Product image of Noliterax (Indapamide, Perindopril Arginine) supplied by GNH India

Noliterax

Active Ingredient:
Indapamide, Perindopril Arginine
Origin:
EU

Noliterax (Indapamide, Perindopril Arginine)

Indapamide, the active ingredient in Noliterax, is a thiazide-like diuretic and ACE inhibitor combination presented as an oral tablet for oral use. It treats hypertension in adult patients.
GNH India supplies Noliterax as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Les Laboratoires Servier (Suresnes)

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Indications & Clinical Uses

Noliterax is an antihypertensive medication that works within the renin‑angiotensin‑aldosterone system and renal sodium handling pathways.

  • Hypertension: lowers systolic and diastolic blood pressure in patients with primary hypertension.
  • Heart failure: assists in blood‑pressure control as part of a physician‑directed regimen for patients with heart failure.
  • Diabetic nephropathy: helps achieve target blood pressure in patients with diabetes, supporting renal protection.

How It Works

  • Indapamide blocks NaCl reabsorption in the distal renal tubule, promoting diuresis and reducing plasma volume. Perindopril inhibits angiotensin‑converting enzyme, decreasing formation of angiotensin II and thereby reducing vasoconstriction and aldosterone secretion. The combined actions lower systemic vascular resistance and blood pressure.

Side Effects

Noliterax may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Persistent dry cough
  • Increased urinary frequency
  • Electrolyte disturbances (e.g., low potassium)
  • Fatigue or weakness

Serious or Rare Side Effects

  • Severe hypotension
  • Angioedema (swelling of face, lips, tongue)
  • Hyperkalemia
  • Acute renal impairment
  • Pancreatitis
  • Blood dyscrasias such as agranulocytosis

Precautions & Warnings

Before initiating Noliterax, several safety considerations should be observed.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Renal function assessment: evaluate serum creatinine and eGFR prior to use.
  • Electrolyte checks: monitor potassium and sodium levels regularly.
  • Contraindication in severe renal impairment: avoid if eGFR is markedly reduced.
  • Caution with potassium‑sparing agents: risk of hyperkalemia.
  • Allergy to ACE inhibitors: discontinue if angioedema occurs.
  • Store at ambient temperature: keep in the original container, protect from moisture.

Avoid Interactions

Noliterax can interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: increased risk of renal dysfunction.
  • Potassium supplements or high‑potassium diet: may cause hyperkalemia.
  • NSAIDs (e.g., ibuprofen, naproxen): can diminish antihypertensive effect and impair renal function.
  • Lithium: risk of lithium toxicity due to reduced clearance.
  • Other potent diuretics: may lead to severe electrolyte imbalance.

Moderate Interactions (Monitor Closely)

  • ARBs or other ACE inhibitors: additive blood‑pressure lowering effect.
  • Beta‑blockers: may enhance hypotensive response.
  • Thiazide diuretics: monitor electrolytes closely.
  • Certain antibiotics (e.g., trimethoprim‑sulfamethoxazole): can increase potassium levels.
  • Glucocorticoids: may counteract antihypertensive effect.

Frequently Asked Questions

Noliterax is prescribed to lower high blood pressure in adults. It combines a thiazide‑like diuretic with an ACE inhibitor, providing a dual mechanism that helps control hypertension and reduce cardiovascular risk when used under medical supervision.

Indapamide reduces sodium and water reabsorption in the kidney’s distal tubule, promoting diuresis and decreasing blood volume. Perindopril blocks the conversion of angiotensin I to angiotensin II, leading to vasodilation and reduced aldosterone secretion. Together they lower vascular resistance and blood pressure.

The specific dose of Noliterax is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and overall health status. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Noliterax is generally not recommended during pregnancy, especially in the second and third trimesters, because ACE inhibitors can affect fetal kidney development. Breastfeeding mothers should consult their healthcare provider, as the drug may be excreted in milk.

To request Noliterax, 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 single‑agent therapies, Noliterax offers the convenience of two complementary mechanisms in one tablet, potentially improving blood‑pressure control and adherence. It may be preferred over separate diuretic and ACE‑inhibitor prescriptions when a combined approach is clinically appropriate.

Noliterax tablets should be stored at ambient temperature, below 25 °C, in their original packaging to protect from moisture and light. Keep the product out of reach of children and avoid storing in humid or excessively hot environments.

Noliterax is taken orally, usually once daily, with or without food, as directed by the prescriber. Swallow the tablet whole with a full glass of water and follow any specific timing instructions provided by the healthcare professional.

Serious risks include severe hypotension, angioedema (which can affect breathing), hyperkalemia, and acute kidney injury. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or a significant drop in urine output.

Noliterax should be avoided in individuals with known hypersensitivity to indapamide, perindopril, or any ACE‑inhibitor components, as well as in patients with severe renal impairment, hyperkalemia, or a history of angioedema related to ACE‑inhibitor therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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