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

Irbesartan + Hidroclorotiazida Generis Phar

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan + Hidroclorotiazida Generis Phar (Hydrochlorothiazide, Irbesartan)

Irbesartan and Hydrochlorothiazide, the active ingredients in Irbesartan + Hidroclorotiazida Generis Phar, are an angiotensin II receptor blocker and a thiazide diuretic presented as an oral tablet for oral use. They are used to lower high blood pressure in adult patients and are indicated for the management of hypertension in patients who require combination therapy.

GNH India supplies Irbesartan + Hidroclorotiazida Generis Phar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide through regulated supply chains.

Manufacturer / TM Owner

Generis Farmacêutica, S.A.

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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide is indicated for the management of hypertension, a condition characterized by elevated arterial pressure.

  • Hypertension: lowers systolic and diastolic blood pressure, helping to reduce cardiovascular risk.
  • Essential hypertension: provides effective blood pressure control when monotherapy is insufficient.
  • Hypertension requiring combination therapy: combines an ARB with a thiazide diuretic to achieve target pressures in patients needing multiple mechanisms.
  • Renal hypertension: assists in blood pressure reduction in patients with mild renal impairment.

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, inhibiting the Na⁺/Cl⁻ cotransporter, which promotes excretion of sodium, chloride, and water, leading to a reduction in plasma volume. The combined actions result in decreased peripheral resistance and lowered blood pressure.

Side Effects

The combination may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Fatigue or weakness
  • Increased urination
  • Electrolyte disturbances (e.g., low potassium)
  • Mild gastrointestinal discomfort

Serious or Rare Side Effects

  • Severe allergic reactions such as angioedema
  • Acute kidney injury
  • Significant drops in blood pressure (hypotension)
  • Elevated blood urea nitrogen or creatinine
  • Pancreatitis
  • Severe skin reactions (e.g., Stevens‑Johnson syndrome)

Precautions & Warnings

When prescribing Irbesartan/HCTZ, clinicians should observe several precautionary measures.

  • Monitor blood pressure: ensure adequate control and avoid hypotension.
  • Assess renal function: check serum creatinine and eGFR before and during therapy.
  • Check electrolytes: especially potassium and sodium levels.
  • Avoid use in pregnancy: drug is classified as pregnancy category D.
  • Use caution in elderly patients: increased sensitivity to blood pressure changes.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Irbesartan/HCTZ can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Concomitant use with ACE inhibitors or aliskiren in diabetic patients: risk of hyperkalemia and renal impairment.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • Lithium: increased lithium levels leading to toxicity.
  • NSAIDs (e.g., ibuprofen, naproxen): may reduce antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives (beta‑blockers, calcium channel blockers): may enhance blood pressure lowering, requiring dose adjustment.
  • CYP2C9 inhibitors (e.g., fluconazole, amiodarone): can increase irbesartan plasma concentrations.
  • Thiazide‑type diuretics: additive electrolyte disturbances.
  • Antidiabetic agents: may require monitoring of blood glucose as blood pressure changes can affect glucose control.

Frequently Asked Questions

It is a prescription combination of irbesartan and hydrochlorothiazide indicated for the treatment of hypertension in adult patients, especially when blood pressure is not adequately controlled with a single agent.

Irbesartan blocks the angiotensin II type 1 (AT1) receptor, preventing angiotensin II‑mediated vasoconstriction and aldosterone release, which leads to relaxation of blood vessels and reduced sodium retention, thereby lowering blood pressure.

The exact dose is determined by the prescribing clinician based on the patient’s blood pressure, renal function, and response to therapy. The prescriber selects the appropriate strength and dosing schedule.

The combination is classified as pregnancy category D, indicating evidence of risk to the fetus, and it is generally contraindicated during pregnancy. Limited data are available for breastfeeding, and a healthcare professional should evaluate the risk‑benefit ratio before use.

Enquiries are submitted via the product page on gnhindia.com, where the required quantity is entered. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Irbesartan/HCTZ combines an angiotensin II receptor blocker with a thiazide diuretic, offering dual mechanisms that can be more effective than monotherapy. Compared with ACE inhibitors, it has a lower incidence of cough, and the thiazide component adds diuretic effect not present in many ARB‑only products.

The product should be stored at room temperature, below 25 °C, in the original packaging to protect it from moisture and light. No refrigeration is required for this oral tablet formulation.

It is taken orally, usually once daily, with or without food, as directed by the prescriber. The tablet should be swallowed whole with a glass of water.

Serious adverse reactions include angioedema, severe hypotension, acute kidney injury, significant electrolyte disturbances (especially hyperkalemia or hyponatremia), and rare severe skin reactions such as Stevens‑Johnson syndrome. Patients should seek immediate medical attention if these occur.

The combination should be avoided in patients with known hypersensitivity to irbesartan, hydrochlorothiazide, or any component of the formulation, in pregnant women, and in individuals with severe renal impairment or uncontrolled electrolyte abnormalities unless closely monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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