Product image of Iruzid (Hydrochlorothiazide, Lisinopril) supplied by GNH India

Iruzid

Active Ingredient:
Hydrochlorothiazide, Lisinopril
Origin:
EU

Iruzid (Hydrochlorothiazide, Lisinopril)

Hydrochlorothiazide / Lisinopril, the active ingredient in Iruzid, is a ACE inhibitor and thiazide diuretic combination presented as an oral tablet for oral use. It treats hypertension in adults.

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

Manufacturer / TM Owner

Belupo D.D.

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Indications & Clinical Uses

Iruzid is indicated for the management of hypertension, a condition involving elevated systemic arterial pressure.

  • Hypertension: reduces elevated blood pressure and helps achieve target levels.
  • Essential hypertension: provides combined ACE inhibition and diuresis to improve control.
  • Renin‑angiotensin system‑mediated hypertension: offers dual mechanism to lower systolic and diastolic pressures.

How It Works

  • Lisinopril blocks the angiotensin‑converting enzyme, decreasing formation of angiotensin II and reducing vasoconstriction, while hydrochlorothiazide inhibits Na⁺/Cl⁻ reabsorption in the distal convoluted tubule, promoting diuresis and lowering plasma volume. The combined actions result in a synergistic reduction of arterial blood pressure.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain in the head region.
  • Cough: dry, persistent cough associated with ACE inhibition.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: mild changes in potassium or sodium levels.
  • Fatigue: general feeling of tiredness.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat that can compromise breathing.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: dangerously high potassium levels.
  • Severe dehydration: excessive fluid loss leading to electrolyte disturbances.
  • Allergic reactions: rash, itching, or anaphylaxis.

Precautions & Warnings

Before initiating Iruzid, several safety considerations should be reviewed.

  • Renal function: monitor serum creatinine and eGFR regularly.
  • Electrolytes: check potassium and sodium levels, especially in patients on other diuretics.
  • Pregnancy: category D; avoid use unless benefits outweigh risks.
  • Concurrent ACE inhibitors or ARBs: increased risk of hyperkalemia and renal impairment.
  • Diabetes mellitus: monitor blood glucose as diuretics may affect control.
  • Store at ambient temperature: keep below 25°C in the original packaging, protected from moisture.

Avoid Interactions

Iruzid can interact with several medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Potassium‑sparing diuretics: risk of hyperkalemia.
  • NSAIDs: may blunt antihypertensive effect and affect renal function.
  • Lithium: increased lithium concentrations leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives: additive blood‑pressure lowering may cause hypotension.
  • Diabetes medications: diuretic effect may alter glucose control.
  • Corticosteroids: may increase sodium retention counteracting diuretic action.

Frequently Asked Questions

Iruzid is a prescription combination of hydrochlorothiazide and lisinopril indicated for the treatment of hypertension in adults. It combines an ACE inhibitor with a thiazide diuretic to lower blood pressure effectively.

Lisinopril blocks the angiotensin‑converting enzyme, reducing angiotensin II formation and vasoconstriction, while hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting diuresis and decreasing plasma volume. Together they produce a synergistic reduction in arterial pressure.

The dosage of Iruzid is individualized by the prescribing healthcare professional based on the patient’s blood pressure, renal function, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose without medical guidance.

Iruzid is classified as pregnancy category D because lisinopril may cause fetal harm; it should be avoided unless the potential benefit justifies the risk. Use during breastfeeding is not recommended unless specifically advised by a physician.

To request Iruzid, 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.

Compared with monotherapy agents, Iruzid offers combined ACE inhibition and thiazide diuresis in a single tablet, which can improve adherence and provide synergistic blood‑pressure reduction. It is an alternative to separate prescriptions of lisinopril and hydrochlorothiazide or to other fixed‑dose combinations such as losartan‑hydrochlorothiazide.

Store Iruzid at ambient temperature, below 25 °C, in the original packaging. Keep the tablets away from moisture, heat and direct sunlight to maintain potency. Do not store in the bathroom or near a kitchen sink.

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

Serious adverse reactions can include angioedema, severe hypotension, acute kidney injury, hyperkalemia, and severe dehydration. Patients should seek immediate medical attention if they experience swelling of the face or throat, dizziness, fainting, or a rapid decline in kidney function.

Iruzid should be avoided in patients with known hypersensitivity to lisinopril, hydrochlorothiazide, or any component of the formulation, in those with a history of angioedema related to ACE inhibitors, and in pregnant women. Caution is also advised for individuals with severe renal impairment or hyperkalemia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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