Product image of Olmesartán/Amlodipino Stada (Amlodipine, Olmesartan) supplied by GNH India

Olmesartán/Amlodipino Stada

Active Ingredient:
Amlodipine, Olmesartan
Origin:
EU

Olmesartán/Amlodipino Stada (Amlodipine, Olmesartan)

Olmesartan and Amlodipine, the active ingredient in Olmesartán/Amlodipino Stada, is an angiotensin II receptor blocker / calcium channel blocker presented as a tablet for oral use. It treats hypertension in adult patients.

GNH India supplies Olmesartán/Amlodipino Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing EU‑sourced quality for global distribution. Our supply chain adheres to stringent regulatory standards, ensuring product integrity from manufacturing to delivery.

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

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

  • Essential hypertension: lowers systolic and diastolic pressure to target levels.
  • Secondary hypertension: assists in controlling blood pressure when caused by underlying disorders.
  • High cardiovascular risk patients: contributes to blood pressure management to reduce the risk of stroke and myocardial infarction.

How It Works

  • Olmesartan selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone release, while amlodipine inhibits calcium influx into vascular smooth‑muscle cells, promoting arterial vasodilation. The combined effect results in reduced peripheral resistance and lowered blood pressure.

Side Effects

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially after the first dose.
  • Peripheral edema: swelling of ankles or feet.
  • Flushing or warmth sensation.
  • Fatigue or generalized weakness.
  • Palpitations or increased heart rate.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat.
  • Severe hypotension: marked drop in blood pressure.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Allergic reactions: rash, itching, or severe skin eruptions.
  • Myocardial infarction: rare but reported in susceptible individuals.
  • Renal impairment: worsening kidney function in predisposed patients.

Precautions & Warnings

Before initiating therapy, clinicians should consider the following precautions:

  • Monitor blood pressure: adjust dosage if target levels are not achieved.
  • Assess renal function: especially in patients with chronic kidney disease.
  • Check electrolytes: potassium and sodium levels may be affected.
  • Avoid use in patients with known hypersensitivity to either component.
  • Pregnancy: only use if clearly needed after risk‑benefit assessment.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Olmesartan/Amlodipine may interact with several medicines. Review the following interactions carefully.

Major Interactions (Avoid)

  • ACE inhibitors or aliskiren: increased risk of hyperkalemia and renal dysfunction.
  • Potassium‑sparing diuretics: potential for dangerous hyperkalemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): may raise amlodipine plasma concentrations.
  • NSAIDs: can blunt antihypertensive effect and affect renal function.
  • Lithium: concurrent use may raise lithium levels and toxicity.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives: additive blood‑pressure lowering effect.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce amlodipine efficacy.
  • Diuretics: may cause electrolyte disturbances, especially potassium.
  • Grapefruit juice: can increase amlodipine exposure, requiring monitoring.

Frequently Asked Questions

Olmesartán/Amlodipino Stada is a fixed‑dose combination of olmesartan and amlodipine used to treat hypertension. The two agents work together to lower elevated blood pressure in adult patients, helping to reduce the risk of cardiovascular events associated with uncontrolled hypertension.

Olmesartan blocks angiotensin II type 1 receptors, preventing vasoconstriction and aldosterone release, while amlodipine inhibits calcium entry into vascular smooth‑muscle cells, causing arterial dilation. The dual action reduces peripheral resistance and lowers both systolic and diastolic blood pressure.

The dosage of Olmesartán/Amlodipino Stada is determined by the prescribing clinician based on the patient’s blood‑pressure profile, comorbidities, and response to therapy. The prescriber selects the appropriate strength and dosing schedule for each individual.

Olmesartan is generally contraindicated in pregnancy because it may harm the fetus, and amlodipine should only be used if the potential benefit justifies the risk. Breastfeeding mothers should consult their healthcare provider, as limited data are available on excretion 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 necessary import documentation.

Compared with single‑agent therapy, the combination of olmesartan and amlodipine offers complementary mechanisms that can achieve better blood‑pressure control with a single tablet. It may reduce the need for multiple pills and improve adherence, while providing a safety profile similar to each component used alone.

Store the tablets at room temperature, below 25 °C, in the original packaging. Protect them from moisture, excessive heat, and direct sunlight to maintain product stability throughout its shelf life.

Olmesartán/Amlodipino Stada is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless otherwise directed by a healthcare professional.

Serious adverse events include angioedema, severe hypotension, hepatic dysfunction, and rare cases of myocardial infarction. Patients should be instructed to seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, or signs of liver injury.

Patients with known hypersensitivity to olmesartan, amlodipine, or any excipients should avoid the product. It is also contraindicated in individuals with severe hepatic impairment, uncontrolled heart failure, or those who are pregnant unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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