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

Olmesartan Medoxomil /Amlodipine Sandoz

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olmesartan Medoxomil /Amlodipine Sandoz (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxil, the active ingredient in Olmesartan Medoxomil /Amlodipine Sandoz, is an angiotensin II receptor blocker (ARB) presented as a fixed‑dose combination tablet 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 Medoxil / Amlodipine Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Sandoz Gmbh

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Indications & Clinical Uses

Olmesartan Medoxil / Amlodipine is an antihypertensive agent that works on the renin‑angiotensin system and calcium‑channel pathways to lower blood pressure.

  • Hypertension: provides combined blockade of angiotensin II receptors and calcium‑channel mediated vasoconstriction to achieve better blood‑pressure control.
  • Hypertension with high cardiovascular risk: reduces systolic and diastolic pressure, contributing to lower risk of stroke and myocardial infarction.
  • Hypertension resistant to monotherapy: offers an additive effect when a single‑agent regimen does not reach target blood pressure.

How It Works

  • Olmesartan medoxil selectively blocks the binding of angiotensin II to the AT‑1 receptor, preventing vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx into vascular smooth‑muscle cells, causing arterial dilation. The combination produces additive blood‑pressure reduction by targeting two complementary pathways involved in vascular tone and fluid balance.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness or light‑headedness, especially after the first dose.
  • Flushing: transient warmth and redness.
  • Fatigue: general feeling of tiredness.
  • Nausea: occasional upset stomach.

Serious or Rare Side Effects

  • Angio‑edema: rapid swelling of face, lips, tongue or throat.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Renal impairment: worsening kidney function, especially in patients with pre‑existing disease.
  • Hyperkalemia: elevated potassium levels, potentially leading to cardiac arrhythmia.

Precautions & Warnings

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

  • Renal function: evaluate creatinine clearance and adjust if necessary.
  • Hepatic function: check liver enzymes in patients with known liver disease.
  • Electrolytes: monitor potassium levels, particularly when used with potassium‑sparing agents.
  • Pregnancy: avoid use during the second and third trimesters; discuss risks if exposure occurs.
  • Concomitant antihypertensives: watch for additive blood‑pressure lowering effects.
  • Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and direct sunlight.

Avoid Interactions

Olmesartan Medoxil / Amlodipine 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, other ARBs): increased risk of hyperkalemia, renal dysfunction.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise amlodipine plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Diuretics: additive hypotensive effect, monitor blood pressure and electrolytes.
  • NSAIDs: may blunt antihypertensive response and affect renal function.
  • Lithium: increased lithium levels, monitor for toxicity.
  • Simvastatin: amlodipine can increase simvastatin exposure; consider dose reduction.

Frequently Asked Questions

Olmesartan Medoxil/Amlodipine is a fixed‑dose oral tablet indicated for the treatment of primary hypertension, especially in patients who need additional blood‑pressure reduction beyond what a single agent can achieve. The combination targets two complementary pathways to improve overall control of systolic and diastolic pressure.

Olmesartan medoxil blocks the angiotensin II type‑1 (AT‑1) receptor, preventing vasoconstriction and aldosterone‑mediated fluid retention. Amlodipine, a dihydropyridine calcium‑channel blocker, inhibits calcium entry into vascular smooth‑muscle cells, causing arterial dilation. Together they provide additive blood‑pressure lowering effects.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s blood‑pressure goals, renal function, and concomitant therapies. The prescriber selects the appropriate strength and titrates according to clinical response.

Olmesartan medoxil is contraindicated in the second and third trimesters of pregnancy because of the risk of fetal toxicity. Amlodipine is generally avoided unless the benefit outweighs the risk. Breastfeeding mothers should consult their healthcare provider, as the drug may pass into milk.

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 required import documentation.

Olmesartan alone lowers blood pressure by blocking the renin‑angiotensin system. Adding amlodipine provides additional vasodilation through calcium‑channel blockade, often achieving greater reductions in systolic pressure and improving control in patients who are not adequately managed with monotherapy.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original packaging to protect from moisture and direct sunlight, and ensure the container is tightly closed until use.

The medication is taken orally, usually once daily, with or without food. Patients should swallow the tablet whole with a glass of water and follow the prescriber’s instructions regarding timing and any dose adjustments.

Serious adverse events include angio‑edema, severe hypotension, hepatic dysfunction, renal impairment, and hyperkalemia. Patients should be educated to seek immediate medical attention if they experience rapid swelling of the face or throat, dizziness leading to fainting, or signs of liver or kidney problems.

The combination should be avoided in patients with known hypersensitivity to either component, in pregnant women during the second and third trimesters, and in individuals with severe hepatic impairment or uncontrolled heart failure unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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