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FDA Approved Meningitis Vaccine 'MenQuadfi' As 'Safe & Effective' Despite Causing 5.3% Serious Adverse Events. 1 out of every 20 children were seriously harmed including death. Previous Meningitis vaccine was used as 'placebo' which caused harm to 1 out of every 30 injected. During the clinical trial, 5.3% of...

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Valerie Anne Smith

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Meningitis Vaccine...FDA Approved For 6 Week Old Infants. The 'safety trials' caused 1 child out of every 20 to suffer a serious vaccine injury. The injection was never tested against a placebo & it causes anaphylaxis, infant death & Guillain Barre 'polio like paralysis.' --MenQuadfi Meningitis Vaccine Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde --Tetanus Toxoid Protein Carrier-- Residual contaminants can exist & cause the risk of contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea (Sudden Infant Death) Heart Palpitations Syncope (fainting) Fever Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --Recommended Frequency Of Injection-- The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life.
1:20

Meningitis Vaccine...FDA Approved For 6 Week Old Infants. The 'safety trials' caused 1 child out of every 20 to suffer a serious vaccine injury. The injection was never tested against a placebo & it causes anaphylaxis, infant death & Guillain Barre 'polio like paralysis.' --MenQuadfi Meningitis Vaccine Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde --Tetanus Toxoid Protein Carrier-- Residual contaminants can exist & cause the risk of contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea (Sudden Infant Death) Heart Palpitations Syncope (fainting) Fever Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --Recommended Frequency Of Injection-- The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life.

Valerie Anne Smith

42,674 Aufrufe • vor 5 Monaten

FDA Approves Meningitis Vaccine 'MenQuadfi' For 6 Week Old Infants. Stamped 'Safe & Effective' Despite Causing 5.3% Serious Adverse Events... 1 Out Of Every 20 Children Were Seriously Harmed Including Death. The 'Placebo' Was Menveo Meningitis Vaccine Causing Harm To 1 in 30... The Licensure & Approval For Meningitis Vaccines Without A Single True Placebo Used: The 1st Meningitis Vaccine, Menomune, was licensed without a proper placebo-controlled trial & was then used as the placebo control to license the next meningitis vaccine, Menactra. This Meningitis Vaccine, Menactra, is then used as the placebo control to license the Meningitis Vaccine, Menveo. And then the Meningitis Vaccine, Menveo, is used as the placebo control to license the new Meningitis Vaccine, MenQuadfi. During the clinical trial, 5.3% of infants receiving MenQuadfi & 3.6% of infants receiving Menveo had a serious adverse reaction. But because these rates were “similar,” this product was deemed “safe” by FDA because it assumes Menveo is “safe.” Serious Adverse Events & Post Marketing Injuries: Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Death MenQuadfi Ingredients & Tetanus Toxoid Information: (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate The Preparation Of Tetanus Toxoid: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. Essentially growing toxin on rancid meat. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting 'Mad Cow Disease', Bovine Spongiform Encephalopathy. -Meningitis only affects 6-8 out of every 100,000 people. - Yet the serious adverse events from the vaccine affects 5,300 out of every 100,000 people. 👇MenQuadfi Package Insert👇 👇FDA Definition Of Serious Adverse Event👇 👇Quad Meningitis Vaccine Adverse Events👇 Speaker: Dr Scott Graves
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FDA Approves Meningitis Vaccine 'MenQuadfi' For 6 Week Old Infants. Stamped 'Safe & Effective' Despite Causing 5.3% Serious Adverse Events... 1 Out Of Every 20 Children Were Seriously Harmed Including Death. The 'Placebo' Was Menveo Meningitis Vaccine Causing Harm To 1 in 30... The Licensure & Approval For Meningitis Vaccines Without A Single True Placebo Used: The 1st Meningitis Vaccine, Menomune, was licensed without a proper placebo-controlled trial & was then used as the placebo control to license the next meningitis vaccine, Menactra. This Meningitis Vaccine, Menactra, is then used as the placebo control to license the Meningitis Vaccine, Menveo. And then the Meningitis Vaccine, Menveo, is used as the placebo control to license the new Meningitis Vaccine, MenQuadfi. During the clinical trial, 5.3% of infants receiving MenQuadfi & 3.6% of infants receiving Menveo had a serious adverse reaction. But because these rates were “similar,” this product was deemed “safe” by FDA because it assumes Menveo is “safe.” Serious Adverse Events & Post Marketing Injuries: Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Death MenQuadfi Ingredients & Tetanus Toxoid Information: (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate The Preparation Of Tetanus Toxoid: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. Essentially growing toxin on rancid meat. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting 'Mad Cow Disease', Bovine Spongiform Encephalopathy. -Meningitis only affects 6-8 out of every 100,000 people. - Yet the serious adverse events from the vaccine affects 5,300 out of every 100,000 people. 👇MenQuadfi Package Insert👇 👇FDA Definition Of Serious Adverse Event👇 👇Quad Meningitis Vaccine Adverse Events👇 Speaker: Dr Scott Graves

Valerie Anne Smith

169,254 Aufrufe • vor 11 Monaten

Meningitis Vaccine...Newly Approved For 6 Week Old Infants. The 'Safety Trials' Caused 1 Child Out Of Every 20 To Suffer A Serious Vaccine Injury. The Injection Was Never Tested Against A Placebo & It Causes Anaphylaxis, Infant Death & Guillain Barre 'Polio Like Paralysis.' --MenQuadfi Meningitis Vaccine--Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate --Tetanus Toxoid Protein Carrier-- Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow, causing a risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea (Sudden Infant Death) Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --Recommended Frequency Of Injection-- The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life. 👇MenQuadfi Package Insert👇 👇Quad Meningitis Vaccine Adverse Events👇 👇SIRVA Shoulder Injury From Meningitis Vaccine👇 Speakers: Del Bigtree & Jefferey Jaxen Podcast: The HighWire
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Meningitis Vaccine...Newly Approved For 6 Week Old Infants. The 'Safety Trials' Caused 1 Child Out Of Every 20 To Suffer A Serious Vaccine Injury. The Injection Was Never Tested Against A Placebo & It Causes Anaphylaxis, Infant Death & Guillain Barre 'Polio Like Paralysis.' --MenQuadfi Meningitis Vaccine--Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate --Tetanus Toxoid Protein Carrier-- Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow, causing a risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea (Sudden Infant Death) Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --Recommended Frequency Of Injection-- The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life. 👇MenQuadfi Package Insert👇 👇Quad Meningitis Vaccine Adverse Events👇 👇SIRVA Shoulder Injury From Meningitis Vaccine👇 Speakers: Del Bigtree & Jefferey Jaxen Podcast: The HighWire

