Black People Are By Nature More Resistant Against HIV-Infection Than White People

UN

By Johan Van Dongen: Micro-Surgeon and Scientist and Joel Savage

The Aids and Ebola epidemic have generated many controversies all over the world, since the outbreak last year, hitting hard Sierra Leone, Guinea, and Liberia, but only a few have access to any inside information on the Aids and Ebola research.

What many people don’t know, according to Professor Johan Van Dongen, the viruses of Ebola and Aids were long created within bacteria factories, with dubious micro-organisms and given different names, such as Reston virus, Belgrade virus, and Marburg virus. It was when the first outbreak of the virus which occurred near a small river in Africa called River Ebola, gave the name of the disease as Ebola. “This is how scientists give names to their findings,” he added.

In Africa, there were varieties of wide experiments of dubious scientists, including a crook called Hillary Koprowski. Later there was a hunt to catch this man. On his normal course of business, he used genetically contaminated engineered vaccines on innocent children in Africa. Not only African children suffered the effect of the contaminated vaccine.

In Australia between 1940 and 1970 hundreds of orphaned children, including babies were used as guinea pigs, to test vaccines against influenza, pertussis, and herpes. This atrocity was confirmed by David Vaux, an expert on infections. In the largest experiment, about 350 children were all injected with doses intended for adults.

Suddenly things started changing positively. Ricardo Veronesi, Professor Emeritus, at the Faculty of Medicine, University Sao Paulo Brasil, together with Dr. Wolff Geisler found out that 97% of the people who have HIV in their bodies, were purposely infected with this virus, which can lead to Aids. The artificially made susceptible was supplied to them in vaccines, drugs, blood transfusions and food. HIV containing microbes were also found in drinking-water and also insecticide spraying pools.

Smallpox vaccine was contaminated or combined with immunodeficiency SCID the precursor of AIDS. Within the continent of Africa, from west to east, more than 100 million children were injected with this vaccine, in cooperation with the World Health Organization (WHO) and Center for Diseases Control (CDC),  financed by the Rockefeller foundation.

In Africa the probability of an early death of HIV patients is three times higher then as were when HIV patients are simultaneously infected with HTLV-1 as described in the Lancet by Page et al in his scientific publication: HTLV-I/II seropositivity and death from Aids among HIV-I seropositive intravenous drug users (Lancet, 1990; 335: 1439-41), an even more extremely important publication for the Aids/HIV theory dissidents. Because especially HTLV-I, among many other HIV viruses, was only demonstrated in Uganda, Ghana, South Africa, and Namibia.

Only in these countries, HIV patients appear simultaneously up till now. According to Wolff Geisler, the concomitant existence of HTLV-I and HIV produces the observed rate of Aids patients in Uganda, Kenya and black-skinned people in Florida, USA and some Caribbean Islands, even though in general black people are by nature more resistant against HIV-infection than pale-skinned people. This means the HIV viruses are genetically engineered as described in our book.

Whoever think Professor Dongen is crazy should seek a psychiatric help. Even an uneducated African living in the remote area without electricity will believe his story. It will be recalled that Professor Johan Van Dongen challenged Belgium’s Professor Van der Groen’s claims that Ebola was invented in the 1960’s in Fort Detrick. Because Professor Dongen proved him a liar, the article which appeared in Diplomatic Aspects Newspaper, link miraculously disappeared from the web.

http://www.amazon.co.uk/Greatest-Medical-History-Against-Mankind-ebook/dp/B016W89W1G

Donald Trump: Why Aren’t You Killed Like Jeffrey Bradstreet Or Other Opponents Of Vaccinations Which Not Only Cause Autism But Also Aids And Ebola?

Donald

Donald Trump

This article is dedicated to Jeffrey Bradstreet: By Johan Van Dongen

The above question is raised by me and many others, because recently in the United States of America, over seven doctors have been murdered or found dead in strange circumstances. I find it very necessary to ask Donald Trump this question, because of the statement he made that: “Vaccines Do Cause Autism.” and also to find an answer to why the disappearance from the medical scene or mysterious deaths of alternative health doctors who have real cures, but opposed and disapproved by the FDA?

