DESCRIPTION:
Edetate calcium disodium is a chelating agent. Because this chelating agent has higher affinity for heavy metal like Pb , Zn , Cd , Mn , Cu and some radioactive metals , that's whys they are capable of removing a heavy metal, such as lead or mercury, from the blood by exchanging with Ca held by it. It is highly ionised , therefore distributed only extracellularly.
PHARMACOKINETICS:
Rapidly excreted in urine by glomerulus filteration carrying the toxic metals along. It is not metabolised. Because of its ic nature , calcium sodium edetate is not absorbed from git.It must be gven parentally. It does not enter brain or CSF.
Half-life: < 1hour.
Half-life: < 1hour.
Route of administration: Preferred route is i.v., i.m. injection is painfull.
ADVERSE REACTION:
1.Hypotension.
2.Cardiac rhythm irregularities.
3.Urinary hesitancy.
4.Pain, fever.
5.Joint pain.
6.Headache.
7.Tremor.
8.Nausea, vomiting.
9.Loss of appetite.
10.Sneezing.
DRUG INTERACTIONS:
1. Steroids + Calcium disodium edetate = Increase Renal toxicity in animals
2. Zinc insulin + calcium sodium edetate = Replace zinc.
CONTRAINDICATIONS:
1.Kidney disease.
2.Hepatitis.
3.Unable to urinate
4.Nephropathy
USES:
It is used in lead poisining.
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