Valerie Anne Smith

49,697 Aufrufe • vor 1 Jahr

🚨SHOCKING: FDA Greenlit MenQuadfi Meningitis Vaccine for 6-Week-Old Babies – But It Triggered Serious Harm in 5.3% of Trial Kids (1 in 19 Suffer Injury or Death!) No Saline Placebo in Sight – 'Vaccine Pyramid Scheme' - They Used *Other Vaccines* as "Controls," Masking Dangers. Only 6 of 100,00 kids gets Meningitis, but the vaccine harms 1 in 19! Package Insert Dirty Details👇 • **Serious Harms from MenQuadfi (Per Package Insert & Post-Marketing Data):** - Guillain-Barré Syndrome (full-body paralysis) - Bell's Palsy (facial paralysis) - SIRVA (shoulder injury causing pain/paralysis) - Anaphylaxis (life-threatening allergic reaction) - Infant apnea, heart palpitations, syncope (fainting) - Acute Disseminated Encephalomyelitis (ADEM – brain inflammation) - Arthralgia (joint pain), convulsions, paresthesia (nerve issues) - Seizures, transverse myelitis (spinal cord inflammation) - DEATH (reported in trials, unrelated per FDA – but you decide) • **Toxic Ingredients in Each Dose:** - 10 mcg each of Meningococcal A, C, W, Y polysaccharides (conjugated to 55 mcg tetanus toxoid carrier) - 3.35 mg sodium chloride - 1.23 mg sodium acetate - Residual synthetic formaldehyde (carcinogen) - Tetanus toxoid grown on rancid beef heart infusion (risk of contaminants like Mad Cow prions) • **No True Safety Tests – Sham "Placebo" Chain for All Meningitis Vax:** - Menomune: Licensed WITHOUT any placebo-controlled trial - Menactra: Used Menomune as "placebo" (both harmful) - Menveo: Used Menactra as "placebo" - MenQuadfi: Used Menveo as "placebo" – 5.3% Serious Adverse Events vs. 3.6% (deemed "similar" & "safe") Parents: Your child's immune system is a powerhouse – don't let Big Pharma override it. Research, question, protect. What do YOU think? RT if this woke you up!
2:22

🚨SHOCKING: FDA Greenlit MenQuadfi Meningitis Vaccine for 6-Week-Old Babies – But It Triggered Serious Harm in 5.3% of Trial Kids (1 in 19 Suffer Injury or Death!) No Saline Placebo in Sight – 'Vaccine Pyramid Scheme' - They Used *Other Vaccines* as "Controls," Masking Dangers. Only 6 of 100,00 kids gets Meningitis, but the vaccine harms 1 in 19! Package Insert Dirty Details👇 • **Serious Harms from MenQuadfi (Per Package Insert & Post-Marketing Data):** - Guillain-Barré Syndrome (full-body paralysis) - Bell's Palsy (facial paralysis) - SIRVA (shoulder injury causing pain/paralysis) - Anaphylaxis (life-threatening allergic reaction) - Infant apnea, heart palpitations, syncope (fainting) - Acute Disseminated Encephalomyelitis (ADEM – brain inflammation) - Arthralgia (joint pain), convulsions, paresthesia (nerve issues) - Seizures, transverse myelitis (spinal cord inflammation) - DEATH (reported in trials, unrelated per FDA – but you decide) • **Toxic Ingredients in Each Dose:** - 10 mcg each of Meningococcal A, C, W, Y polysaccharides (conjugated to 55 mcg tetanus toxoid carrier) - 3.35 mg sodium chloride - 1.23 mg sodium acetate - Residual synthetic formaldehyde (carcinogen) - Tetanus toxoid grown on rancid beef heart infusion (risk of contaminants like Mad Cow prions) • **No True Safety Tests – Sham "Placebo" Chain for All Meningitis Vax:** - Menomune: Licensed WITHOUT any placebo-controlled trial - Menactra: Used Menomune as "placebo" (both harmful) - Menveo: Used Menactra as "placebo" - MenQuadfi: Used Menveo as "placebo" – 5.3% Serious Adverse Events vs. 3.6% (deemed "similar" & "safe") Parents: Your child's immune system is a powerhouse – don't let Big Pharma override it. Research, question, protect. What do YOU think? RT if this woke you up!

Valerie Anne Smith

28,610 Aufrufe • vor 8 Monaten

🚨PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System.
2:31

🚨PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System.

Valerie Anne Smith

22,102 Aufrufe • vor 1 Monat

PREVNAR Pneumonia Vaccine...If People Read The Package Insert, No One Would Get This Injection. No Safety Studies Using A Placebo For All 5 Pneumonia Shots. Warning Of Sudden Death From Apnea Following Injection. 44,240 Shots Are Required To Prevent Only 41 Cases Of Pneumonia. --Ingredients-- Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein: Beef Heart Infusion (BHI) is used as a culture medium to grow diphtheria toxoid, the bacterium that produces diphtheria toxin. The infusion is prepared by suspending minced beef heart in water, heated to boiling & putrid environment allows the diphtheria toxin to grow. The diphtheria toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant: Known Neurotoxin permeating the Blood Brain Barrier to cause diseases such as Autism, Alzheimer's & MS. This vaccine has 8X the toxic limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5mcg/per kg of weight as max aluminum limit. Polysorbate 80: Weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of Pneumovax 23 was the HEP-A & HEP-B vaccines. The safety trial 'placebo' used to prove the safety of Prevnar 20 was the Prevnar 13 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 13 was the Prevnar 9 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 9 was the Prevnar 7 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 7 was the DTP-HIB vaccine. --Serious Adverse Events & Post Market Injuries-- Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. The adult, without warning, will stop breathing & the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Guillain Barre Syndrome(full body paralysis) Lymphadenopathy Cyanosis(cardiac distress) Hypotonia Vascular Disease Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Systemic Inflammatory Response System(SIRS) 👇Prevnar Package Insert👇 👇Pneumonia Vaccine Serious Adverse Events👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD
0:59

PREVNAR Pneumonia Vaccine...If People Read The Package Insert, No One Would Get This Injection. No Safety Studies Using A Placebo For All 5 Pneumonia Shots. Warning Of Sudden Death From Apnea Following Injection. 44,240 Shots Are Required To Prevent Only 41 Cases Of Pneumonia. --Ingredients-- Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein: Beef Heart Infusion (BHI) is used as a culture medium to grow diphtheria toxoid, the bacterium that produces diphtheria toxin. The infusion is prepared by suspending minced beef heart in water, heated to boiling & putrid environment allows the diphtheria toxin to grow. The diphtheria toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant: Known Neurotoxin permeating the Blood Brain Barrier to cause diseases such as Autism, Alzheimer's & MS. This vaccine has 8X the toxic limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5mcg/per kg of weight as max aluminum limit. Polysorbate 80: Weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of Pneumovax 23 was the HEP-A & HEP-B vaccines. The safety trial 'placebo' used to prove the safety of Prevnar 20 was the Prevnar 13 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 13 was the Prevnar 9 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 9 was the Prevnar 7 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 7 was the DTP-HIB vaccine. --Serious Adverse Events & Post Market Injuries-- Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. The adult, without warning, will stop breathing & the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Guillain Barre Syndrome(full body paralysis) Lymphadenopathy Cyanosis(cardiac distress) Hypotonia Vascular Disease Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Systemic Inflammatory Response System(SIRS) 👇Prevnar Package Insert👇 👇Pneumonia Vaccine Serious Adverse Events👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