When I saw the interview of Dr. Jeff Bradstreet, nothing shows a possible suicide as mentioned by US governmental institutions. During this interview, Bradstreet showed his engagement, for he was not a person who would give up easily. It was a very optimistic person with a normal attitude. He was laughing, joking and celebrating because his autistic son just graduated from high-school.
The supposed reason for his “suicide” – an FDA raid on his clinic – is nothing new for him. There was nothing new in his life that would have been a reason for him to want to end his own life, only new things that would encourage him to live his life and perhaps encourage others that want to take their lives. Now we have to wait and see what happens to Donald Trump.

The overall conclusion

“Dr. Jeffrey Bradstreet has been under attack by big pharma for his success during all his professional life, so there is no way he would have committed suicide for just another attack. He was murdered; the FDA were clearly involved, and the other suspect is the MMR vaccine corporations, who work with the FDA. Dr. Bradstreet loudly published the fact we all know: The MMR jab, which makes billions of profit, causes autism.”

It isn’t only autism which is caused by vaccines but also Aids and Ebola. For decades Africa is used as a bio-warfare laboratory of German and Japanese war criminals under the guidance of the USA because they protect these Nazi bastards. This makes the USA the land of evil, so once Donald Trump becomes president of the United States, there is a lot work to do by replacing black prisoners with white pharmaceutical criminals in three piece suits.

The horrific Aids pandemic tremendously has generated scientific controversies within and outside the scientific establishment. Only a minority of scientists and other engaged people have access to inside information concerning (bio-warfare) Aids and Ebola research.

As an experimental micro-surgeon in the early seventies, almost at the beginning of the multiple organ transplantation eras, I have carried out thousands of experimental organ transplantations. In order to deal with organ rejection, I administered, radiation and sera for diminishing the immunity of the organ receiver. Besides that, I also administered uncountable agents to recipients of organs in order to trigger, diminish or completely wipe out the immune capacity which can be compared with Aids.

During my university and hospital appointments in the early seventies, and later undercover in the pharmaceutical industry, I discovered at that time that animals didn’t die because of rejection of the transplanted organ but because of multiple infections which can be compared with human Aids victims. So, I noticed that Aids can be induced by radiation, aflatoxins, Immuran/prednisolone combination, anti-lymphocyte sera and many other bio-warfare agents.

Dormant HIV virus

As head of the Department of Experimental Microsurgery, and involved in all transplantation and immunological experiments, I also have been involved in many controversies. Especially the connection of my work and the polemic concerning the transmission of HIV in many ways. I discovered not only in experiments but also in the extensive scientific literature the role of an obligatory co-factor that trans-activates the “Dormant” virus HIV in specific human cells.

This obligatory co-factor which trans-activates the “Dormant” virus in specific human cells are deliberately introduced into mostly black-skinned African people, governed by massive environmental factors as you can read in our book: “Aids and Ebola the greatest crime in medical history against mankind,” in order to depopulate Africa and other parts of the world.

This article is to enlighten readers about the real origin of Aids and the true nature of famous international researchers as Robert Gallo. As far as Gallo is concerned, Ricardo Veronesi, professor of the Faculty of Medicine at the University of Sao Paulo, was personally informed about the true nature of Gallo’s research long before this controversy turned into a public scandal and as a consequence thousands of scientific Aids dissidents.

It was no less than Francoise Barré-Sinoussi of the French Pasteur Institute who revealed the criminal intention of Gallo. Not only she became an Aids dissident? but also the discoverer of the HIV virus Luc Montagnier disputed Gallo, the fake discoverer of the HIV virus.

In their opinion, the major bursts in the common scientific approach of lies in its ignoring that the pathogenicity of the HIV indeed is governed by multiple deliberate environmental factors and one of these determinant factors are the PCR test (Polymerase Chain Reaction Test).

Using and extrapolation of these kinds of techniques we can conclude that people who have HIV in their bodies, were purposely infected with this virus which can lead to Aids. Bio-warfare scientists are able to make black-skinned people ‘Africans) artificially susceptible for HIV or Ebola by using controllable diseases as a cover-up.

