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 diuretic (thiazide‑like) and ACE inhibitor combination presented as an oral tablet for oral use. It is indicated for the management of 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 acts on blood pressure regulation pathways.

  • Hypertension: lowers systolic and diastolic blood pressure in patients with elevated readings.
  • Essential hypertension: provides sustained control of primary high blood pressure.
  • High blood pressure: contributes to reduced cardiovascular risk by maintaining target pressures.

How It Works

  • Indapamide blocks sodium reabsorption in the distal renal tubule, increasing urinary sodium and water excretion, while Perindopril arginine inhibits angiotensin‑converting enzyme, decreasing angiotensin II formation and reducing systemic vascular resistance. The combined actions produce additive blood‑pressure‑lowering effects.

Side Effects

Noliterax may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

  • Dizziness: feeling light‑headed, especially after standing.
  • Headache: mild to moderate intensity.
  • Cough: dry, persistent throat irritation.
  • Fatigue: general tiredness or lack of energy.
  • Increased urination: more frequent need to void.
  • Electrolyte imbalance: changes in potassium or sodium levels.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat.
  • Severe hypotension: markedly low blood pressure causing faintness.
  • Renal impairment: worsening kidney function.
  • Hyperkalemia: elevated potassium concentration in blood.
  • Neutropenia: reduced white blood cell count.
  • Hepatic dysfunction: abnormal liver enzyme elevations.

Precautions & Warnings

Before initiating Noliterax, clinicians should consider several safety factors.

  • Blood pressure monitoring: check regularly to avoid excessive lowering.
  • Renal function assessment: evaluate serum creatinine and eGFR.
  • Electrolyte surveillance: monitor potassium and sodium levels.
  • Caution in diabetes: watch for changes in glucose control.
  • Avoid in severe hepatic impairment: limited data support use.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Noliterax can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Potassium‑sparing diuretics: risk of hyperkalemia.
  • Aliskiren in diabetic patients: additive renin‑angiotensin blockade.
  • Lithium: increased lithium levels and toxicity.
  • NSAIDs: may blunt antihypertensive effect and impair renal function.
  • ACE inhibitor with other ACE inhibitors or ARBs: heightened risk of renal dysfunction.

Moderate Interactions (Monitor Closely)

  • Thiazide‑type diuretics: additive electrolyte disturbances.
  • Other antihypertensives: may cause excessive blood pressure drop.
  • Diuretics causing dehydration: monitor volume status.
  • Antidiabetic agents: potential enhancement of hypoglycaemia.
  • Antimicrobials (e.g., trimethoprim): may increase potassium levels.

Frequently Asked Questions

Noliterax is prescribed to lower high blood pressure in adults. It combines a thiazide‑like diuretic with an ACE inhibitor to provide complementary antihypertensive effects, helping to achieve target blood pressure levels and reduce cardiovascular risk.

Indapamide increases urine output by inhibiting sodium reabsorption in the kidney’s distal tubule, while Perindopril arginine blocks the conversion of angiotensin I to angiotensin II, decreasing vascular resistance. Together they lower blood pressure through diuresis and vasodilation.

The specific dose of Noliterax is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and other individual factors. Patients should follow the dosage instructions provided by their healthcare professional.

Safety of Noliterax in pregnancy or while breastfeeding has not been established. Healthcare providers should evaluate the potential benefits against possible risks before prescribing it to pregnant or nursing women.

To place an order, 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.

Noliterax offers a fixed‑dose combination of a diuretic and an ACE inhibitor, which can simplify therapy compared with taking separate agents. This dual mechanism may provide more consistent blood‑pressure control and improve adherence relative to monotherapy, though individual response varies.

Noliterax tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Noliterax is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious risks include angioedema (swelling of the face, lips, tongue, or throat), severe hypotension, significant renal impairment, and hyperkalemia. Patients should seek immediate medical attention if they experience symptoms such as difficulty breathing, sudden swelling, or marked dizziness.

Noliterax is contraindicated in patients with known hypersensitivity to indapamide, perindopril, or any component of the formulation, as well as in individuals with a history of angioedema related to ACE‑inhibitor therapy. It should also be avoided in severe renal or hepatic impairment unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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