Edetate disodium
Edetate disodium Uses, Dosage, Side Effects, Food Interaction and all others data.
Edetate disodium is a polyvalent chelating agent used to treat hypercalcemia and digitalis toxicity associated ventricular arrhythmias.
Edetate disodium is a polyvalent ion chelator that reduces blood concentrations of calcium or digitalis. It has a long duration of action as patients are generally given 1 daily dose. The therapeutic index is wide, as high doses are generally well tolerated. Patients should be counselled regarding the risk of postural hypotension, effects of myocardial contractility, hypokalemia, hypomagnesemia, and hypoglycemia.
Trade Name | Edetate disodium |
Generic | Edetate disodium anhydrous |
Edetate disodium anhydrous Other Names | Edetate disodium |
Type | |
Formula | C10H14N2Na2O8 |
Weight | Average: 336.2063 Monoisotopic: 336.054554784 |
Groups | Approved, Vet approved |
Therapeutic Class | |
Manufacturer | |
Available Country | |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Edetate disodium is a polyvalent ion chelator indicated for emergency treatment of hypercalcemia and digitalis toxicity associated ventricular arrhythmias.
Edetate disodium is indicated for emergency treatment of hypercalcemia and digitalis toxicity associated ventricular arrhythmias.
Edetate disodium is also used to associated treatment for these conditions: Hypercalcemia, Arrhythmia of ventricular origin
How Edetate disodium works
Edetate disodium chelates divalent and trivalent ions such as magnesium, zinc, and calcium. The chelate is excreted in the urine, reducing concentrations of these ions in the blood.
Toxicity
Patients experiencing an overdose may present with calcium deficiency. Treat overdose with symptomatic and supportive treatment, which may include intravenous calcium gluconate.
Food Interaction
No interactions found.Volume of Distribution
Data regarding the volume of distribution of edetate disodium anhydrous is not readily available.
Clearance
The mean clearance of edetate in 1 month olds is 54.6mL/min/1.73m2. 2-17 year olds have a mean clearance of 113.9 ± 24.4 mL/min/1.73m2
Elimination Route
After intravenous administration, 95% of the dose is recovered in the urine after 24 hours. Oral administration in rats leads to 5.3% recovery in urine and 88.5% recovery in feces.
Innovators Monograph
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