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Repres SR 1.5 mg is a Product of the Generic Indapamide

Repres SR 1.5 mg belongs to the generic category of Indapamide. This medicine should be used according to a doctor's advice. We have provided detailed information about the uses, dosage, effectiveness, side effects, precautions, drug interactions, storage conditions, and other important details of Repres SR 1.5 mg. Our goal is to present essential medicine information in one place for patients, caregivers, and healthcare professionals. To better understand Indapamide and ensure the safe use of this medicine, please read the information below carefully and consult a healthcare professional when necessary.

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Rx

Repres SR 1.5 mg

Square Pharmaceuticals PLC · Tablet (Sustained Release)

Generic

Indapamide

Strength1.5 mg
Total Strip3
Strip Size10
Unit Price
5

/ Piece

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Description of Repres SR 1.5 mg

Repres SR 1.5 mg may be available as a prescription or over-the-counter medicine, depending on local regulations and medical recommendations. It is used for the treatment and management of specific conditions or symptoms. The way this medicine is used may vary depending on the patient's condition and the advice of a healthcare provider. Detailed information about the approved uses, therapeutic applications, and other relevant details of Repres SR 1.5 mg is provided below to help users gain a clear understanding of this medicine.

What Is Repres SR 1.5 mg Indications and Uses?

Indapamide tablet is indicated in the treatment of essential hypertension. It is effective in treating hypertension in patients with renal function impairment, although its diuretic effect is reduced. Indapamide is also indicated for the treatment of salt and fluid retention associated with congestive heart failure. One tablet daily, preferably in the morning. In more severe cases, Indapamide tablet can be combined with other categories of antihypertensive agents.


Pharmacology (Source, Chemical and Physical Composition) Of Repres SR 1.5 mg

Indapamide is an oral antihypertensive agent. The mechanism whereby Indapamide exerts its antihypertensive action has not been completely elucidated; both vascular and renal actions have been implicated. The possible beneficial pharmacological effects of Indapamide in the treatment of hypertension include a reduction in cardiac hypertrophy and a reduction in the thickening of arterial walls, a prevention of the accumulation of the embryonic isoform of fibronectin in coronary vessels, free radical scavenging leading to stimulation of vasodilator eicosanoid formation, and interaction with renal carbonic anhydrase. The renal site of action of Indapamide is the proximal segment of the distal tubule. Indapamide appears to have natriuretic properties (sodium and chloride being excreted in equivalent amounts) with less effect on kaliuresis or uric acid excretion. Only at doses greater than 1.5 mg Indapamide sustained release tablet/day is an appreciable increase in urinary volume observed in man. No significant changes in plasma sodium levels have been observed in clinical studies. Significant hypokalemia (plasma potassium <3.2 mmol/L) has been reported in 4% of patients.Absorption: The fraction of Indapamide released is rapidly and totally absorbed via the gastrointestinal digestive tract. Ingestion with food slightly increases the rate and extent of absorption. These changes are unlikely to be clinically significant. Peak serum level following a single dose occurs about 12 hours after ingestion; repeated administration reduces the variation in serum levels between 2 doses. Distribution: Indapamide is widely distributed throughout the body, with extensive binding to some specific sites. In blood, it is highly bound to red blood cells (80%) and more specifically to carbonic anhydrase (98%) without having any significant inhibiting activity on this enzyme. Binding of Indapamide to plasma proteins is 79%. The plasma elimination half-life is 14 to 24 hours (mean 18 hours). The drug has a volume of distribution of approximately 60L. Steady state is achieved after 7 days. Repeated administration does not lead to accumulation. Metabolism: The drug is extensively metabolized in the liver, with only 5 to 7% of the dose excreted in the urine as unchanged drug.Elimination: Elimination is essentially urinary (70% of the dose) and faecal (22%) in the form of inactive metabolites.


Dosage And Administration of Repres SR 1.5 mg

One tablet daily preferably in the morning. In more sever case Indapamide can be combine with other categories of anti-hypertensive agent. The safety and effectiveness in pediatric patients have not been established.Use in Pediatric Patients: The safety and effectiveness in pediatric patients have not been established.


Drug Interactions of Repres SR 1.5 mg

Other Antihypertensive: Indapamide may add to or potentiate the action of other antihypertensive drugs. In limited controlled trials that compared the effect of Indapamide combined with other antihypertensive drugs with the effect of the other drugs administered alone, there was no notable change in the nature or frequency of adverse reactions associated with the combined therapy.Norepinephrine: Indapamide, like the thiazides, may decrease arterial responsiveness to norepinephrine, but this diminution is not sufficient to preclude effectiveness of the pressor agent for therapeutic use.


Side Effects of Repres SR 1.5 mg

Side effects include dizziness, headache, anorexia, nausea, vomiting, constipation, diarrhea and postural hypotension. Electrolyte imbalances include hypochloremic alkalosis, hyponatremia, hypokalemia and hyperuricemia; hypersensitivity reactions which include skin rashes, cholestatic jaundice and blood dyscrasias including thrombocytopenia, leucopenia, aplastic anemia.


Use During Pregnancy and Lactation

There is no adequate and well-controlled studies in pregnant women and so Indapamide is not recommended. Mothers taking Indapamide should not breastfeed.


Precautions And Warnings for Repres SR 1.5 mg

The drug should be used cautiously in the following situations- disturbed water/electrolyte balance, diabetes, gout and kidney problems. Monitoring of potassium and uric acid serum levels is also recommended.


Therapeutic Class

Thiazide diuretics & related drugs


Storage Conditions of It

Store in a cool and dry place. Protect from light and moisture.

Data Source: Data source of Indications and Usages, Pharmacology, Dosage & Administration, Drug Interactions, Side Effects, Use during Pregnancy & Lactation, Precautions & Warnings, Use in Special Populations, Therapeutic Class, and Storage Conditions is the concerned medicine company or respective organization.

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The information provided on All Samadhan is intended for general informational purposes only and is prepared based on our best practices. It is not a substitute for professional medical advice, diagnosis, or treatment. While we strive to keep the information accurate and up to date, we do not guarantee its completeness or accuracy. The absence of specific information or warnings about any medicine or service should not be considered as an assurance or endorsement by All Samadhan. All Samadhan shall not be held responsible for any consequences arising from the use of this information. We strongly recommend consulting a qualified healthcare professional or physician for any medical concerns, questions, or clarifications.All Samadhan is a digital healthcare software platform operated by MS Genius Experts. We provide technology solutions for pharmacies and healthcare providers; we are not a direct seller or dispenser of prescription medicines

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