136,945 Aufrufe • vor 1 Jahr

PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System. 👇Penta 5-in-1 Vaccines Death Study👇 👇Pentacel Vaccine Package Insert👇 👇Vaccine Excipient Summary List👇 Speaker: Dr Jeffrey Barke, MD
2:37

PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System. 👇Penta 5-in-1 Vaccines Death Study👇 👇Pentacel Vaccine Package Insert👇 👇Vaccine Excipient Summary List👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

209,935 Aufrufe • vor 1 Jahr

"The Most Damning Of All Evidence Is That The DTaP Vaccine Will Kill You 30X More Than The Disease Itself." Dr Paul Thomas, MD "Whooping Cough Vaccine Primes Your Body To Contract Pertussis Multiple Times, Over & Over, For Life." Safety Tested For Only 14 Days With No Placebo. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. The Placebos used to 'safety test' the Pertussis vaccine were the Tetanus & Diphtheria vaccines. Tested for only 14 days before US FDA & CDC approval. Warnings: The vaccine does not stop transmission or infection. Whooping cough outbreaks occur within the vaccinated because natural contraction of whooping cough provides lifelong immunity. The risk of a serious adverse event after vaccination is 1 in 25, including SIDS Apnea: SIDS is now being called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. How The 3 Components Are Grown & Cultured: Tetanus: C. Tetani Toxoid is grown in heated & putrefied Beef Heart Infusion, known as BHI. The tetanus toxin is treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Neomycin Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Dr Paul Thomas, MD Video: Children’s Health Defense
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"The Most Damning Of All Evidence Is That The DTaP Vaccine Will Kill You 30X More Than The Disease Itself." Dr Paul Thomas, MD "Whooping Cough Vaccine Primes Your Body To Contract Pertussis Multiple Times, Over & Over, For Life." Safety Tested For Only 14 Days With No Placebo. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. The Placebos used to 'safety test' the Pertussis vaccine were the Tetanus & Diphtheria vaccines. Tested for only 14 days before US FDA & CDC approval. Warnings: The vaccine does not stop transmission or infection. Whooping cough outbreaks occur within the vaccinated because natural contraction of whooping cough provides lifelong immunity. The risk of a serious adverse event after vaccination is 1 in 25, including SIDS Apnea: SIDS is now being called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. How The 3 Components Are Grown & Cultured: Tetanus: C. Tetani Toxoid is grown in heated & putrefied Beef Heart Infusion, known as BHI. The tetanus toxin is treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Neomycin Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Dr Paul Thomas, MD Video: Children’s Health Defense

Valerie Anne Smith

62,758 Aufrufe • vor 1 Jahr

Pertussis (Whooping Cough) Vaccine...Shocking Facts Everyone Should Know. The Vaccine Does Not Stop Infection Or Transmission. It Has Never Been Safety Tested With A Placebo & The Risk Of Serious Adverse Injury Is 1 in 25. Whooping Cough Outbreaks Occur Within The Vaccinated. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. Pertussis Vaccine is only available combined with Tetanus Toxoid & Diphtheria. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. Institute Of Medicine Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid Vaccine Manufacture: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. Minced beef heart is heated to boiling & the putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria Toxin Vaccine Manufacture: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis Antigen Vaccine Manufacture: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Facial palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder Placebo Safety Testing In Clinical Trials: Neither DTaP nor TDap were clinical safety tested against a true saline placebo. Each individual component was safety tested against the other 2 used as placebo. Pertussis safety trials used Diphtheria Toxoid & Tetanus Toxoid as placebos, thus skewing results with vaccine injuries in both groups making the pertussis vaccine appear safe. NNV Number Needed To Vaccinate For Efficacy: (The number of people needed to receive vaccination in order to prevent death or hospitalization.) 1,000,000 million people need to be vaccinated to prevent 1 death from pertussis. 100,000 people need to be vaccinated to prevent 1 ICU hospital admission. 10,000 people need to be vaccinated to prevent 1 hospital admission. 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Ted Kuntz & Nico Laganiere Video: Vaccine Choice Canada
0:54

Pertussis (Whooping Cough) Vaccine...Shocking Facts Everyone Should Know. The Vaccine Does Not Stop Infection Or Transmission. It Has Never Been Safety Tested With A Placebo & The Risk Of Serious Adverse Injury Is 1 in 25. Whooping Cough Outbreaks Occur Within The Vaccinated. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. Pertussis Vaccine is only available combined with Tetanus Toxoid & Diphtheria. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. Institute Of Medicine Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid Vaccine Manufacture: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. Minced beef heart is heated to boiling & the putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria Toxin Vaccine Manufacture: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis Antigen Vaccine Manufacture: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Facial palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder Placebo Safety Testing In Clinical Trials: Neither DTaP nor TDap were clinical safety tested against a true saline placebo. Each individual component was safety tested against the other 2 used as placebo. Pertussis safety trials used Diphtheria Toxoid & Tetanus Toxoid as placebos, thus skewing results with vaccine injuries in both groups making the pertussis vaccine appear safe. NNV Number Needed To Vaccinate For Efficacy: (The number of people needed to receive vaccination in order to prevent death or hospitalization.) 1,000,000 million people need to be vaccinated to prevent 1 death from pertussis. 100,000 people need to be vaccinated to prevent 1 ICU hospital admission. 10,000 people need to be vaccinated to prevent 1 hospital admission. 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Ted Kuntz & Nico Laganiere Video: Vaccine Choice Canada

