TxMatt
Member
I will reveal the manufacturers that dispense their H1N1 vaccines to Europe and the us what kind of toxic substances are in them. Secondly, I will home in on those substances and expand on the nature of their respective toxicities.
Focetria (Novartis)
What Focetria contains
- Active Substance:
Influenza virus surface antigens (haemagglutinin and neuraminidase)* of strain:
A/California/7/2009 (H1N1)v like strain (X-179A) 7.5 micrograms** per 0.5 ml dose
* propagated in eggs
** expressed in microgram haemagglutinin.
This vaccine complies with the WHO recommendation and EU decision for the pandemic.
- Adjuvant:
The vaccine contains an ‘adjuvant’ (MF59C.1) to stimulate a better response. MF59C.1 is an oil/water emulsion containing 9.75 mg squalene, 1.175 mg polysorbate 80 and 1.175 mg sorbitan trioleate in a citrate buffer.
- Other Ingredients:
The other ingredients are: thiomersal (multidose vial only), sodium chloride, potassium chloride, potassium dihydrogen phosphate, disodium phosphate dihydrate, magnesium chloride hexahydrate, calcium chloride dihydrate, sodium citrate, citric acid and water for injections.
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Pandemrix (GlaxoSmithKline)
What Pandemrix contains
• Active substance:
Split influenza virus, inactivated, containing antigen* equivalent to:
A/California/7/2009 (H1N1)v-like strain (X-179A) 3.75 micrograms** per 0.5 ml dose
*propagated in eggs
** expressed in microgram haemagglutinin
This vaccine complies with the WHO recommendation and EU decision for the pandemic.
• Adjuvant:
The vaccine contains an ‘adjuvant’ AS03 to stimulate a better response. This adjuvant contains
squalene (10.69 milligrams), DL-α-tocopherol (11.86 milligrams) and polysorbate 80 (4.86
milligrams).
• Other ingredients:
The other ingredients are: polysorbate 80, octoxynol 10, thiomersal, sodium chloride, disodium
hydrogen phosphate, potassium
-------------------------------------------------------------
Celvapan (Baxter)
What Celvapan contains
Active substance:
Whole virion influenza vaccine, inactivated, containing antigen of pandemic strain*:
A/California/07/2009 (H1N1) 7.5 micrograms**
per 0.5 ml dose
* propagated in Vero cells (continuous cell line of mammalian origin)
** haemagglutinin
This vaccine complies with the WHO recommendation and EU decision for the pandemic.
Other ingredients:
The other ingredients are: trometamol, sodium chloride, water for injections, polysorbate 80.
---------------------------------------------------------------------
The Different Poisons
-----------------------------------------------------
Mercury (Thimerosal or Thiomersal)
Thiomersal (INN) (C9H9HgNaO2S), or sodium ethylmercurithiosalicylate, commonly known in the United States as thimerosal, is an organomercury compound (approximately 49% mercury by weight) used as an antiseptic and antifungal agent.
It was invented and patented by Morris Kharasch. The pharmaceutical corporation Eli Lilly and Company gave it the trade name Merthiolate and it has been used as a preservative in vaccines, immunoglobulin preparations, skin test antigens, antivenins, ophthalmic and nasal products, and tattos inks. The compound is being phased out from routine childhood vaccines in the United States, the European Union, and a few other countries
-----------------------------------------------------------------
Here are two quotes from the CDC and the National Academies stating that thimerosal in vaccines is basically all fine and dandy
Thimerosal
“Thimerosal is a mercury-containing preservative used in some vaccines and other products since the 1930s. No harmful effects have been reported from thimerosal at doses used in vaccines, except for minor reactions like redness and swelling at the injection site. However, in July 1999, the Public Health Service (PHS) agencies, the American Academy of Pediatrics (AAP), and vaccine manufacturers agreed that thimerosal should be reduced or eliminated in vaccines as a precautionary measure. Today, with the exception of some influenza (flu) vaccines, none of the vaccines used in the U.S. to protect preschool children against 12 infectious diseases contain thimerosal as a preservative.” Centers for Disease Control and Prevention
“Based on a thorough review of clinical and epidemiological studies, neither the mercury-based vaccine thimerosal nor the measles-mumps-rubella (MMR) vaccine are associated with autism… Five large epidemiological studies in the United States, the United Kingdom, Denmark, and Sweden since 2001 consistently provided evidence that there is no association between thimerosal-containing vaccines and autism… ” National Academies press release about the IOM report “Immunization Safety Review: Vaccines and Autism,” May 18, 2004
----------------------------------------------------------------------------------
Regarding the first quote, if “no harmful effects have been reported from thimerosal at doses used in vaccines” then, while reading the next sentence, why promote the push to eliminate it from vaccines? The quote of and by itself by its mere formulation is oxymoronic and therefore suspicion raising.
