Product image of Irbesartan/Hydrochlorothiazide Evolugen Pharma (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbesartan/Hydrochlorothiazide Evolugen Pharma

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan/Hydrochlorothiazide Evolugen Pharma (Hydrochlorothiazide, Irbesartan)

Irbesartan/Hydrochlorothiazide, the active ingredient in Irbesartan/Hydrochlorothiazide Evolugen Pharma, is an angiotensin II receptor blocker and thiazide diuretic combination presented as an oral tablet for oral use. It treats hypertension in adult patients.

GNH India supplies Irbesartan/Hydrochlorothiazide Evolugen Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Evolupharm

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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide is used to manage hypertension, a condition characterized by elevated arterial pressure.

  • Hypertension: lowers systolic and diastolic blood pressure, helping to reduce cardiovascular risk.
  • Essential hypertension: provides sustained blood pressure control when monotherapy is insufficient.
  • Hypertension with renal impairment: assists in blood pressure management while supporting renal protection.

How It Works

  • Irbesartan selectively blocks angiotensin II type 1 (AT₁) receptors, preventing vasoconstriction and aldosterone‑mediated sodium retention. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit Na⁺/Cl⁻ reabsorption, promoting diuresis and reducing plasma volume. The combined effect decreases peripheral vascular resistance and blood volume, producing an additive antihypertensive response that is greater than either component alone.

Side Effects

Irbesartan/Hydrochlorothiazide may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Increased urination
  • Mild electrolyte disturbance (e.g., low potassium)

Serious or Rare Side Effects

  • Severe dehydration or electrolyte imbalance
  • Acute kidney injury
  • Allergic reactions such as rash or angioedema

Precautions & Warnings

When prescribing Irbesartan/Hydrochlorothiazide, clinicians should observe several safety considerations.

  • Monitor blood pressure: ensure adequate control without excessive hypotension.
  • Assess renal function: check serum creatinine and eGFR before initiation and periodically.
  • Check electrolytes: especially potassium and sodium levels.
  • Use caution in patients with diabetes: monitor glucose as the diuretic may affect glycaemic control.
  • Avoid in severe hepatic impairment: limited safety data are available.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Irbesartan/Hydrochlorothiazide can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Concomitant use with potassium‑sparing diuretics or supplements: risk of hyperkalaemia.
  • Strong CYP2C9 inhibitors (e.g., fluconazole): may increase irbesartan concentrations.
  • Lithium: thiazide component can raise lithium levels, leading to toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect and affect renal function.
  • ACE inhibitors or other ARBs: additive risk of hyperkalaemia and renal impairment.
  • Antidiabetic drugs: thiazide may increase blood glucose, requiring dose adjustment.

Frequently Asked Questions

Irbesartan/Hydrochlorothiazide is prescribed to lower high blood pressure (hypertension). By combining an angiotensin II receptor blocker with a thiazide diuretic, it provides a dual mechanism that helps achieve better blood‑pressure control than either component alone, reducing the risk of cardiovascular complications.

Irbesartan blocks the angiotensin II type 1 (AT₁) receptors on blood‑vessel walls, preventing angiotensin II from causing vasoconstriction and stimulating aldosterone release. This leads to relaxed vessels and reduced sodium‑water retention, contributing to lower blood pressure.

The appropriate dose is determined by the prescribing clinician based on the patient’s blood‑pressure readings, kidney function, and other individual factors. Dosage may be adjusted over time to achieve target blood‑pressure goals while minimizing side effects.

Safety data for this combination in pregnancy are limited, and it is generally avoided unless the potential benefit outweighs the risk. Breastfeeding mothers should consult their healthcare provider, as the drug may pass into breast milk and affect the infant.

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 (including any cold‑chain requirements) and necessary import documentation.

Compared with single‑agent therapy, the Irbesartan/Hydrochlorothiazide combo offers additive blood‑pressure reduction by targeting both the renin‑angiotensin system and fluid volume. This can improve efficacy in patients who need more than one mechanism, while simplifying the regimen into a single tablet.

Store the tablets at ambient temperature, preferably below 25 °C, in the original packaging. Keep them away from excess moisture, heat and direct sunlight to maintain potency throughout the shelf life.

The medication is taken orally, usually once daily, with a full glass of water. It can be taken with or without food, but patients should follow the specific instructions provided by their prescriber.

Serious risks include severe dehydration or electrolyte imbalance, acute kidney injury, marked hypotension, and allergic reactions such as rash or angioedema. Patients should seek immediate medical attention if they experience symptoms like fainting, swelling, or sudden changes in urine output.

The combination should be avoided in individuals with known hypersensitivity to either component, severe renal impairment, uncontrolled hyperkalaemia, or severe hepatic disease. It is also contraindicated in patients who are pregnant unless the benefits clearly outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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