Product image of Irbesartan/Hydroklortiazid Actavis (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbesartan/Hydroklortiazid Actavis

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan/Hydroklortiazid Actavis (Hydrochlorothiazide, Irbesartan)

Irbesartan, the active ingredient in Irbesartan/Hydrochlorothiazide Actavis, is an angiotensin II receptor blocker presented as a tablet for oral use. It treats hypertension in adults, often combined with hydrochlorothiazide to enhance blood‑pressure control.

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

Manufacturer / TM Owner

Actavis Group Ptc Ehf.

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Indications & Clinical Uses

  • Irbesartan/Hydrochlorothiazide is an antihypertensive combination that acts on the renin‑angiotensin system and renal sodium handling to lower blood pressure.
  • Essential hypertension: reduces systolic and diastolic blood pressure in patients with primary hypertension.
  • Hypertension requiring combined ARB and diuretic therapy: provides dual mechanism for improved control when monotherapy is insufficient.
  • Resistant hypertension: used as part of a multi‑drug regimen for patients whose blood pressure remains elevated despite other treatments.

How It Works

  • Irbesartan selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone‑mediated sodium retention. Hydrochlorothiazide inhibits Na+/Cl‑ reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, thereby reducing plasma volume. The combined actions produce additive reductions in systemic vascular resistance and circulating fluid volume, resulting in lower arterial pressure.

Side Effects

Common Side Effects

  • Dizziness or light‑headedness, especially after the first dose.
  • Headache.
  • Increased frequency of urination.
  • Fatigue or mild weakness.
  • Electrolyte disturbances such as low potassium.
  • Mild gastrointestinal discomfort.

Serious or Rare Side Effects

  • Severe dehydration or electrolyte imbalance.
  • Acute kidney injury or worsening renal function.
  • Hyperkalemia, especially when used with potassium‑sparing agents.
  • Angioedema or severe allergic reaction.
  • Significant drops in blood pressure (hypotension).
  • Blood dyscrasias such as agranulocytosis or thrombocytopenia.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess baseline blood pressure, renal function, and electrolyte status.
  • Monitor blood pressure regularly: adjust therapy based on response.
  • Check renal function: evaluate serum creatinine and eGFR before and during treatment.
  • Assess electrolytes: especially potassium and sodium levels.
  • Avoid use in severe renal impairment: contraindicated when creatinine clearance is markedly reduced.
  • Use caution in elderly patients: increased sensitivity to hypotension and electrolyte shifts.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Irbesartan/Hydrochlorothiazide may interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • ACE inhibitors or aliskiren in pregnancy: risk of angioedema and renal dysfunction.
  • Potassium‑sparing diuretics or supplements: can cause dangerous hyperkalemia.
  • Lithium: increased lithium levels and toxicity.
  • NSAIDs: may blunt antihypertensive effect and impair renal function.
  • Cyclosporine or tacrolimus: heightened risk of nephrotoxicity.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives (beta‑blockers, calcium channel blockers): may enhance hypotensive effect.
  • Additional thiazide or loop diuretics: increase risk of electrolyte disturbances.
  • Antidiabetic agents: diuretic‑induced changes in glucose may require dose adjustment.
  • CYP2C9 inhibitors (e.g., fluconazole): may raise irbesartan plasma levels.
  • Antacids containing aluminum or magnesium: may affect absorption of hydrochlorothiazide.

Frequently Asked Questions

Irbesartan/Hydrochlorothiazide is prescribed to lower high blood pressure. The combination provides an angiotensin II receptor blocker together with a thiazide diuretic, offering two mechanisms that help control hypertension in adults.

Irbesartan blocks AT1 receptors for angiotensin II, preventing vasoconstriction and reducing aldosterone‑driven sodium retention. This leads to relaxed blood vessels and lower systemic resistance, contributing to blood‑pressure reduction.

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

Safety in pregnancy and lactation has not been established for this combination. It is generally avoided in pregnant women, especially during the second and third trimesters, and used only if the potential benefit outweighs the risk. Breastfeeding mothers should consult 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 single‑agent therapies, the Irbesartan/Hydrochlorothiazide combo offers dual action—vascular relaxation from the ARB and diuresis from the thiazide—often achieving better blood‑pressure control with a single pill. It may be preferred when monotherapy does not reach target pressures.

Store the tablets at temperatures below 25 °C in their original container. 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. Patients should swallow the tablet whole with a full glass of water and follow the dosing instructions provided by their prescriber.

Serious risks include severe dehydration, acute kidney injury, hyperkalemia, and angioedema. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden weakness, or a marked drop in urine output.

The combination should be avoided in patients with severe renal impairment, known hypersensitivity to either component, or those taking contraindicated medications such as aliskiren in pregnancy. Clinicians must evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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