Hexachlorocyclopentadiene Velsicol Chemical/Hubei Chemical from Rosemont Illinois- Hubei China and Mind Controlhttp://www.google.com/url?sa=t&source=web&ct=res&cd=2&ved=0CAkQFjAB&url=http%3A%2F%2Fwww.epa.gov%2Foppt%2Fchemtest%2Fpubs%2Fnote47.pdf&rct=j&q=hexachlorocyclopentadiene+marshall+illinois&ei=te7ySrXuKsL_8AbohcTgAQ&usg=AFQjCNFxhOGmIsgC52Bee9iL4Fgr86go0QHubei Chemical Company also makes Sodium Benzoate that goes into all soda pops in the USA as well as other drinks. Google Sodium Benzoate "Mind Control"Hubei Chemical also makes table salt for the USA as well.[PDF]

EPA/Hexachlorocyclopentadiene; Response to the Interagency Testing ...

File Format: PDF/Adobe Acrobat - www.epa.gov/oppt/chemtest/pubs/note47.pdf+hexachloro+cyclopentadiene+velsicol&cd=3&hl=en&ct=clnk&gl=us" onmousedown="return rwt(this,'','','html','3','AFQjCNES91W9P4AA0B4C0t9eCQ8v5r26yQ','')">View as HTML
Mutagencity of hexachlorocyclopentadiene in the mouse dominant lethal assay. LBI Project. No. 20862. Submitted by Velsicol Chemical. Corporation. .. http://www.google.com/#hl=en&q=hexachloro+cyclopentadiene+%22mind+control%22&aq=f&aqi=&oq=&fp=642c18fb4411ca2e
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  • Coca-cola to phase out controversial chemical linked to hyperactivity and gene damage
    http://www.dailymail.co.uk/news/article-1021809/Coca-cola-phase-con...

    Side effects of Sodium Benzoate http://www.drugs.com/cons/sodium-benzoate-and-sodium-phenylacetate....

    Soft drink giant Coca-Cola is phasing out a controversial additive that has been linked to hyperactivity and causing damage to DNA.

    The chemical Sodium Benzoate, also known as E211, is used to stop fizzy drinks going mouldy.

    But recent research has shown that the chemical can deactivate parts of DNA, the genetic code in the cells of living creatures.

    Coca-Cola said it was withdrawing the additive from Diet Coke in response to consumer demand for more natural products.

    The move will mean that by the end of the year no can will contain E211 - and it plans to remove it from its other products as soon as possible.

    But the company said at present it had not found a satisfactory alternative to replace the additive in some soft drinks with a higher juice content including Fanta and Dr Pepper.

    Other fizzy drinks made by rival companies, such as Irn-Bru, Pepsi Max and Lucozade will continue to contain the additive.

    While the chemical occurs naturally in some fruits, such as prunes, apples and cranberries, it is used in much greater strengths by the soft drinks industry.

    Peter Piper, a professor of molecular biology research at Sheffield University found that the additive could switch off vital parts of DNA that could be linked to cirrhosis of the liver and Parkinson's disease.

    He has also called for further research into the chemical.

    In combination with vitamin C (CORR) sodium benzoate can form a potentially cancer-causing substance, benzene.

    However the government-backed Committee on Mutagenicity - which investigates whether chemicals cause cancer - has dismissed the research.

    The panel argue that while Sodium Benzoate has been shown to be harmful to yeast cells, it argues that human cells are stronger.

    But Professor Piper called the dismissal a 'whitewash' that failed to take into account modern techniques of monitoring DNA damage.

    Research by Southampton University found that sodium benzoate was one of seven additives - the six others being food colours -that can lead to hyperactivity.

    The Food Standards Agency called for the six colours to be withdrawn from UK products - although sodium benzoate has been allowed to remain.

    Coca-Cola said it had begun removing sodium benzoate from Diet Coke production in January.

    A company spokesperson said: 'We are continuously looking at emerging trends and listening to our consumers thoughts about ingredients.

