Indapamide, the active ingredient in Idatix SR, is an oral antihypertensive agent. Its mechanism of action is not entirely understood but involves both vascular and renal effects. Potential benefits of Indapamide in treating hypertension include reducing cardiac hypertrophy and arterial wall thickening, preventing fibronectin accumulation in coronary vessels, scavenging free radicals to stimulate vasodilator eicosanoid production, and interacting with renal carbonic anhydrase. Its primary site of action in the kidney is the proximal segment of the distal tubule, where it promotes sodium and chloride excretion with minimal impact on potassium or uric acid levels. Urinary volume increase is noticeable only at doses exceeding 1.5 mg per day. Clinical studies have not observed significant changes in plasma sodium levels, although hypokalemia (potassium <3.2 mmol/L) has been reported in 4% of patients.
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Indapamide is widely distributed in the body, with strong binding to red blood cells (80%) and carbonic anhydrase (98%). Plasma protein binding is 79%. The drug has a half-life of 14 to 24 hours (mean 18 hours) and reaches steady-state concentration after seven days without accumulation.
Indapamide undergoes extensive liver metabolism, with only 5-7% excreted unchanged in the urine.
The drug is primarily eliminated through urine (70%) and feces (22%) in the form of inactive metabolites.
The safety and effectiveness of Idatix SR in children have not been determined.
Take medication only as advised by a registered physician.
The standard dosage is one tablet daily, preferably in the morning. In severe cases, Idatix SR can be combined with other antihypertensive medications. The safety and efficacy of this medication in pediatric patients have not been established.
Possible side effects include dizziness, headache, nausea, vomiting, anorexia, constipation, diarrhea, and postural hypotension. Electrolyte imbalances may occur, such as hypochloremic alkalosis, hyponatremia, hypokalemia, and hyperuricemia. Hypersensitivity reactions, including skin rashes, cholestatic jaundice, and blood disorders (e.g., thrombocytopenia, leukopenia, and aplastic anemia), have also been reported.
Adequate and well-controlled studies in pregnant women are lacking; therefore, Indapamide is not recommended during pregnancy. Breastfeeding mothers should avoid taking this medication.
Caution is advised in patients with disturbed water or electrolyte balance, diabetes, gout, or kidney problems. Regular monitoring of serum potassium and uric acid levels is recommended.
Store in a cool, dry place, protected from light and moisture.
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