Product image of Irbesartan/Hydrocholorthiazide Teva (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbesartan/Hydrocholorthiazide Teva

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan/Hydrocholorthiazide Teva (Hydrochlorothiazide, Irbesartan)

Irbesartan/Hydrochlorothiazide, the active ingredient in Irbesartan/Hydrochlorothiazide Teva, is an angiotensin II receptor blocker / thiazide diuretic presented as an oral tablet for systemic use. It is prescribed to lower elevated blood pressure in adult patients with hypertension and to help reduce cardiovascular risk.

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide is used within the antihypertensive drug class to manage high blood pressure.

  • Primary hypertension: reduces systolic and diastolic pressure in patients with essential hypertension.
  • Secondary hypertension: assists in controlling blood pressure when hypertension is caused by another underlying condition.
  • Hypertensive urgency (as part of combination therapy): helps achieve target blood pressure when rapid reduction is needed under medical supervision.

How It Works

  • Irbesartan selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone release, while hydrochlorothiazide inhibits Na⁺/Cl⁻ reabsorption in the distal convoluted tubule, promoting sodium and water excretion. The combined actions lower peripheral vascular resistance and plasma volume, resulting in a sustained reduction of arterial blood pressure.

Side Effects

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
  • Hepatic dysfunction or jaundice

Precautions & Warnings

Before initiating therapy, clinicians should assess patient history and monitor relevant parameters.

  • Renal function: evaluate serum creatinine and eGFR prior to and during treatment.
  • Electrolytes: check potassium and sodium levels regularly.
  • Diabetes: monitor blood glucose as diuretics may affect glycemic control.
  • Hepatic impairment: use with caution in patients with severe liver disease.
  • Pregnancy and lactation: avoid unless clearly indicated by a physician.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Irbesartan/Hydrochlorothiazide may interact with several medicines; careful review is essential.

Major Interactions (Avoid)

  • Aliskiren in patients with diabetes or renal impairment
  • Potassium‑sparing diuretics or supplements (risk of hyperkalemia)
  • Lithium (increased lithium toxicity)
  • ACE inhibitors or other ARBs (excessive hypotension, renal dysfunction)
  • NSAIDs (reduced antihypertensive effect, renal risk)

Moderate Interactions (Monitor Closely)

  • Other antihypertensives (additive blood pressure lowering)
  • CYP2C9 inhibitors (e.g., fluconazole) may increase irbesartan levels
  • Loop diuretics (enhanced diuretic effect, electrolyte loss)
  • Antidiabetic agents (possible need for dose adjustment)

Frequently Asked Questions

Irbesartan/Hydrochlorothiazide is an oral antihypertensive medication used to treat high blood pressure (hypertension) in adults. By lowering blood pressure, it helps reduce the risk of cardiovascular events such as stroke and heart attack.

Irbesartan blocks angiotensin II type 1 (AT1) receptors, preventing the hormone from causing blood vessels to narrow and from stimulating aldosterone release. This results in vasodilation and reduced fluid retention, contributing to lower blood pressure.

The specific dose of Irbesartan/Hydrochlorothiazide is determined by the prescribing clinician based on the patient’s condition, response, and other medical factors. Patients should follow the dosage instructions provided by their healthcare professional.

Safety in pregnancy and lactation has not been fully established. The medication should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified 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 monotherapy agents, the Irbesartan/Hydrochlorothiazide combination offers dual mechanisms—angiotensin receptor blockade and diuretic action—providing more consistent blood‑pressure control for many patients. It is often preferred when a single agent does not achieve target pressures.

The product should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the tablets away from excessive heat and humidity to maintain stability.

Irbesartan/Hydrochlorothiazide is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a glass of water; do not crush or chew unless instructed otherwise.

Serious risks include severe dehydration, electrolyte imbalances (especially low potassium), acute kidney injury, hyperkalemia, and rare cases of angioedema. Patients should report symptoms such as rapid weight loss, muscle weakness, swelling of the face or throat, or sudden drops in blood pressure.

Patients with known hypersensitivity to irbesartan, hydrochlorothiazide, or any component of the formulation should avoid the drug. It is also contraindicated in individuals with severe renal impairment, anuria, or those taking aliskiren in combination with an ACE inhibitor or ARB.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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