Valerie Anne Smith

35,435 Aufrufe • vor 1 Jahr

2.23 Million-Person Study Finds Pneumococcal Vaccines Increase Risk Of Pneumonia & Death. Rather Than Prevention, Risk Of Pneumonia Increased +83% & Risk Of Death Increased +91%. There Have Been 5 Pneumonia Vaccines, All Were 'Safety Tested' Using Another Vaccine As 'Placebo.' The pneumococcal vaccines that are given to nearly every US child & senior adult are linked to higher pneumonia & death rates in one of the largest real-world studies ever conducted. Health authorities have promoted getting a Pneumonia Vaccine as a 'crucial' tool to prevent serious bacterial pneumonia. Tens of millions of doses are given every year. Infants receive a 4 dose series & adults over 50 are urged to get vaccinated. Now, a landmark population-based study published in BMC Infectious Diseases has completely dismantled the rationale for current pneumococcal conjugate vaccine (PCV) recommendations. The study authors found that recipients were significantly more likely to be hospitalized for pneumonia & more likely to die from pneumonia-related causes compared to their unvaccinated counterparts. Risk of pneumonia increased +83% & risk of death increased +91%. All 5 Pneumococcal Vaccines are built on the same biological platform. Each newer version contains all of the same serotypes included in PCV13, plus additional ones, using the same diphtheria-derived carrier protein (CRM197) & aluminum adjuvant system. Safety Study Placebos Used For Each Vaccine... Pneumovax 23 used the HEP-A & HEP-B vaccines as placebo. Prevnar 20 used the Prevnar 13 vaccine as placebo. Prevnar 13 used the Prevnar 9 vaccine as placebo. Prevnar 9 used the Prevnar 7 vaccine as placebo. Prevnar 7 used the DTP-HIB vaccine as placebo. Harmful Ingredients In Each Of The Pneumonia Vaccines... 1⃣ Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein, which carries the risk of Bovine Spongiform Encephalopathy also known as Mad Cow Disease, because of how the diphtheria toxoid is 'grown.' 2⃣ Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant, is a known neurotoxin. The amount in the vaccine, 125 mcg, is 8X the limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5 mcg/per kg of weight as max aluminum limit. 3⃣ Polysorbate 80 weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events. Post Marketing Injuries... 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. In the infant, the death will be classified as SIDS. In the adult, the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Serious Adverse Events... Guillain Barre Syndrome(full body paralysis) Cyanosis(cardiac distress) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant & Adult Sudden Apnea Heart Palpitations Acute Disseminated Encephalomyelitis (ADEM) Convulsions Seizure Transverse myelitis Systemic Inflammatory Response System (SIRS) 👇Vaccines Increase Risk Of Pneumonia & Death👇 👇Prevnar 20 Package Insert👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD
0:58

2.23 Million-Person Study Finds Pneumococcal Vaccines Increase Risk Of Pneumonia & Death. Rather Than Prevention, Risk Of Pneumonia Increased +83% & Risk Of Death Increased +91%. There Have Been 5 Pneumonia Vaccines, All Were 'Safety Tested' Using Another Vaccine As 'Placebo.' The pneumococcal vaccines that are given to nearly every US child & senior adult are linked to higher pneumonia & death rates in one of the largest real-world studies ever conducted. Health authorities have promoted getting a Pneumonia Vaccine as a 'crucial' tool to prevent serious bacterial pneumonia. Tens of millions of doses are given every year. Infants receive a 4 dose series & adults over 50 are urged to get vaccinated. Now, a landmark population-based study published in BMC Infectious Diseases has completely dismantled the rationale for current pneumococcal conjugate vaccine (PCV) recommendations. The study authors found that recipients were significantly more likely to be hospitalized for pneumonia & more likely to die from pneumonia-related causes compared to their unvaccinated counterparts. Risk of pneumonia increased +83% & risk of death increased +91%. All 5 Pneumococcal Vaccines are built on the same biological platform. Each newer version contains all of the same serotypes included in PCV13, plus additional ones, using the same diphtheria-derived carrier protein (CRM197) & aluminum adjuvant system. Safety Study Placebos Used For Each Vaccine... Pneumovax 23 used the HEP-A & HEP-B vaccines as placebo. Prevnar 20 used the Prevnar 13 vaccine as placebo. Prevnar 13 used the Prevnar 9 vaccine as placebo. Prevnar 9 used the Prevnar 7 vaccine as placebo. Prevnar 7 used the DTP-HIB vaccine as placebo. Harmful Ingredients In Each Of The Pneumonia Vaccines... 1⃣ Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein, which carries the risk of Bovine Spongiform Encephalopathy also known as Mad Cow Disease, because of how the diphtheria toxoid is 'grown.' 2⃣ Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant, is a known neurotoxin. The amount in the vaccine, 125 mcg, is 8X the limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5 mcg/per kg of weight as max aluminum limit. 3⃣ Polysorbate 80 weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events. Post Marketing Injuries... 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. In the infant, the death will be classified as SIDS. In the adult, the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Serious Adverse Events... Guillain Barre Syndrome(full body paralysis) Cyanosis(cardiac distress) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant & Adult Sudden Apnea Heart Palpitations Acute Disseminated Encephalomyelitis (ADEM) Convulsions Seizure Transverse myelitis Systemic Inflammatory Response System (SIRS) 👇Vaccines Increase Risk Of Pneumonia & Death👇 👇Prevnar 20 Package Insert👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

41,576 Aufrufe • vor 9 Monaten

The American Academy of Pediatrics Wants To Ban All Religious & Philosophical Vaccine Exemptions. Mandating The 72 Doses On The Childhood Vaccine Schedule Assures Pediatricians Of Their Continued 50% Revenue Stream. Making Vaxelis 6-in-1 Vaccine Mandatory Is Criminal & Unjust. If Parents Read The Package Insert, No One In Their Right Mind Would Ever Inject Their Child Again. Not A Single Safety Study Against A Placebo & 6 Infants Died During The Trial. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. 'Institute Of Medicine' Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Ingredients: Each dose, in a 3 injection series Diphtheria Vaccine Tetanus Toxoid Vaccine Pertussis Vaccine Polio Vaccine HIB & Hep-B Vaccines Polysorbate 80 Formaldehyde Aluminum Phosphate Amorphous Aluminium Hydroxyphosphate Sulfate Recombinant DNA Yeast Vero African Green Monkey Kidney cell line, Ammonium Thiocyanate Glutaraldehyde Neomycin Streptomycin Polymyxin B Bovine serum albumin Clinical Safety Trial Studies: 6 clinical trials were all run without an inert placebo. One group received the Vaxelis 6 in 1 experimental vaccine. The other group received the 5 in 1 Penta vaccine with added Hep-B. Both groups received the same 6 vaccines. There was no placebo group to compare vaccine injuries. Clinical Safety Trial Deaths: In one of the 6 safety studies, 68 infants suffered a serious adverse event. Of these adverse event injuries, 6 infants died. The reported 'causes of death' were: Sepsis, SIDS & Hydrocephalus. Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇AAP Calls To Ban Vaccine Exemptions👇 👇Hexavalent Vaccines & Sudden Death👇 👇National Vaccine Information Center👇 👇Vaxelis Vaccine Package Insert For Physicians👇 Speaker: Dr Jeffrey Barke, MD
2:33

