Product image of Malidum (Eplerenone) supplied by GNH India

Malidum

Active Ingredient:
Eplerenone
Origin:
EU

Malidum (Eplerenone)

Eplerenone, the active ingredient in Malidum, is a selective aldosterone receptor antagonist presented as an oral tablet for oral use. It is used to manage hypertension and to treat heart failure in adult patients, helping to control blood pressure and reduce fluid overload.

GNH India supplies Malidum as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare Polska Sp. Z O.O.

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Indications & Clinical Uses

Malidum (eplerenone) acts on the mineralocorticoid pathway to control fluid balance and vascular tone.

  • Hypertension: lowers blood pressure by reducing sodium and water retention.
  • Heart failure: improves cardiac function and reduces hospitalizations by decreasing fluid overload.
  • Post‑myocardial infarction with reduced ejection fraction: helps prevent adverse remodeling and further cardiovascular events.

How It Works

  • Eplerenone selectively blocks aldosterone binding at mineralocorticoid receptors in the distal nephron, kidneys, and cardiovascular tissues. This inhibition reduces sodium reabsorption and potassium excretion, leading to decreased extracellular fluid volume and lower arterial pressure, while also attenuating aldosterone‑mediated cardiac remodeling.

Side Effects

Eplerenone may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Hyperkalaemia: elevated serum potassium levels.
  • Dizziness or light‑headedness.
  • Headache.
  • Fatigue.
  • Gastrointestinal discomfort such as nausea or abdominal pain.
  • Cough.

Serious or Rare Side Effects

  • Severe hyperkalaemia leading to cardiac arrhythmia.
  • Acute renal impairment or worsening kidney function.
  • Angioedema or severe allergic reactions.
  • Hepatic injury with elevated liver enzymes.
  • Life‑threatening hypotension.
  • Myocardial infarction in susceptible patients.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor key parameters.

  • Monitor serum potassium: check levels regularly, especially after dose changes.
  • Assess renal function: evaluate creatinine and eGFR before and during treatment.
  • Avoid in patients with existing hyperkalaemia: contraindicated when potassium >5.0 mmol/L.
  • Caution in elderly: increased sensitivity to blood‑pressure lowering effects.
  • Review concomitant potassium‑sparing agents: adjust therapy to prevent excess potassium.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Eplerenone can interact with several medicines, altering electrolyte balance or renal function.

Major Interactions (Avoid)

  • ACE inhibitors or ARBs combined with eplerenone: markedly increase risk of hyperkalaemia and renal dysfunction.
  • Potassium supplements or potassium‑rich salt substitutes: may cause dangerous potassium accumulation.
  • NSAIDs (e.g., ibuprofen, naproxen): can impair renal function and exacerbate hyperkalaemia.

Moderate Interactions (Monitor Closely)

  • Loop or thiazide diuretics: may require potassium monitoring and dose adjustments.
  • Digoxin: altered serum levels may occur; monitor for toxicity.
  • Lithium: reduced clearance may increase lithium toxicity risk.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can raise eplerenone concentrations, necessitating closer monitoring.

Frequently Asked Questions

Malidum contains eplerenone, which is prescribed to treat hypertension and to manage chronic heart failure. It may also be used after a myocardial infarction when left‑ventricular function is reduced, helping to lower blood pressure and reduce fluid retention.

Eplerenone selectively blocks aldosterone from binding to mineralocorticoid receptors in the kidneys and cardiovascular system. This blockade reduces sodium reabsorption and potassium loss, leading to decreased fluid volume, lower blood pressure, and less cardiac remodeling.

The appropriate dose of Malidum is determined by the prescribing clinician based on the patient’s medical condition, kidney function, and serum potassium levels. Dosage adjustments are made individually and should follow the prescriber’s instructions.

The safety of eplerenone in pregnancy and lactation has not been fully established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Malidum, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Compared with non‑selective mineralocorticoid antagonists such as spironolactone, eplerenone offers a more selective receptor profile, which may reduce the incidence of hormonal side effects like gynecomastia. However, both drug classes share similar risks of hyperkalaemia and require careful monitoring.

Malidum should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the tablets away from moisture, excessive heat, and direct sunlight to maintain product stability.

Malidum is taken orally, usually once daily, with or without food, as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

The most serious risks include severe hyperkalaemia, which can cause cardiac arrhythmias, and acute renal impairment. Patients should be monitored regularly for serum potassium and kidney function, especially when starting therapy or adjusting doses.

Malidum is contraindicated in patients with known hypersensitivity to eplerenone, those with severe hyperkalaemia (serum potassium >5.0 mmol/L), and individuals with significant renal impairment (eGFR <30 mL/min/1.73 m²) unless closely supervised by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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