Most of the biowarfare research using viruses which cause Aids and Ebola is predominantly carried out in Germany and Japan until 1945 and since then mainly in the USA and France, using Nazi and Japanese (military) scientific war criminals.

Autism/Aids/HIV Theory Dissidents Like Jeffrey Bradstreet

The official scientific origin of the diverse HIV-strains has been placed somewhere between 1938 and 1948 when scientist T.F. Smith et al, published an article in the authoritative medical journal Nature, is 1988, captioned: “The phylogenetic history of immunodeficiency virus.”

He wasn’t the only scientists who revealed the true nature of the HIV virus. Smith’s efforts to reveal the real origin of HIV was followed, to name a few, by Sharp et al with his article: “Understanding the origins of Aids viruses,” also in Nature, followed by Meyers et all with: “The phylogenetic analysis of the HIVs.” But the most important article is described in the top of the bill of medical journals the Lancet,  by scientist L.A. Evans et al who discovered the; “Simultaneous isolation of HIV-1 and HIV-2 from an Aids patient”.

All these mentioned scientists agreed that the distribution of the HIV virus was an intentional action. Their findings make it very conceivable that this distribution was intentional, because sometimes both the new viruses HIV-1 and HIV-2, respectively HTLV-IV, are existing in one and the same person according to Evans. And because his publication is checked by the editing and scientific boards of the Lancet, the outcome of his investigation was true. This counts also for thousands of publications in other medical journals as described in our book “Aids and Ebola the greatest crime in medical history against mankind.”

According to the famous Aids/HIV theory dissident Wolff Geisler, further evidence of the intentional distribution, out of the mentioned simultaneous infection of the same persons, it was described as a second Aids epidemic in the same black-skinned population, by an inefficient transmission of the HIV virus. The appearance of this extreme rare retrovirus among the African Aids patients is so conspicuous that some world famous scientists uttered a sentence about it. They alleged this to be; “Only another acquired opportunistic infection but rather an additional death sentence.” But is it?

In Africa the probability of an early death of HIV patients is three times higher than elsewhere when HIV patients are simultaneously infected with HTLV-1 as described in the Lancet by Page et al in his scientific publication: HTLV-I/II seropositivity and death from Aids among HIV-Seropositiveintravenous drug users (Lancet, 1990; 335: 1439-41), an even more extremely important publication for the Aids/HIV theory dissidents. Because, especially HTLV-I, among many other HIV viruses, was only demonstrated in Uganda, Ghana, South Africa, and Namibia.

Only in these countries, HIV patients appear simultaneously up till now. According to Wolff Geisler, the concomitant existence of HTLV-I and HIV produces the observed rate of Aids patients in Uganda, Kenya and black-skinned people in Florida, USA and some Caribbean Islands, even though in general black people are by nature more resistant against HIV-infection than pale-skinned persons (see below). This means the HIV viruses are genetically engineered as describe in our book.

No less than Luc Montagnier et al, the discoverer of the HIV virus stated that this virus is made out of the Nazi eugenics and  a genetically engineered experiment as well as the development of Aids-causing viruses in horses. In a very talked about an article he described in the authoritative Annals of Virology: “A new type of retrovirus from patients presenting with lymphadenopathy and acquired immune deficiency syndrome”: Structural and anti-genetic relatedness with Equine Infectious Anemia Virus EIAV (horse Aids), 1984; 135E: 119-31.

Equine Infectious Anemia Virus EIAV (HIV/Horse-Aids) made by Nazi Germany

If we compare these findings to our references in:“Aids the greatest crime in medical history against mankind” the book now available at Amazon, the HLA-A, B, C, DR3 and DR5 loci, is examined by the Nazi’s led by Otmar Verschuer.

In 1956, he joined the American Eugenics Society and worked under auspices of the Rockefeller-fund. He was also head of the Department of the Kaiser Wilhelm Institute in Germany.

Furthermore, we have to take into account that within people who have blood type HLA-DR3 Aids, it is much less common than in people who have the HLA-DR5 type. Under the Nazi’s research, it is important to note that precisely the HLA-DR5 type occurs mainly in Jews. The HLA-DR3 type contrast is most common in dark-colored Africans.