The American Academy of Pediatrics Wants To Ban All Religious & Philosophical Vaccine Exemptions. Mandating The 72 Doses On The Childhood Vaccine Schedule Assures Pediatricians Of Their Continued 50% Revenue Stream. Making Vaxelis 6-in-1 Vaccine Mandatory Is Criminal & Unjust. If Parents Read The Package Insert, No One In Their Right Mind Would Ever Inject Their Child Again. Not A Single Safety Study Against A Placebo & 6 Infants Died During The Trial. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. 'Institute Of Medicine' Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Ingredients: Each dose, in a 3 injection series Diphtheria Vaccine Tetanus Toxoid Vaccine Pertussis Vaccine Polio Vaccine HIB & Hep-B Vaccines Polysorbate 80 Formaldehyde Aluminum Phosphate Amorphous Aluminium Hydroxyphosphate Sulfate Recombinant DNA Yeast Vero African Green Monkey Kidney cell line, Ammonium Thiocyanate Glutaraldehyde Neomycin Streptomycin Polymyxin B Bovine serum albumin Clinical Safety Trial Studies: 6 clinical trials were all run without an inert placebo. One group received the Vaxelis 6 in 1 experimental vaccine. The other group received the 5 in 1 Penta vaccine with added Hep-B. Both groups received the same 6 vaccines. There was no placebo group to compare vaccine injuries. Clinical Safety Trial Deaths: In one of the 6 safety studies, 68 infants suffered a serious adverse event. Of these adverse event injuries, 6 infants died. The reported 'causes of death' were: Sepsis, SIDS & Hydrocephalus. Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇AAP Calls To Ban Vaccine Exemptions👇 👇Hexavalent Vaccines & Sudden Death👇 👇National Vaccine Information Center👇 👇Vaxelis Vaccine Package Insert For Physicians👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

317,898 Aufrufe • vor 1 Jahr

If People Were Properly Informed About Tetanus & The 'Vaccine'...No One Would Ever Get This Injection. 4 Truths That Everyone Should Know About Tetanus & The 'Vaccine.' Before Your Doctor Pressures You To Get The Shot, Consider The Facts Carefully & Make An Informed Decision. 1⃣ Tetanus Toxoid Vaccine Manufacture: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. 2⃣ There Is No Single Tetanus Vaccine: The Tetanus vaccine was discontinued in 2012. When a Tetanus vaccine is given, it is actually the TDaP Vaccine, which is Tetanus, Diphtheria & Pertussis. Doctors & Pharmacists do not disclose this fact when they administer a 'Tetanus Shot.' Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP. Many cases of fatal anaphylaxis are caused by this. 3⃣ Tetanus (Clostridium Tetani) Is An Anaerobic Bacterial Spore: It resides in the intestinal tract of ruminant animals & in their feces. If your wound was not in an area where cattle, sheep or horses graze you will not get Tetanus. Tetanus is an anaerobic bacteria that cannot survive in the presence of oxygen. The bacterial spore dies when it's oxygenated. Blood carries oxygen, so a bleeding wound that is cleaned thoroughly will not have living Tetanus spores. ✳️Tetanus does not live on knives or scissors in your kitchen. ✳️Tetanus does not live on nails you brought home from the hardware store. ✳️Tetanus does not live on the wood splinter that entered your foot in your home. ✳️Tetanus does not live on the shards of glass that broke in your sink. 4⃣ The Tetanus Shot Will Not Help An Active Tetanus Infection: It takes a minimum of 3 weeks & possibly up to 8 weeks to build antibodies from the Tetanus vaccine within TDaP. An active injury & Tetanus infection will not be helped at all by getting vaccinated. It is pointless to get the shot & harmful side effects are well known from TDaP. Actual Tetanus bacterial infection is rare. In the US there are less than 30 cases annually. And the risk of dying from Tetanus is 1 in 44 million. The good news is, Tetanus as C. Tetani, is easily treated & eradicated from the body: *⃣ 1 Gram of Vitamin C (whole acerola complex) per day for 5-7 days kills the Tetanus bacterial spores. As shown in clinical trials as 100% reversal with no fatalities when Vitamin C is used as prevention & treatment for Tetanus bacterial infection. The Tetanus vaccine did not eradicate Tetanus. 98% of Tetanus cases were eradicated in the early 1900s, PRIOR to the invention of the Tetanus Toxoid Vaccine. Simple community & street wide sanitation improvements cleared Tetanus Bacterial Spores from streets filled with horse feces & barns full of cattle feces. 👇The Manufacture Process Of Tetanus Toxoid👇 👇Tetanus Research Document Substack👇 👇Vitamin C Prevents & Treats Tetanus Infection👇 Speaker: Dennis Echelbarger
1:28

If People Were Properly Informed About Tetanus & The 'Vaccine'...No One Would Ever Get This Injection. 4 Truths That Everyone Should Know About Tetanus & The 'Vaccine.' Before Your Doctor Pressures You To Get The Shot, Consider The Facts Carefully & Make An Informed Decision. 1⃣ Tetanus Toxoid Vaccine Manufacture: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. 2⃣ There Is No Single Tetanus Vaccine: The Tetanus vaccine was discontinued in 2012. When a Tetanus vaccine is given, it is actually the TDaP Vaccine, which is Tetanus, Diphtheria & Pertussis. Doctors & Pharmacists do not disclose this fact when they administer a 'Tetanus Shot.' Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP. Many cases of fatal anaphylaxis are caused by this. 3⃣ Tetanus (Clostridium Tetani) Is An Anaerobic Bacterial Spore: It resides in the intestinal tract of ruminant animals & in their feces. If your wound was not in an area where cattle, sheep or horses graze you will not get Tetanus. Tetanus is an anaerobic bacteria that cannot survive in the presence of oxygen. The bacterial spore dies when it's oxygenated. Blood carries oxygen, so a bleeding wound that is cleaned thoroughly will not have living Tetanus spores. ✳️Tetanus does not live on knives or scissors in your kitchen. ✳️Tetanus does not live on nails you brought home from the hardware store. ✳️Tetanus does not live on the wood splinter that entered your foot in your home. ✳️Tetanus does not live on the shards of glass that broke in your sink. 4⃣ The Tetanus Shot Will Not Help An Active Tetanus Infection: It takes a minimum of 3 weeks & possibly up to 8 weeks to build antibodies from the Tetanus vaccine within TDaP. An active injury & Tetanus infection will not be helped at all by getting vaccinated. It is pointless to get the shot & harmful side effects are well known from TDaP. Actual Tetanus bacterial infection is rare. In the US there are less than 30 cases annually. And the risk of dying from Tetanus is 1 in 44 million. The good news is, Tetanus as C. Tetani, is easily treated & eradicated from the body: *⃣ 1 Gram of Vitamin C (whole acerola complex) per day for 5-7 days kills the Tetanus bacterial spores. As shown in clinical trials as 100% reversal with no fatalities when Vitamin C is used as prevention & treatment for Tetanus bacterial infection. The Tetanus vaccine did not eradicate Tetanus. 98% of Tetanus cases were eradicated in the early 1900s, PRIOR to the invention of the Tetanus Toxoid Vaccine. Simple community & street wide sanitation improvements cleared Tetanus Bacterial Spores from streets filled with horse feces & barns full of cattle feces. 👇The Manufacture Process Of Tetanus Toxoid👇 👇Tetanus Research Document Substack👇 👇Vitamin C Prevents & Treats Tetanus Infection👇 Speaker: Dennis Echelbarger

