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

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Accord

Active Ingredient:
Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide
Origin:
EU

Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Accord (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Accord, is a angiotensin II receptor blocker presented as a combination tablet for oral use. It treats hypertension, often in patients who require multiple mechanisms of blood pressure control. GNH India supplies Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

GNH India supplies Olmesartan Medoxomil/Amlodipine/Hydrochlorothiazide 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 Medoxil/Amlodipine/Hydrochlorothiazide is used in the management of hypertension, targeting several physiological pathways that regulate blood pressure.

  • Hypertension: improves blood pressure control when monotherapy is insufficient.
  • Hypertensive heart disease: reduces cardiac workload and risk of progression.
  • Chronic kidney disease with hypertension: helps slow renal function decline associated with high blood pressure.

How It Works

  • The combination product contains three agents that act synergistically: olmesartan medoxil blocks the angiotensin II type 1 receptor, preventing vasoconstriction; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, producing arterial dilation; and hydrochlorothiazide increases urinary sodium and water excretion, lowering plasma volume. Together they lower systemic vascular resistance and cardiac output, resulting in reduced arterial pressure.

Side Effects

Adverse reactions may vary depending on the individual component and patient characteristics.

Common Side Effects

  • Dizziness or light‑headed headache.
  • Peripheral edema, especially related to amlodipine.
  • Cough or mild upper‑respiratory irritation.
  • Increased urination or electrolyte changes.
  • Fatigue or general weakness.
  • Mild gastrointestinal discomfort.

Serious or Rare Side Effects

  • Severe hypotension or syncope.
  • Acute kidney injury or significant rise in serum creatinine.
  • Hyperkalemia or severe electrolyte imbalance.
  • Angio‑edema involving the face, lips or airway.
  • Hepatotoxicity presenting as jaundice or abnormal liver enzymes.
  • Blood dyscrasias such as agranulocytosis or thrombocytopenia.

Precautions & Warnings

When prescribing this combination, clinicians should consider patient history, comorbidities, and concurrent therapies.

  • Renal impairment: adjust monitoring and avoid excessive diuretic use.
  • Hepatic dysfunction: use with caution; monitor liver enzymes.
  • Electrolyte disturbances: check serum potassium and sodium regularly.
  • Pregnancy: contraindicated in the second and third trimesters; avoid use.
  • Elderly patients: start at lower doses and monitor for orthostatic hypotension.
  • Store below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide may interact with several drug classes.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): risk of renal failure and hyperkalaemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): increase amlodipine levels.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive effect and impair renal function.
  • Lithium: increased risk of lithium toxicity.
  • Antidiabetic agents: may enhance hypoglycaemic effect.
  • Antacids containing aluminium or magnesium: may affect absorption of olmesartan.
  • Alcohol: additive vasodilatory effect leading to dizziness.

Frequently Asked Questions

Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide Accord is a fixed‑dose combination indicated for the treatment of hypertension, especially when blood pressure is not adequately controlled with a single‑agent therapy. It targets multiple mechanisms that regulate vascular tone and fluid balance to achieve better blood‑pressure control.

Olmesartan medoxil blocks the angiotensin II type‑1 receptor, preventing the hormone from causing vasoconstriction and aldosterone release. This action reduces systemic vascular resistance and fluid retention, contributing to lower arterial pressure when combined with amlodipine‑induced vasodilation and hydrochlorothiazide‑induced diuresis.

The specific dose of Olmesartan Medoxil/Amlodipine/Hydrochlorothiazide Accord is determined by the prescribing clinician based on the patient’s blood‑pressure readings, comorbid conditions, and response to therapy. Dosage adjustments are made individually and are not standardized in public literature.

Olmesartan medoxil is contraindicated in the second and third trimesters of pregnancy because of the risk of fetal toxicity. Use during breastfeeding is not recommended unless the benefit outweighs the potential risk, and the decision should be made by a healthcare professional.

To place an 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.

Compared with single‑agent therapy, this three‑component tablet offers broader blood‑pressure control by simultaneously blocking the renin‑angiotensin system, providing calcium‑channel mediated vasodilation, and promoting diuresis. It can reduce pill burden versus taking each agent separately, but clinicians must consider the combined side‑effect profile.

Store the tablets at or below 25 °C in a dry place, protected from moisture and light. Keep them in the original container with the lid tightly closed until use.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Swallow the tablet whole with a glass of water and do not split or crush it unless specifically instructed.

Serious adverse events can include severe hypotension, acute kidney injury, hyperkalaemia, angio‑edema, and rare blood‑cell disorders. Patients should be monitored for signs such as dizziness, rapid weight loss, swelling of the face or throat, and abnormal laboratory values.

Patients with known hypersensitivity to any component, those in the second or third trimester of pregnancy, individuals with severe renal or hepatic impairment, and patients taking other potent renin‑angiotensin system blockers should avoid this combination unless a physician determines it is safe.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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