--------------------------------------------------------
Here’s a Material Safety Data Sheet of thimerosal:
Primary Physical and Health Hazards: Skin Permeable. Toxic. Mutagen. Irritant (eyes).
Allergen. Nervous System and Reproductive Effects.
Caution Statement: Thimerosal may enter the body through the skin, is toxic, alters genetic material, may be irritating to the eyes, and causes allergic reactions. Effects of exposure may include numbness of extremities, fetal changes, decreased offspring survival, and lung tissue changes.
Routes of Entry: Inhalation and skin absorption.
Effects of Overexposure: Topical allergic dermatitis has been reported. Thimerosal contains
mercury. Mercury poisoning may occur and topical hypersensitivity reactions may be seen. Early signs
of mercury poisoning in adults are nervous system effects, including narrowing of the visual field and
numbness in the extremities. Exposure to mercury in utero and in children may cause mild to severe mental retardation and mild to severe motor coordination impairment. Based on animal data, may be irritating to the eyes.
----------------------------------------------------------------------
So what’s the meaning of these codes? The pictograms and hazard codes page indicates that T+ stands for “Extremely toxic” and N stands for “Dangerous for the environment.” Does that sound like stuff you want to have injected straight into your system?
Here is a portion of the abstract of a new peer-reviewed scientific study investigating thimerosal neurotoxicity. It states quite clearly that thimerosal induces autism-like neurotoxicity:
-------------------------------------------------------------
Thimerosal-induced cellular damage as evidenced by concentration- and time-dependent mitochondrial damage, reduced oxidative-reduction activity, cellular degeneration, and cell death in the in vitro human neuronal and fetal model systems studied. Thimerosal at low nanomolar (nM) concentrations induced significant cellular toxicity in human neuronal and fetal cells. Thimerosal-induced cytoxicity is similar to that observed in AD pathophysiologic studies. Thimerosal was found to be significantly more toxic than the other metal compounds examined
-------------------------------------------------------------------
Squalene
Squalene is a natural organic compound originally obtained for commercial purposes primarily from shark liver oil, though botanic sources (primarily vegetable oils) are used as well, including amaranth seed, rice bran, wheat germ, and olives. All higher organisms produce squalene, including humans. It is a hydrocarbon and a triterpene. Squalene is a natural and vital part of the synthesis of cholesterol, steroid hormones, and vitamin D in the human body.[1] Squalene is used in cosmetics, and more recently as an immunologic adjuvant in vaccines.
Looks pretty benign, no? Well, that seems to be the case if you consume it through regular channels, that is by eating or drinking it. The situation changes unfortunately when you have the stuff injected straight into your system. Now the substance suddenly is being perceived far from benign. You see when injected, squalene is then registered by your immune system as a foreign substance, i.e. something that should not be there. As a consequence, an immune response is triggered, meaning that your immune system will proceed with attacking squalene
---------------------------------------------------------
here’s the abstract of a scientific study which shows that Gulf War era troops suffering from GWS, whether or not they were deployed in the actual Gulf War, almost all had antibodies to squalene:
Antibodies to squalene in Gulf War syndrome.