    'For a number of years we have been moving towards non-artificial colours, flavours and preservatives where possible in our drinks.

    'We are looking to phase out the use of sodium benzoate where technically possible.'

    The company stressed that E211 was an approved additive by many worldwide bodies including the European Food Standards Agency.


    Side effects of Sodium Benzoate http://www.drugs.com/cons/sodium-benzoate-and-sodium-phenylacetate....

    sodium benzoate and sodium phenylacetate (Oral route)


    SOE-dee-um BEN-zoe-ate, SOE-dee-um fen-il-AS-e-tate

    Commonly used brand name(s):

    In the U.S.

    • Ucephan

    Available Dosage Forms:

    • Solution

    Therapeutic Class: Hyperammonemia Agent




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    Uses For sodium benzoate and sodium phenylacetate

    Sodium benzoate and sodium phenylacetate combination is used to treat a condition caused by too much ammonia in the blood (hyperammonemia). sodium benzoate and sodium phenylacetate works by causing less ammonia to be produced by the body.

    Ammonia is formed from the breakdown of protein in the body. If the ammonia cannot be removed by the body, then a buildup may cause serious unwanted effects.


    Sodium benzoate and sodium phenylacetate combination is available only with your doctor's prescription.

    Before Using sodium benzoate and sodium phenylacetate

    In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For sodium benzoate and sodium phenylacetate, the following should be considered:

    Allergies

    Tell your doctor if you have ever had any unusual or allergic reaction to sodium benzoate and sodium phenylacetate or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

    Pediatric


    sodium benzoate and sodium phenylacetate has been tested in children and, in effective doses, has not been shown to cause different side effects or problems than it does in adults.

    Geriatric

    Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults or if they cause different side effects or problems in older people. There is no specific information comparing the use of sodium benzoate and sodium phenylacetate in the elderly with use in other age groups.

    Interactions with Medicines

    Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.

    Interactions with Food/Tobacco/Alcohol

    Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


    Other Medical Problems

    The presence of other medical problems may affect the use of sodium benzoate and sodium phenylacetate. Make sure you tell your doctor if you have any other medical problems, especially:

    • Cancer—Use of sodium benzoate and sodium phenylacetate may increase your chance of side effects
    • Edema (swelling) or
    • Heart disease—Increased retention of water may make these conditions worse
    • Kidney disease or
    • Liver disease—May increase the amount of medicine in your body


    Proper Use of sodium benzoate and sodium phenylacetate

    It is important that you follow any special instructions from your doctor, such as following a low protein diet. If you have any questions about this, check with your doctor.


    Dosing

    The dose of sodium benzoate and sodium phenylacetate will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of sodium benzoate and sodium phenylacetate. If your dose is different, do not change it unless your doctor tells you to do so.

    The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

    • For injection dosage form (solution):
      • Treatment of too much ammonia in the blood:
        • Adults and children—The dose is based on body weight and must be determined by the doctor.

    Missed Dose

    If you miss a dose of sodium benzoate and sodium phenylacetate, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.

    Storage

    Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

    Keep out of the reach of children.

    Do not keep outdated medicine or medicine no longer needed.

    Precautions While Using sodium benzoate and sodium phenylacetate


    Your doctor should check your progress at regular visits to make sure that sodium benzoate and sodium phenylacetate is working properly.

    sodium benzoate and sodium phenylacetate Side Effects

    Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

    Stop taking sodium benzoate and sodium phenylacetate and get emergency help immediately if any of the following effects occur:

