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

Olmesartanmedoxomil/Amlodipine Accord

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olmesartanmedoxomil/Amlodipine Accord (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxil, the active ingredient in Olmesartan/Amlodipine Accord, is an angiotensin II receptor blocker presented as a tablet for oral use. It is combined with amlodipine, a calcium‑channel blocker, to treat hypertension in adults when monotherapy is insufficient.

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

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Olmesartan/Amlodipine Accord is a fixed‑dose combination that targets the renin‑angiotensin system and vascular smooth‑muscle calcium channels to control high blood pressure.

  • Hypertension: provides additive blood‑pressure reduction for patients not adequately controlled on a single agent.
  • Essential hypertension: achieves target systolic and diastolic pressures with once‑daily dosing.
  • Resistant hypertension (as adjunct): offers an alternative pathway when additional agents are needed.

How It Works

  • Olmesartan medoxil selectively blocks the angiotensin II type 1 (AT1) receptor, preventing vasoconstriction and aldosterone release. Amlodipine inhibits L‑type calcium channels in vascular smooth muscle, causing arterial dilation. The combined blockade reduces peripheral vascular resistance and lowers both systolic and diastolic blood pressure more effectively than either component alone.

Side Effects

Adverse reactions may occur with any antihypertensive therapy.

Common Side Effects

  • Dizziness: transient light‑headedness, especially after the first dose.
  • Headache: mild to moderate intensity, often resolves with continued use.
  • Peripheral edema: swelling of ankles or feet due to vasodilation.
  • Flushing: temporary warmth and reddening of the skin.
  • Fatigue: general tiredness without exertion.
  • Palpitations: awareness of heartbeat, usually benign.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue, or airway requiring emergency care.
  • Severe hypotension: marked drop in blood pressure leading to fainting or shock.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Myocardial infarction: rare occurrence of heart attack, especially in patients with existing coronary disease.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor for adverse events.

  • Renal impairment: assess kidney function and adjust dose if necessary.
  • Hepatic impairment: use with caution; monitor liver enzymes.
  • Pregnancy: contraindicated due to risk of fetal toxicity; avoid in women of child‑bearing potential.
  • Elderly: start at the lowest dose and titrate slowly.
  • Electrolyte imbalance: monitor serum potassium, especially when combined with diuretics.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/Amlodipine may interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • ACE inhibitors: combined use can increase risk of hyperkalemia and renal dysfunction.
  • Potassium‑sparing diuretics: may precipitate dangerous hyperkalemia.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): raise amlodipine plasma levels, increasing hypotension risk.
  • NSAIDs: can blunt antihypertensive effect and affect renal function.

Moderate Interactions (Monitor Closely)

  • Thiazide or loop diuretics: additive blood‑pressure lowering; monitor for volume depletion.
  • Other antihypertensives: may enhance hypotensive effect; adjust dose as needed.
  • Rifampin: induces CYP3A4, reducing amlodipine concentrations.
  • Grapefruit juice: can increase amlodipine exposure; advise limited consumption.

Frequently Asked Questions

Olmesartan/Amlodipine Accord is a fixed‑dose combination of an angiotensin II receptor blocker and a calcium‑channel blocker. It is prescribed to lower elevated blood pressure in adults, particularly when a single antihypertensive agent does not achieve target levels.

Olmesartan medoxil selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. This leads to relaxation of blood vessels and reduced fluid retention, contributing to lower systemic blood pressure.

The prescribed dose is determined by the treating clinician based on the patient’s blood‑pressure goals, renal function, and concomitant medications. Dosage adjustments are made individually; patients should follow the prescriber’s instructions.

The combination is contraindicated in pregnancy because angiotensin‑II receptor blockers can cause fetal harm. Safety during breastfeeding has not been established, and a healthcare professional should be consulted before use.

Enquiries are submitted via the product page on gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Olmesartan/Amlodipine offers dual‑mechanism blood‑pressure control in a single tablet, reducing pill burden compared with separate ARB and calcium‑channel blocker prescriptions. It provides more consistent BP reduction than monotherapy and is often preferred when patients need additional control without adding multiple agents.

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

The medication is taken orally, usually once daily with or without food. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed by a healthcare professional.

Serious adverse events include angioedema, severe hypotension, and hepatic dysfunction. Patients should seek immediate medical attention if they experience swelling of the face or throat, fainting, or signs of liver injury such as jaundice.

The product should be avoided in individuals with known hypersensitivity to either component, pregnant women, and patients with severe hepatic impairment. Caution is also advised for those with significant renal dysfunction or a history of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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