Asa PB, Cao Y, Garry RF.
Department of Microbiology, Tulane Medical School, 1430 Tulane Avenue, New Orleans, Louisiana, 70112, USA. PMBA@aol.com
Gulf War Syndrome (GWS) is a multisystemic illness afflicting many Gulf War-era veterans. The molecular pathological basis for GWS has not been established. We sought to determine whether the presence of antibodies to squalene correlates with the presence of signs and symptoms of GWS. Participants in this blinded cohort study were individuals immunized for service in Desert Shield/Desert Storm during 1990-1991. They included 144 Gulf War-era veterans or military employees (58 in the blinded study), 48 blood donors, 40 systemic lupus erythematosus patients, 34 silicone breast implant recipients, and 30 chronic fatigue syndrome patients. Serum antibodies to squalene were measured. In our small cohort, the substantial majority (95%) of overtly ill deployed GWS patients had antibodies to squalene. All (100%) GWS patients immunized for service in Desert Shield/Desert Storm who did not deploy, but had the same signs and symptoms as those who did deploy, had antibodies to squalene. In contrast, none (0%) of the deployed Persian Gulf veterans not showing signs and symptoms of GWS have antibodies to squalene. Neither patients with idiopathic autoimmune disease nor healthy controls had detectable serum antibodies to squalene. The majority of symptomatic GWS patients had serum antibodies to squalene. Copyright 2000 Academic Press.
----------------------------------------------------------------------------
Polysorbate 80 (TWEEN 80)
What is this stuff?
Polysorbate 80
Polysorbate 80 (commercially also known as Tween® 80) is a nonionic detergent and emulsifier derived from sorbitol and oleic acid, and is often used in foods, especially pickles. Polysorbate 80 is a viscous water soluble yellow liquid. The hydrophilic groups in this compound are polyethers which are polymers of ethylene oxide.
Polysorbate 80 is often used in ice cream to prevent milk proteins from completely coating the fat droplets. This allows them to join together in chains and nets, to hold air in the mixture, and provide a firmer texture, holding its shape as the ice cream melts.
Other names
Polyoxyethylene sorbitan monooleate
(x)-sorbitan mono-9-octadecenoate poly(oxy-1,2-ethanediyl)
-----------------------------------
Can it do harm? Yes, it can:
Polysorbate 80 in medical products and nonimmunologic anaphylactoid reactions.
Coors EA, Seybold H, Merk HF, Mahler V.
Department of Dermatology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
Polyoxyethylene-sorbitan-20-monooleate (also known as polysorbate 80 and Tween 80) is a solubilizing agent ubiquitously used in nutritives, creams, ointments, lotions, and multiple medical preparations (e.g., vitamin oils, vaccines, and anticancer agents) and as an additive in tablets. Whereas its relevance as a contact allergen has declined during the past decades, it is of current relevance as a “hidden” inductor of anaphylactoid reactions. OBJECTIVE: To identify polysorbate 80 (generally believed to be an inert vehicle) as an inductor of a severe anaphylactoid reaction. METHODS: Skin prick testing, enzyme-linked immunosorbent assay, IgE immunoblotting, and flow cytometric detection of basophil activation were performed in controls and in a patient with a medical history of anaphylactic shock due to intravenous administration of a multivitamin product during pregnancy. RESULTS: Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Polysorbate specific IgE antibodies were not identified in enzyme-linked immunosorbent assay and immunoblot examinations, confirming the nonimmunologic nature of the anaphylactoid reaction. CONCLUSIONS: Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.
ncbi.nlm.nih.gov
==============================
Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.
Gajdová M, Jakubovsky J, Války J.
Institute of Preventive and Clinical Medicine, Limbová, Bratislava.
