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

Olmesartan Stada

Active Ingredient:
Olmesartan Medoxomil
Origin:
EU

Olmesartan Stada (Olmesartan Medoxomil)

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

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

Manufacturer / TM Owner

Thornton & Ross Ltd

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Indications & Clinical Uses

Olmesartan medoxil is used to treat high blood pressure by blocking the renin‑angiotensin system.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Heart failure: used as part of combination therapy to improve symptoms and outcomes.
  • Diabetic nephropathy: helps slow progression of kidney damage associated with diabetes.

How It Works

  • Olmesartan medoxil selectively blocks the binding of angiotensin II to the AT1 receptor on vascular smooth‑muscle cells and adrenal tissue. This inhibition prevents vasoconstriction and aldosterone release, leading to reduced peripheral resistance, lower blood pressure, and decreased sodium and water retention.

Side Effects

Olmesartan medoxil may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dizziness
  • Headache
  • Fatigue
  • Nasal congestion
  • Diarrhea
  • Back pain

Serious or Rare Side Effects

  • Angio‑edema
  • Hyperkalemia
  • Acute kidney injury
  • Severe hypotension
  • Liver enzyme elevation
  • Bullous skin reactions

Precautions & Warnings

When prescribing Olmesartan Stada, clinicians should consider several safety aspects.

  • Renal function monitoring: assess baseline creatinine and eGFR before initiation.
  • Electrolyte balance: check potassium levels periodically, especially if combined with potassium‑sparing diuretics.
  • Pregnancy: contraindicated in the second and third trimesters due to fetal toxicity.
  • Concomitant NSAID use: may blunt antihypertensive effect and increase renal risk.
  • Elderly patients: start at lower dose and monitor for orthostatic symptoms.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Olmesartan medoxil can interact with several medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Aliskiren (in diabetic patients): risk of renal dysfunction, hyperkalemia, and hypotension.
  • Potassium‑supplement supplements: may cause dangerous hyperkalemia.

Moderate Interactions (Monitor Closely)

  • NSAIDs (e.g., ibuprofen): may diminish blood‑pressure‑lowering effect and affect kidney function.
  • Diuretics (especially thiazides): can increase risk of electrolyte disturbances.
  • Lithium: may raise serum lithium levels, risking toxicity.
  • ACE inhibitors or other ARBs: combined use can lead to excessive hypotension and renal impairment.

Frequently Asked Questions

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

Olmesartan medoxil selectively blocks AT‑1 receptors, preventing angiotensin II from causing vasoconstriction and aldosterone release. This leads to relaxed blood vessels, reduced fluid retention, and ultimately lower arterial pressure.

The appropriate dose of Olmesartan Stada is determined by the prescribing clinician based on the patient’s blood‑pressure readings, kidney function, and overall health profile. Dosage adjustments are made during follow‑up visits.

Olmesartan Stada is contraindicated in pregnancy, especially in the second and third trimesters, because it can cause fetal toxicity. Limited data are available for breastfeeding; the drug is generally avoided unless the benefit outweighs potential risk.

To order, submit an enquiry on the product page at gnhindia.com with 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.

Olmesartan Stada belongs to the ARB class, which unlike ACE inhibitors does not commonly cause a dry cough. Compared with calcium‑channel blockers, ARBs provide a more direct blockade of the renin‑angiotensin system, offering similar blood‑pressure control with a distinct side‑effect profile.

Store Olmesartan Stada tablets at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Keep out of reach of children and do not use after the expiry date.

Olmesartan Stada is taken orally, usually once daily, with or without food. Patients should swallow the tablet whole with a glass of water and follow the prescriber’s instructions regarding timing and any concomitant medications.

Serious risks include angio‑edema, severe hypotension, hyperkalemia, and acute kidney injury. Patients should seek immediate medical attention if they experience swelling of the face, lips or throat, sudden dizziness, or a marked drop in blood pressure.

Olmesartan Stada should not be used by individuals with known hypersensitivity to olmesartan or any tablet excipients, pregnant women in the second or third trimester, and patients with severe renal artery stenosis without close medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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