Product image of Modamide (Amiloride Hydrochloride Dihydrate) supplied by GNH India

Modamide

Active Ingredient:
Amiloride Hydrochloride Dihydrate
Origin:
EU

Modamide (Amiloride Hydrochloride Dihydrate)

Amiloride, the active ingredient in Modamide, is a potassium-sparing diuretic presented as an oral tablet for oral use. It treats hypertension, edema associated with congestive heart failure, and nephrotic syndrome in adult patients.

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

Manufacturer / TM Owner

Substipharm

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Indications & Clinical Uses

Modamide is a potassium‑sparing diuretic used in conditions where sodium retention contributes to fluid overload.

  • Hypertension: helps lower blood pressure by reducing sodium reabsorption while preserving potassium.
  • Congestive heart‑failure edema: decreases fluid accumulation in the lungs and peripheral tissues.
  • Nephrotic syndrome: limits protein‑loss‑related edema by promoting modest diuresis without worsening potassium loss.

How It Works

  • Amiloride blocks epithelial sodium channels (ENaC) located in the distal convoluted tubule and collecting duct of the nephron. By inhibiting sodium entry through these channels, the drug reduces sodium reabsorption, leading to a modest increase in urinary sodium excretion while sparing potassium, thereby producing a mild diuretic effect without significant potassium loss.

Side Effects

Adverse reactions may occur with any medication and should be monitored by the prescriber.

Common Side Effects

  • Dizziness
  • Headache
  • Nausea or upset stomach
  • Fatigue
  • Muscle cramps
  • Mild hyperkalemia (elevated potassium)

Serious or Rare Side Effects

  • Severe hyperkalemia leading to cardiac arrhythmia
  • Acute renal impairment
  • Significant hypotension
  • Allergic skin reactions (rash, urticaria)
  • Metabolic acidosis
  • Pulmonary edema in rare cases

Precautions & Warnings

Before initiating therapy, clinicians should assess patient‑specific factors and monitor relevant parameters.

  • Monitor serum potassium: avoid excessive accumulation, especially with other potassium‑sparing agents.
  • Assess renal function: dose adjustment may be required in reduced clearance.
  • Use caution in diabetic patients: potassium shifts can affect glucose control.
  • Avoid in severe renal impairment unless benefits outweigh risks.
  • Adjust dose in elderly patients due to altered pharmacodynamics.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Amiloride can affect the pharmacodynamics of several co‑administered drugs.

Major Interactions (Avoid)

  • ACE inhibitors or ARBs: may cause dangerous hyperkalemia.
  • Other potassium‑sparing diuretics (e.g., spironolactone): increase risk of severe hyperkalemia.
  • Potassium supplements or salt substitutes containing potassium.
  • Trimethoprim: additive effect on potassium levels.
  • Lithium: may increase lithium toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: can reduce diuretic efficacy and impair renal function.
  • Thiazide diuretics: may cause additive electrolyte disturbances.
  • Digoxin: altered serum potassium can affect digoxin toxicity.
  • Corticosteroids: may counteract diuretic effect.
  • Antidiabetic agents: potassium shifts may influence glucose control.

Frequently Asked Questions

Modamide, containing amiloride, is prescribed for hypertension, edema linked to congestive heart failure, and fluid retention in nephrotic syndrome. It helps lower blood pressure and reduce excess fluid while preserving potassium levels.

Amiloride blocks epithelial sodium channels (ENaC) in the distal nephron, decreasing sodium reabsorption. This modestly increases sodium excretion and retains potassium, producing a mild diuretic effect that assists in controlling blood pressure and fluid overload.

The specific dose of Modamide is determined by the prescribing clinician based on the patient’s condition, renal function, and response to therapy. Dosage adjustments are individualized and should follow the prescriber’s instructions.

Modamide is classified as Pregnancy Category B, indicating no evidence of risk in animal studies but lacking well‑controlled studies in pregnant women. It should be used only if the potential benefit justifies the potential risk. Breastfeeding decisions should be made in consultation with a healthcare professional.

To request Modamide, 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 necessary import documentation.

Unlike loop or thiazide diuretics, amiloride is a potassium‑sparing agent that provides modest diuresis without causing significant potassium loss. It is often combined with other diuretics to balance fluid removal while minimizing hypokalemia, making it a useful adjunct in resistant hypertension or heart‑failure regimens.

Modamide should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and extreme heat to maintain its stability and potency.

Modamide is taken orally, usually as a tablet, with or without food as directed by the prescriber. The exact timing and frequency depend on the individual treatment plan and should be followed exactly as prescribed.

The most serious risks include severe hyperkalemia, which can cause cardiac arrhythmias, and acute renal impairment. Patients should be monitored regularly for serum potassium and kidney function, especially when used with other potassium‑affecting medications.

Modamide is contraindicated in patients with severe renal impairment, hyperkalemia, or known hypersensitivity to amiloride. Caution is also advised for individuals on multiple potassium‑sparing agents or those with conditions predisposing them to high potassium levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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