The two evidence or references are enough to let you know vividly what took place. In general you can say that it is harder for blacks to get Aids than as it is for whites, but blacks have been made susceptible for a broad spectrum of brand new diseases caused by Germans, partly under the auspices of the South African Apartheid regime, and after the war under the guidance of the U.S.A.

Nowadays we now know that monkeys do not get Aids when infected with the human Aids virus. The same goes for tuberculosis until the moment that monkeys in a laboratory made receptive. Therefore black-skinned people are under no circumstances contaminated with Aids by monkeys with or without eating them. That is so to speak a criminal WHO/ CDC / FDA scientific fairy tale.

 

 

Bio-warfare Laboratories Of German And Japanese War Criminals Under The Guidance Of USA: The Revealing Voices of AIDS/HIV Theory Dissidents

Case

By Johan van Dongen and Joel Savage

The horrific Aids pandemic, tremendously has generated scientific controversies within and outside the scientific establishment. Only a minority of scientists, like Johan van Dongen, and other engaged people have access to inside information concerning (bio-warfare) Aids and Ebola research.

As an experimental micro-surgeon in the early seventies, almost at the beginning of the multiple organ transplantation era,  Micro-Surgeon Johan van Dongen did carried out thousands of experimental organ transplantation. In order to deal with organ rejection, he administered, radiation and sera for diminishing the immunity of the organ receiver. Besides that he also administered uncountable agents to recipients of organs in order to trigger, diminish or completely wipe out the immune capacity which can be compared with Aids.

During his university and hospital appointments in the early seventies, and later undercover in the pharmaceutical industry, he discovered that animals didn’t die because of rejection of the transplanted organ but because of multiple infections which can be compared with human Aids victims. So, Johan van Dongen noticed that Aids can be induced by radiation, aflatoxins, Immuran/prednisolone combination, anti-lymphocyte sera, and many other bio-warfare agents.

Dormant HIV virus

As head of the Department of Experimental Microsurgery, and involved in all transplantation and immunological experiments, Johan also had been involved in many controversies. Especially the connection of his work and the polemic concerning the transmission of HIV.  In many ways, he discovered not only in his experiments but also in the extensive scientific literature the role of an obligatory co-factor that trans-activates the “Dormant” virus HIV in specific human cells. This obligatory co-factor which trans-activates the “Dormant” virus in specific human cells are deliberately introduced into mostly black-skinned people, collectively, Africans, governed by massive environmental factors, as you can read in our book: “Aids and Ebola the greatest crime in medical history against mankind,” in order to depopulate Africa.

Therefore we will always like to enlighten readers about the real origin of Aids and the true nature of famous international researchers as Robert Gallo. And as far as Gallo is concerned, Ricardo Veronesi, professor of the Faculty of Medicine at the University of Sao Paulo, was personally informed about the true nature of  Gallo’s research long before this controversy turned into a public scandal and as a consequence thousands of scientific Aids dissidents.

It was no less than Francoise Barré-Sinoussi of the French Pasteur Institute, who revealed the criminal intention of Gallo. And not only she became an Aids dissident but also the discovery of the HIV virus Luc Montagnier disputed Gallo, the fake discoverer of the HIV virus. In their opinion, the major bursts in the common scientific approach lie in its ignoring that the pathogenic of the HIV. Indeed it is governed by multiple deliberate environmental factors and one of these determinant factors is the PCR test (Polymerase Chain Reaction Test).

Polymerase Chain Reaction Test

This test is a technology in molecular biology used to amplify a single copy or a few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence. Especially the diagnosis of hereditary diseases; the identification of genetic fingerprints, used in forensic sciences and paternity testing; and the detection and diagnosis of infectious diseases. The PCR test can be used to investigate the connection of diseases to the specific black race. Moreover, PCR can be extensively modified to perform a wide array of genetic manipulations not only in humans but also from microorganisms which cause Aids and Ebola.

Using an extrapolation of these kinds of techniques we can conclude that almost all persons who have HIV in their bodies, were purposely infected with this virus which can lead to Aids. Bio-warfare scientists are able to make black people artificially susceptible to HIV or Ebola by using controllable diseases as a cover-up.

