Product image of Olmesardipin Mylan Plus (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide) supplied by GNH India

Olmesardipin Mylan Plus

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

Olmesardipin Mylan Plus (Olmesartan Medoxomil, Amlodipine, Hydrochlorothiazide)

Olmesartan medoxomil, amlodipine, hydrochlorothiazide, the active ingredient in Olmesardipin Mylan Plus, is a combination antihypertensive presented as a tablet for oral use. It treats high blood pressure in adults, often when single‑agent therapy does not provide adequate control.

GNH India supplies Olmesardipin Mylan Plus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Mylan Germany Gmbh

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Indications & Clinical Uses

Olmesardipin Mylan Plus is a combination antihypertensive that addresses several pathways involved in blood pressure regulation.

  • Hypertension: Provides additive blood pressure reduction when monotherapy is insufficient.
  • Resistant hypertension: Helps achieve target pressures in patients who have not responded to two or more antihypertensive agents.
  • Hypertensive patients with edema: The amlodipine component mitigates calcium‑channel‑mediated vasodilation while hydrochlorothiazide adds diuretic effect.

How It Works

  • The formulation combines three mechanisms: olmesartan medoxomil blocks angiotensin II type‑1 receptors, preventing vasoconstriction; amlodipine inhibits calcium influx into vascular smooth‑muscle cells, promoting arterial relaxation; and hydrochlorothiazide reduces plasma volume by inhibiting sodium‑chloride reabsorption in the distal convoluted tubule, together producing a synergistic antihypertensive effect.

Side Effects

Adverse reactions may occur with any antihypertensive combination. Monitoring for side effects is recommended.

Common Side Effects

  • Dizziness: Light‑headed sensation, especially after standing.
  • Peripheral edema: Swelling of ankles or feet.
  • Headache: Mild to moderate intensity.
  • Fatigue: General feeling of tiredness.
  • Increased urination: Due to diuretic action.
  • Flushing: Warm sensation, often transient.

Serious or Rare Side Effects

  • Angio‑edema: Swelling of face, lips, or throat requiring immediate care.
  • Severe hypotension: Marked drop in blood pressure with fainting risk.
  • Electrolyte imbalance: Abnormal potassium or sodium levels.
  • Acute kidney injury: Reduced renal function, especially in volume‑depleted patients.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient history and laboratory parameters.

  • Renal function: Assess creatinine clearance, adjust if impaired.
  • Hepatic impairment: Use caution; monitor liver enzymes.
  • Electrolytes: Check potassium and sodium levels regularly.
  • Pregnancy: Contraindicated in the second and third trimesters; avoid unless benefits outweigh risks.
  • Concomitant drugs: Review for potential interactions, especially other antihypertensives.
  • Store below 25°C: Keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesardipin Mylan Plus may interact with several medication classes. Awareness of major and moderate interactions helps optimise safety.

Major Interactions (Avoid)

  • Aliskiren (dual renin‑angiotensin blockade) – risk of hyperkalemia and renal dysfunction.
  • Potassium‑sparing diuretics or supplements – may cause dangerous hyperkalemia.
  • Lithium – increased lithium levels and toxicity.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) – may blunt antihypertensive effect and affect renal function.
  • Other antihypertensives (beta‑blockers, ACE inhibitors) – risk of additive hypotension.
  • CYP3A4 inhibitors (e.g., itraconazole) – can raise amlodipine concentrations.

Frequently Asked Questions

Olmesardipin Mylan Plus is a fixed‑dose combination of olmesartan medoxomil, amlodipine and hydrochlorothiazide indicated for the treatment of hypertension, including cases where blood pressure is not adequately controlled with single‑agent therapy or in resistant hypertension.

Olmesartan medoxomil is an angiotensin II type‑1 receptor blocker; it prevents angiotensin II from binding to its receptor on vascular smooth muscle, reducing vasoconstriction and aldosterone‑mediated sodium retention, which helps lower blood pressure.

The prescribed dose of Olmesardipin Mylan Plus is determined by the treating physician based on the patient’s blood pressure response, renal function, and overall clinical profile. Dosage adjustments are made individually and are not standardized in public literature.

Olmesartan medoxomil and hydrochlorothiazide are contraindicated in the second and third trimesters of pregnancy, and caution is advised in the first trimester. Amlodipine is generally avoided unless benefits outweigh risks. Breastfeeding mothers should consult a healthcare professional before use.

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.

Compared with other fixed‑dose combos such as lisinopril/hydrochlorothiazide or valsartan/amlodipine, Olmesardipin Mylan Plus adds a thiazide diuretic to an ARB and calcium‑channel blocker, offering three complementary mechanisms that may provide stronger blood‑pressure reduction in patients needing multiple pathways addressed.

Store tablets below 25 °C in their original container, protected from moisture and direct sunlight. Do not expose to extreme temperatures or humidity, and keep out of reach of children.

Olmesardipin Mylan Plus is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a glass of water.

Serious risks include angio‑edema, severe hypotension, electrolyte disturbances such as hyper‑ or hypokalemia, and acute kidney injury, particularly in patients with pre‑existing renal impairment or those taking interacting medications.

Patients with known hypersensitivity to any component, severe renal or hepatic impairment, pregnant women in the second or third trimester, and those taking contraindicated drugs such as aliskiren (in combination with an ARB) should avoid this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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