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

Olmesartan/Amlodipine Eg

Active Ingredient:
Amlodipine, Olmesartan
Origin:
EU

Olmesartan/Amlodipine Eg (Amlodipine, Olmesartan)

Olmesartan and amlodipine, the active ingredients in Olmesartan/Amlodipine EG, are a calcium‑channel blocker and an angiotensin II receptor blocker presented as a fixed‑dose oral tablet for once‑daily use. They are indicated for the treatment of hypertension in adult patients, helping to lower systolic and diastolic blood pressure and reduce cardiovascular risk.

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

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Olmesartan/Amlodipine EG is indicated for the management of hypertension, acting on the renin‑angiotensin system and vascular smooth‑muscle tone.

  • Hypertension: provides sustained blood‑pressure reduction and improves cardiovascular outcomes.
  • Hypertension in patients requiring combination therapy: offers convenient dual‑mechanism control when monotherapy is insufficient.
  • Hypertension with comorbidities such as diabetes: assists in achieving target blood pressure while minimizing metabolic impact.

How It Works

  • Amlodipine selectively inhibits L‑type calcium channels in vascular smooth muscle, producing arterial vasodilation and reduced peripheral resistance. Olmesartan blocks the angiotensin II type 1 (AT1) receptor, preventing vasoconstriction, aldosterone secretion, and sympathetic activation. The combined actions result in additive blood‑pressure lowering through decreased vascular tone and inhibition of the renin‑angiotensin system.

Side Effects

Common Side Effects

  • Headache: mild to moderate pain often occurring early in therapy.
  • Peripheral edema: swelling of the ankles or lower legs.
  • Flushing: transient warmth and redness of the skin.
  • Dizziness: sensation of light‑headedness, especially when standing.
  • Fatigue: general feeling of tiredness.
  • Palpitations: awareness of heartbeats.

Serious or Rare Side Effects

  • Hypotension: marked drop in blood pressure causing faintness.
  • Angioedema: swelling of face, lips, tongue, or throat requiring urgent care.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Severe allergic reaction: rash, itching, or anaphylaxis.
  • Myocardial infarction: rare occurrence of heart attack.
  • Renal impairment: worsening kidney function in susceptible individuals.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Blood pressure monitoring: ensure adequate control and avoid excessive hypotension.
  • Renal function assessment: adjust dosing in patients with impaired kidney function.
  • Hepatic impairment: use with caution in moderate to severe liver disease.
  • Pregnancy: avoid use; teratogenic risk associated with angiotensin receptor blockers.
  • Elderly patients: start at lower dose and monitor for orthostatic effects.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Olmesartan/Amlodipine EG may interact with several medicines.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., clarithromycin): increase amlodipine exposure.
  • Concurrent antihypertensives: risk of additive hypotension.
  • Potassium‑sparing diuretics or supplements with ARBs: may cause hyperkalaemia.
  • High‑dose simvastatin: increased risk of myopathy when combined with amlodipine.
  • Lithium: elevated lithium levels and toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect.
  • Diuretics: can potentiate electrolyte disturbances.
  • CYP3A4 inducers (e.g., rifampin): reduce amlodipine concentrations.
  • Grapefruit juice: may raise amlodipine plasma levels.
  • Antacids containing aluminum or magnesium: may affect absorption of olmesartan.

Frequently Asked Questions

Olmesartan/Amlodipine EG is a fixed‑dose oral tablet used to treat hypertension. By combining a calcium‑channel blocker with an angiotensin II receptor blocker, it helps lower blood pressure in adult patients who need more than one medication to achieve target levels.

The amlodipine component blocks L‑type calcium channels in vascular smooth muscle, causing vasodilation. Olmesartan blocks the AT1 receptor for angiotensin II, preventing vasoconstriction and aldosterone release. Together they reduce peripheral resistance and lower blood pressure through complementary mechanisms.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s blood‑pressure goals, renal function, and other medications. The product is supplied as a once‑daily tablet, but the exact strength is individualized by the healthcare professional.

Olmesartan/Amlodipine EG is not recommended for use in pregnancy because the angiotensin receptor blocker component can cause fetal toxicity. Safety during breastfeeding has not been established, and the product should be avoided unless the benefits clearly outweigh the risks.

To place an order, submit an enquiry on the product page at gnhindia.com, indicating 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 monotherapy, the combination offers additive blood‑pressure reduction, simplifying regimens and improving adherence. It provides a broader mechanism of action than either a calcium‑channel blocker or an ARB alone, and may be more effective than increasing the dose of a single agent.

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

Olmesartan/Amlodipine EG is taken orally, usually once daily, with or without food. Swallow the tablet whole with a glass of water. Follow the prescribing clinician’s instructions regarding timing and any dose adjustments.

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

The product should be avoided in patients with known hypersensitivity to either component, pregnant women, those with severe hepatic impairment, and individuals with a history of angioedema related to ARB therapy. Clinicians should also assess renal function before initiating treatment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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