Product image of Noliprel Bi-Forte A (Indapamide, Perindopril Arginine) supplied by GNH India

Noliprel Bi-Forte A

Active Ingredient:
Indapamide, Perindopril Arginine
Origin:
EU

Noliprel Bi-Forte A (Indapamide, Perindopril Arginine)

Indapamide, Perindopril arginine, the active ingredients in Noliprel Bi-Forte A, constitute a combination antihypertensive presented as a tablet for oral use. This EU‑market product combines a thiazide‑like diuretic with an ACE‑inhibitor to lower blood pressure in adult patients with primary hypertension.

GNH India supplies Noliprel Bi-Forte A as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU GMP standards and provides regulatory documentation for importers. Our global logistics network ensures timely delivery across continents.

Manufacturer / TM Owner

Anpharm Przedsiębiorstwo Farmaceutyczne Spółka Akcyjna

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Indications & Clinical Uses

Noliprel Bi-Forte A is indicated for hypertension, acting through combined diuretic and ACE‑inhibitor mechanisms.

  • Hypertension: lowers systolic and diastolic blood pressure in adult patients.
  • Isolated systolic hypertension: improves pulse‑pressure control especially in elderly individuals.
  • Essential (primary) hypertension: provides sustained blood pressure reduction when monotherapy is insufficient.
  • High‑risk hypertensive patients: contributes to cardiovascular risk reduction as part of a comprehensive treatment plan.
  • Hypertensive patients with peripheral edema: the diuretic component helps reduce fluid retention.
  • Patients requiring fixed‑dose combination therapy: simplifies dosing and may improve adherence.

How It Works

  • Indapamide acts on the distal renal tubule to inhibit sodium and chloride reabsorption, promoting diuresis and reducing plasma volume. Perindopril arginine blocks the angiotensin‑converting enzyme, decreasing formation of angiotensin II, leading to vasodilation, reduced aldosterone secretion, and lower systemic vascular resistance. The combined effect results in a synergistic reduction of arterial blood pressure.

Side Effects

Adverse reactions may occur with any antihypertensive therapy.

Common Side Effects

  • Dizziness or light‑headedness, especially after the first dose.
  • Headache.
  • Cough, often dry.
  • Fatigue or weakness.
  • Nausea or abdominal discomfort.
  • Electrolyte disturbances such as low potassium.

Serious or Rare Side Effects

  • Angioedema or swelling of the face, lips, tongue, or throat.
  • Severe hypotension leading to fainting.
  • Acute renal impairment or rise in serum creatinine.
  • Hyperkalemia, particularly when combined with potassium‑sparing agents.
  • Hepatic dysfunction or jaundice.
  • Severe allergic reactions (e.g., Stevens‑Johnson syndrome).

Precautions & Warnings

Before initiating therapy, clinicians should assess patient‑specific factors and monitor for potential complications.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Renal function: evaluate serum creatinine and eGFR before and during treatment.
  • Electrolyte balance: monitor potassium and sodium levels, especially in patients on other diuretics.
  • History of angioedema: avoid use in individuals with prior ACE‑inhibitor–related swelling.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk; consult obstetric guidance.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Drug‑drug interactions may modify efficacy or increase toxicity.

Major Interactions (Avoid)

  • Aliskiren combined with an ACE inhibitor in diabetic patients: risk of renal dysfunction and hyperkalemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: thiazide component may increase lithium levels, risking toxicity.
  • Other antihypertensives (beta‑blockers, calcium channel blockers): additive blood‑pressure lowering effect; monitor for hypotension.
  • CYP450 inhibitors (e.g., itraconazole): may increase perindopril plasma concentrations; adjust dose if needed.

Frequently Asked Questions

Noliprel Bi-Forte A is a prescription‑only oral tablet that combines indapamide and perindopril arginine to treat primary hypertension. The fixed‑dose combination lowers elevated blood pressure by promoting diuresis and inhibiting the renin‑angiotensin system, providing a convenient option for patients who need both a thiazide‑like diuretic and an ACE inhibitor.

Indapamide reduces sodium and water reabsorption in the distal renal tubules, increasing urine output and decreasing plasma volume. Perindopril arginine blocks the angiotensin‑converting enzyme, lowering angiotensin II levels, which leads to vasodilation and reduced aldosterone secretion. Together they produce a synergistic reduction in systemic vascular resistance and arterial pressure.

The specific dose of Noliprel Bi-Forte A is determined by the prescribing clinician based on the patient’s blood‑pressure profile, renal function, and overall health status. Dosage adjustments may be required during therapy, and patients should follow the exact regimen provided by their healthcare professional.

Safety in pregnancy and lactation has not been fully established for this combination. Perindopril, an ACE inhibitor, is generally contraindicated in the second and third trimesters due to fetal toxicity. Indapamide also carries risks. Use only if the potential benefit outweighs the potential risk and after consulting a qualified obstetrician.

To place an order, visit the product page on gnhindia.com, enter the required quantity, and submit the enquiry form. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.

Compared with single‑agent therapy, the fixed‑dose combination of indapamide and perindopril offers the convenience of one tablet and synergistic blood‑pressure control. It may improve adherence relative to taking separate diuretic and ACE‑inhibitor tablets. However, clinicians must consider individual patient tolerance, renal function, and potential drug interactions when selecting therapy.

Store the tablets at room temperature, preferably below 25 °C, in the original blister pack or container. Protect them from moisture, excessive heat, and direct sunlight. Do not refrigerate or freeze the product, and keep it out of reach of children.

Noliprel Bi-Forte A is taken orally, usually once daily, with or without food, as directed by the prescribing physician. Swallow the tablet whole with a full glass of water. Do not crush, chew, or split the tablet unless specifically instructed by a healthcare professional.

Patients should be alert for signs of angioedema (swelling of the face, lips, tongue, or throat), severe hypotension (dizziness, fainting), rapid decline in kidney function (decreased urine output, swelling), and hyperkalemia (muscle weakness, irregular heartbeat). Any of these symptoms require immediate medical attention.

The medication is contraindicated in individuals with a known hypersensitivity to indapamide, perindopril, or any component of the formulation, as well as those with a history of angioedema related to ACE‑inhibitor therapy. It should also be avoided in patients with severe renal impairment, hyperkalemia, or in the second and third trimesters of pregnancy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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