Product image of Irbesartán/Hidroclorotiazida Tecnigen (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbesartán/Hidroclorotiazida Tecnigen

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartán/Hidroclorotiazida Tecnigen (Hydrochlorothiazide, Irbesartan)

Irbesartan/Hydrochlorothiazide, the active ingredient in Irbesartán/Hidroclorotiazida Tecnigen, is an angiotensin II receptor blocker/thiazide diuretic combination presented as an oral tablet for systemic use. It is indicated for the management of hypertension in adult patients, providing blood‑pressure reduction through dual mechanisms that address vascular tone, sodium balance and fluid volume. The combination is approved across the European Union and is commonly prescribed when monotherapy does not achieve target blood pressure.

GNH India supplies Irbesartán/Hidroclorotiazida Tecnigen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Tecnimede España Ind. Fca., S.A.

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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide is used to treat hypertension, acting on the renin‑angiotensin system and fluid balance.

  • Essential hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Hypertension requiring diuretic therapy: adds diuretic effect to improve blood‑pressure control in volume‑dependent cases.
  • Hypertension with concomitant cardiovascular risk: helps achieve target pressures in patients with additional risk factors such as dyslipidaemia or smoking.

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 NaCl reabsorption, increasing urinary excretion of sodium and water, which reduces plasma volume. This dual action also attenuates sympathetic activation and improves endothelial function, contributing further to antihypertensive efficacy.

Side Effects

Irbesartan/Hydrochlorothiazide may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after the first doses.
  • Headache: mild to moderate intensity, often transient.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance (low potassium): mild hypokalaemia may occur.
  • Fatigue: general feeling of tiredness.
  • Mild gastrointestinal upset: nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Severe dehydration: marked fluid loss requiring medical attention.
  • Hyperkalemia: elevated potassium levels that can affect heart rhythm.
  • Acute kidney injury: sudden decline in renal function.
  • Angioedema: swelling of face, lips, tongue or airway.
  • Severe hypotension: dangerous drop in blood pressure.
  • Allergic reactions: rash, itching, or anaphylaxis.

Precautions & Warnings

Before initiating therapy with Irbesartan/Hydrochlorothiazide, several precautions should be considered.

  • Monitor blood pressure: ensure adequate control and avoid excessive hypotension.
  • Check electrolytes: especially potassium and sodium levels during treatment.
  • Assess renal function: periodic serum creatinine and eGFR measurements are recommended.
  • Use caution in severe hepatic impairment: dose adjustments may be required.
  • Consider elderly patients: increased sensitivity to blood‑pressure changes and electrolyte disturbances.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Irbesartan/Hydrochlorothiazide can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Aliskiren: combined renin‑angiotensin blockade may increase risk of renal impairment and hyperkalaemia.
  • Potassium‑sparing diuretics (e.g., spironolactone): can cause dangerous hyperkalaemia.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and worsen renal function.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or other ARBs: additive blood‑pressure lowering and potassium rise.
  • Lithium: thiazide component may increase lithium levels, risking toxicity.
  • Antidiabetic agents: diuretic effect can affect glucose control.
  • CYP2C9 inhibitors (e.g., fluconazole): may raise irbesartan concentrations.
  • High‑dose corticosteroids: can counteract antihypertensive action.

Frequently Asked Questions

Irbesartan/Hydrochlorothiazide is prescribed to lower high blood pressure in adult patients. The combination targets both vascular tone and fluid volume, making it effective for essential hypertension and cases where additional diuretic action is needed to achieve target blood‑pressure levels.

Irbesartan blocks angiotensin II type 1 receptors, preventing vasoconstriction and aldosterone‑driven sodium retention. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, increasing urinary excretion of water and electrolytes. Together they reduce peripheral resistance and plasma volume, producing an additive antihypertensive effect.

The specific dose is determined by the prescribing clinician based on the patient’s blood‑pressure readings, renal function, and other clinical factors. Physicians typically start with a low dose and may adjust it to achieve optimal control while monitoring safety parameters.

Safety data are limited, and the combination is generally not recommended for use during pregnancy or while breastfeeding unless the potential benefit outweighs the risk. Patients who are pregnant, planning pregnancy, or nursing should discuss alternatives with their healthcare provider.

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.

Compared with irbesartan alone, the combination adds a thiazide diuretic, offering greater blood‑pressure reduction in patients who need volume control. Compared with hydrochlorothiazide alone, it provides additional vasodilatory effect via AT1‑receptor blockade, often achieving target pressures with lower diuretic doses and fewer electrolyte disturbances.

The product should be stored at room temperature, below 25 °C, in its original packaging. It must be kept away from moisture, direct sunlight, and sources of heat. No special refrigeration is required for this oral tablet formulation.

Irbesartan/Hydrochlorothiazide is taken orally, usually as a whole tablet swallowed with a glass of water. It can be taken with or without food, but patients should follow the prescribing physician’s instructions regarding timing and any dietary considerations.

Serious risks include severe dehydration, hyperkalaemia, acute kidney injury, angioedema, and profound hypotension. Patients should be educated to seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, marked weakness, or any signs of kidney dysfunction.

The combination should be avoided in patients with severe renal impairment, uncontrolled hyperkalaemia, known hypersensitivity to either component, and in women who are pregnant. Caution is also advised for individuals with severe hepatic disease or those taking interacting medications that could raise potassium levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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