Neonatal female rats were injected ip (0.1 ml/rat) with Tween 80 in 1, 5 or 10% aqueous solution on days 4-7 after birth. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle, and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea, and had degenerative follicles. ncbi.nlm.nih.gov
Focetria (Novartis)
What Focetria contains
- Active Substance:
Influenza virus surface antigens (haemagglutinin and neuraminidase)* of strain:
A/California/7/2009 (H1N1)v like strain (X-179A) 7.5 micrograms** per 0.5 ml dose
* propagated in eggs
** expressed in microgram haemagglutinin.
This vaccine complies with the WHO recommendation and EU decision for the pandemic.
- Adjuvant:
The vaccine contains an ‘adjuvant’ (MF59C.1) to stimulate a better response. MF59C.1 is an oil/water emulsion containing 9.75 mg squalene, 1.175 mg polysorbate 80 and 1.175 mg sorbitan trioleate in a citrate buffer.
- Other Ingredients:
The other ingredients are: thiomersal (multidose vial only), sodium chloride, potassium chloride, potassium dihydrogen phosphate, disodium phosphate dihydrate, magnesium chloride hexahydrate, calcium chloride dihydrate, sodium citrate, citric acid and water for injections.
--------------------------------------------------------------------
Pandemrix (GlaxoSmithKline)
What Pandemrix contains
• Active substance:
Split influenza virus, inactivated, containing antigen* equivalent to:
A/California/7/2009 (H1N1)v-like strain (X-179A) 3.75 micrograms** per 0.5 ml dose
*propagated in eggs
** expressed in microgram haemagglutinin
This vaccine complies with the WHO recommendation and EU decision for the pandemic.
• Adjuvant:
The vaccine contains an ‘adjuvant’ AS03 to stimulate a better response. This adjuvant contains
squalene (10.69 milligrams), DL-α-tocopherol (11.86 milligrams) and polysorbate 80 (4.86
milligrams).
• Other ingredients:
The other ingredients are: polysorbate 80, octoxynol 10, thiomersal, sodium chloride, disodium
hydrogen phosphate, potassium
-------------------------------------------------------------
Celvapan (Baxter)
What Celvapan contains
Active substance:
Whole virion influenza vaccine, inactivated, containing antigen of pandemic strain*:
A/California/07/2009 (H1N1) 7.5 micrograms**
per 0.5 ml dose
* propagated in Vero cells (continuous cell line of mammalian origin)
** haemagglutinin
This vaccine complies with the WHO recommendation and EU decision for the pandemic.
Other ingredients:
The other ingredients are: trometamol, sodium chloride, water for injections, polysorbate 80.
---------------------------------------------------------------------
The Different Poisons
-----------------------------------------------------
Mercury (Thimerosal or Thiomersal)
Thiomersal (INN) (C9H9HgNaO2S), or sodium ethylmercurithiosalicylate, commonly known in the United States as thimerosal, is an organomercury compound (approximately 49% mercury by weight) used as an antiseptic and antifungal agent.
It was invented and patented by Morris Kharasch. The pharmaceutical corporation Eli Lilly and Company gave it the trade name Merthiolate and it has been used as a preservative in vaccines, immunoglobulin preparations, skin test antigens, antivenins, ophthalmic and nasal products, and tattos inks. The compound is being phased out from routine childhood vaccines in the United States, the European Union, and a few other countries
-----------------------------------------------------------------
Here are two quotes from the CDC and the National Academies stating that thimerosal in vaccines is basically all fine and dandy
Thimerosal
“Thimerosal is a mercury-containing preservative used in some vaccines and other products since the 1930s. No harmful effects have been reported from thimerosal at doses used in vaccines, except for minor reactions like redness and swelling at the injection site. However, in July 1999, the Public Health Service (PHS) agencies, the American Academy of Pediatrics (AAP), and vaccine manufacturers agreed that thimerosal should be reduced or eliminated in vaccines as a precautionary measure. Today, with the exception of some influenza (flu) vaccines, none of the vaccines used in the U.S. to protect preschool children against 12 infectious diseases contain thimerosal as a preservative.” Centers for Disease Control and Prevention
“Based on a thorough review of clinical and epidemiological studies, neither the mercury-based vaccine thimerosal nor the measles-mumps-rubella (MMR) vaccine are associated with autism… Five large epidemiological studies in the United States, the United Kingdom, Denmark, and Sweden since 2001 consistently provided evidence that there is no association between thimerosal-containing vaccines and autism… ” National Academies press release about the IOM report “Immunization Safety Review: Vaccines and Autism,” May 18, 2004
----------------------------------------------------------------------------------
Regarding the first quote, if “no harmful effects have been reported from thimerosal at doses used in vaccines” then, while reading the next sentence, why promote the push to eliminate it from vaccines? The quote of and by itself by its mere formulation is oxymoronic and therefore suspicion raising.
