions on face and skin.
Ant-t.: When Thuja fails and Silica is not indicated.
Sulph.: When Sulphur symptoms prevail.
Sep.: When Sepia symptoms prevail
To prevent side effects Hyp./Led.
Attenuierter Lebendimpfstoff
Lebendimpfstoffe enthalten abgeschwächte (attenuierte) Viren/Bakterien, die sich noch vermehren können und eine Immunantwort auslösen, in der Regel jedoch keine Erkrankung. Ein attenuierter Lebendimpfstoff ist in der Regel deutlich wirksamer als ein Totimpfstoff.
In seltenen Fällen kann es nach der Anwendung eines solchen Impfstoffes bei der möglichen Vermehrung der Erreger zu einer Mutation in Richtung der nicht abgeschwächten Ausgangsform kommen, durch die dann doch die Erkrankung eintreten kann. Beispiele hierfür sind die in Europa aufgegebene Polio-Schluckimpfung (hat sehr selten Impfpoliomyelitis ausgelöst), der MMR-Impfstoff/BCG/Gelbfieber.
Zur Typhus-Impfung stehen sowohl Lebend- als auch Totimpfstoffe zur Verfügung.
Lebendimpfstoffe werden unterschieden in
1. kälte-adaptierte Stämme, die sich nur bei Temperaturen um 25 °C vermehren können, was die Viren auf die oberen Atemwege beschränkt, und
2. temperatur-sensitive Stämme, deren Replikation auf einen Temperaturbereich von 38 - 39°C beschränkt ist; es kommt auch hier nicht zum Befall der unteren Atemwege.
Totimpfstoff
Totimpfstoffe enthalten inaktivierte o. abgetötete Viren o. Bakterien o. Teile von Viren/Bakterien/Giftstoffen. Diese können sich im Körper nicht mehr weitervermehren oder vergiften, wie es das Tetanospasmin könnte, Aber sie lösen ebenfalls eine Abwehrreaktion (Immunreaktion) aus.
Beispiele sind die Toxoidimpfstoffe und Impfstoffe gegen Influenza/Cholera/Beulenpest = Haffkine/Hepatitis A./Masern/Mumps/Röteln/Typhus.
1. Toxoide: = entgiftete Toxine krankheitserregender Mikroorganismen. Diese Impfstoffe werden
verwendet in denen Toxine die Krankheitssymptome verursachen, nicht die Erreger selbst (Tetanus/und Diphtherie).
2. Inaktivierte Ganzpartikelimpfstoffe: Inaktivierung der Viren mittels einer Anwendung von Formaldehyd + beta-Propiolacton + Psoralen
3. Teilpartikelimpfstoffe: Zerstörung der Virusoberfläche mit Detergentien/starken organischen Lösungsmitteln
4. Untereinheitimpfstoffe o. Spaltvakzine: Oberfläche wird vollständig aufgelöst und spezifische Komponenten (Hämagglutinin- und Neuraminidase-Proteine) herausgereinigt. Eine andere Möglichkeit besteht darin, die Untereinheiten rekombinant herzustellen. Untereinheitimpfstoffe sind wenig immunogen mit geringen Nebenwirkungen.
The live Mycobacterium tuberculosis vaccine developed by Calmette and Guérin is not made of a contagious strain, but contains a virulently modified strain called "BCG" used to elicit immunogenicity to the vaccine.
Toxoid vaccines are made from inactivated toxic compounds that cause illness rather than the micro-organism. Examples of toxoid-based vaccines include tetanus and diphtheria. Toxoid vaccines are known for their efficacy. Not all toxoids are for micro-organisms; for example, Crotalus atrox toxoid is used to vaccinate dogs against rattlesnake bites.
Jedes 4e Jahr ist der Grippeimpfung nicht die reale Umständen angepasst.
Informationen:
www.impfschäden.info.de
1. The
problem of vaccinations and new vaccine preparations:
We must try
to understand why a child is oversensitive and then expose the practical
attitude to our everyday practice.
Suggestions
proposed by Madeleine Bastide, professor in immunology University of
Montpellier.
* 1st the
adverse effects obtained with certain vaccinations (Hepat B) are due to certain
relationships between viral antigens and self antigens.
* 2nd the
special method of preparing the vaccinating antigene (producer cells) may be
responsible for the wrong response of the body to the vaccination. Producer
cells are the basis for the fabrication of the latest vaccinations. The Hep B
vaccination is cultivitated on cancerous, undifferential cells called producer
cells.
* 3rd the
organism is not capable of analysing the" strangeness" of those new
vaccinations/so producing a self-immune response.
Now back to
the origins of the vaccinations and Pasteur’s initial approach.
Sure
Pasteur’s attitude to vaccination is now been totally bypassed/swept away.
Pasteur worked on a real identity: the vaccine itself was the pathogenetic
agent, and it was diluted or killed and simply attenuated. This is different in
the new vaccinations. They are genetically engineered/cultivated on producer
cells/the pathogenic agent is not found in these vaccination.
Pasteur’s
principle of identity has been abamdoned and so the immunity system has to
adapt to a certain extent and sometimes it responds in a perverse way. This
explains the greater number of accidents linked to vaccination (connected with
self-immune diseases).
There is a
real problem with the new vaccinations.
The new
vaccination against Hep A/Pert tends to improve with each personal vaccination,
but the immunity system can only try to adapt as much as it can take and
adverse effects may multiply.
Vaccination
should only be done when there is a complete agreement between the physician
and the patient. This explains why the character of legal obligation is not
really acceptable from point of view of the patients freedom. We live in
democracies/each family should be able to evaluate the advantage/risk ratio, as
in other pathologies, decide on the vaccination or not.
Pert. has
been implicated in the causation of juvenile onset diabetes as the vaccine acts
directly on the islets of Langerhans/BCG is compulsary only in France (last country
in Europe). It is an interesting example because the incidence of this
pathology in France is the same as in countries where the vaccination is not
compulsary.
Vaccination
program must be discussed with the parents/it concerns their children and help
them to take all aspects in consideration. A vaccination program should be set
up for their child as it is very important for their health, and each child is
different and needs a different approach.
To cure
cases of oversensitive reaction to vaccinations we can give antidotes to
vaccination.
In a
certain way we reverse what Pasteur would have done 100 years ago on the
perverse effects of the vaccination in order to have an adequate response to
vaccination.