Valerie Anne Smith

41,566 Aufrufe • vor 1 Jahr

🚨BREAKING: 6 INFANTS DIED in VAXELIS 6-in-1 Childhood Vaccine Trials—NO PLACEBO Safety Study! AAP American Academy of Pediatrics Pushes Mandates, Calls For Exemptions To Be Banned, While Hiding THESE DEATHS? Parents, Please WAKE UP Before It's Too Late! • **Allergies Alert:** Package warns of anaphylaxis—epinephrine MUST be ready! Risk of severe hypersensitivity reactions. ⚠️ • **IOM Bombshell:** Institute of Medicine confirms Tetanus Toxoid causes Brachial Neuritis (arm paralysis) & Guillain-Barré (full-body paralysis mimicking polio). Paralyzing truth! 🛑 • **Apnea Nightmare:** Aluminum adjuvants trigger "Aluminum Adjuvant Apnea"—stops breathing, mislabeled as SIDS. Silent killer in shots? 💔 • **Toxic Ingredients:** Formaldehyde, Polysorbate 80, Aluminum salts, Monkey kidney cells, Fetal bovine blood, Human organ DNA, Neomycin, Streptomycin, Glutaraldehyde—poison cocktail for babies! ☠️ Full list in insert. • **Flawed Trials:** ZERO inert placebo groups! Compared to another multi-vax, masking real harms. 68 serious Adverse Events in one study—6 infant deaths (SIDS, sepsis, hydrocephalus). Criminal cover-up? ❌ • **Post-Market Horrors:** Reports of GBS paralysis, myocarditis, encephalitis, Bell's palsy, anaphylaxis, apnea, autoimmune disorders. VAERS hides the iceberg—demand transparency! 📈
2:26

🚨BREAKING: 6 INFANTS DIED in VAXELIS 6-in-1 Childhood Vaccine Trials—NO PLACEBO Safety Study! AAP American Academy of Pediatrics Pushes Mandates, Calls For Exemptions To Be Banned, While Hiding THESE DEATHS? Parents, Please WAKE UP Before It's Too Late! • **Allergies Alert:** Package warns of anaphylaxis—epinephrine MUST be ready! Risk of severe hypersensitivity reactions. ⚠️ • **IOM Bombshell:** Institute of Medicine confirms Tetanus Toxoid causes Brachial Neuritis (arm paralysis) & Guillain-Barré (full-body paralysis mimicking polio). Paralyzing truth! 🛑 • **Apnea Nightmare:** Aluminum adjuvants trigger "Aluminum Adjuvant Apnea"—stops breathing, mislabeled as SIDS. Silent killer in shots? 💔 • **Toxic Ingredients:** Formaldehyde, Polysorbate 80, Aluminum salts, Monkey kidney cells, Fetal bovine blood, Human organ DNA, Neomycin, Streptomycin, Glutaraldehyde—poison cocktail for babies! ☠️ Full list in insert. • **Flawed Trials:** ZERO inert placebo groups! Compared to another multi-vax, masking real harms. 68 serious Adverse Events in one study—6 infant deaths (SIDS, sepsis, hydrocephalus). Criminal cover-up? ❌ • **Post-Market Horrors:** Reports of GBS paralysis, myocarditis, encephalitis, Bell's palsy, anaphylaxis, apnea, autoimmune disorders. VAERS hides the iceberg—demand transparency! 📈

Valerie Anne Smith

41,136 Aufrufe • vor 8 Monaten

"No Vaccine On The Childhood Schedule Has Ever Been Tested Against A True Placebo." Del Bigtree "No Vaccine Has Ever Been Thoroughly Safety Tested." The Hep-B Vaccine Used Injected Aluminum As The 'Placebo...' 'Safety Tested' On 147 Children For Only 5 Days Before Approval. Every Single⏬Vaccine Safety Trial Period Is Listed In The Package Insert Under Section 6.1, Which States How Long The Trial Participants Were Observed To 'Prove Safety Of The Vaccine' Before Given CDC & FDA Approval. Think the vaccines have gone thru a long robust safety trial to prove they are 'safe & effective'? All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, not vaccines... Hep-B Vaccine: Administered to 147 infants & children who were monitored for 5 days, then granted approval. Gardasil HPV Vaccine: Safety was evaluated using vaccination report card (VRC)- aided surveillance for 14 days. Hep-A Vaccine: Test subjects were followed for safety for 14 days. Influenza A Vaccine: Participants were monitored for adverse events for 28 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored daily for 7 days. DTaP & TDaP Vaccines: Participants were monitored for 14 days. Chicken Pox Vaccine: Subjects were observed for adverse reactions for 42 days. Shingles Vaccine: Test subjects were followed for 7 days. Prevnar Pneumonia Vaccine: Participants were monitored for 7 days. RSV Vaccine: Safety monitored for 30 days. MMR Vaccine: Participants were followed for 42 days. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. No true placebo in a vaccine clinical trial skews all results & makes all vaccines appear "safe & effective" because the adverse events, side effects & Injuries in both groups are the same. List⏬Of 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo Was Injected Aluminum Adjuvant. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine. Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. COVID-19 Vaccine Clinical Trial...Placebo Was Meningitis Vaccine. 👇Hep-B Vaccine Package Insert👇 👇Gardasil HPV Vaccine Package Insert👇 👇Hep-A Vaccine Package Insert👇 Speaker: Alex Clark & Del Bigtree Podcast: Alex Clark
1:15

"No Vaccine On The Childhood Schedule Has Ever Been Tested Against A True Placebo." Del Bigtree "No Vaccine Has Ever Been Thoroughly Safety Tested." The Hep-B Vaccine Used Injected Aluminum As The 'Placebo...' 'Safety Tested' On 147 Children For Only 5 Days Before Approval. Every Single⏬Vaccine Safety Trial Period Is Listed In The Package Insert Under Section 6.1, Which States How Long The Trial Participants Were Observed To 'Prove Safety Of The Vaccine' Before Given CDC & FDA Approval. Think the vaccines have gone thru a long robust safety trial to prove they are 'safe & effective'? All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, not vaccines... Hep-B Vaccine: Administered to 147 infants & children who were monitored for 5 days, then granted approval. Gardasil HPV Vaccine: Safety was evaluated using vaccination report card (VRC)- aided surveillance for 14 days. Hep-A Vaccine: Test subjects were followed for safety for 14 days. Influenza A Vaccine: Participants were monitored for adverse events for 28 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored daily for 7 days. DTaP & TDaP Vaccines: Participants were monitored for 14 days. Chicken Pox Vaccine: Subjects were observed for adverse reactions for 42 days. Shingles Vaccine: Test subjects were followed for 7 days. Prevnar Pneumonia Vaccine: Participants were monitored for 7 days. RSV Vaccine: Safety monitored for 30 days. MMR Vaccine: Participants were followed for 42 days. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. No true placebo in a vaccine clinical trial skews all results & makes all vaccines appear "safe & effective" because the adverse events, side effects & Injuries in both groups are the same. List⏬Of 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo Was Injected Aluminum Adjuvant. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine. Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. COVID-19 Vaccine Clinical Trial...Placebo Was Meningitis Vaccine. 👇Hep-B Vaccine Package Insert👇 👇Gardasil HPV Vaccine Package Insert👇 👇Hep-A Vaccine Package Insert👇 Speaker: Alex Clark & Del Bigtree Podcast: Alex Clark