--------------------------------------------------------
Here’s a Material Safety Data Sheet of thimerosal:
Primary Physical and Health Hazards: Skin Permeable. Toxic. Mutagen. Irritant (eyes).
Allergen. Nervous System and Reproductive Effects.
Caution Statement: Thimerosal may enter the body through the skin, is toxic, alters genetic material, may be irritating to the eyes, and causes allergic reactions. Effects of exposure may include numbness of extremities, fetal changes, decreased offspring survival, and lung tissue changes.
Routes of Entry: Inhalation and skin absorption.
Effects of Overexposure: Topical allergic dermatitis has been reported. Thimerosal contains
mercury. Mercury poisoning may occur and topical hypersensitivity reactions may be seen. Early signs
of mercury poisoning in adults are nervous system effects, including narrowing of the visual field and
numbness in the extremities. Exposure to mercury in utero and in children may cause mild to severe mental retardation and mild to severe motor coordination impairment. Based on animal data, may be irritating to the eyes.
----------------------------------------------------------------------
So what’s the meaning of these codes? The pictograms and hazard codes page indicates that T+ stands for “Extremely toxic” and N stands for “Dangerous for the environment.” Does that sound like stuff you want to have injected straight into your system?
Here is a portion of the abstract of a new peer-reviewed scientific study investigating thimerosal neurotoxicity. It states quite clearly that thimerosal induces autism-like neurotoxicity:
-------------------------------------------------------------
Thimerosal-induced cellular damage as evidenced by concentration- and time-dependent mitochondrial damage, reduced oxidative-reduction activity, cellular degeneration, and cell death in the in vitro human neuronal and fetal model systems studied. Thimerosal at low nanomolar (nM) concentrations induced significant cellular toxicity in human neuronal and fetal cells. Thimerosal-induced cytoxicity is similar to that observed in AD pathophysiologic studies. Thimerosal was found to be significantly more toxic than the other metal compounds examined
-------------------------------------------------------------------
Squalene
Squalene is a natural organic compound originally obtained for commercial purposes primarily from shark liver oil, though botanic sources (primarily vegetable oils) are used as well, including amaranth seed, rice bran, wheat germ, and olives. All higher organisms produce squalene, including humans. It is a hydrocarbon and a triterpene. Squalene is a natural and vital part of the synthesis of cholesterol, steroid hormones, and vitamin D in the human body.[1] Squalene is used in cosmetics, and more recently as an immunologic adjuvant in vaccines.
Looks pretty benign, no? Well, that seems to be the case if you consume it through regular channels, that is by eating or drinking it. The situation changes unfortunately when you have the stuff injected straight into your system. Now the substance suddenly is being perceived far from benign. You see when injected, squalene is then registered by your immune system as a foreign substance, i.e. something that should not be there. As a consequence, an immune response is triggered, meaning that your immune system will proceed with attacking squalene
---------------------------------------------------------
here’s the abstract of a scientific study which shows that Gulf War era troops suffering from GWS, whether or not they were deployed in the actual Gulf War, almost all had antibodies to squalene:
Antibodies to squalene in Gulf War syndrome.