We realise
in pediatrics that most of our patients with immunological disorders or
allergic states, need antidotes to their vaccinations to allow the action of
the similimum.
If the
bloquage state caused by vaccination on a sensitive organism is not taken away
by antidote, the result of a well prescribed remedy will have no effect.
As a
conclusion to these frequent problems, it seems important to remember here that
vaccinations initially have brought progress and relief for severe diseases
(small pocks!/Polio/Tetanus).
But
vaccination can not solve all our health problems/multiplying sophisticated
vaccinations is leading to saturation of our immunities.
It is also
important to consider that cancers/self immune diseases/AIDS are deeply linked
to saturation of immunity.
Immunology
as a speciality must be considered the most holistically as possible. Its
comprehension and function should lead to a very different way of healing and
open way to giving alternative medecines their proper place in this field.
2°
Immunology and homeopathy:
We all know
that the immune system has a function of defense.
It is a
system less systemisable as its anatomical and functionnal process is present
in the whole body (thymus/marrow/ganglions).
This
explains why several unconventional therapies, far from a mechanical allopathic
therapy, seem esp. well adapted to correcting the impairments of the immunity
system.
3 fundamental points that can help us to
understand this:
* The
immunity system of mamals is totally adapted to defending its own biological system/it
is a hybrid system: ½ mechanical + ½ informational/it can produce double-faced
molecules seving as mediators between mechanics and information (cells that
have a function of representing the outside world to the body).
* The
immunity system that works on the model of the identy law (meaning pain curing
pain) and that adapts to the defense processes of the virus or the bacteria
that is different from it, can then develop wrong responses when vaccinations
are made with cells identified as agressor (virus/bacteria)
But if the
law of similarity seeks to recognise strangers, maybe the components of the
vaccinations do not represent sufficently the agressor . Therefore the immune
system can reply in a perverse way (self immune
disease or allergy).
Vakzins
Attenuation
(abgeschwächt) reduces the virulence of a pathogen, while keeping it viable (or
'alive')
Ist
counterpart is a vaccine produced by 'killing' the virus (= inactivated)
Examples of
live vaccines include:
* viral: polio vaccine (Sabin
vaccine), Morb. Pert. rubella vaccine/Varicellinum o. Varicell (= chicken pox vaccine)/yellow fever
vaccine
* bacterial: BCG vaccine, typhoid
vaccine
Viruses may
be attenuated via passage of the virus through a foreign host, such as: tissue
culture/embryonated eggs/live animals/the initial viral population is applied
to the foreign host. In all likelihood one of these will possess a mutation
that enables it to infect the new host. However this mutant will normally have
a lower virulence in the original host, as the rest of the genetic information
for interacting with the host hasn't changed, enabling it to infect them, but
cause less damage, and so it acts as a vaccine/in an attenuated vaccine live
virus particles with very low virulence are administered/they will reproduce,
but very slowly/they do reproduce and continue to present antigens beyond the
initial vaccination, so boosters are required less often. These vaccines are
produced by growing the virus in tissue cultures that will select for less
virulent strains, or by mutagenesis or targeted deletions in genes required for
virulence. There is a small? risk of reversion the virulence, this risk is
smaller in vaccines with deletions. Attenuated vaccines also cannot be used by
immunocompromised (= mit geschwächtem Immunsystem) individuals.
Advantages
of attenuated vaccines: activates all phases of the immune system (for instance
IgA local antibodies are produced)/provides more durable immunity; boosters are
required less frequently/low cost/quick immunity/easy to transport/administer
Disadvantages
of attenuated Vaccines: Secondary mutation can cause a reversion to
virulence/can still cause disease, particularly in immunocompromised patients
(AIDS)/can be difficult to transport due to requirement to maintain conditions
(i.e. temperature) at which the virus can "survive".
*
Self-immunity can have a mechanic explanation by the presence of true cross
reactions against bacteria which, by provoking antibodies responses would give
way to self-immune disorders through antigenic patterns.
In a
different approach, to global awareness, it can be a deeper disease in the
organism, with a true loss of identity of the patient, who’s immunity system in
its function of protection of the living can no longer differentiate, the self
from the extraneous agressors.
The
elimination process would therefore be this error in identification on what an
agressor can be.
We must try
and go ahead in our thinking and learning of homeopathy and realise how to feed
the fire (sulfur fire of course): this will then leed us to entire
satisfaction.
Tinus Smits († 27-4-2010)
‡
Folgendes hat
anthroposofische Einschlüße ‡
Frei nach: Hans-Ulrich Albonico, M.D.
Swiss Campaign against Measles, Mumps and Rubella Immunization
When the campaign was initiated in 1987, the USA was cited as an example because 20 years of enforced vaccination in the States had reduced the incidence of measles by 99%. Recent developments in the USA give pause for thought, however.
Major measles epidemics have developed repeatedly since 1982. Adolescents are increasingly affected, in spite of vaccination, and so are infants, because mothers no longer confer adequate immunity. Childhood diseases are more dangerous for both these age groups than for other children. According to official statements, measles mortality has increased by a factor of 10 in the USA. American experts refer to this as an unexpected and partly inexplicable development. Warning voices are increasingly heard among vaccination experts.
It may be said that the incidence in the U.S. is still much lower than in the period preceding the mass immunization campaign. One thing is abundantly clear there are compulsive elements to the MMR immunization campaign that inevitably intervene profoundly in the sphere of the individual. When obligatory immunization had enforced high levels of compliance in many places, the unexpected epidemics necessitated rigorous measures including quarantaine, exclusion from school, house-to-house immunization. MMR re-immunization has already been made obligatory. Similar reports are coming from other countries with high immunization rates.
Recent investigations in Switzerland and other countries have also shown that in practice it is impossible to eradicate measles, rubella and mumps. This deprives MMR vaccination strategies based on mass immunization of young children of any kind of rational basis.
In Switzerland, measles, rubella and mumps cannot be said to represent an emergency situation that would justify such rigorous government intervention. Prevention of the serious complications of these three childhood diseases relates to three entirely different spheres, and a single combination vaccine cannot do justice to these.
The Medical Group for Differentiated MMR Immunization and the Groupe Medical de Reflexion sur le Vaccin ROR are not against immunization as such. They do, however, advocate a cautious approach, taking account of the individual situation and of the specific problems of each of the three childhood diseases, avoiding fundamental changes to their epidemiology and respecting parents' freedom of decision.
