Product image of Olmesartan Medoxomil Mylan (Olmesartan Medoxomil) supplied by GNH India

Olmesartan Medoxomil Mylan

Active Ingredient:
Olmesartan Medoxomil
Origin:
EU

Olmesartan Medoxomil Mylan (Olmesartan Medoxomil)

Olmesartan Medoxomil, the active ingredient in Olmesartan Medoxomil Mylan, is an Angiotensin II receptor blocker presented as an oral tablet for oral use. It treats hypertension in adult patients.
GNH India supplies Olmesartan Medoxomil Mylan as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mylan S.P.A.

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Indications & Clinical Uses

Olmesartan Medoxil is used to manage hypertension, a condition characterized by elevated arterial pressure.

  • Hypertension: lowers blood pressure by blocking the effects of angiotensin II, helping to reduce the risk of cardiovascular events.
  • Essential hypertension: provides sustained blood pressure control in patients requiring long‑term therapy.
  • Primary hypertension: improves vascular tone and reduces cardiac workload.

How It Works

  • Olmesartan Medoxomil selectively antagonizes the angiotensin II type 1 (AT1) receptor, preventing angiotensin II from binding. This inhibition blocks vasoconstriction and aldosterone secretion, leading to relaxation of vascular smooth muscle, reduced peripheral resistance, and ultimately a decrease in systemic blood pressure.

Side Effects

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain in the head region.
  • Fatigue: feeling unusually tired or lacking energy.
  • Abdominal pain: discomfort or cramping in the stomach area.

Serious or Rare Side Effects

  • Angioedema: swelling of the face, lips, tongue, or throat that may impair breathing.
  • Hyperkalemia: elevated potassium levels that can affect heart rhythm.
  • Renal impairment: worsening kidney function, indicated by increased creatinine.
  • Severe hypotension: markedly low blood pressure causing faintness or shock.

Precautions & Warnings

Olmesartan Medoxomil requires careful monitoring and patient education.

  • Blood pressure monitoring: regularly check to ensure therapeutic effect and avoid excessive lowering.
  • Renal function assessment: evaluate kidney function before initiating and during therapy.
  • Serum potassium check: monitor potassium levels, especially when combined with potassium‑sparing agents.
  • Pregnancy avoidance: do not use during pregnancy due to risk of fetal toxicity.
  • Elderly caution: start at lower doses and monitor for orthostatic hypotension.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan Medoxomil may interact with several drug classes.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): combined use can increase risk of renal dysfunction.
  • Potassium‑sparing diuretics (e.g., spironolactone): may cause dangerous hyperkalemia.
  • ACE inhibitors (e.g., enalapril): concurrent use heightens risk of hypotension and hyperkalemia.
  • NSAIDs (e.g., ibuprofen): can blunt antihypertensive effect and affect renal function.

Moderate Interactions (Monitor Closely)

  • Thiazide diuretics: may enhance blood‑pressure‑lowering effect, requiring dose adjustment.
  • Lithium: can increase lithium levels, necessitating serum monitoring.
  • Other antihypertensives (e.g., beta‑blockers): may require careful titration to avoid excessive hypotension.

Frequently Asked Questions

Olmesartan Medoxomil Mylan is prescribed to treat hypertension, helping to lower elevated blood pressure and reduce the risk of cardiovascular complications in adult patients.

The active ingredient, Olmesartan Medoxomil, selectively blocks the angiotensin II type 1 (AT1) receptor, preventing vasoconstriction and aldosterone release, which leads to relaxation of blood vessels and a decrease in systemic blood pressure.

The appropriate dose is determined by the prescribing healthcare professional based on the individual’s blood‑pressure response, renal function, and overall clinical condition.

Olmesartan Medoxomil is classified as pregnancy category D, indicating potential risk to the fetus. It should be avoided during pregnancy and used with caution while breastfeeding, following a physician’s advice.

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 necessary import documentation.

Olmesartan belongs to the angiotensin II receptor blocker (ARB) class, offering a similar blood‑pressure‑lowering effect to ACE inhibitors but with a lower incidence of cough. Compared with calcium‑channel blockers, ARBs act on the renin‑angiotensin system rather than directly on vascular smooth muscle.

Store the tablets at room temperature, below 25 °C, in the original container to protect them from moisture and light. Keep out of reach of children and do not use if the packaging is damaged.

Olmesartan Medoxomil is taken orally, usually once daily, with or without food, as directed by a healthcare professional.

Serious adverse reactions can include angioedema, severe hypotension, hyperkalemia, and renal impairment. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or signs of kidney dysfunction.

Olmesartan should be avoided in patients with known hypersensitivity to the drug, those who are pregnant, and individuals with severe renal artery stenosis or severe hepatic impairment unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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