Date:   11/18/2009 6:48:44 AM ( 15 y ago)
Hits:   12,676
URL:   https://www.curezone.org/forums/fm.asp?i=1525734

thanks for your input. This is the company with the high parts per million silver I am looking at

http://www.ultrasilver.com/Ultra-Silver.html


as far as the Mercury goes, DMPS has a track record decades long as the most effective mercury chelation agent in the world. It has literally brought people back from the brink of death as shown here. This is just one of many such studies done

Note that there were no negative side effects reported. I have had none myself, only good has come from using this drug. I think there is a chance I would be dead now without it. That is not an exaggeration


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Mercury Kinetics in a Case of Severe Mercuric Chloride Poisoning Treated with Dimercapto-1-propane Sulphonate (DMPS)
A.E. Toet

National Poison Control Center, National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven, Department of Intensive Care and Clinical Toxicology, University Hospital Utrecht, P.O. Box 85500, 3508 GA Utrecht

A. van Dijk

Department of Hospital Pharmacy, University Hospital Utrecht, P.O. Box 85500, 3508 GA Utrecht, The Netherlands

T.J.F. Savelkoul

National Poison Control Center, National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven, Department of Intensive Care and Clinical Toxicology, University Hospital Utrecht, P.O. Box 85500, 3508 GA Utrecht

J. Meulenbelt

National Poison Control Center, National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven, Department of Intensive Care and Clinical Toxicology, University Hospital Utrecht, P.O. Box 85500, 3508 GA Utrecht

1 A case of severe mercuric chloride poisoning with clinical signs of mucosal damage of the gastrointestinal tract and anuric renal failure, is presented. The initial whole blood mercury concentration was 14,300 ?g 1-1. This concentration is supposed to be associated with fatal outcome due to multiple organ failure.

2 Because of anuric renal failure, haemodialysis was necessary. Kidney function returned to normal within 10 days. Haemodialysis proved to be ineffective with regard to total mercury elimination.

3 Treatment with DMPS was started because of very severe poisoning, anuric renal failure and optimistic reports on the 'new' chelating agent 2,3-dimercapto-1-propanesulphonic acid (DMPS) in mercury poisoning. DMPS was administered by parenteral route initially and was continued thereafter by oral route, until whole blood and urine mercury concentrations had decreased below a level considered as toxic. Except for a temporary pruritic erythema of the skin, no side effects of DMPS treatment were observed.

4 The clinical course was mild, despite continuing high whole blood mercury concentrations, Recovery was uneventful and complete. DMPS treatment, administered by intravenous and oral route, was shown to be an effective alternative for BAL in life-threatening mercuric chloride intoxication.

5 The pharmacokinetic data presented in this case report suggest that non-renal mercury clearance may considerably exceed renal mercury clearance.

Human & Experimental Toxicology, Vol. 13, No. 1, 11-16 (1994)
DOI: 10.1177/096032719401300103

 

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