Most of the biowarfare research using viruses which cause Aids and Ebola was predominantly carried out in Germany and Japan until 1945 and since then mainly in the USA and France, using Nazi and Japanese (military) scientific war criminals.

The Revealing Voices of Aids/HIV Theory Dissidents

The official scientific origin of the diverse HIV-strains has been placed somewhere between 1938 and 1948 when scientist T.F. Smith et al published an article in the authoritative medical journal Nature about this period in 1988 named: “The phylogenetic history of immunodeficiency virus”.

He wasn’t the only scientists who revealed the true nature of the HIV virus. Smith’s efforts to reveal the real origin of HIV was followed, to name a few, by Sharp et al with his article: “Understanding the origins of Aids viruses”, also in Nature, followed by Meyers et all with: “The phylogenetic analysis of the HIVs”. But the most important article is described in the top of the bill of medical journals the Lancet by scientist L.A. Evans et al who discovered the; “Simultaneous isolation of HIV-1 and HIV-2 from an Aids patient”.

All these mentioned scientists agreed that the distribution of the HIV virus was an intentional action. Their findings make it very conceivable that this distribution was intentional because sometimes both the new viruses HIV-1 and HIV-2, respectively HTLV-IV, are existing in one and the same person according to Evans. And because his publication is checked by the editing and scientific boards of the Lancet the outcome of his investigation was true. This counts also for thousands of publications in other medical journals as described in our book “Aids and Ebola the greatest crime in medical history against mankind.”

German scientist Wolff Geisler

According to the famous Aids/HIV theory dissident Wolff Geisler, further evidence of the intentional distribution, out of the mentioned simultaneous infection of the same persons, it was described as a second Aids epidemic in the same black-skinned population, by an inefficient transmission of the HIV virus. The appearance of this extremely rare retrovirus among the African Aids patients is so conspicuous that some world-famous scientists uttered a sentence about it. They alleged this to be; “Only another acquired opportunistic infection but rather an additional death sentence”. But is it?

In Africa, the probability of an early death of HIV patients is three times bigger than elsewhere when HIV patients are simultaneously infected with HTLV-1 as described in the Lancet by Page et al in his scientific publication: HTLV-I/II seropositivity and death from Aids among HIV-I seropositive intravenous drug users (Lancet, 1990; 335: 1439-41), an even more extremely important publication for the Aids/HIV theory dissidents. Because especially HTLV-I, among many other HIV viruses, was only demonstrated in Uganda, Ghana, South Africa, and Namibia.  HIV patients only in these countries appear simultaneously up till now.

According to Wolff Geisler, the concomitant existence of HTLV-I and HIV produces the observed rate of Aids patients in Uganda, Kenya and black-skinned people in Florida, USA and some Caribbean Islands, even though in general black people are by nature more resistant against HIV-infection than pale-skinned persons (see below). This means the HIV viruses are genetically engineered as described in our book.

No less than Luc Montagnier et al, the discoverer of the HIV virus stated that this virus is made out of the Nazi eugenics and genetic engineered experiments as well as the development of Aids-causing viruses in horses. In a very talked about an article he described in the authoritative Annals of Virology: “A new type of retrovirus from patients presenting with lymphadenopathy and acquired immune deficiency syndrome”: Structural and anti-genetic relatedness with Equine Infectious Anemia Virus EIAV (horse Aids), 1984; 135E: 119-31.

Equine Infectious Anemia Virus EIAV (HIV/Horse-Aids) made by Nazi Germany.

If we compare these findings to our references in “Aids the greatest crime in medical history against mankind” the book now available at Amazon, the HLA-A, B, C, DR3 and DR5 loci, is examined by the Nazi’s led by Otmar Verschuer.

In 1956 he joined the American Eugenics Society and worked under auspices of the Rockefeller-fund. He was also head of the Department of the Kaiser Wilhelm Institute in Germany.

