Product image of Mozartan (Losartan Potassium) supplied by GNH India

Mozartan

Active Ingredient:
Losartan Potassium
Origin:
EU

Mozartan (Losartan Potassium)

Losartan Potassium, the active ingredient in Mozartan, is an Angiotensin II receptor blocker (ARB) presented as a strength/form for oral use. It treats hypertension and related cardiovascular conditions in adults.

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

Manufacturer / TM Owner

Vocate Φαρμακευτικη Αε

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Indications & Clinical Uses

Losartan Potassium is an ARB that lowers blood pressure and protects target organs in several cardiovascular and renal conditions.

  • Hypertension: reduces systolic and diastolic pressure, decreasing risk of stroke and myocardial infarction.
  • Heart failure: improves symptoms and survival by lowering after‑load.
  • Diabetic nephropathy: slows progression of renal impairment in patients with type 2 diabetes.
  • Stroke risk reduction in left ventricular hypertrophy: lowers incidence of cerebrovascular events in hypertensive patients with LVH.

How It Works

  • Losartan Potassium selectively blocks angiotensin II type 1 (AT1) receptors, preventing angiotensin II from inducing vasoconstriction, aldosterone release, and sympathetic activation. This antagonism leads to vasodilation, reduced sodium and water retention, and lower blood pressure, thereby mitigating cardiovascular strain and protecting end‑organ function.

Side Effects

Common Side Effects

  • Dizziness: feeling light‑headed, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness without exertion.
  • Nasal congestion: stuffy or runny nose.
  • Upper respiratory infection: mild cold‑like symptoms.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat requiring immediate medical attention.
  • Hyperkalemia: elevated serum potassium that can cause cardiac arrhythmias.
  • Acute renal impairment: sudden decrease in kidney function, especially when combined with other nephrotoxic agents.
  • Hepatic injury: abnormal liver enzymes or jaundice.
  • Severe hypotension: markedly low blood pressure leading to dizziness or fainting.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient-specific factors and monitor relevant parameters.

  • Blood pressure monitoring: ensure adequate control and avoid excessive hypotension.
  • Renal function assessment: check serum creatinine and eGFR periodically.
  • Serum potassium measurement: monitor for hyperkalemia, especially with potassium‑sparing agents.
  • Pregnancy avoidance: Losartan is contraindicated in pregnancy due to fetal toxicity.
  • Elderly caution: start at lower doses and monitor for orthostatic effects.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Losartan may interact with several medicines, requiring dose adjustments or avoidance.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: increased risk of renal dysfunction and hyperkalemia.
  • Concurrent ACE inhibitors or other ARBs: additive effect on potassium and renal function.
  • Potassium‑sparing diuretics (e.g., spironolactone): heightened hyperkalemia risk.
  • NSAIDs (e.g., ibuprofen): may blunt antihypertensive effect and impair renal perfusion.

Moderate Interactions (Monitor Closely)

  • Loop or thiazide diuretics: may enhance hypotensive response.
  • Lithium: losartan can raise lithium levels, risking toxicity.
  • CYP2C9 inhibitors (e.g., fluconazole): may increase losartan plasma concentrations.
  • Rifampin: may reduce losartan effectiveness by inducing metabolism.

Frequently Asked Questions

Mozartan contains losartan potassium, an angiotensin II receptor blocker that is prescribed for hypertension, heart failure, diabetic nephropathy, and to lower stroke risk in patients with hypertension and left ventricular hypertrophy.

Losartan potassium selectively blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction and aldosterone release. This results in vasodilation, reduced sodium and water retention, and ultimately lower blood pressure.

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

Losartan potassium is classified as Pregnancy Category D, indicating evidence of fetal risk. It should not be used during pregnancy. Limited data are available for breastfeeding; the decision to continue therapy should be made by a healthcare professional weighing potential benefits and risks.

To place an order, submit an enquiry on the Mozartan 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 ACE inhibitors, losartan offers a similar blood‑pressure‑lowering effect but a lower incidence of cough and angioedema. Unlike calcium‑channel blockers, it directly blocks the renin‑angiotensin system, providing renal‑protective benefits especially in diabetic patients.

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

Mozartan is taken orally, usually as a tablet, with or without food. Patients should swallow the tablet whole with a full glass of water and follow the dosing schedule prescribed by their healthcare provider.

Serious risks include angioedema, severe hyperkalemia, acute renal impairment, and marked hypotension. Patients should seek immediate medical attention if they experience swelling of the face or throat, rapid heartbeat, or a sudden drop in blood pressure.

Mozartan is contraindicated in patients with known hypersensitivity to losartan or any ARB, in pregnant women, and in individuals with severe hepatic impairment. Caution is advised for patients with renal artery stenosis or those taking multiple potassium‑increasing agents.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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