The critical studies of the Swiss MMR immunization campaign published in the two papers mentioned below result from three years of fundamental research done by the Medical Group for Differentiated MMR Immunization and the Groupe medical de Reflexion sur le Vaccin ROR. Essentially they base on the following:
- Documents from the Swiss Federal Department of Health (BAG) relating to the MMR campaign, especially information material for the medical profession issued in 1987 and 1989.
- 30-page correspondence between the Group and BAG.
- Detailed study of the specialist literature on the subject.
- A. Tschumper and Th. Abelin's study of the literature entitled Die Impfstrategien gegen Masem, Mumps und Roetein (MMR-Impfung) im Lichte der epidemiologischen Literatur. Bern, December 1988.
- Correspondence and discussions with experts in Switzerland, Germany, the USA - esp. the US Centers of Disease Control (CDC) - on the subject of protective immunization, and Prof. Dr. D. Jachertz in Bern (on matters of epidemiclogical concern).
- The professional experience of the c. 240 physicians in the two groups.
The Medical Group for Differentiated MMR Immunization (est. in 1987) and the Groupe Medical de Reflexion sur Ie Vaccin ROR (est. in 1988) include c. 240 Swiss medical practitioners whose aim is to gain acceptance for a differentiated MMR immunization practice.
The fundamental aspects are presented in leaflets for parents published by the groups which are entitled "Masem-, Mumps- und Roeteln- Impfung - Warum die Eitern mitentscheiden sollen" and "Vaccination ROR - Parents vous etes con-ceme's" (MMR immunization - why parents should have a part in the decision). They may be obtained from the Secretariat, Postfach 3009 Bern, Switzerland.
Smallpox = Pocken
Tb. have been
linked to the smallpox vaccine.
Iimportant
in understanding the significance of smallpox vaccination is that smallpox and
other communicable diseases were declining before vaccination programs were
enforced. This may be attributed to the sanitation reforms and nutritional
teachings instituted around the mid-1800’s as much as to the vaccination
programs as these other communicable diseases, for which there was no
vaccination, were also declining at the same rate.
However the
incidence of smallpox actually increased once vaccination programs were
instituted. In Jenner’s time, there were only a few hundred cases of smallpox
in UK. After more than 15 years of mandatory vaccinations, in 1870/1871 alone
more than 23.000 people died from the disease. Later, in Japan, nearly 29.000
people died in 7 years under a stringent compulsory (re)vaccination program.
This
increase in smallpox deaths was associated with a noticeable lack of protection
- not the best combination of events. In Germany over 124.000 people died of
smallpox during the same epidemic. All had been vaccinated. Additionally,
(unaltered) hospital records consistently show that about 90 % of all smallpox
cases occurred after vaccination.
This lack
of efficiency and increase in disease incidence, while other communicable
diseases were declining, led to the refusal of smallpox vaccination by some
countries. This resulted in a drop of the incidence of the disease that is
quite remarkable. In Australia, when 2 children died from their smallpox shots,
the government terminated compulsory vaccinations. As a result, smallpox
virtually disappeared in that country (3 cases in 15 years). When UK began to
reject vaccination, then the incidence of smallpox deaths decreased
accordingly.
Assumed is
that vaccination has made a difference in incidence. Facts: from 1923 to 1953,
before the Salk killed-virus vaccine was introduced, the polio death rate in
U.S. and UK had already declined on its own by 47% and 55% respectively.
Statistics show a similar decline in other European countries. When the vaccine
became available, many European countries questioned its effectiveness and
refused to systematically inoculate their citizens. Yet, polio epidemics also
ended in these countries as well.
Additionally,
as with smallpox vaccine, the number of reported cases of polio following mass
inoculations with the killed-virus vaccine was significantly greater than
before mass inoculations. Though these facts are readily available, the mass
vaccination against polio has continued with the result that most of the cases
of this dread disease are now attributed to the vaccine.
In 1976,
Dr. Jonas Salk testified that the live-virus vaccine, used almost exclusively
in the US since the early 1960’s, was “the principle if not the sole cause” of
all reported polio cases in the US since 1961.
The Federal
Centers for Disease Control recently (Feb. 1992) admitted that the livevirus
vaccine has become the dominant cause of polio in the US today. According to
CDC figures, 87% of all cases of polio between 1973 and 1983 were caused by the
vaccine. More recently, from 1980 through 1989, every case of polio in the U.S.
was caused by the vaccine. During this same time period, 3 of 5 people that
caught polio during foreign travel were previously vaccinated against the
disease.
Begleitend zu Polioimpfung: Sagitario sagitifolia,
Is very
similar to canine distemper. The measles vaccine was introduced in 1963, yet in
the U.S./U.K.from 1915 to 1958, a greater than 95 % decline in the measles
death rate had already occurred. In addition, the death rate from measles in
the mid-1970’s (which was several years post-vaccine) remained exactly the same
as in the early 1960’s (pre-vaccine), e.g.,
.03 deaths per 100.000. Again, the efficacy of vaccination in prevention
of this disease has not been established. According to a study conducted by the
W.H.O., chances are 14x greater that measles will be contracted by those
vaccinated against the disease than those who are left alone. According to Dr.
Atkinson of the CDC, “measles transmission has been clearly documented among
vaccinated persons. In some large outbreaks.... over 95% of cases have a
history of vaccination...”
In
addition, of all reported cases of measles in the U.S. in 1984, more than 58 %
of the school age children were “adequately” vaccinated. In 1985, the federal
government reported 1.984 non-preventable cases of measles. But 80% of these so-called
“non-preventable” cases occurred in people who had been properly vaccinated.
More recent outbreaks continue to occur throughout the country,
sometimes
among 100% vaccinated populations. In spite of the evidence for lack of
efficacy of this vaccine it is still strongly promoted. This continued use of a
useless vaccine, is not without its price. It has been determined that the
measles vaccine may cause ataxia/learning disability/retardation/aseptic
meningitis/seizure disorders/paralysis/death. It has also been investigated as
a possible cause of or cofactor for MS/Reye’s syndrome/Guillain-Barre
syndrome/blood clotting disorders/juvenile-onset diabetes.