Furthermore, we have to take into account that within people who have blood type HLA-DR3 Aids, it is much less common than in people who have the HLA-DR5 type. Under the Nazi’s research, it is important to note that precisely the HLA-DR5 type occurs mainly in Jews. The HLA-DR3 type contrast is most common in dark-colored Africans.

These two shreds of evidence or references are enough to let you know vividly what took place. In general, you can say that it is harder for blacks to get Aids than as it is for whites, but blacks have been made susceptible for a broad spectrum of brand new diseases caused by Germans, partly under the auspices of the South African Apartheid regime, and after the war under guidance of the U.S.A.

Nowadays we now know that monkeys do not get Aids when infected with the human Aids virus. The same goes for tuberculosis until the moment that monkeys in a laboratory made receptive. Therefore black-skinned people are under no circumstances contaminated with Aids by monkeys with or without eating them. That is so to speak a criminal scientific fairy tale.

Pharmaceutical Disease Producing Factories Administered Dangerous Isoniazide And Sulfadiazide To Spread Tuberculosis

“Pharmaceuticals Companies Make Business With Intentionally Created Diseases In Africa”- Professor Johan Van Dongen.

Johan 2

Professor Johan Van Dongen, the former Micro-Surgeon.

According to the German scientist Wolff Geisler, thousands of Aids patients affected with tuberculosis in Africa, are not caused by the HIV virus. In my opinion he is right, because the increase of the number of tuberculosis patients in Africa, is a result of intended spread of the disease through dangerous medicines like Isoniazid and Sulfadianozide , given to Africans in tuberculosis clinics in African countries, such as Burundi, the former Belgian Congo, Uganda and Zambia. Instead of curing, the two mentioned medicines rather cause a tremendous acceleration of HIV infections amongst African people.

The WHO/IUATLD Working Group And Wolff Geisler

In 1989, the WHO/IUATLD working group declared in the “Bulletin International Union Tuberculosis Lung Disease” that HIV in TB-hospitals could have been spread as a result of unhygienic anti-tuberculosis injections, but as a former micro-surgeon, I, Johan van Dongen challenge them to prove that statement.

Again according to Wolff Geisler, remarkably horrendous numbers of HIV-infections originate only from US American or British financed and managed hospitals in the respectively mentioned countries. For instance in hospitals in Kitgum and Kagando in Uganda (where there was no recognizable USA or British finance), 10% of the TB patients, normally an average of 15% of the total population were HIV infected.

Aids Causing Factories

According to the World Health Organization, in Africa 17-55% of TB patients have HIV-antibodies. The WHO expert Slutkin mentioned 30-60% in some of the developing countries, a clear sign of intentional infection of tuberculosis patients in Zambia with HIV. The same evidence was provided by the same expert in the Chinkala Hospital, TB patients Mazubuku. 23% of the TB patients in the middle of 1987 were also infected with HIV.

Six months later, the virus was located in 50% of patients within the same hospital, after administering Isoniazid and Sulfadiazide. The same figures slightly increased in 58% of TB patients in Ndola, and in 60% of TB patients in the University Teaching Hospital in Lusaka, Zambia.

In the Makalala Sanatorium in Kinshasa, Zaire, 33% of TB patients had HIV antibodies (among the staff: 4-8%), and in Chinkankata 36%. In Malawi, 50-66% of TB patients also had HIV antibodies. In the TB clinic, Centre Anti Tuberculeux de Bujumbura in Burundi, 55% of TB patients were HIV-infected in 1986, and in the Mwanza region of Tanzania, 25% of TB patients had HIV-antibodies. Moreover, the patients were treated with forbidden drugs, because in New York, 1972, about 21 people who were taking intravenous agents had succumbed to inexplicable tuberculosis before 1972.

Already written in a previous article, in contrast, patient with a cellular deficiency hypersensitivity following the polio- and cowpox vaccinations, are particularly prone to certain bacterial, viral and protozoal infections caused by Mycobacterium tuberculosis TB. And then the pharmaceutical disease producing factories appear by using deadly toxic agents such as Isoniazid, produced by Teva Netherlands BV (Holland, and Sulfadiazide, produced by Pfizer in Germany.

What Is Tuberculosis?

