Product image of Irbesartan + Hidroclorotiazida Basi (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbesartan + Hidroclorotiazida Basi

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan + Hidroclorotiazida Basi (Hydrochlorothiazide, Irbesartan)

Irbesartan, the active ingredient in Irbesartan + Hidroclorotiazida Basi, is an Angiotensin II receptor blocker (ARB) presented as an oral tablet for systemic use. It is combined with hydrochlorothiazide, a thiazide diuretic, to treat hypertension in adult patients when monotherapy is insufficient. The combination works to lower blood pressure by reducing vascular resistance and decreasing fluid volume, offering a synergistic approach for patients with moderate to severe hypertension.

GNH India supplies Irbesartan + Hidroclorotiazida Basi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratórios Basi – Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Irbesartan/HCTZ acts on the renin‑angiotensin‑aldosterone system and fluid balance to control elevated blood pressure.

  • Hypertension: lowers systolic and diastolic pressure in patients with primary hypertension.
  • Resistant hypertension: adds diuretic effect when an ARB alone does not achieve target blood pressure.
  • Cardiovascular risk reduction: contributes to decreased risk of stroke and myocardial infarction in hypertensive individuals.

How It Works

  • Irbesartan selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release, which reduces peripheral resistance. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, promoting diuresis and decreasing extracellular fluid volume. The combined actions result in additive blood‑pressure‑lowering effects.

Side Effects

Adverse reactions may occur with any medication. The following list reflects reported events.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain in the head region.
  • Fatigue: feeling unusually tired or weak.
  • Increased urination: more frequent need to void.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss requiring medical attention.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: elevated blood potassium levels that can affect heart rhythm.
  • Anaphylactic reaction: severe allergic response requiring emergency care.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Monitor renal function: assess serum creatinine and eGFR regularly.
  • Assess electrolytes: watch for hyponatremia, hypokalemia, or hyperkalemia.
  • Avoid in severe hepatic impairment: use only if benefits outweigh risks.
  • Pregnancy: risk category unknown; avoid unless clearly needed.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Irbesartan/HCTZ can interact with several medicines. Review patient medication lists carefully.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: combined use may increase renal risk.
  • Dual RAAS blockade (e.g., ACE inhibitors, other ARBs): may cause excessive hypotension or kidney injury.
  • Potassium‑sparing diuretics or supplements: risk of dangerous hyperkalemia.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect and affect kidney function.
  • Lithium: concurrent use can raise lithium concentrations, risking toxicity.

Frequently Asked Questions

Irbesartan + Hidroclorotiazida Basi is a fixed‑dose oral tablet that combines an angiotensin II receptor blocker with a thiazide diuretic. It is prescribed to lower high blood pressure in adult patients, especially when a single agent does not achieve adequate control.

Irbesartan blocks AT1 receptors, preventing angiotensin II from causing blood‑vessel constriction and aldosterone release. This leads to vasodilation and reduced sodium retention, helping to lower systemic vascular resistance and blood pressure.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s blood‑pressure level, renal function, and overall health status. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of this combination in pregnancy has not been established, and it is generally avoided unless the potential benefit justifies the risk. Breastfeeding mothers should consult their healthcare provider, as the drug may be excreted in breast milk.

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 monotherapy using either an ARB or a thiazide alone, the combination offers additive blood‑pressure reduction, often achieving target levels with a single tablet. It may reduce pill burden versus separate agents, but clinicians must consider individual patient tolerance and potential drug interactions.

Store the tablets at room temperature, below 25 °C, in the original packaging. Protect them from moisture, excessive heat, and direct sunlight to maintain potency throughout the shelf life.

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

Serious adverse events include severe dehydration, acute kidney injury, hyperkalemia, and anaphylactic reactions. Patients should be educated to report sudden drops in urine output, swelling, muscle weakness, or signs of an allergic reaction promptly.

Patients with known hypersensitivity to irbesartan, hydrochlorothiazide, or any component of the formulation should avoid the product. It is also contraindicated in individuals with severe renal impairment, anuria, or those taking prohibited drug combinations such as aliskiren in diabetes.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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