Another
additional harmful effect is that the disease has changed form, and now affects
primarily a different age group. The peak incidence of measles no longer occurs
in children, but in adolescents and young adults. The risk of complications of
pneumonia (3%) and liver abnormality (20%) have increased as a result.
Before the
vaccine was introduced, it was extremely rare for an infant to contract
measles. However by 1993 more than 25 % of all measles cases were occurring in
babies under 1 year. Centre for Disease Control anticipates a worsening of this
situation and attributes it to the growing number of mothers who were
vaccinated during the last 30 years and therefore have no natural immunity to
pass on to their children.
Whooping
Cough (Pertussis)
Pertussis
vaccine been connected with juvenile onset diabetes as the vaccine acts
directly on the islets of Langerhans (=
insulin-secreting parts of the pancreas).
1.
hypoglycæmia, 2. diabetes. This emphasises the link between candidiasis and
diabetes + Cand assimilating/fermentating sugar. Use of Foll. successfully in
candidiasis underlines the connection with female sex hormones.
Incidence
and severity of whooping cough had begun to decline long before the pertussis
vaccine was introduced in the 1940’s. From 1900 to 1935, in US/UK, before the
pertussis vaccine was introduced, the death rate from pertussis had already
declined by 79 % and 82 %, respectively.
Some
studies indicate that the effectiveness of the pertussis vaccine may be as low
as 40- 45 + evidence indicates that immunity is not sustained. During an
epidemic in 1978, of 85 fully vaccinated children, 46 (= 54%) developed
whooping cough.
During a 10
month period in 1984, the state of Washington reported 162 cases in age 3
months to 6 years, 49% had been fully vaccinated against the disease. In the
same year, of the 560 cases reported to CDC in the age bracket of 7 months to 6
years with known vaccination status, 46 % had received vaccine protection. In
1986, in Kansas, 1300 cases of pertussis were reported. Of the patients whose
vaccination
status was known, 90 % were “adequately” vaccinated.
There are
several known or suspected harmful effects from this vaccine. Includeding SIDS
(Sudden Infant Death Syndrome - research shows that children die at a rate 8x
greater than normal within 3 days after getting a DPT shot), encephalitis (the
pertussis vaccine is used in animal experiments to help produce anaphylactic
shock/to cause an acute auto immune encephalomyelitis), retardation and
learning
disorders/fever as high as 106 degrees - with pain/swelling/diarrhea/projectile
vomiting/sleePY/high-pitched
screaming/inconsolable crying bouts/seizures/convulsions, collapse/shock.
In the 20
months prior to July 31, 1992 - 250 deaths and 7,200 adverse reactions linked
to whooping cough vaccinations had been reported to CDC. In addition, the US
Public Health Service announced that as of Nov. 16, 1992, some 3,200 pertussis
vaccine claims against the US government had been filed.
Vaccination
question looked at from several aspects. We have looked at the way in which I
think that routine vaccinations can result in the production of chronic disease
in animals and I have made some specific suggestions of the symptoms that
result. Also, we have considered the question of vaccine effectiveness with the
surprising evidence that vaccines do not actually protect populations from
disease - though they do seem to modify the pattern in which the acute disease
manifests.
Lebendimpfstoffe enthalten abgeschwächte (attenuierte) Viren/Bakterien, die sich noch vermehren können und eine Immunantwort auslösen, in der Regel jedoch keine Erkrankung. Ein attenuierter Lebendimpfstoff ist in der Regel deutlich wirksamer als Totimpfstoff.
In seltenen Fällen kann es nach der Anwendung eines solchen Impfstoffes bei der möglichen Vermehrung der Erreger zu einer Mutation in Richtung der nicht abgeschwächten Ausgangsform kommen, durch die dann doch die Erkrankung eintreten kann. Beispiele hierfür sind die in Europa aufgegebene Polio-Schluckimpfung, welche sehr selten die Impfpoliomyelitis ausgelöst hat, der MMR-Impfstoff, der Bacillus Calmette-Guérin sowie Impfstoffe gegen Gelbfieber.
Totimpfstoffe enthalten inaktivierte o. abgetötete Viren o. Bakterien o. Bestandteile von Viren, Bakterien o. Giftstoffen. Diese können sich im Körper nicht mehr weitervermehren o. ihn vergiften, wie es das Tetanospasmin könnte, Aber sie lösen ebenfalls eine Abwehrreaktion (Immunreaktion) aus. Beispiele sind die Toxoidimpfstoffe und Impfstoffe gegen Influenza, Cholera, Beulenpest oder Hepatitis A.
Totimpfstoffe werden unterschieden in:
* Toxoide: sind entgiftete Toxine krankheitserregender Mikroorganismen. Diese Impfstoffe werden in Fällen verwendet, in denen nicht die Erreger selbst, sondern vor allem deren Toxine die Krankheitssymptome verursachen (Tetanus/Diph).
* Inaktivierte Ganzpartikelimpfstoffe: Inaktivierung der Viren mittels einer kombinierten Anwendung von Formaldehyd, beta-Propiolacton und Psoralen
* Teilpartikelimpfstoffe: Zerstörung der Virusoberfläche mit Detergentien o. starken organischen Lösungsmitteln
* Untereinheitimpfstoffe o. Spaltvakzine: die Oberfläche wird vollständig aufgelöst und spezifische Komponenten (Hämagglutinin- und Neuraminidase-Proteine) herausgereinigt. Eine andere Möglichkeit besteht darin, die Untereinheiten rekombinant herzustellen. Untereinheitimpfstoffe sind nur wenig immunogen, besitzen dafür aber geringe Nebenwirkungen.
Lebendimpfstoffe wirken effizienter als Totimpfstoffe, da sie neben humoraler Immunität (eine durch in den Körperflüssigkeiten zirkulierende Antikörper bewirkte Form der Immunität) auch bis zu lebenslang anhaltende zelluläre Immunantworten auslösen.
Allerdings sind sie etwas schlechter in der Verträglichkeit und bergen das (sehr geringe) Risiko einer Rückmutation in Krankheitserreger und damit der Auslösung einer (meist abgeschwächten) Form der Erkrankung, gegen die sie ursprünglich schützen sollten.
