Product image of Olmesartan Medoxomil/Amlodipine Accord Healthcare Ireland (Olmesartan Medoxomil, Amlodipine) supplied by GNH India

Olmesartan Medoxomil/Amlodipine Accord Healthcare Ireland

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olmesartan Medoxomil/Amlodipine Accord Healthcare Ireland (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil/Amlodipine Accord Healthcare Ireland, is a angiotensin II receptor blocker presented as a combination tablet for oral use. It treats hypertension, often in combination with other antihypertensive agents, and is suitable for adults. GNH India supplies Olmesartan Medoxomil/Amlodipine Accord Healthcare Ireland as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

GNH India supplies Olmesartan Medoxomil/Amlodipine Accord Healthcare Ireland as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Accord Healthcare Ireland Limited

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Indications & Clinical Uses

Olmesartan medoxomil and amlodipine is used in the management of cardiovascular conditions that involve elevated blood pressure.

  • Hypertension: improves blood pressure control when monotherapy is insufficient.
  • Chronic kidney disease with hypertension: slows progression of renal impairment.
  • Heart failure with preserved ejection fraction: assists in afterload reduction and symptom management.
  • Post‑myocardial infarction hypertension: helps maintain target blood pressure to reduce recurrent events.
  • High‑risk cardiovascular patients: contributes to overall cardiovascular risk reduction when combined with lifestyle measures.

How It Works

  • Olmesartan medoxil binds selectively to angiotensin II type 1 (AT1) receptors, blocking the vasoconstrictive and aldosterone‑secreting effects of angiotensin II. Amlodipine, a dihydropyridine calcium‑channel blocker, inhibits calcium influx into vascular smooth‑muscle cells, causing arterial vasodilation. The combined action reduces systemic vascular resistance and lowers blood pressure more effectively than either component alone.

Side Effects

Common Side Effects

  • Peripheral edema: mild swelling of the ankles or feet.
  • Headache: transient, often resolves with continued therapy.
  • Dizziness: especially upon standing quickly.
  • Flushing: warm sensation, typically short‑lived.
  • Fatigue: general tiredness without other cause.
  • Palpitations: awareness of heartbeat, usually benign.

Serious or Rare Side Effects

  • Angio‑edema: rapid swelling of face, lips, tongue, or throat.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Acute kidney injury: sudden reduction in renal function.
  • Myocardial infarction: rare occurrence of heart attack.
  • Blood dyscrasias: abnormal blood counts such as neutropenia.

Precautions & Warnings

Before initiating therapy, evaluate patient history and concomitant medications.

  • Renal impairment: adjust dose and monitor kidney function regularly.
  • Hepatic disease: use with caution; monitor liver enzymes.
  • Electrolyte disturbances: check potassium and sodium levels.
  • Pregnancy: avoid use; drug is contraindicated in the second and third trimesters.
  • Elderly patients: start at lower dose and titrate slowly.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan medoxomil/amlodipine may interact with several drug classes.

Major Interactions (Avoid)

  • Potassium‑rich supplements or potassium‑sparing diuretics: risk of hyper‑kalemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): increase amlodipine levels.
  • NSAIDs (high dose): may blunt antihypertensive effect and affect renal function.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance hypotensive effect, requiring dose adjustment.
  • Lithium: increased lithium levels, monitor serum concentrations.
  • Antidiabetic agents: may require adjustment of glucose‑lowering therapy.

Frequently Asked Questions

Olmesartan Medoxomil/Amlodipine is a fixed‑dose combination tablet indicated for the treatment of hypertension, either when monotherapy does not achieve target blood pressure or when additional cardiovascular risk reduction is desired. It is prescribed for adults who need both an angiotensin‑II receptor blocker and a calcium‑channel blocker in a single pill.

Olmesartan medoxomil blocks the angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone release. Amlodipine inhibits calcium entry into vascular smooth‑muscle cells, causing arterial dilation. Together they lower systemic vascular resistance and reduce blood pressure.

The prescribed dose is individualized by the treating physician based on the patient’s blood pressure, response, and tolerability. The prescriber determines the appropriate strength and titration schedule; patients should follow the specific instructions provided on the prescription label.

This medication is contraindicated in pregnancy, particularly in the second and third trimesters, because angiotensin‑II receptor blockers can cause fetal harm. Limited data are available for breastfeeding; therefore, it should be used only if the potential benefit justifies the potential risk to the infant.

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 pharmacologic effects as taking the two agents separately but simplifies the regimen, potentially improving adherence. It provides consistent dosing of both components, which can be advantageous for patients who require both an ARB and a calcium‑channel blocker.

Store the tablets at temperatures below 25°C in their original packaging, protecting them from moisture and direct sunlight. Do not expose the product to excessive heat or humidity, as this may affect tablet integrity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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