Valerie Anne Smith

46,282 Aufrufe • vor 1 Jahr

FLUZONE Flu Vaccine...Approved For 6 Month Old Infants. Causes Guillain Barre Syndrome Paralysis. Contains Neurotoxin Formaldehyde Which Causes Leukemia. 4 Flu Strains Grown In Fertilized Chicken Egg--Warning For Future Egg Allergy. No Clinical Safety Study Prior To Approval. ---Ingredients--- 4 Strains of influenza Fertilized embryonic chicken egg (causes egg allergy) Formaldehyde (neurotoxin & causes leukemia) Triton X-100 (detergent/hormone disruptor) Hemagglutinin HA Antigen (harmful host cell) Phosphate solution (toxic to bones) ---European Union Bans Triton X-100--- Triton™ X-100, a detergent with a hydrophilic polyethylene oxide chain has found widespread use in the biopharmaceutical industry. Even though it is used heavily throughout the industry, the degradation products from Triton™ X-100 exhibit long-lasting estrogenic properties in fish, birds & mammals, causing chronic harm to their endocrine systems. ---Hemagglutinin HA Antigen--- Influenza virus hemagglutinin facilitates infection by allowing the virus to bind to & enter host cells, making the virus dangerous. ---Warnings & Precautions--- Causal for Guillain Barre Syndrome Paralysis like Polio. Do not administer to anyone with an egg allergy, if egg allergy is known in a 6 month old infant. Emergency procedures must be in place in case of anaphylaxis. ---Clinical Trials--- No clinical trial was done, no safety trial & no placebo. 1,419 children age 6 months thru 35 months were injected & then blood serum tested to check for antibody titers. ---Post Marketing Adverse Events & Injuries--- Guillain-Barré syndrome (GBS) Convulsions Myelitis Encephalomyelitis Transverse myelitis Facial palsy (Bell’s Palsy) Optic neuritis/neuropathy Brachial neuritis (paralysis) Syncope Anaphylaxis Angioedema Thrombocytopenia Lymphadenopathy Vasculitis Stevens Johnson Syndrome High fever Loss of appetite Extreme fatigue Apnea ---Vaxxed Verses Unvaxxed Studies--- 2025 flu vaccine efficacy rate is only 32%. Studies on inactivated influenza vaccines show 4.4 times greater risk of getting the flu after a flu vaccination as compared to those unvaccinated. 👇Fluzone Vaccine Package Insert👇 👇Influenza Vaccine Adverse Events Reports👇 👇Flu Vaccine Increases Risk Of Getting The Flu👇 Speaker: Dr Jeffrey Barke, MD
2:07

FLUZONE Flu Vaccine...Approved For 6 Month Old Infants. Causes Guillain Barre Syndrome Paralysis. Contains Neurotoxin Formaldehyde Which Causes Leukemia. 4 Flu Strains Grown In Fertilized Chicken Egg--Warning For Future Egg Allergy. No Clinical Safety Study Prior To Approval. ---Ingredients--- 4 Strains of influenza Fertilized embryonic chicken egg (causes egg allergy) Formaldehyde (neurotoxin & causes leukemia) Triton X-100 (detergent/hormone disruptor) Hemagglutinin HA Antigen (harmful host cell) Phosphate solution (toxic to bones) ---European Union Bans Triton X-100--- Triton™ X-100, a detergent with a hydrophilic polyethylene oxide chain has found widespread use in the biopharmaceutical industry. Even though it is used heavily throughout the industry, the degradation products from Triton™ X-100 exhibit long-lasting estrogenic properties in fish, birds & mammals, causing chronic harm to their endocrine systems. ---Hemagglutinin HA Antigen--- Influenza virus hemagglutinin facilitates infection by allowing the virus to bind to & enter host cells, making the virus dangerous. ---Warnings & Precautions--- Causal for Guillain Barre Syndrome Paralysis like Polio. Do not administer to anyone with an egg allergy, if egg allergy is known in a 6 month old infant. Emergency procedures must be in place in case of anaphylaxis. ---Clinical Trials--- No clinical trial was done, no safety trial & no placebo. 1,419 children age 6 months thru 35 months were injected & then blood serum tested to check for antibody titers. ---Post Marketing Adverse Events & Injuries--- Guillain-Barré syndrome (GBS) Convulsions Myelitis Encephalomyelitis Transverse myelitis Facial palsy (Bell’s Palsy) Optic neuritis/neuropathy Brachial neuritis (paralysis) Syncope Anaphylaxis Angioedema Thrombocytopenia Lymphadenopathy Vasculitis Stevens Johnson Syndrome High fever Loss of appetite Extreme fatigue Apnea ---Vaxxed Verses Unvaxxed Studies--- 2025 flu vaccine efficacy rate is only 32%. Studies on inactivated influenza vaccines show 4.4 times greater risk of getting the flu after a flu vaccination as compared to those unvaccinated. 👇Fluzone Vaccine Package Insert👇 👇Influenza Vaccine Adverse Events Reports👇 👇Flu Vaccine Increases Risk Of Getting The Flu👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

69,163 Aufrufe • vor 1 Jahr

Dr Fauci Admits, "We Don't Do True Placebo Trials On Vaccines." Del Bigtree, CEO, I.C.A.N. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. Shocking List Of 'Placebos' Used In Vaccine Clinical Trials. FDA, WHO & CDC Approved Vaccine Trial "Placebo": Thimerosal Mercury & Aluminum Oxide Other Already Approved Vaccines Clinical Trial Vaccines & What Placebo Was Used: HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Hepatitis A Clinical Trial...Placebo Was Aluminum Adjuvant. Prevnar-9 Pneumonia Clinical Trial...Placebo Was DTP-Hib Vaccine. Cholera Vaccine Clinical Trial...Placebo Was K-12 E.Coli Vaccine. Prevnar-23 Pneumonia Vaccine...Placebo Was Hep A & Hep-B Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. Some COVID-19 Vaccine Clinical Trials...Placebo Was Meningitis Vaccine. The Government believes, "Testing a new vaccine against a saline injection is considered unethical." The Government believes, "Depriving half of the trial participants of an older vaccine(which is approved to use as placebo) & giving them a true saline placebo instead would not be fair: it would actually be unethical." The Government believes, "Saline injections don’t cause a sore arm, which might unwittingly reveal to the 'double blind volunteers' that they are in the placebo group. Those who get the experimental vaccine & those who get placebo must be kept secret." This is the most flagrant violation of human rights. causing harm to both children & adults. Crimes against humanity with no informed consent & no true placebo skews all results & makes all vaccines appear "safe & effective" because the adverse events & side effects in both groups are similar. 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 Speaker: Del Bigtree ICAN - Informed Consent Action Network @MAHAalliance
1:42

