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

Olmesartan/Amlodipine/Hct Eg

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

Olmesartan/Amlodipine/Hct Eg (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxil, the active ingredient in Olmesartan/Amlodipine/Hct Eg, is a angiotensin II receptor blocker presented as a fixed‑dose combination tablet for oral use. It treats hypertension in adults, often when monotherapy does not achieve target blood pressure.

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

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Olmesartan/Amlodipine/Hct Eg is prescribed for hypertension and related cardiovascular risk management pathways.

  • Hypertension: helps achieve target blood pressure when single‑agent therapy is insufficient.
  • Hypertensive heart disease: reduces cardiac workload and may limit disease progression.
  • Chronic kidney disease with hypertension: assists in slowing renal function decline associated with high blood pressure.

How It Works

  • The combination product provides three complementary actions: olmesartan blocks the angiotensin II type‑1 receptor, preventing vasoconstriction and aldosterone release; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, producing arterial dilation; and hydrochlorothiazide promotes renal sodium and water excretion, decreasing plasma volume. Together they lower systemic vascular resistance and cardiac output, resulting in blood‑pressure reduction.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Peripheral edema
  • Flushing
  • Fatigue
  • Increased urination

Serious or Rare Side Effects

  • Severe hypotension
  • Electrolyte disturbances (e.g., low potassium)
  • Acute kidney injury
  • Angio‑edema
  • Liver function abnormalities
  • Blood cell count changes

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Renal function: assess baseline creatinine and eGFR, adjust if impaired.
  • Electrolytes: monitor potassium and sodium levels, especially with diuretic component.
  • Hepatic function: use caution in patients with liver disease.
  • Pregnancy: contraindicated in the second and third trimesters; avoid use.
  • Elderly patients: start at lower dose and monitor for orthostatic hypotension.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Olmesartan/Amlodipine/Hct Eg can interact with several drug classes; awareness helps prevent adverse events.

Major Interactions (Avoid)

  • Potassium‑rich supplements or potassium‑sparing diuretics: risk of hyper‑kalemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): increase amlodipine exposure.
  • Lithium: may increase lithium levels and toxicity risk.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect.
  • ACE inhibitors or other ARBs: additive blood‑pressure lowering, risk of renal dysfunction.
  • Antidiabetic agents: monitor glucose as diuretic may affect glycemic control.

Frequently Asked Questions

Olmesartan/Amlodipine/Hct Eg is a fixed‑dose combination tablet used to lower high blood pressure in adults, especially when a single antihypertensive agent does not achieve the desired blood‑pressure target.

Olmesartan blocks the angiotensin II type‑1 receptor, which prevents vasoconstriction and reduces aldosterone‑mediated sodium retention, contributing to lower systemic vascular resistance and blood pressure.

The prescribed dose is individualized by the treating clinician based on the patient’s blood‑pressure level, response, and tolerability. The prescriber determines the appropriate strength and dosing schedule.

Olmesartan/Amlodipine/Hct Eg is contraindicated in the second and third trimesters of pregnancy because of potential fetal harm, and it is not recommended while breastfeeding due to limited safety data.

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

Compared with single‑agent therapy, the Olmesartan/Amlodipine/Hct Eg combo offers three complementary mechanisms—ARB, calcium‑channel blockade, and diuresis—allowing more effective blood‑pressure control with a single tablet, potentially improving adherence versus multiple separate drugs.

Store the tablets at ambient temperature, below 25 °C, in the original container, protected from moisture and direct light to maintain stability.

The medication is taken orally, usually once daily, with or without food, as directed by the prescribing healthcare professional.

Serious risks include severe hypotension, electrolyte imbalances such as hyper‑kalemia, acute kidney injury, angio‑edema, and rare liver function abnormalities; patients should be monitored for these events.

Patients with known hypersensitivity to any component, those in the second or third trimester of pregnancy, and individuals with severe renal impairment or uncontrolled electrolyte disturbances should avoid this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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