Asa PB, Cao Y, Garry RF.
Department of Microbiology, Tulane Medical School, 1430 Tulane Avenue, New Orleans, Louisiana, 70112, USA. PMBA@aol.com
Gulf War Syndrome (GWS) is a multisystemic illness afflicting many Gulf War-era veterans. The molecular pathological basis for GWS has not been established. We sought to determine whether the presence of antibodies to squalene correlates with the presence of signs and symptoms of GWS. Participants in this blinded cohort study were individuals immunized for service in Desert Shield/Desert Storm during 1990-1991. They included 144 Gulf War-era veterans or military employees (58 in the blinded study), 48 blood donors, 40 systemic lupus erythematosus patients, 34 silicone breast implant recipients, and 30 chronic fatigue syndrome patients. Serum antibodies to squalene were measured. In our small cohort, the substantial majority (95%) of overtly ill deployed GWS patients had antibodies to squalene. All (100%) GWS patients immunized for service in Desert Shield/Desert Storm who did not deploy, but had the same signs and symptoms as those who did deploy, had antibodies to squalene. In contrast, none (0%) of the deployed Persian Gulf veterans not showing signs and symptoms of GWS have antibodies to squalene. Neither patients with idiopathic autoimmune disease nor healthy controls had detectable serum antibodies to squalene. The majority of symptomatic GWS patients had serum antibodies to squalene. Copyright 2000 Academic Press.
----------------------------------------------------------------------------
Polysorbate 80 (TWEEN 80)
What is this stuff?
Polysorbate 80
Polysorbate 80 (commercially also known as Tween® 80) is a nonionic detergent and emulsifier derived from sorbitol and oleic acid, and is often used in foods, especially pickles. Polysorbate 80 is a viscous water soluble yellow liquid. The hydrophilic groups in this compound are polyethers which are polymers of ethylene oxide.
Polysorbate 80 is often used in ice cream to prevent milk proteins from completely coating the fat droplets. This allows them to join together in chains and nets, to hold air in the mixture, and provide a firmer texture, holding its shape as the ice cream melts.
Other names
Polyoxyethylene sorbitan monooleate
(x)-sorbitan mono-9-octadecenoate poly(oxy-1,2-ethanediyl)
-----------------------------------
Can it do harm? Yes, it can:
Polysorbate 80 in medical products and nonimmunologic anaphylactoid reactions.
Coors EA, Seybold H, Merk HF, Mahler V.
Department of Dermatology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
Polyoxyethylene-sorbitan-20-monooleate (also known as polysorbate 80 and Tween 80) is a solubilizing agent ubiquitously used in nutritives, creams, ointments, lotions, and multiple medical preparations (e.g., vitamin oils, vaccines, and anticancer agents) and as an additive in tablets. Whereas its relevance as a contact allergen has declined during the past decades, it is of current relevance as a “hidden” inductor of anaphylactoid reactions. OBJECTIVE: To identify polysorbate 80 (generally believed to be an inert vehicle) as an inductor of a severe anaphylactoid reaction. METHODS: Skin prick testing, enzyme-linked immunosorbent assay, IgE immunoblotting, and flow cytometric detection of basophil activation were performed in controls and in a patient with a medical history of anaphylactic shock due to intravenous administration of a multivitamin product during pregnancy. RESULTS: Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Polysorbate specific IgE antibodies were not identified in enzyme-linked immunosorbent assay and immunoblot examinations, confirming the nonimmunologic nature of the anaphylactoid reaction. CONCLUSIONS: Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.
ncbi.nlm.nih.gov
==============================
Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.
Gajdová M, Jakubovsky J, Války J.
Institute of Preventive and Clinical Medicine, Limbová, Bratislava.
Neonatal female rats were injected ip (0.1 ml/rat) with Tween 80 in 1, 5 or 10% aqueous solution on days 4-7 after birth. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle, and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea, and had degenerative follicles. ncbi.nlm.nih.gov