    More common
    • Confusion
    • convulsions
    • decreased urine
    • dry mouth
    • headache
    • increase in frequency of seizures
    • increased thirst
    • irregular heartbeat
    • loss of appetite
    • mood changes
    • muscle pain or cramps
    • nausea
    • numbness or tingling in hands, feet, or lips
    • problems with movement, walking or speech
    • shortness of breath
    • swelling of face
    • unusual tiredness or weakness
    • vomiting
    • yellow eyes or skin
    Less common
    • Blood in stools
    • blood in urine
    • bruising
    • change in consciousness
    • coughing or vomiting blood
    • difficulty in breathing
    • drowsiness
    • loss of consciousness
    • mental changes
    • muscle cramps in hands, arms, feet, legs, or face
    • muscle tremors
    • persistent bleeding or oozing from puncture sites, mouth, or nose
    • rapid, deep breathing
    • rash
    • restlessness
    • shortness of breath
    • stomach cramps
    • tightness in chest
    • tremor
    • troubled breathing
    • wheezing
    Frequency unknown
    • Abnormally slow deep breathing
    • blue lips, fingernails, or skin
    • blurred vision
    • bulging soft spot on head of an infant
    • change in ability to see colors, especially blue or yellow
    • chest pain or discomfort
    • dizziness or fainting
    • injection site hemorrhage
    • insomnia
    • irregular, fast or slow, or shallow breathing
    • lightheadedness
    • severe headache
    • shakiness
    • sleepiness
    • slow heartbeat
    • slow to respond
    • slurred speech
    • unconsciousness

    Symptoms of overdose
    • Agitation
    • back pain
    • blue lips, fingernails, or skin
    • blurred vision
    • bulging soft spot on head of an infant
    • change in ability to see colors, especially blue or yellow
    • chest pain or discomfort
    • chills
    • cold, clammy, pale skin
    • coma
    • confusion
    • continuing nausea or vomiting
    • cough
    • deep or fast breathing with dizziness
    • difficult or troubled breathing
    • dizziness, faintness, or lightheadedness when getting up from a lying or sitting position suddenly
    • drowsiness
    • fainting
    • fast heartbeat
    • fever
    • general feeling of discomfort or illness
    • hallucinations
    • headache
    • high blood pressure
    • insomnia
    • irregular, fast or slow, or shallow breathing
    • irregular heartbeats
    • irritability
    • lightheadedness
    • loss of appetite
    • mood or mental changes
    • muscle twitching
    • no blood pressure
    • not alert
    • numbness to feet, hands and around mouth
    • rapid, shallow breathing
    • restlessness
    • seizures
    • slow heart rate
    • stiff neck
    • sweating
    • swelling of face
    • swelling of feet or lower legs
    • thickening of bronchial secretions
    • trouble with coordination
    • unusual tiredness or weakness
    • vomiting
    • weakness
    • yellow eyes or skin

    Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

    More common

    • Changes in skin color
    • cold hands and feet
    • confusion or excitement
    • cough or hoarseness;
    • dry mouth;
    • fever or chills
    • flushed, dry skin;
    • fruit-like breath odor
    • increased hunger
    • increased thirst
    • increased urination
    • lower back or side pain
    • mental depression or anxiety
    • nightmares or unusually vivid dreams
    • painful or difficult urination
    • pain, redness, or swelling in arm or leg
    • skin disorders
    • sweating
    • unexplained weight loss
    Less common
    • Bladder pain
    • bleeding, blistering, burning, coldness, discoloration of skin, feeling of pressure, hives, infection; inflammation, itching, lumps, numbness, pain, rash, redness, scarring, soreness, stinging, swelling, tenderness, tingling, ulceration, or warmth at site
    • decrease in urine-concentrating ability
    • diarrhea
    • difficult, burning, or painful urination
    • frequent urge to urinate
    • hyperventilation
    • nervousness
    • pale skin
    • shaking
    • troubled breathing with exertion
    • trouble sleeping
    • unusual bleeding or bruising
    Frequency unknown
    • Blister
    • full or bloated feeling or pressure in the stomach
    • itching skin
    • rash with flat lesions or small raised lesions on the skin
    • swelling of abdominal or stomach area
    • uncontrolled jerking movement

    Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.

    The information contained in the Thomson Healthcare (Micromedex) products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.

    The use of the Thomson Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Healthcare does not assume any responsibility or risk for your use of the Thomson Healthcare products.

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