Dr Fauci Admits, "We Don't Do True Placebo Trials On Vaccines." Del Bigtree, CEO, I.C.A.N. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. Shocking List Of 'Placebos' Used In Vaccine Clinical Trials. FDA, WHO & CDC Approved Vaccine Trial "Placebo": Thimerosal Mercury & Aluminum Oxide Other Already Approved Vaccines Clinical Trial Vaccines & What Placebo Was Used: HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Hepatitis A Clinical Trial...Placebo Was Aluminum Adjuvant. Prevnar-9 Pneumonia Clinical Trial...Placebo Was DTP-Hib Vaccine. Cholera Vaccine Clinical Trial...Placebo Was K-12 E.Coli Vaccine. Prevnar-23 Pneumonia Vaccine...Placebo Was Hep A & Hep-B Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. Some COVID-19 Vaccine Clinical Trials...Placebo Was Meningitis Vaccine. The Government believes, "Testing a new vaccine against a saline injection is considered unethical." The Government believes, "Depriving half of the trial participants of an older vaccine(which is approved to use as placebo) & giving them a true saline placebo instead would not be fair: it would actually be unethical." The Government believes, "Saline injections don’t cause a sore arm, which might unwittingly reveal to the 'double blind volunteers' that they are in the placebo group. Those who get the experimental vaccine & those who get placebo must be kept secret." This is the most flagrant violation of human rights. causing harm to both children & adults. Crimes against humanity with no informed consent & no true placebo skews all results & makes all vaccines appear "safe & effective" because the adverse events & side effects in both groups are similar. 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 Speaker: Del Bigtree ICAN - Informed Consent Action Network @MAHAalliance

Valerie Anne Smith

1,082,646 Aufrufe • vor 1 Jahr

"It Is A Myth That Vaccines Are Safe & Necessary...If I Had My Young Children Today, They Would Not Get A Single Vaccine." Dr Pierre Kory, MD "SIDS Occurs At 2, 4 & 6 Months Of Age...Right After Vaccination." "The Gov't Refuses To Do A True Placebo Safety Trial On Any Vaccine." Vaccines have not gone thru a long robust safety trial to prove they are 'safe & effective.' All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, but vaccines are not safety monitored this way. Hep-B Vaccine: Tested on only 147 infants & children, then monitored for 5 days & granted CDC approval. Hep-A Vaccine: Subjects were monitored for safety, 14 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored for 7 days. Prevnar Pneumonia Vaccine: Study volunteers were monitored for 7 days. MMR Vaccine: Subjects were followed for 42 days. RSV Vaccine: Participants were monitored for 30 days. DTaP & TDaP Vaccines: Subjects were monitored for 14 days. Gardasil HPV Vaccine: Trial participants were surveilled for 14 days. Vaccines have not been safety trialed against a saline placebo. They have all used Aluminum adjuvant or another vaccine as the placebo in clinical trials. Gardasil HPV Clinical Trial: placebo was the Hep-A Vaccine & Aluminum Adjuvant. Hepatitis A Clinical Trial: placebo was the Hep-B Vaccine. Influenza A Clinical Trial: placebo was the Influenza B Vaccine. Meningitis Vaccine Clinical Trial: placebo was the DTaP Vaccine. Pertussis Vaccine Clinical Trial: placebo was the Tetanus & Diphtheria Vaccine. Polio Vaccine Clinical Trial: placebo was Diluted Polio Vaccine. Vaxelis 6 in 1 Vaccine Trial: placebo was the DTaP, Polio, HIB & Hep-B Vaccines. Hepatitis B Clinical Trial: placebo was Aluminum Adjuvant. The countries that have the most infant vaccines on their childhood schedules, have the highest infant mortality. The United States is #1 in infant vaccines & #1 in infant mortality, of all industrialized nations. 97% of infants who die of SIDS, do so within 7 days being vaccinated. 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 👇Health Outcomes: Vaxxed Versus UnVaxxed👇 Speaker: Dr Pierre Kory, MD Video: @that_barefootgirlv
2:03

"It Is A Myth That Vaccines Are Safe & Necessary...If I Had My Young Children Today, They Would Not Get A Single Vaccine." Dr Pierre Kory, MD "SIDS Occurs At 2, 4 & 6 Months Of Age...Right After Vaccination." "The Gov't Refuses To Do A True Placebo Safety Trial On Any Vaccine." Vaccines have not gone thru a long robust safety trial to prove they are 'safe & effective.' All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, but vaccines are not safety monitored this way. Hep-B Vaccine: Tested on only 147 infants & children, then monitored for 5 days & granted CDC approval. Hep-A Vaccine: Subjects were monitored for safety, 14 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored for 7 days. Prevnar Pneumonia Vaccine: Study volunteers were monitored for 7 days. MMR Vaccine: Subjects were followed for 42 days. RSV Vaccine: Participants were monitored for 30 days. DTaP & TDaP Vaccines: Subjects were monitored for 14 days. Gardasil HPV Vaccine: Trial participants were surveilled for 14 days. Vaccines have not been safety trialed against a saline placebo. They have all used Aluminum adjuvant or another vaccine as the placebo in clinical trials. Gardasil HPV Clinical Trial: placebo was the Hep-A Vaccine & Aluminum Adjuvant. Hepatitis A Clinical Trial: placebo was the Hep-B Vaccine. Influenza A Clinical Trial: placebo was the Influenza B Vaccine. Meningitis Vaccine Clinical Trial: placebo was the DTaP Vaccine. Pertussis Vaccine Clinical Trial: placebo was the Tetanus & Diphtheria Vaccine. Polio Vaccine Clinical Trial: placebo was Diluted Polio Vaccine. Vaxelis 6 in 1 Vaccine Trial: placebo was the DTaP, Polio, HIB & Hep-B Vaccines. Hepatitis B Clinical Trial: placebo was Aluminum Adjuvant. The countries that have the most infant vaccines on their childhood schedules, have the highest infant mortality. The United States is #1 in infant vaccines & #1 in infant mortality, of all industrialized nations. 97% of infants who die of SIDS, do so within 7 days being vaccinated. 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 👇Health Outcomes: Vaxxed Versus UnVaxxed👇 Speaker: Dr Pierre Kory, MD Video: @that_barefootgirlv

Valerie Anne Smith

261,486 Aufrufe • vor 11 Monaten