Tuberculosis is a chronically infectious disease which generally affects the lungs. The causing agent, tubercle bacilli, is mostly passed on from person to person through coughing of droplets from the respiratory tract (lungs), and can also be transmitted onto the skin, eyes of persons in the immediate vicinity. Tubercles also can penetrate the body through drinking.

A striking phenomenon! Side Effects Of Isoniazid And Sulfadiozanide.

Hospitals, including Mbare Hospital in Harare, were suddenly full of tuberculosis patients and the people were suffering from venereal diseases at the same time, as a side effect consequence, because Isoniazid and Sulfadiazide made them susceptible for these. It is obvious that Isoniazid and Sulfadiazide are the cause of these venereal diseases because it appears in almost all infected children under the age of ten.

As described before, in Africa tuberculosis and HIV go hand in hand, but the mass spread of tuberculosis infections in Africans with Aids is not caused by HIV-infection at all. The increase in the number of African TB patients is the result of intended spread of special tuberculosis agents, and patients treated with Sulfadiozanide and Isoniazid at the end caught Aids!

Disease Factories Using Isoniazid And Sulfadiozanide

The two medicines, Isoniazid and Sulfadiazide, shouldn’t have been used as medications against TB and most certainly not in Aids patients. Only the long list of side effects gives you the shivers. Therefore we will describe a list with side effects causing a huge amount of invented new diseases in order to sell more medicines against these side effects……

TB 3

Tuberculosis patients in a hospital.

Side Effects Caused By Isoniazid And Sulfadiazide There we go! And We Are starting With:

“Anxiety, blurred vision, changes in menstrual periods, chills, cold sweats, coma, confusion, cool, pale skin, decreased sexual ability in males, depression, dizziness, ‘dry’ puffy skin, fast heartbeat, feeling cold, headache, increased hunger, nausea, nervousness, nightmares, seizures, shakiness, slurred speech, swelling of front part of the neck, unusual tiredness or weakness and last but not least: weight gain.”

There You Have It. And If You Think This List Of Side Effects Is Completed, Not at all! There Is More: Let’s continue:

“Abdominal or stomach pain, back- leg- or stomach pains, ‘black’ tarry stools, bleeding gums, bleeding under the skin, blindness or vision changes, “blistering, peeling, or loosening” of the skin, bloating, blood in the urine or stools, “bluish-colored lips, fingernails or palms”, burning of the face or mouth, –burning, crawling, itching, numbness, painful, prickling, “pins and needles”, or tingling feelings–, chest pain, cloudy urine, clumsiness or unsteadiness.

Constipation, continuing ringing or buzzing or other unexplained noise in the ears, cough or hoarseness, cracks in the skin, darkened urine, decrease in the amount of urine, diarrhea, difficulty with breathing, difficulty with moving, dizziness or lightheadedness, feeling of discomfort, fever with or without chills, general body swelling, general feeling of tiredness or weakness, headache, hearing loss.

Indigestion, itching- joint or muscle pain, light-colored stools, loss of appetite and weight, loss of heat from the body, lower back or side pain, muscle pain or stiffness, nosebleeds, not able to pass urine, pain or burning while urinating, painful or difficult urination, “pains in the stomach side or abdomen and possibly radiating to the back”, pale skin, pinpoint red or purple spots on the skin, rapid heart rate, rash, “red skin lesions often with a purple center.”

Red irritated eyes, red swollen skin, redness of the white part of the eyes, scaly skin, “seeing, hearing, or feeling things that are not there”, seizures, shakiness and unsteady walk, shortness of breath, sore throat, soreness of the muscles, sores, ulcers, or white spots on the lips or in the mouth, sudden decrease in amount of urine, swelling around the eyes.

“Swelling of the face, hands, legs, and feet”, swelling or inflammation of the mouth, swollen lymph glands, swollen or painful glands, tightness in the chest, “unsteadiness, trembling, or other problems with muscle control or coordination”, unusual bleeding or bruising, upper right abdominal pain, vision changes, vomiting, weakness in the hands or feet, wheezing, yellow eyes or skin.”

