Product image of Irbesartan Accord (Irbesartan) supplied by GNH India

Irbesartan Accord

Active Ingredient:
Irbesartan
Origin:
EU

Irbesartan Accord (Irbesartan)

Irbesartan, the active ingredient in Irbesartan Accord, is an angiotensin II receptor blocker presented as an oral tablet for oral use. It belongs to the ARB class and works by selectively blocking AT1 receptors, leading to vasodilation and reduced aldosterone secretion. It is used to treat high blood pressure and to protect kidney function in patients with diabetic kidney disease.

GNH India supplies Irbesartan Accord as a licensed, GDP‑compliant international pharmaceutical supplier, providing quality‑assured products to hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Irbesartan is indicated for conditions related to the renin‑angiotensin system, primarily hypertension and diabetic kidney disease.

  • Hypertension: lowers elevated blood pressure, reducing cardiovascular risk.
  • Diabetic nephropathy: slows progression of kidney damage in patients with type 2 diabetes.
  • Proteinuria: decreases urinary protein excretion associated with diabetic kidney disease.

How It Works

  • Irbesartan selectively antagonizes angiotensin II type 1 (AT1) receptors on vascular smooth muscle, adrenal glands, and renal tubular cells. By blocking AT1 activation, it prevents angiotensin II‑mediated vasoconstriction, aldosterone release, and sodium‑water retention, producing vasodilation, reduced blood volume, and lowered systemic blood pressure while also attenuating pathological cardiac and renal remodeling.

Side Effects

Like other ARBs, Irbesartan may be associated with a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after initial dosing.
  • Headache: mild to moderate intensity.
  • Hyperkalaemia: elevated blood potassium levels.

Serious or Rare Side Effects

  • Angioedema: swelling of the face, lips, tongue or throat that may impair breathing.
  • Acute renal failure: sudden decline in kidney function.
  • Hepatic injury: signs of liver dysfunction such as jaundice.

Precautions & Warnings

When prescribing Irbesartan, clinicians should consider several safety measures to minimize risks.

  • Monitor blood pressure: check regularly to ensure therapeutic control and avoid hypotension.
  • Assess renal function: evaluate serum creatinine and eGFR before initiation and during therapy.
  • Check serum potassium: periodic testing to detect hyperkalaemia.
  • Use caution in hepatic impairment: dose adjustments may be required in patients with liver disease.
  • Avoid in known hypersensitivity: discontinue if allergic reactions occur.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Irbesartan can interact with other medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Concomitant use with aliskiren in patients with diabetes: increased risk of renal impairment, hyperkalaemia, and hypotension.
  • Combined therapy with ACE inhibitors or other ARBs: may cause excessive reduction in blood pressure and renal function.

Moderate Interactions (Monitor Closely)

  • Potassium‑sparing diuretics (e.g., spironolactone): may raise serum potassium levels.
  • NSAIDs (e.g., ibuprofen): can diminish antihypertensive effect and worsen renal function.
  • Lithium: may increase lithium concentrations, risking toxicity.

Frequently Asked Questions

Irbesartan Accord contains the ARB irbesartan and is prescribed to lower high blood pressure and to slow the progression of kidney damage in patients with diabetic nephropathy. It helps reduce cardiovascular risk associated with uncontrolled hypertension.

Irbesartan blocks angiotensin II type 1 (AT1) receptors, preventing the hormone from causing blood‑vessel constriction and aldosterone release. This leads to vasodilation, reduced fluid retention, and ultimately lower systemic blood pressure.

The appropriate dose of Irbesartan Accord is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Irbesartan is generally not recommended for use during pregnancy because it may affect fetal renal development. Safety during breastfeeding has not been established, so clinicians usually advise against its use unless the benefits outweigh potential risks.

To order Irbesartan Accord, submit an enquiry on the product page at gnhindia.com indicating 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.

Irbesartan belongs to the ARB class, which specifically blocks AT1 receptors. Compared with ACE inhibitors, ARBs have a lower incidence of cough and angio‑edema. Compared with calcium‑channel blockers or diuretics, ARBs target the renin‑angiotensin system and are often combined with those agents for additive blood‑pressure control.

Irbesartan Accord should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Irbesartan Accord is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare provider.

Serious risks include angio‑edema (swelling of the face, lips, tongue or throat), acute renal failure, and severe hyperkalaemia. If any signs of swelling, sudden loss of kidney function, or markedly high potassium levels occur, medical attention should be sought immediately.

Irbesartan Accord should be avoided in individuals with known hypersensitivity to irbesartan or any component of the formulation, in patients with severe hepatic impairment, and in those who are pregnant. Clinicians should also exercise caution in patients with existing renal dysfunction or high serum potassium.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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