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

Olmesartan /Amlodipine Mylan

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olmesartan /Amlodipine Mylan (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxil, the active ingredient in Olmesartan /Amlodipine Mylan, is a angiotensin II receptor blocker presented as a fixed‑dose combination for oral use. It treats hypertension, often in patients who require additional blood pressure control beyond what a single agent can provide.

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

Manufacturer / TM Owner

Viatris Limited

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Indications & Clinical Uses

Olmesartan /Amlodipine Mylan is used in cardiovascular therapy to manage high blood pressure through combined angiotensin receptor blockade and calcium‑channel antagonism.

  • Hypertension: Improves blood pressure control when monotherapy is insufficient.
  • Hypertensive patients with concomitant edema: Reduces peripheral edema associated with calcium‑channel blocker therapy.
  • High‑risk cardiovascular patients: Lowers the risk of stroke and myocardial infarction by achieving target blood pressure levels.

How It Works

  • Olmesartan medoxil selectively blocks the AT1 subtype of angiotensin II receptors, preventing vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation. The combination produces additive blood‑pressure‑lowering effects by reducing peripheral resistance and volume overload.

Side Effects

Adverse reactions may occur with any antihypertensive regimen and should be monitored during therapy.

Common Side Effects

  • Dizziness or light‑headedness
  • Peripheral edema
  • Headache
  • Flushing
  • Fatigue
  • Palpitations

Serious or Rare Side Effects

  • Angio‑edema
  • Severe hypotension
  • Hepatic enzyme elevation
  • Acute kidney injury
  • Myocardial infarction in patients with severe aortic stenosis
  • Hyperkalemia

Precautions & Warnings

Before initiating therapy, clinicians should assess patient history and monitor relevant parameters.

  • Renal function: Evaluate baseline creatinine and adjust if impairment is present.
  • Hepatic function: Use caution in patients with liver disease.
  • Electrolytes: Monitor potassium levels, especially if combined with potassium‑sparing diuretics.
  • Pregnancy: Contraindicated in the second and third trimesters; avoid use.
  • Elderly: Start at lower dose and titrate slowly.
  • Store at below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Olmesartan /Amlodipine Mylan may interact with several drug classes; careful review of a patient’s medication list is essential.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, aliskiren) – increased risk of renal dysfunction and hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole) – may raise amlodipine levels.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) – can blunt antihypertensive effect and affect renal function.
  • Diuretics – may enhance hypotensive response.
  • Lithium – increased risk of lithium toxicity.
  • Simvastatin – amlodipine may increase statin concentration, raising myopathy risk.

Frequently Asked Questions

Olmesartan /Amlodipine Mylan is a fixed‑dose oral tablet that combines an angiotensin II receptor blocker with a calcium‑channel blocker. It is prescribed to lower high blood pressure in adults, especially when a single‑agent regimen does not achieve target blood pressure levels.

Olmesartan medoxil blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Amlodipine relaxes arterial smooth muscle by inhibiting calcium entry, producing vasodilation. Together they provide complementary blood‑pressure reduction.

The specific dose is determined by the prescribing clinician based on the patient’s blood‑pressure readings, comorbidities, and response to therapy. Dosage forms are available in several strength combinations, and the prescriber selects the appropriate one.

Use of this product is contraindicated in the second and third trimesters of pregnancy because of potential fetal toxicity. Limited data exist for breastfeeding; therefore, it should be used only if the potential benefit justifies the possible risk to the infant.

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 any necessary import documentation.

Compared with monotherapy, the fixed‑dose combo offers additive blood‑pressure reduction, potentially improving adherence by reducing pill burden. It may be preferred over separate tablets of an ARB and a calcium‑channel blocker when both mechanisms are needed, but clinicians consider individual patient factors and cost.

Store the tablets below 25°C in their original container, protecting them from moisture and light. Do not expose the product to excessive heat or humidity, and keep it out of reach of children.

The medication is taken orally, usually once daily, with or without food. Patients should follow the prescribing information and avoid crushing or splitting tablets unless specifically instructed by a healthcare professional.

Serious adverse events include angio‑edema, severe hypotension, acute kidney injury, and hyper‑kalemia. Patients should seek immediate medical attention if they experience swelling of the face, lips or throat, faintness, or a sudden decline in kidney function.

Individuals with known hypersensitivity to olmesartan, amlodipine or any excipients in the tablet should avoid this product. It is also contraindicated in pregnant women during the second and third trimesters and in patients with severe aortic stenosis where rapid blood‑pressure reduction could be hazardous.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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