“Some side effects do not need medication, because of fear, you will pay a visit to a doctor, you have to pay consultation fee, you also have to pay for the prescription and medicines and together we pay billions of dollars to the pharmaceutical industry, and  in turn they pay scientists, pharmacists and everybody else who wants to be paid in order to sell medicines for causing the above-mentioned side effects for the production of diseases.”

Pharmacists, Doctors And Scientist Paid By The Pharmaceutical Industry

Some Sulfadiazine side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects but do check with them if any of the following side effects continue, or if you are concerned about them.

And for each and every one of these checks, because of side effects you will pay a visit to a doctor, you have to pay for the consultation fee, you also will have to pay for the prescription and medicines and together we pay billions of dollars to the pharmaceutical industry and the pharmaceutical industry pay scientists, pharmacists and everybody else, who wants to be paid in order to sell medicines for causing the above-mentioned side effects for the production of diseases.

Incidence Side Effects Not known

Feeling of constant movement of self or the surroundings, hives or welts, the sensation of spinning, restlessness, and trouble with sleeping.

Healthcare Professionals Applies To Sulfadiazine: Compounding Powder, Oral Tablet Causing Hypersensitivity

Hypersensitivity side effects include urticarial rash (most common), allergic myocarditis, anaphylactoid reactions, anaphylaxis, arthralgia, conjunctival and scleral injection, drug fever and chills, epidermal necrolysis, erythema multiforme, exfoliative dermatitis, generalized skin eruptions, periorbital edema, photosensitization, serum sickness, Stevens-Johnson syndrome, and urticaria.

The use of sulfonamide antibiotics, including sulfadiazine, is associated with large increases in the risk of Stevens-Johnson syndrome and toxic epidermal necrolysis, although these phenomena are rare as a whole.

Hematologic

Hematologic side effects include agranulocytosis (0.1%), aplastic anemia, hemolytic anemia (0.05%), hypoprothrombinemia, leukopenia, methemoglobinemia, and purpura. Hemolytic anemia occurs less often with sulfadiazine than with other sulfonamides. Aplastic anemia may be more likely in patients with poor bone marrow reserves.

Gastrointestinal Side Effects

Gastrointestinal side effects include nausea, vomiting, abdominal pain, diarrhea, anorexia, pancreatitis, and stomatitis.

Hepatic Side Effects

Hepatic side effects are rare but can be serious. Isolated cases of hepatitis and jaundice due to cholestasis have been associated with sulfadiazine. Elevated liver function tests (with a negative hepatitis panel) have been reported in at least one case associated with psychosis.

Psychiatric Side Effects

Psychosis associated with Sulfadiazine and Pyrimethamine therapy in patients with AIDS and CNS toxoplasmosis has been described in two separate case reports. In each case, tremulousness and disorientation developed within three days to two weeks after starting therapy, despite partial resolution of the size of the intracranial T Gondii lesions. No other obvious cause for mental status changes was found.

The delirium resolved upon discontinuation of therapy in each case and was reproducible upon re-challenged. In one case, the patient had elevated liver function tests (hepatitis panel was negative), which were reversible upon discontinuation of therapy. Psychiatric side effects include frank psychosis in patients with AIDS and CNS toxoplasmosis. Tremulousness, disorientation, and delirium have been reported.

Nervous System Side Effects

Nervous system side effects include ataxia, convulsions, hallucinations, headache, insomnia, mental depression, peripheral neuritis, tinnitus, and vertigo.

Renal Side Effects

Renal side effects include crystalluria, lupus erythematosus, periarteritis nodosa, toxic nephrosis with oliguria and anuria, and acute renal failure secondary to crystalluria or tubulointerstitial nephritis.

Genitourinary Side Effects

In one case, analysis of the stone fragments showed a composition of 100% acetylated 2-sulfanilamidopyrimidine, a metabolite of sulfadiazine.

Genitourinary side effects include urolithiasis.

Metabolic Side Effects

Metabolic side effects have included hypoglycemia.

Endocrine side effects

Endocrine side effects associated with sulfonamides have rarely included diuresis, goiter production, and sialadenitis.

If you swallow Isoniazid and Sulfadianozide or AZT as mentioned in one of our previous articles, then you are a lunatic.

References:

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