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Reply #37: And all the other crap that people have severe reactions to? Have they taken all that out too? [View All]

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TalkingDog Donating Member (1000+ posts) Send PM | Profile | Ignore Sun Nov-18-07 10:44 AM
Response to Reply #22
37. And all the other crap that people have severe reactions to? Have they taken all that out too?
Having known people who ended up hospitalized because the nurse LIED and said she was given a vaccine with no gluten in it (probably in the form of MSG. MSG has been shown to cause brain damage in laboratory animals.) , I am dubious about the safety and efficacy of entire process, from creation to injection.

Based on federal recommendations an 18-month-old-child could receive 22 shots of 12 vaccine in 32 doses.

Read a few of the inserts from those injections and tell me this is acceptable.

http://www.vaccineawareness.org/concerns.htm

"IVAC is concerned with the cross-species in the culture mediums, i.e., chicken embryos, guinea pig cells, monkey kidney cells. SV40, implicated in many cancers, was in the polio vaccines from 1955-1962"


Measles, Mumps and Rubella (German measles) Live virus Vaccine

M-M-R II, vaccine package insert summary, Merck & Co., Whitehouse Station, NJ October 2003

Ingredients

-Attenuvax: live measles virus from Eders’ weakened Edmonston strain grown in chick embryo cell culture;

-Mumpsvax: Jerry Lynn (B level) strain of live mumps virus grown in chick embryo cell culture;

-Meruvax:Wistar RA 27/3 strain of live weakened rubella virus grown in WI-38 aborted human lung fibroblasts (connective tissue cells);

-fetal bovine serum;

-hydrolyzed gelatin;

-glutamate;

-human albumin (processed using Cohn cold ethanol fractionation,

-medium 199

-Minimum Essential Medium;

-neomycin;

-sodium chloride;

-sodium phosphate;

-sorbitol;

-sucrose;

Contraindications

-hypersensitivity reaction to ingredients including gelatin;

-no vaccination for pregnant women; unknown vaccine effects on fetus;

-pregnancy avoided for 3 months after vaccination;

-respiratory fever; active fever infection

Warnings

-elevated fever may occur after vaccination;

-remote risk of viral disease from albumin, derivative of human blood;

-theoretical risk of Creutzfeldt-Jacob disease (CJD);

-hypersensitivity to ingredients including eggs, neomycin;

-people with thrombocytopenis (low platelets resulting in bleeding and easy bruising);

Precautions

-epinephrine available for possible allergic reaction;

-transmission of rubella virus through breast milk;

-unknown if measles or mumps virus excreted in breast milk;

-deferred vaccination (3 months or longer) after transfusions or human immune globulin;

-live rubella virus excretion from nose or throat of susceptible people 7-28 days after vaccination, transmission through close contact , accepted as theoretical risk, not regarded as a significant risk;

-reports of individual measles, mumps, rubella vaccines may result in temporary depression of tuberculin skin sensitivity;

-no studies on effect of measles vaccine on untreated tuberculosis children;

-no vaccination for people with active, untreated tuberculosis;

-no evaluation for carcinogenicity, mutagenicity or fertility impairment;

-no animal reproduction studies;

-unknown if vaccine can cause fetal harm when injected into a pregnant woman or can affect reproduction capacity;

-pregnancy avoided for 3 months after vaccination;

-safety and effectiveness to established for measles vaccine in infants under 6 months;

-safety ad effectiveness not established for mumps and rubella vaccine in infants less than 12 months;

-M-M-R II given one month before or after other live virus vaccines;

-limited data, thus not recommended, for simultaneous vaccination with diphtheria/pertussis/tetanus (DPT) and or oral polio vaccine (OPV);


Adverse Reactions: arthritis, atypical measles, brain disease, convulsions, cough, death (reported rarely, no established causal link), diabetes, diarrhea, dizziness, ear, (middle infection) and nerve deafness, edema, eye paralysis, fainting, fever, Guillain-Barre Syndrome, headache, injection site-burning, redness, stinging, swelling, tenderness, tissue hardening, irritability, itchiness, hives, meningitis (aseptic), sclerosis (brain), nausea, nerve inflammation, nose inflammation, pitting of abdomen & thigh, pneumonia, rash, seizures, sore throat, testes inflammation, upper respiratory infection, visual disturbances, vomiting, weakness. More adverse reactions are listed.


(Pneumoccal 7-valent vaccine, Diphtheria Protein)

Prevnar, vaccine package insert summary, Wyeth Pharmaceuticals. Inc., Philadelphia, PA, January 2004

Ingredients:

-Streptococcus pneumoniae stereotypes 4, 6B, 9V, 14, 18C, 19F, 23F

joined to diphtheria CRM protein isolated from cultures of Coynebacterium diphtheria strain C7 (B197);

-aluminum phosphate;

-ammonium sulfate

-casamioacids;

-soy peptone broth

-yeast;

Contraindications

-hypersensitivity reaction to ingredients including diptherua weakened toxin;

-delay for severe or moderate fever;

Warnings

-no protection from diseases caused by serotypes unrelated to those vaccine;

-package contains dry natural rubber;

-Sudden Infant Death Syndrome (SIDS) mentioned in specific studies;

Precautions

-fever and seizure reported after vaccination;

-acetaminophen may be given to reduce possibility of post-vaccination fever;

-given with caution for children on anti-coagulant therapy;

-unknown clinical relevance for inconsistent differences in response to pertussis atingens;

-unavailable immune data for MMR and chickenpox vaccine with Prevnars

-no evaluation for carciogeicity, mutageicity or fertility impairment;

-no animal reproduction studies;

-unknown if vaccine can cause fetal harm when injected into a pregnant woman or can affect reproduction capacity;

-not recommended for pregnant women;

-unknown whether vaccine is excreted in breast milk;

-not recommended for nursing mothers;

-safety and effectiveness not established for children below 6 weeks or over 10 years;

-no immune response studies on premature infants;

-not recommended for adults;

Adverse Reactions: apnea, appetite-decrease, breath-shortness, brocospasm, diarrhea, drowsiness, edema, face edema, fever, injection site: hives, itching, lymph system, redness, irritability, seizure, shock, sleep-restless, vomiting. More adverse reactions are listed.



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