Product image of Hizaar (Losartan Potassium, Hydrochlorothiazide) supplied by GNH India

Hizaar

Active Ingredient:
Losartan Potassium, Hydrochlorothiazide
Origin:
EU

Hizaar (Losartan Potassium, Hydrochlorothiazide)

Hizaar is an oral prescription medication that combines the active ingredients losartan potassium and hydrochlorothiazide. It is formulated as a tablet and marketed in the European Union. The product belongs to the angiotensin II receptor blocker and thiazide diuretic combination class, and it is used to manage elevated blood pressure in adults. Hizaar provides a dual mechanism to help lower systemic hypertension.

Manufacturer / TM Owner

Organon Italia S.R.L.

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Indications & Clinical Uses

Hizaar is indicated for the treatment of hypertension, particularly when monotherapy does not achieve target blood pressure. It may be considered in patients who require both an angiotensin receptor blocker and a diuretic.

  • Hypertension that is uncontrolled with a single antihypertensive agent.
  • Patients needing combined RAAS inhibition and diuretic therapy.
  • Adjunct therapy for resistant high blood pressure.
  • Situations where a once‑daily oral tablet simplifies regimen adherence.
  • Use in adults as part of a comprehensive blood pressure management plan.

How It Works

  • Losartan potassium selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone‑mediated sodium retention, which reduces peripheral resistance. Hydrochlorothiazide acts on the distal convoluted tubule to inhibit NaCl reabsorption, increasing urinary excretion of sodium and water, thereby decreasing plasma volume. The combined actions result in lowered arterial pressure through reduced vascular tone and decreased fluid overload.

Side Effects

Adverse reactions to Hizaar can vary in frequency and severity.

Common

  • Dizziness or light‑headedness, especially after the first dose.
  • Headache.
  • Fatigue or tiredness.
  • Increased urination.
  • Electrolyte disturbances such as low potassium.
  • Mild gastrointestinal upset.

Serious

  • Severe hypotension.
  • Acute kidney injury.
  • Hyperkalemia.
  • Allergic reactions including rash, itching, or swelling.
  • Pancreatitis.
  • Liver function abnormalities.

Precautions & Warnings

Before starting Hizaar, certain health considerations should be reviewed to ensure safe use.

  • Assess renal function and electrolyte levels, especially potassium and sodium.
  • Monitor blood pressure regularly to avoid excessive lowering.
  • Use caution in patients with a history of gout, as thiazides may increase uric acid.
  • Evaluate liver function, as both components are metabolized hepatically.
  • Discuss pregnancy or breastfeeding plans with a healthcare professional.
  • Review any history of angioedema or hypersensitivity to ARBs or thiazides.
  • Adjust dose or discontinue if significant hypotension or renal impairment develops.

Avoid Interactions

Hizaar can interact with several other medicines, affecting its efficacy or safety.

Avoid

  • Concomitant use with other potent antihypertensives that may cause additive hypotension.
  • Potassium‑sparing diuretics or supplements, which can lead to hyperkalemia.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that may reduce renal clearance.
  • Lithium, as thiazides can increase lithium levels.
  • Strong CYP2C9 inhibitors that may raise losartan concentrations.

Use with caution

  • ACE inhibitors or other ARBs, monitoring for renal function and potassium.
  • Digoxin, due to potential changes in serum potassium.
  • Antidiabetic agents, as blood pressure changes may affect glucose control.
  • Anticoagulants, because of possible alterations in plasma volume.
  • Certain antibiotics (e.g., macrolides) that may affect drug metabolism.

Frequently Asked Questions

Hizaar is prescribed to lower high blood pressure (hypertension) by combining an angiotensin II receptor blocker with a thiazide diuretic.

Losartan blocks AT1 receptors, preventing angiotensin II from causing blood vessels to narrow and reducing aldosterone‑driven sodium retention.

Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal tubule, increasing urine output and lowering plasma volume, which helps reduce blood pressure.

Kidney function should be evaluated before starting Hizaar; dose adjustments or alternative therapy may be needed for significant renal impairment.

The safety of Hizaar in pregnancy has not been established; pregnant individuals should discuss alternative antihypertensive options with their clinician.

Common adverse effects include dizziness, headache, fatigue, increased urination, mild electrolyte changes, and occasional gastrointestinal discomfort.

Severe hypotension, acute kidney injury, hyperkalemia, allergic reactions such as rash or swelling, pancreatitis, and significant liver enzyme elevations should be reported promptly.

Avoid NSAIDs and potassium supplements without medical advice, as they can affect blood pressure control and potassium balance.

Blood pressure should be checked regularly, especially after initiating therapy or adjusting the dose, to ensure target levels are achieved without excessive lowering.

Hizaar may be used with other antihypertensives, but clinicians should monitor for additive effects on blood pressure and renal function.

Baseline and periodic assessments of serum electrolytes, kidney function (creatinine, eGFR), and liver enzymes are recommended.

Thiazide diuretics can raise uric acid levels, potentially increasing gout risk; patients with a history of gout should be monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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