Product image of Olmesartán Aurovitas (Olmesartan Medoxomil) supplied by GNH India

Olmesartán Aurovitas

Active Ingredient:
Olmesartan Medoxomil
Origin:
EU

Olmesartán Aurovitas (Olmesartan Medoxomil)

Olmesartan Medoxomil, the active ingredient in Olmesartán Aurovitas, is an angiotensin II receptor blocker presented as a tablet for oral use. It is employed in the management of hypertension in adult patients. GNH India supplies Olmesartán Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

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

Manufacturer / TM Owner

Aurovitas Spain,s.A.U.

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Indications & Clinical Uses

Olmesartan Medoxomil is an antihypertensive agent that works within the renin‑angiotensin‑aldosterone system to lower blood pressure.

  • Hypertension: helps achieve target blood pressure and reduces cardiovascular risk.
  • Diastolic heart failure: assists in decreasing afterload and improving symptoms.
  • Chronic kidney disease with proteinuria: slows progression by lowering intraglomerular pressure.

How It Works

  • Olmesartan Medoxomil selectively blocks the binding of angiotensin II to the AT1 receptor on vascular smooth‑muscle and adrenal cells. This inhibition prevents vasoconstriction and aldosterone secretion, leading to reduced peripheral resistance, lower blood volume, and ultimately a decrease in systemic blood pressure.

Side Effects

Adverse reactions to olmesartan are generally mild to moderate and vary among individuals.

Common Side Effects

  • Dizziness: especially after the first dose or when standing quickly.
  • Headache: mild to moderate intensity.
  • Fatigue: feeling of tiredness without exertion.
  • Nasal congestion: mild blockage of the nasal passages.
  • Diarrhea: loose, watery stools.
  • Cough: non‑productive cough.

Serious or Rare Side Effects

  • Angioedema: swelling of the face, lips, tongue or throat that may compromise breathing.
  • Hyperkalemia: elevated potassium levels that can affect heart rhythm.
  • Acute kidney injury: sudden decline in renal function.
  • Severe hypotension: markedly low blood pressure causing faintness or shock.
  • Liver enzyme elevation: increased ALT/AST indicating hepatic stress.
  • Allergic rash: widespread skin eruption with itching or hives.

Precautions & Warnings

When using olmesartan, clinicians should assess patient history and monitor relevant parameters.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Renal function: evaluate serum creatinine and eGFR before initiation and during therapy.
  • Electrolyte balance: monitor potassium levels, especially if combined with potassium‑sparing agents.
  • Pregnancy: contraindicated in the second and third trimesters due to fetal toxicity.
  • Drug interactions: review concomitant medications for potential additive hypotensive effects.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan may interact with several medicines, requiring attention to dosage and monitoring.

Major Interactions (Avoid)

  • Aliskiren: combined use in diabetic patients can increase risk of renal impairment and hyperkalemia.
  • Potassium‑sparing diuretics: may cause dangerous elevations in serum potassium.
  • Lithium: concurrent use can raise lithium concentrations and risk toxicity.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and affect renal function.
  • ACE inhibitors: additive blood‑pressure lowering effect; monitor for hypotension.
  • Thiazide diuretics: can enhance antihypertensive response and increase risk of electrolyte disturbances.

Frequently Asked Questions

Olmesartán Aurovitas contains olmesartan medoxomil, an angiotensin II receptor blocker that is prescribed to lower high blood pressure (hypertension) and to reduce the risk of cardiovascular events associated with sustained hypertension.

Olmesartan medoxomil selectively blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction and aldosterone release. This results in relaxed blood vessels, reduced blood volume, and a gradual decline in systemic blood pressure.

The specific dose is determined by the prescribing clinician based on the individual’s blood‑pressure readings, kidney function, and overall health status. Only a qualified health‑care professional should set the dosage regimen.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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