A substantial new Bill to require meningitis vaccine for 7th graders and ALL college students is gaining momentum in Albany, New York
http://www.healthfreedomusa.org/?p=5472
Bill S7156 passed the Senate Health Committee and is due for a floor vote.
Bill A10313 will be voted on the Assembly Health Committee any given Tuesday.
http://www.ncsl.org/IssuesResearch/Health/MeningitisLegislationandLaws/tabid/13960/Default.aspx
Assuming this Bill is rammed through the Senate & Health Committee which seems inevitable the public must be alerted immediately to the serious risks associated with this vaccine. If New York buckles under pressure then other States & countries around the world are sure to follow. There are 3 Meningitis Vaccines being promoted by the WHO & CDC for distribution in this campaign including:
1) MENACTRA (Manufactured by Sanofi Pasteur Inc.)
Menactra®, Meningococcal (Groups A, C, Y and W-135) Polysaccharide Diphtheria Toxoid Conjugate Vaccine, is a sterile, intramuscularly administered vaccine that contains Neisseria meningitidis serogroup A, C, Y and W-135 capsular polysaccharide antigens individually conjugated to diphtheria toxoid protein. N meningitidis A, C, Y and W-135 strains are cultured on Mueller Hinton agar (1) and grown in Watson Scherp(2) media. The polysaccharides are extracted from the N meningitidis cells and purified by centrifugation, detergent precipitation, alcohol precipitation, solvent extraction and diafiltration. To prepare the polysaccharides for conjugation, they are depolymerized, derivatized, and purified by diafiltration. Corynebacterium diphtheriae cultures are grown in a modified Mueller and Miller medium (3) and detoxified with formaldehyde. The diphtheria toxoid protein is purified by ammonium sulfate fractionation and diafiltration.
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM131170.pdf
Package Insert: General Warnings –
NURSING MOTHERS: It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Menactra vaccine is administered to a nursing woman.
PEDIATRIC USE: Safety and effectiveness of Menactra vaccine in children below the age of 2 years have not been established.
GERIATRIC USE: Safety and effectiveness of Menactra vaccine in adults older than 55 years have not been established
CARCINOGENESIS, MUTAGENESIS – IMPAIRMENT OF FERTILITY: Menactra vaccine has not been evaluated in animals for its carcinogenic or mutagenic potentials or for impairment of fertility.
CONTRAINDICATIONS: Known hypersensitivity to any component of Menactra vaccine including diphtheria toxoid, or a life-threatening reaction after previous administration of a vaccine containing similar components, are contraindications to vaccine administration.
GUILLAIN-BARRE SYNDROME: Guillain-Barré syndrome has been reported in temporal relationship following administration of Menactra vaccine. An evaluation of post-marketing adverse events suggests a potential for an increased risk of GBS following Menactra vaccination. Persons previously diagnosed with GBS should not receive Menactra vaccine.
LATEX: The stopper of the vial contains dry natural rubber latex, which may cause allergic reactions in latex-sensitive individuals. There is no latex in any component of the syringe.
2) MENOMUNE (Manufactured by Sanofi Pasteur Inc.)
Menomune® – A/C/Y/W-135, Meningococcal Polysaccharide Vaccine, Groups A, C, Y and W-135 Combined, for subcutaneous use, is a freeze-dried preparation of the group-specific polysaccharide antigens from Neisseria meningitidis, Group A, Group C, Group Y and Group W-135. N meningitidis are cultivated with Mueller Hinton agar1 and Watson Scherp2 media. The purified polysaccharide is extracted from the Neisseria meningitidis cells and separated from the media by procedures which include centrifugation, detergent precipitation, alcohol precipitation, solvent or organic extraction and diafiltration.
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM131653.pdf
Package Insert: General Warnings –
IT IS A CONTRAINDICATION TO ADMINISTER MENOMUNE – A/C/Y/W-135 VACCINE TO INDIVIDUALS KNOWN TO BE SENSITIVE TO THIMEROSAL OR ANY OTHER COMPONENT OF THE VACCINE.
FOR INDIVIDUALS SENSITIVE TO THIMEROSAL, ADMINISTER THE ONE DOSE PACKAGE SIZE AND RECONSTITUTE WITH THE 0.78 ML VIAL OF DILUENT THAT CONTAINS NO PRESERVATIVE.
WARNING: This product contains dry natural latex rubber as follows: The stopper to the vial contains dry natural latex rubber.
If the vaccine is used in persons receiving immunosuppressive therapy, the expected immune response may not be obtained.
VACCINE INTERACTIONS – Menomune should NOT be given at the same time as whole-cell pertussis or whole-cell typhoid vaccines due to combined endotoxin content.20,21
PRECAUTIONS: EPINEPHRINE INJECTION (1:1000) MUST BE IMMEDIATELY AVAILABLE TO COMBAT UNEXPECTED ANAPHYLACTIC OR OTHER ALLERGIC REACTIONS.
DRUG INTERACTIONS: If Menomune – A/C/Y/W-135 vaccine is administered to immunosuppressed persons or persons receiving immunosuppressive
therapy, an adequate immunologic response may not be obtained.
CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: Menomune – A/C/Y/W-135 vaccine has not been evaluated in animals for its carcinogenic, mutagenic potentials or impairment
of fertility.
