Product image of Olmesartanmedoxomil/Amlodipine Stada (Amlodipine, Olmesartan) supplied by GNH India

Olmesartanmedoxomil/Amlodipine Stada

Active Ingredient:
Amlodipine, Olmesartan
Origin:
EU

Olmesartanmedoxomil/Amlodipine Stada (Amlodipine, Olmesartan)

Olmesartan, the active ingredient in Olmesartanmedoxomil/Amlodipine Stada, is an angiotensin II receptor blocker presented as a fixed‑dose combination tablet for oral use. It treats hypertension, often in combination with a calcium‑channel blocker, and is indicated for adults.
GNH India supplies Olmesartanmedoxomil/Amlodipine Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Olmesartanmedoxomil/Amlodipine Stada is used in cardiovascular therapy, targeting blood‑pressure regulation pathways.

  • Hypertension: provides additive blood‑pressure reduction by combining an ARB with a calcium‑channel blocker.
  • Isolated systolic hypertension in the elderly: improves systolic control where vascular stiffness predominates.
  • Hypertension with concomitant edema risk: mitigates calcium‑channel blocker‑induced peripheral edema through vasodilatory synergy.

How It Works

  • The combination pairs olmesartan medoxomil, a prodrug that converts to olmesartan and selectively blocks the angiotensin II type 1 (AT1) receptor, preventing vasoconstriction and aldosterone release, with amlodipine, a dihydropyridine calcium‑channel antagonist that inhibits L‑type calcium channels in vascular smooth muscle, producing arterial dilation and lowering peripheral resistance.

Side Effects

Adverse reactions may occur with any antihypertensive regimen and should be monitored during therapy.

Common Side Effects

  • Dizziness or light‑headedness
  • Peripheral edema, especially with amlodipine component
  • Headache
  • Flushing
  • Fatigue
  • Nasal congestion

Serious or Rare Side Effects

  • Angio‑edema involving face, lips or airway
  • Severe hypotension or syncope
  • Acute kidney injury or rising serum creatinine
  • Hyperkalemia
  • Hepatic enzyme elevation
  • Myocardial infarction in patients with unstable coronary disease

Precautions & Warnings

When prescribing this fixed‑dose combination, clinicians should consider several safety aspects.

  • Monitor blood pressure: ensure adequate control without excessive lowering.
  • Assess renal function: adjust use in patients with impaired kidney function.
  • Check electrolytes: watch for potassium abnormalities.
  • Evaluate for heart failure: use cautiously in decompensated states.
  • Review concomitant medications: avoid additive hypotensive agents.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartanmedoxomil/Amlodipine Stada can interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): increased risk of hyperkalaemia and renal impairment.
  • Potassium‑sparing diuretics or supplements: may precipitate hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): raise amlodipine levels, risking hypotension.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can blunt antihypertensive effect and affect renal function.
  • Diuretics (especially thiazides): may enhance hypotensive response.
  • Simvastatin or other statins metabolised by CYP3A4: increased risk of myopathy.
  • Lithium: may increase serum lithium concentrations.
  • Alcohol: additive central nervous system depression and blood‑pressure lowering.

Frequently Asked Questions

Olmesartanmedoxomil/Amlodipine Stada is a fixed‑dose oral tablet that combines an angiotensin‑II receptor blocker with a calcium‑channel blocker. It is prescribed to lower high blood pressure in adult patients, including those with isolated systolic hypertension or who are prone to edema from calcium‑channel‑blocker therapy alone.

Olmesartan medoxomil is a prodrug that is converted to olmesartan, which selectively blocks the angiotensin II type‑1 (AT1) receptor. This inhibition prevents vasoconstriction and reduces aldosterone‑mediated sodium and water retention, contributing to lower systemic vascular resistance and blood‑pressure reduction.

The dosage is individualized by the prescribing clinician based on the patient’s blood‑pressure profile, renal function and concomitant therapies. The prescriber determines the appropriate strength and titration schedule according to clinical guidelines.

Both olmesartan and amlodipine are classified as contraindicated in pregnancy because they may affect fetal development and cause hypotension. Breastfeeding is not recommended without medical advice, as drug excretion in milk is possible. Consultation with a healthcare professional is essential.

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 any necessary import documentation.

The fixed‑dose combination offers the same therapeutic agents in a single tablet, simplifying dosing regimens and improving patient adherence. Pharmacologically, the effect is equivalent to taking the individual components separately, but the combo reduces pill burden and may provide more consistent blood‑pressure control.

Store the tablets at ambient temperature, below 25 °C, in the original container. Protect them from moisture, excessive heat and direct sunlight to maintain potency throughout the shelf‑life.

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

Serious adverse events include angio‑edema, severe hypotension, acute kidney injury and hyperkalaemia. Patients should seek immediate medical attention if they experience swelling of the face or throat, dizziness leading to fainting, or a sudden decline in kidney function.

The combination is contraindicated in individuals with known hypersensitivity to olmesartan, amlodipine or any tablet excipients, as well as in patients with severe hepatic impairment, pregnancy, or those already receiving dual renin‑angiotensin system blockade.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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