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

Olmesartan Medoxomil/Amlodipine Ascend

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olmesartan Medoxomil/Amlodipine Ascend (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil/Amlodipine Ascend, 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 Olmesartan Medoxomil/Amlodipine Ascend as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

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

Manufacturer / TM Owner

Ascend Gmbh

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Indications & Clinical Uses

Olmesartan medoxomil/amlodipine is indicated for the management of hypertension, a condition characterized by elevated arterial pressure.

  • Hypertension: provides additive blood pressure reduction by combining an angiotensin II receptor blocker with a calcium‑channel blocker.
  • High cardiovascular risk patients: helps achieve target blood pressure when monotherapy is insufficient.
  • Elderly patients with hypertension: offers once‑daily oral control with a favorable tolerability profile.

How It Works

  • The combination pairs olmesartan medoxomil, an angiotensin II receptor blocker that prevents angiotensin II from binding to AT1 receptors, with amlodipine, a dihydropyridine calcium‑channel blocker that relaxes vascular smooth muscle by inhibiting calcium influx. Together they produce complementary vasodilation, lowering systemic vascular resistance and arterial pressure.

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
  • Nasal congestion

Serious or Rare Side Effects

  • Angio‑edema involving the face, lips or tongue
  • Severe hypotension
  • Hepatic enzyme elevation
  • Acute kidney injury
  • Heart block or severe bradycardia
  • Allergic skin reactions such as Stevens‑Johnson syndrome

Precautions & Warnings

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

  • Renal impairment: adjust dose or monitor renal function regularly.
  • Hepatic disease: use with caution and observe liver enzymes.
  • Electrolyte disturbances: check potassium and sodium levels.
  • Concomitant diuretics: monitor for excessive blood pressure fall.
  • Pregnancy: contraindicated in the second and third trimesters.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Olmesartan medoxomil/amlodipine may interact with several drug classes; careful review of the medication list is essential.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): risk of hyperkalaemia and renal dysfunction.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase amlodipine exposure.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and affect renal function.
  • Potassium‑sparing diuretics or supplements: monitor serum potassium.
  • Lithium: may increase lithium levels, requiring serum monitoring.
  • Simvastatin: amlodipine can raise statin concentrations, increasing myopathy risk.
  • Alcohol: may enhance hypotensive effects.

Frequently Asked Questions

Olmesartan Medoxomil/Amlodipine Ascend is a fixed‑dose combination tablet used to lower high blood pressure in adults, especially when a single antihypertensive agent does not achieve target levels. It combines an angiotensin II receptor blocker with a calcium‑channel blocker to provide complementary blood‑pressure reduction.

Olmesartan medoxomil blocks the binding of angiotensin II to AT1 receptors on blood vessels and adrenal tissue, preventing vasoconstriction and aldosterone‑mediated sodium retention. This action reduces systemic vascular resistance and helps lower blood pressure.

The prescribed dose is determined by the treating physician based on the patient’s blood‑pressure readings, age, renal function and other clinical factors. The prescriber selects the appropriate strength and dosing schedule for each individual.

The combination is contraindicated in pregnancy, particularly in the second and third trimesters, because angiotensin‑II receptor blockers can cause fetal toxicity. Limited data are available for breastfeeding; therefore, use is generally not recommended unless the benefit outweighs potential risk.

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.

The fixed‑dose combination offers the same pharmacologic actions as taking the two agents separately but simplifies the regimen to a single tablet, which can improve adherence. It also ensures a consistent dose ratio, reducing the risk of dosing errors that may occur with separate tablets.

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

The medication is taken orally, usually once daily, with or without food. Patients should follow the prescribing clinician’s instructions regarding timing and whether the tablet should be swallowed whole or can be taken with a glass of water.

Serious adverse events include angio‑edema, severe hypotension, acute kidney injury and significant liver enzyme elevations. Patients should seek immediate medical attention if they experience swelling of the face or throat, dizziness, fainting, or signs of liver dysfunction.

Individuals with known hypersensitivity to olmesartan, amlodipine or any tablet excipients, those in the second or third trimester of pregnancy, and patients with severe hepatic impairment should avoid this medication. Clinicians should also exercise caution in patients with advanced renal disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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