PREGNANCY CATEGORY C: Animal reproduction studies have not been conducted with Meningococcal Polysaccharide Vaccine, Groups A, C, Y and W-135. It is also not known whether Meningococcal Polysaccharide Vaccine, Groups A, C, Y and W-135 can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Meningococcal Polysaccharide Vaccine, Groups A, C, Y
and W-135 should be given to a pregnant woman only if clearly needed.
NURSING MOTHERS: It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Menomune – A/C/Y/W-135 vaccine is administered to a nursing woman.
PEDIATRIC USE SAFETY AND EFFECTIVENESS OF MENOMUNE – A/C/Y/W-135 VACCINE IN CHILDREN BELOW THE AGE OF 2 YEARS HAVE NOT BEEN ESTABLISHED.
3) MENVEO (Manufatured by Novartis Vaccines and Diagnostics, Inc.)
Menveo® [Meningococcal (Groups A, C, Y and W-135) Oligosaccharide Diphtheria CRM197 Conjugate Vaccine] is a sterile liquid vaccine administered by intramuscular injection that contains N. meningitidis serogroup A, C, Y and W-135 oligosaccharides conjugated individually to Corynebacterium diphtheriae CRM197 protein. The polysaccharides are produced by bacterial fermentation of N. meningitidis (serogroups A, C, Y or W-135). N. meningitidis strains A, C, Y and W-135 are each cultured and grown on Franz Complete medium and treated with formaldehyde. MenA, MenW-135 and MenY polysaccharides are purified by several extraction and precipitation steps. MenC polysaccharide is purified by a combination of chromatography and precipitation steps.
The protein carrier (CRM197) is produced by bacterial fermentation and is purified by a series of chromatography and ultrafiltration steps. C. diphtheriae is cultured and grown on CY medium containing yeast extracts and amino acids.
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM201349.pdf
*NOTE: C. diphtheriae is cultured and grown on CY medium containing yeast extracts refers to genetically modified yeast. Anyone with an allergy to gluten will be adversely affected by this process.
Package Insert: General Warnings –
PRECAUTIONS: Management of Acute Allergic Reactions Appropriate medical treatment must be available should an acute allergic reaction, including an anaphylactic reaction, occur following administration of MENVEO.
SYNCOPE: Because vaccinees may develop syncope, sometimes resulting in falling with injury, observation for 15 minutes after administration is recommended. Syncope, sometimes associated with tonic-clonic movements and other seizure-like activity, has been reported following vaccination with MENVEO. When syncope is associated with tonic-clonic movements, the activity is usually transient and typically responds to restoring cerebral perfusion by maintaining a supine or Trendelenburg position.
Altered Immunocompetence Safety and effectiveness of MENVEO have not been evaluated in immunocompromised persons. If MENVEO is administered to immunocompromised persons, including those receiving immunosuppressive therapy, the expected immune response may not be obtained.
GUILLAIN-BARRE SYNDROME: Following vaccination with a U.S.-licensed meningococcal quadrivalent polysaccharide conjugate vaccine, an evaluation of post-marketing adverse events suggested a potential for an increased risk of Guillain-Barré Syndrome (GBS). Data are not available to evaluate the potential risk of GBS following administration of MENVEO.
BLEEDING DISORDERS: MENVEO should not be administered to persons with any bleeding disorder, or persons receiving anticoagulant therapy, unless the potential benefit outweighs the risk of administration.
Complete list of Meningitis Vaccines Found Here
http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm093830.htm
MENINGITIS: THE FACTS – These days, when a vaccinee develops poliomyelitis, it may not be called poliomyelitis; instead, it may be called viral or aseptic meningitis, ascending paralysis (Guillain-Barre syndrome), cerebral palsy (over 75 per cent of cases are not diagnosed at birth but after six months) or other such names. According to MMWR (1997; 32[29]:384-385), there are 30,000 to 50,000 cases of aseptic meningitis every year in the United States. Considering that the vast majority (99 per cent) of the reported cases in the pre-vaccine era were non-paralytic and would have corresponded to aseptic or aviral meningitis, then vaccination has actually increased the incidence of poliomyelitis. In the pre-vaccine era, such high numbers only occurred in some epidemics. Now, such numbers occur every year, year by year.
http://www.whale.to/vaccines/meningitis2.htm
The Department of Health has refused to carry out a review into the safety of the meningitis C vaccine despite fears it is unsafe. New figures show that almost 5,000 children have suffered adverse reactions to the vaccine since it was introduced. The Chiron jab was introduced in June of 2000, a year ahead of schedule, as a protection against the meningitis C strain. It has been given to 13m children and university students across the UK. But according to figures from the Medical Controls Agency there were 4,764 reports of adverse reactions to the vaccine up to the beginning of June. A further 10,202 suspected reactions have been reported while an investigation has been launched into the deaths of eight children to see if there is a link to the vaccine.
http://www.nccn.net/~wwithin/meningitisc.htm
GRASSROOTS COMMUNITY ORGANIZING TO COUNTER LEGISLATION: Stop Stealth Mandatory Meningitis Vaccine Bill In New York. Come to Albany on Tuesday, June 1
http://capwiz.com/a-champ/issues/alert/?alertid=15089571
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