Ferner sind nach aktuellen Empfehlungen des in Deutschland dafür zuständigen Robert-Koch-Instituts Lebendimpfungen ab 3 Monaten vor einer und während der gesamten Schwangerschaft kontraindiziert. Dagegen können fällige Impfungen mit Totimpfstoffen den werdenden Müttern im 2en und 3en Drittel der Schwangerschaft bedenkenlos verabreicht werden; im 1en Drittel sollten zum Ausschluss jeglichen Risikos für das Kind dagegen nur diejenigen Totstoff-Impfungen vorgenommen werden, die individuell dringend indiziert sind. In der anschließenden Stillzeit sind Impfungen generell ohne Beschränkungen möglich.
Unterschiedliche Lebendimpfstoffe können ohne Weiteres simultan verabreicht werden. Bei nicht gleichzeitiger Impfung soll der Abstand zwischen zwei Lebendimpfungen allerdings mindestens vier Wochen betragen. Totimpfstoffe oder eine Kombination mit ihnen betrifft dies nicht.
Impfung mit Endotoxine: (= in der Apotheke frei erhältlich) Bestandteil der äußeren Zellmembran von gramnegativen Bakterien/Blaualgen. Im Gegensatz zu den Bakterien, aus denen sie stammen, sind Endotoxine sehr hitzestabil (Sterilisierung).
Endotoxine gehören zu den Pyrogenen, sie können bei Kontakt mit Schleimhäuten und bei Übertritt ins Blut bei Menschen und manchen Tierarten Fieber erzeugen/aktivieren eine Reihe von Signalwegen von immunkompetenten Zellen, die entweder zu einer Entzündung o. zu einem programmierten Zelltod (Apoptose) dieser Zellen führen können. Sie sind schon in niedrigsten Konzentrationen (unterer pg/mL-Bereich) biologisch wirksam.
http://www.remedia.at/homoeopathie/suche.html?q=&gruppe=21
Arzneien in Gruppe Impfstoff
6- facher Impfstoff
ACT-HIB-plus-DPT
BCG Vaccine
Beriglobin P*
Bovigrip.
Bovilis BVD-MD
Bovilis IBR Marker
Diph Pert Tet Vaccinum
Diph Tet Vaccine
Dipht Tet Pert Hib Vaccine
Dipht Tet Pert IPV HIB Vacc.
Dipht Tet Pert IPV Vacc.
Dipht Tet Pert Polio - Vaccine
Dipht Tet Polio Vaccine (Pert.: Effekten danach)
FSME Vacc.
Gelbfieber
Grippe 2010/2011 #1
Grippe 2010/2011 #2
Grippe 2010/2011 #3
Grippeimpfstoff 2001/2002
Grippeimpfstoff 2002/2003
Grippeimpfstoff 98/99
Haemophilus B - Hepatitis B Vacc.
Haemophylus influenzae B Vacc.
Hepatitis A + B Vaccine, Erwachsene
Hepatitis A + B Vaccine, Kinder
Hepatitis A Impfstoff für Kinder
Hepatitis-B Vaccine
Humaner Papillomavirus Impfstoff
Influenza Virus Vaccine
Meningokokkenimpfstoff
MMR Vacc.
MMR-Impfstoff
Pneumococcen Vaccine A
Polio Sabin
Polio Vaccine
Rota Corona Vacc.
Tetanus Vaccine
Typhus Impfstoff oral
Vaccininum
Varizellen Lebendimpfstoff
Liste von Impfstoffen und enthaltene Zusatzstoffen:
Acel-Immune DTaP - Diphtheria-Tetanus-Pertussis Wyeth-Ayerst 800.934.5556
diphtheria and tetanus toxoids and acellular pertussis adsorbed, formaldehyde, aluminum hydroxide, aluminum phosphate, thimerosal, and polysorbate 80 (Tween-80) gelatin Act HIB
Haemophilus - Influenza B Connaught Laboratories 800.822.2463
Haemophilus influenza Type B, polyribosylribitol phosphate ammonium sulfate, formalin, and sucrose
Attenuvax - Measles Merck & Co., Inc. 800-672-6372
measles live virus neomycin sorbitol hydrolized gelatin, chick embryo
Biavax - Rubella Merck & Co., Inc. 800-672-6372
rubella live virus neomycin sorbitol/hydrolized gelatin/human diploid cells from aborted fetal tissue
BioThrax - Anthrax Adsorbed BioPort Corporation 517.327.1500
nonencapsulated strain of Bacillus anthracis aluminum hydroxide, benzethonium chloride, and formaldehyde
DPT - Diphtheria-Tetanus-Pertussis GlaxoSmithKline 800.366.8900 x5231
diphtheria and tetanus toxoids and acellular pertussis adsorbed, formaldehyde, aluminum phosphate, ammonium sulfate, and thimerosal, washed sheep RBCs
Dryvax - Smallpox (not licensed d/t expiration) Wyeth-Ayerst 800.934.5556
live vaccinia virus, with "some microbial contaminants," according to the Working Group on Civilian Biodefense polymin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate glycerin, and phenol (obtained by distillation of coal tar vesicle fluid from calf skins) Engerix-B
Recombinant Hepatitis B GlaxoSmithKline 800.366.8900 x5231
genetic sequence of the hepatitis B virus that codes for the surface antigen (HbSAg), cloned into GMO yeast, aluminum hydroxide, and thimerosal
Fluvirin Medeva Pharmaceuticals 888.MEDEVA 716.274.5300
influenza virus, neomycin, polymyxin, beta-propiolactone, chick embryonic fluid
FluShield Wyeth-Ayerst 800.934.5556
trivalent influenza virus, types A&B gentamicin sulphate formadehyde, thimerosal, and polysorbate 80 (Tween-80) chick embryonic fluid
Havrix - Hepatitis A GlaxoSmithKline 800.366.8900 x5231
hepatitis A virus, formalin, aluminum hydroxide, 2-phenoxyethanol, and polysorbate 20 residual MRC5 proteins - human diploid cells from aborted fetal tissue
HiB Titer - Haemophilus Influenza B Wyeth-Ayerst 800.934.5556
haemophilus influenza B, polyribosylribitol phosphate, yeast, ammonium sulfate, thimerosal, and chemically defined yeast-based medium
Imovax Connaught Laboratories 800.822.2463
rabies virus adsorbed, neomycin sulfate, phenol, red indicator human albumin, human diploid cells from aborted fetal tissue
IPOL Connaught Laboratories 800.822.2463
3 types of polio viruses neomycin, streptomycin, and polymyxin B formaldehyde, and 2-phenoxyethenol continuous line of monkey kidney cells
JE-VAX - Japanese Ancephalitis Aventis Pasteur USA 800.VACCINE
Nakayama-NIH strain of Japanese encephalitis virus, inactivated formaldehyde, polysorbate 80 (Tween-80), and thimerosal mouse serum proteins, and gelatin
LYMErix - Lyme GlaxoSmithKline 888-825-5249
recombinant protein (OspA) from the outer surface of the spirochete Borrelia burgdorferi kanamycin aluminum hydroxide, 2-phenoxyethenol, phosphate buffered saline
