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

Irbesartan + Hidroclorotiazida Farmoz

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan + Hidroclorotiazida Farmoz (Hydrochlorothiazide, Irbesartan)

Irbesartan/Hydrochlorothiazide, the active ingredient in Irbesartan + Hidroclorotiazida Farmoz, is an angiotensin II receptor blocker / thiazide diuretic presented as an oral tablet for oral use. It is used to lower high blood pressure in adult patients.

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

Manufacturer / TM Owner

Farmoz - Sociedade Técnico Medicinal, S.A.

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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide acts on the renin‑angiotensin‑aldosterone system to control elevated blood pressure.

  • Hypertension: reduces systolic and diastolic blood pressure in patients with primary hypertension.
  • Hypertension with fluid retention: provides additional diuretic effect to manage volume overload.
  • Hypertension uncontrolled by monotherapy: offers combined ARB and thiazide action for patients needing two agents.

How It Works

  • Irbesartan selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, increasing urinary excretion of water and electrolytes, which together lower peripheral resistance and plasma volume, resulting in reduced arterial pressure.

Side Effects

Common side effects are generally mild and may resolve with continued therapy.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain in the head region.
  • Increased urination: more frequent need to void due to diuretic action.
  • Electrolyte imbalance: low potassium or sodium levels.
  • Fatigue: feeling unusually tired or weak.
  • Mild gastrointestinal upset: nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss leading to low blood pressure.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: dangerously high potassium levels.
  • Angioedema: swelling of face, lips, tongue, or throat.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Allergic reactions: rash, itching, or anaphylaxis.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Blood pressure monitoring: ensure target levels are achieved without excessive drop.
  • Renal function assessment: check serum creatinine and eGFR periodically.
  • Electrolyte surveillance: monitor potassium and sodium levels, especially in patients on other diuretics.
  • Hepatic impairment: use with caution in patients with liver disease.
  • Pregnancy and lactation: safety not established; avoid unless benefits outweigh risks.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Irbesartan/Hydrochlorothiazide may interact with several drug classes.

Major Interactions (Avoid)

  • ACE inhibitors: combined use can increase risk of hyperkalemia and renal dysfunction.
  • Lithium: diuretic component may raise lithium concentrations, leading to toxicity.
  • Potassium‑sparing diuretics: additive effect on serum potassium, risking hyperkalemia.
  • Rifampin: enzyme induction may reduce irbesartan plasma levels.
  • NSAIDs: may blunt antihypertensive effect and impair renal function.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives: additive blood‑pressure lowering may require dose adjustment.
  • CYP2C9 inhibitors (e.g., fluconazole): may increase irbesartan exposure.
  • Antidiabetic agents: diuretic‑induced changes in glucose may affect glycemic control.
  • High‑dose corticosteroids: can counteract antihypertensive effect.
  • Alcohol: may enhance dizziness and hypotensive effects.

Frequently Asked Questions

Irbesartan + Hidroclorotiazida Farmoz is a fixed‑dose combination of an angiotensin II receptor blocker and a thiazide diuretic. It is prescribed to lower elevated blood pressure in adults, particularly when a single agent does not achieve 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, contributing to lower blood pressure.

The appropriate dose is determined by the prescribing clinician based on the patient’s blood‑pressure level, renal function, and other individual factors. Dosage adjustments are made according to therapeutic response and safety monitoring.

Safety in pregnancy and lactation has not been established. The product should be avoided unless the potential benefit justifies the potential risk to the fetus or infant, and it should be used only under close medical supervision.

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 required import documentation.

Compared with monotherapy, the Irbesartan/Hydrochlorothiazide combination offers dual mechanisms—vascular relaxation and diuresis—in a single tablet, which can improve adherence and provide stronger blood‑pressure reduction than either component alone.

Store at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing healthcare professional. Swallow the tablet whole with a glass of water; do not crush or chew it.

Serious risks include severe dehydration, acute kidney injury, hyperkalemia, angioedema, and marked hypotension. Patients should be monitored for signs of these conditions, especially during the initiation phase or when dose changes occur.

The combination is contraindicated in patients with known hypersensitivity to irbesartan, hydrochlorothiazide, or any component of the formulation, and in those with severe renal impairment, anuria, or severe electrolyte disturbances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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