Product image of Irbésartan/Hydrochlorothiazide Cristers (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbésartan/Hydrochlorothiazide Cristers

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbésartan/Hydrochlorothiazide Cristers (Hydrochlorothiazide, Irbesartan)

Irbesartan, the active ingredient in Irbésartan/Hydrochlorothiazide Cristers, is an Angiotensin II receptor blocker presented as a fixed‑dose oral tablet for oral use. It is combined with hydrochlorothiazide, a thiazide diuretic, to treat hypertension in adult patients.

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

Manufacturer / TM Owner

Cristers

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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide is an antihypertensive combination that lowers elevated blood pressure through dual mechanisms.

  • Hypertension: provides sustained reduction of systolic and diastolic blood pressure in patients with primary hypertension.
  • Essential hypertension: improves blood‑pressure control when monotherapy is insufficient.
  • High blood pressure: assists in achieving target blood‑pressure goals as part of a comprehensive treatment plan.

How It Works

  • Irbesartan selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release, which lowers peripheral resistance. Hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion, thereby reducing plasma volume. The combined actions result in additive blood‑pressure lowering effects.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

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

Serious or Rare Side Effects

  • Severe dehydration or electrolyte imbalance
  • Acute kidney injury or worsening renal function
  • Hyperkalemia or severe hypokalemia
  • Angioedema or severe allergic reaction
  • Significant hypotension leading to syncope
  • Blood dyscrasias such as agranulocytosis

Precautions & Warnings

Patients should be monitored for safety and appropriate use.

  • Blood pressure monitoring: check regularly to ensure therapeutic response.
  • Renal function assessment: evaluate serum creatinine and eGFR before and during therapy.
  • Electrolyte surveillance: monitor potassium and sodium levels, especially with concomitant drugs.
  • Pregnancy avoidance: contraindicated in pregnancy due to fetal risk.
  • Elderly caution: start at lower dose and monitor for orthostatic hypotension.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Irbesartan/Hydrochlorothiazide may interact with several medicines.

Major Interactions (Avoid)

  • Aliskiren: combined use can increase risk of renal impairment and hyperkalemia.
  • Lithium: thiazide component may raise lithium levels, leading to toxicity.
  • ACE inhibitors or other ARBs: additive effects on potassium and renal function.
  • Potassium‑sparing diuretics or supplements: risk of hyperkalemia.
  • NSAIDs: may blunt antihypertensive effect and worsen renal function.

Moderate Interactions (Monitor Closely)

  • Other diuretics: monitor electrolytes and volume status.
  • Antihypertensive agents (beta‑blockers, calcium channel blockers): may enhance blood‑pressure lowering.
  • CYP2C9 inhibitors (e.g., fluconazole): can increase irbesartan plasma concentrations.
  • Antidiabetic drugs: diuretic‑induced changes in glucose may require dose adjustment.

Frequently Asked Questions

Irbésartan/Hydrochlorothiazide 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 when a single agent does not provide adequate control.

Irbesartan blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction and aldosterone release. This leads to relaxed blood vessels and reduced fluid retention, helping to lower blood pressure.

The specific dose is determined by the prescribing clinician based on the patient’s blood‑pressure level, renal function, and other individual factors. Only a qualified health professional should set the dosage regimen.

The product is classified as Pregnancy Category D, indicating evidence of fetal risk. It should not be used during pregnancy. Safety during breastfeeding has not been established, so use is generally discouraged unless the benefit outweighs the risk.

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, the combination offers additive blood‑pressure reduction by targeting two pathways: the renin‑angiotensin system and sodium‑water balance. This can improve control in patients who need more than one agent, while simplifying the pill burden.

Store the tablets at room temperature, below 25 °C, in the original blister pack. Protect them from moisture, heat and direct sunlight to maintain potency and stability.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole with a full glass of water.

Serious risks include severe dehydration, electrolyte disturbances (especially low potassium), acute kidney injury, hyperkalemia, and rare cases of angioedema or severe hypotension. Patients should be monitored for these events, particularly during the initial treatment period.

The combination is contraindicated in patients with known hypersensitivity to irbesartan, hydrochlorothiazide, or any component of the formulation, as well as in pregnant women. Caution is advised in severe renal impairment, hyperkalemia, and in patients taking interacting medications such as aliskiren or lithium.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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