MMR - Measles-Mumps-Rubella Merck & Co., Inc. 800.672.6372
measles, mumps, rubella live virus, neomycin sorbitol, hydrolized gelatin, chick embryonic fluid, and human diploid cells from aborted fetal tissue
M-R-Vax - Measles-Rubella Merck & Co., Inc. 800.672.6372
measles, rubella live virus neomycin sorbitol hydrolized gelatin, chick embryonic fluid, and human diploid cells from aborted fetal tissue
Menomune - Meningococcal Connaught Laboratories 800.822.2463
freeze-dried polysaccharide antigens from Neisseria meningitidis bacteria, thimerosal, and lactose
Meruvax I - Mumps Merck & Co., Inc. 800.672.6372
mumps live virus neomycin sorbitol hydrolized gelatin
NYVAC - (new smallpox batch, not licensed) Aventis Pasteur USA 800.VACCINE
highly-attenuated vaccinia virus, polymin B, sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate glycerin, and phenol -a compound obtained by distillation of coal tar vesicle fluid from calf skins
Orimune - Oral Polio Wyeth-Ayerst 800.934.5556
3 types of polio viruses, attenuated neomycin, streptomycin sorbitol monkey kidney cells and calf serum
Pneumovax - Streptococcus Pneumoniae Merck & Co., Inc. 800.672.6372
capsular polysaccharides from polyvalent (23 types), pneumococcal bacteria, phenol,
Prevnar Pneumococcal - 7-Valent Conjugate Vaccine Wyeth Lederle 800.934.5556
saccharides from capsular Streptococcus pneumoniae antigens (7 serotypes) individually conjugated to diphtheria CRM 197 protein aluminum phosphate, ammonium sulfate, soy protein, yeast
RabAvert - Rabies Chiron Behring GmbH & Company 510.655.8729
fixed-virus strain, Flury LEP neomycin, chlortetracycline, and amphotericin B, potassium glutamate, and sucrose human albumin, bovine gelatin and serum "from source countries known to be free of bovine spongioform encephalopathy," and chicken protein
Rabies Vaccine Adsorbed GlaxoSmithKline 800.366.8900 x5231
rabies virus adsorbed, beta-propiolactone, aluminum phosphate, thimerosal (= Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff in Impfungen), and phenol, red rhesus monkey fetal lung cells
Recombivax - Recombinant Hepatitis B Merck & Co., Inc. 800.672.6372
genetic sequence of the hepatitis B virus that codes for the surface antigen (HbSAg), cloned into GMO yeast, aluminum hydroxide, and thimerosal (= Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff in Impfungen)
RotaShield - Oral Tetravalent Rotavirus (recalled) Wyeth-Ayerst 800.934.5556
1 rhesus monkey rotavirus, 3 rhesus-human reassortant live viruses neomycin sulfate, amphotericin B potassium monophosphate, potassium diphosphate, sucrose, and monosodium glutamate (MSG) rhesus monkey fetal diploid cells, and bovine fetal serum smallpox (not licensed due to expiration)
40-yr old stuff "found" in Swiftwater, PA freezer Aventis Pasteur USA 800.VACCINE
live vaccinia virus, with "some microbial contaminants," according to the Working Group on Civilian Biodefense polymin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate glycerin, and phenol -a compound obtained by distillation of coal tar vesicle fluid from calf skins
Smallpox (new, not licensed) Acambis, Inc. 617.494.1339 in partnership with Baxter BioScience
highly-attenuated vaccinia virus, polymin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate glycerin, and phenol -a compound obtained by distillation of coal tar vesicle fluid from calf skins
TheraCys BCG (intravesicle -not licensed in US for tuberculosis) Aventis Pasteur USA 800.VACCINE
live attenuated strain of Mycobacterium bovis monosodium glutamate (MSG), and polysorbate 80 (Tween-80)
Tripedia - Diphtheria-Tetanus-Pertussis Aventis Pasteur USA 800.VACCINE
Corynebacterium diphtheriae and Clostridium tetani toxoids and acellular Bordetella pertussis adsorbed aluminum potassium sulfate, formaldehyde, thimerosal (= Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff in Impfungen), and polysorbate 80 (Tween-80) gelatin, bovine extract
US-sourced Typhim Vi - Typhoid Aventis Pasteur USA SA 800.VACCINE
cell surface Vi polysaccharide from Salmonella typhi Typ2 strain, aspartame, phenol, and polydimethylsiloxane (silicone)
Varivax - Chickenpox Merck & Co., Inc. 800.672.6372
varicella live virus neomycin phosphate, sucrose, and monosodium glutamate (MSG) processed gelatin, fetal bovine serum, guinea pig embryo cells, albumin from human blood, and human diploid cells from aborted fetal tissue
YF-VAX - Yellow Fever Aventis Pasteur USA 800.VACCINE
17D strain of yellow fever virus sorbitol chick embryo, and gelatin
Adjuvantien für Humanimpfstoffe
Bezeichnung/Handelsname Typ, Zusammensetzung/Aufbau Beschreibung, Verwendung
Aluminiumhydroxid Anorganische Verbindung, Gelstruktur. Aluminiumhydroxid bindet das Antigen durch Adsorption und setzt es langsam frei. Verwendung als Adsorptionsmittel in Tetanus-/Diphtherie-/Pertussis-/Hepatitis A-Impfstoff
MF59 Öl-in-Wasser-Emulsion. Squalen/Polysorbat 80/Sorbitantrioleat Nach Injektion geht MF59 schnell in das Lymphsystem über und beschleunigt die Aufnahme der Antigene in das Immunsystem. Verwendung als Wirkverstärker in Influenza-Impfstoffen
AS03 Öl-in-Wasser-Emulsion. Squalen/Polysorbat 80/DL-α-Tocopherol Verwendung als Wirkverstärker in Influenza-Impfstoffen wie z. B. Pandemischer Influenza-Impfstoff A/H1N1 (Pandemrix)
MPL Monophosphoryl-Lipid A (gereinigtes Derivat von Lipopolysacchariden aus Bakterienzellwänden von Salmonella minnesota). Bestandteil von kombinierten Adjuvantien (Adjuvant Systems, AS)
QS21 Oberflächenaktiver Stoff (Saponin) aus Rinde von Quill Verwendung als Matrix in den sogenannten ISCOMs (immunstimulating complexes) und in den kombinierten Adjuvantien
AS04 Kombiniertes Adjuvans.
Komplex aus MPL und Aluminiumhydroxid bzw. Aluminiumphosphat Aktivierung des Toll-like-Rezeptors TLR4. Bestandteil in Fendrix (Hepatitis B-Impfstoff), Cervarix (HPV-Impfstoff)
AS01 Kombiniertes Adjuvans.
Liposomen, MPL und QS21. Aktivierung von Toll-like-Rezeptoren, experimentelle Verwendung
AS02 Kombiniertes Adjuvans.
Öl-in-Wasser-Emulsion, MPL und QS21. Aktivierung von Toll-like-Rezeptoren, experimentelle Verwendung (Entwicklung Malaria-Impfstoff)
IC31 Kombination des Peptids KLK mit dem Oligodesoxynukleotid ODN1 Aktivierung des Toll-like-Rezeptors TLR9. Experimentelle Verwendung (Entwicklung von Impfstoffen gegen Malaria/Influenza/Tb)
CpG ODN Immunstimulierende DNA-Sequenzen (ISS) aus synthetisch hergestellten Oligonukleotiden mit CpG-Motiven experimentelle Verwendung in der Entwicklung von Hepatits B- und Influenza-Impfstoffen
ISCOMATRIX Hersteller: CSL Behring. Besteht aus dem gereinigtem Quillariasaponin QS21, Cholesterol und Phospholipiden der Zellmembran, welche unter geeigneten Bedingungen 40-50 nm große "Käfigstrukturen" ausbilden experimentelle Verwendung in Humanimpfstoffen (zugelassen in Impfstoffen gegen Pferdeinfluenza)
Virosomen Doppelmembran aus Phospholipiden (Liposomen), in die die die viralen Antigenstrukturen (z.B. Influenzavirus A-Hämagglutinin und Neuraminidase) eingebaut werden; rekonstituierte („künstliche“) Virushülle. Einsatz in Hepatitis A-Impfstoffen wie HAVpur und Epaxal
SALK-Vakzine (= Lebendvakzin des Polios/hergestellt mit Form).
Thimerosal (= Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff in Impfungen)/Quelle: Remedia.at
Using Thimerosal as a remedy could be considered allopathic thinking. It's treating the cause of the illness. In homeopathy, sometimes "why" is not necessarily as important. Classical homeopathy addresses the symptom picture and finds the one simillimum to match. Unless you consider the thousands of children who have been vaccinated with thimerosal containing vaccines and the resulting disorders the proving, thimerosal would probably not be considered a simillimum.
Arguing that these children *are*
the proving of Thimerosal. And while it may or may not be their simillimum, is
a false picture of who they are. In other words, the thimerosal masks the true
constitution. Believing a person's constitution can change and never more so
than when an artificial substance has effected them. A person is completely
different drunk from being sober. The alcohol would cover up who the person
really is and what his real traits and characteristics are. Unless perpetually
drunk, the effects of the alcohol are temporary. This cannot be said for the
effects of Thimerosal (and other vaccines).
There are some homeopaths who
have had astounding success treating children (and adults) the very way described.
Tinus Smits has some truly impressive cure stories and his understanding of
autism is admirable (check out the new article on autism on his site, including
a good grasp of glutathione). And there are also homeopaths practicing what is
considered sequential homeopathy who address the vaccine insults. I cannot
attest to their successes as I have no experience of it although I have read
reports of improvements from other parents on various lists. But their approach
is very different than classical homeopathy.
Given my son recovered from an
"isopath" (the DPT remedy), I can only attest it worked for him. However,
it has been his "one" remedy for a little over 3 years. It could be
reasoned, the DPT remedy *is* his simillimum which some would argue is the only
way the isopath would bring true cure. As a side note, I find it curious others
refer to the DPT remedy as a nosode as it is not made from the diseases
themselves. It is made from one ingredient like other remedies. It is made from
the actual DPT shot with thimerosal. I know there are homeopaths who feel this
isn't good homeopathic practice and in their experience, people treated with a
nosode or anything other than a traditional constitutional remedy may not
experience the long lasting, permanent "cures" but a temporary
amelioration. Only time will tell if that is true for us.
In the mean time, it is my own
personal opinion that like anything else, with time, we learn to improve upon
our knowledge. To be rigid in treatment, may miss an opportunity for healing
for many. Hahnemann himself (the founder of homeopathy) revised his methods
during his lifetime leading to several editions of the Organon. (Note to
newbies: the Organon is the book written by Hahnemann outlining the principles
of homeopathy and its practice.) Water dosing was a "new" development
from him which went unnoticed for years and years. Now, many homeopaths will
only dose in water because it is seen as superior to dry dosing. This doesn't
mean dry dosing doesn't work. Of course it does. But what it means is that
Hahnemann was continuing to learn and improve upon his craft. I believe this type
of learning and growing should continue in homeopathy.
Never before in our time, have
our children been subjected to such an assault to their vital force. The
majority have been injected with unclean antigens and adjuvants in the form of
vaccine at birth! Most major hospitals in the US made it policy to inject Hep B
(which did contain thimerosal) into babies within 24 hours of birth.
Additionally, almost all babies in the states are injected with Vitamin K which
contains its own adjuvants. Their immune systems are not only fully
undeveloped, but they are not even as yet fully incarnated. Add to that the
routine use of ultrasound, pitocin, brethine, and all the other drugs and
interventions given to women during pregnancy these days and it is no wonder we
are facing a nation of ill children. Couple that with air pollution, fish
pollution, and the unhealthy state of many diets, it is almost inevitable.
Moreover, as each generation
evolves, I think we are seeing children who are "more" of everything
- more sensitive, more intelligent, and more susceptible. We need to evolve
with these changes and how we address them.
This does not mean I think every parent should run out and give their child Thimerosal remedy. It is so important to work with a qualified homeopath who has the training and experience to know what to do. We are only at the tip of the iceberg when it comes to treating spectrum disorders. But I do think keeping an open mind is critical for success.
Zu den ältesten immunologischen Emulsionsadjuvantien zählen das inkomplette Freund-Adjuvans (IFA), eine mit einem Emulgator stabilisierte experimentell verwendete Wasser-in-Öl-Emulsion auf Mineralölbasis und das Adjuvans 65, eine Wasser-in-Öl-Emulsion mit Erdnussöl. Beide führen wegen ihrer ausgeprägt öligen Eigenschaften zu einer starken Gewebereizung.
Mit Gentechnik hergestellt sind Vaccin Hepatitis B und Vaccin Pertussinum
Impfungsnosoden:
DiTePo (Diphterie, Tetanus, Polio)
DiTePoPe (Diphterie, Tetanus, Polio, Pertussin)
MMR (Mumps. Masern, Röteln)
DiTe (Diphterie, Tetanus)
(alle Schmidt-Nagel)
Diph-pert-t.= Impfung DPT
Diph-t-tpt = Impfung DTTP
Impffolgen vorbeugen: Mit 1er Impfung warten bis Kind mündlich angeben kann, dass es Kopfschmerz hat. (ist meist 1er Beschwerde bei Impfschade).
Impffolgen Akut: Acon: FieBER, trockne Haut/DURST/Unruhe
Ant-t: Impfung während Atemwegebeschwerden wenn Thuj. versagt und Sil. nicht angezeigt ist.
Apis: Impfstelle HEIß/geschwollen/Ausschlag (Erypsel/schmerzlose Durchfall)/frösTELT + < warmes Zimmer/durstlos
Ars: SCHWACH/Atemnot/langsames FieBER/ängstlicher Ausdruck/unruhig
Crot-h: Haut entzündet/dunklen Bläschen/brennen
Echi: Impfung aus Tierserum/Blutvergiftung
Gun: Allgemein Empfinden SCHLECHT, Abszessen rezidivierend, Blutvergiftung
Hep: Abszess/Eiterung
Kali-m: AppeTIT + Essen = unverträglich/schläfrig nach essen, schwach + reizbar
Malan: Pustulösen Ausschlag/Kopfschmerz/Rückengradschmerz
Mez: Juckender Ausschlag = < Wärme/Waschen, Krusten + Eiter
Perla = Zuchtperle
Rhus-t: Ausschlag (Bläschen mit rotem Hof), BrenNEN + jucKEN
Sars: Hautausschlag trocken o. ätzEND, < waschen/nass-kaltes Wetter/Periode Kratzen lässt Juckreiz Ort wechseln, Abmagerung
Sil: Fieber, Hirn-/Ohrenentzündung, geimpftes Körperteil = geschwollen/Impfstelle entzündet, Abszess/Geschwür an Lymphknotem, Bläschen
Ohren/Gesicht/Beinen. Krampf
Thuj: durchfall
Vacc: Chronische Depression/Psychose/lauNISCH, weinerlich/vergesslich,
KopfSCHMERZ, schwach, Appetitverlust + Nahrungsmittelunverträglichkeit
Vario: Herpes + SCHMERZ, Muskeln tun weh/Fieber
Impffolgen chronisch: Bufo. Cars. Syph. Stram. Tub.
After vaccination:
Mind: anxiety: thuj.
Head: Inflamed brain from suppressed eruption (eczema) from vaccination: bac.
headache in general from vaccination: thuj.
Eyes: Inflammation (in conjunctivae): thuj. Of cornea, keratitis: vac. vario.
Stomach: Pain in general: Thuj.
Nausea: Sil.
Rectum: Diarrhea: ant-t. apis, sil, thuj.
Stool: apisin. thuj.
Respiration: asthmatic: thuj. (children)
Cough: thuj.
Extremities: Emaciation of upper limbs: maland. thuj.
Eruptions: Pustules on Leg: sulph./like varicella: syc-co.
Paralysis of lower limbs: thuj.
Suppuration of finger nails: Thuj.
Felon/onchyia/paronhia run-around: Thuj.
Swelling of shoulder: apis, thuj./of upper arm: sil. sulph. thuj.
Sleep: Restless: thuj.
Sleepless: mez. thuj.
Skin: Eruptions in general: crot-h. maland. mez. sars. skook. sulph. vario.
Eczema: ammc. kali-m. maland. mez.
Generalities: acon. ant-t. apis, ars. bac. bapt. bcg, bell. bufo, carc. crot-h. diph. echi. graph. gun. hep. kali-chl. lac-v. lepro. Maland. med. merc. merc-cy. Mez. nat-bic. ped. phos. psor. rhus-t. sabin. sarr. sars. sep. SIL. skook. SULPH. syc-co. THUJ. Tub. Vac. vario.
after diphtheria injections: diph. merc-cy.
After Yellow fever vaccination: ars.
after Meningitis injections: apis
Begleitend zu Polioimpfung: Sagitario sagitifolia,
After Smallpox vaccination: maland. thuj.
after Typhus: bapt.
Prophylactic: sulph. thuj. vario.
Convulsions: Sil. thuj.
Vaccinations: Use the Isode of the vaccination given.
Wirkung: sycotisch
Allerlei:
Perla Künstliche Entstehung: Herstellung von Zuchtperlen geschieht durch Implantierung eines mit Epithelzellen einer anderen Perlmuschel beschichteten Zuchtkerns ins Muschelinnere („Wie Impfung“)
Sechsfachimpfstoff (= Hexavalente Impfstoff): Polio (Kinderlähmung)/Diphtherie/Tetanus/Pertus (Keuchhusten)/Haemophilus influenzae Typ B/Hepatitis B.
Durch Lebendimpfstoff kann bei der möglichen Vermehrung der Erreger zu einer Mutation in Richtung der nicht abgeschwächten Ausgangsform kommen, durch die dann die Erkrankung eintreten kann. Z.b. Polio-Schluckimpfung/MMR-Impfstoff/Bacillus Calmette-Guérin/Impfstoffe gegen Gelbfieber/Schweinegrippe.
Vorwort/Suchen Zeichen/Abkürzungen Impressum