Product image of Icomb 10 Mg/10 Mg (Ramipril, Amlodipine Besilate) supplied by GNH India

Icomb 10 Mg/10 Mg

Active Ingredient:
Ramipril, Amlodipine Besilate
Origin:
EU

Icomb 10 Mg/10 Mg (Ramipril, Amlodipine Besilate)

Ramipril and Amlodipine besilate, the active ingredients in Icomb 10 Mg/10 Mg, are an ACE inhibitor and a calcium‑channel blocker presented as a 10 mg/10 mg oral tablet for oral use. They are indicated for the treatment of hypertension in adult patients, helping to lower elevated blood pressure.

GNH India supplies Icomb 10 Mg/10 Mg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product is sourced from the European Union market and meets stringent quality and regulatory standards, ensuring reliable access for global healthcare providers.

Manufacturer / TM Owner

Egis Pharmaceuticals Plc

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Indications & Clinical Uses

Icomb 10 Mg/10 Mg combines ramipril and amlodipine besilate to manage hypertension, an elevated blood pressure condition.

  • Essential hypertension: reduces systolic and diastolic blood pressure to target levels.
  • Isolated systolic hypertension: provides sustained control of high systolic pressure.
  • Diastolic hypertension: helps lower elevated diastolic pressure and improve overall cardiovascular risk.

How It Works

  • Ramipril inhibits the angiotensin‑converting enzyme, decreasing formation of angiotensin II and thereby reducing vasoconstriction and aldosterone‑mediated sodium retention. Amlodipine besilate blocks L‑type calcium channels in vascular smooth muscle, causing arterial vasodilation. The combined actions result in additive reduction of peripheral vascular resistance and blood pressure, offering effective control of hypertension. This dual mechanism also improves endothelial function and reduces cardiac afterload.

Side Effects

Icomb 10 Mg/10 Mg may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Cough: dry or persistent cough often reported with ACE inhibitors.
  • Dizziness: light‑headedness, especially after the first dose.
  • Peripheral edema: swelling of ankles or feet due to vasodilation.
  • Headache: mild to moderate headache.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue or throat, potentially life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing fainting.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.

Precautions & Warnings

When prescribing Icomb 10 Mg/10 Mg, clinicians should consider several precautionary measures to ensure safe use.

  • Monitor blood pressure: adjust dose if target not achieved.
  • Assess renal function: dose may need adjustment in renal impairment.
  • Check electrolytes: especially potassium levels.
  • Caution in heart failure: may exacerbate fluid retention.
  • Avoid in known hypersensitivity: discontinue if allergic reaction occurs.
  • Store at room temperature: keep in original packaging, protect from moisture.

Avoid Interactions

Icomb 10 Mg/10 Mg can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Concomitant use with other ACE inhibitors or ARBs: risk of additive renal dysfunction and hyperkalemia.
  • Aliskiren in diabetic patients: increased risk of hypotension, renal impairment.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): may raise amlodipine levels, leading to excessive vasodilation.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance hypotensive effect, monitor volume status.
  • Lithium: may increase serum lithium concentrations, monitor levels.

Frequently Asked Questions

Icomb 10 Mg/10 Mg is a fixed‑dose combination of ramipril and amlodipine besilate indicated for the treatment of hypertension in adult patients, helping to lower elevated systolic and diastolic blood pressure.

Ramipril is an ACE inhibitor that blocks the conversion of angiotensin I to angiotensin II, reducing vasoconstriction, aldosterone release and sodium retention, which together lower blood pressure.

The prescribed dose is determined by the treating physician based on the patient’s blood pressure, renal function and concomitant therapies; dosing adjustments are made according to clinical response and safety considerations.

Safety in pregnancy and lactation has not been established; the product should be used only if the potential benefit justifies the potential risk to the fetus or infant, and alternative therapies are generally preferred.

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 monotherapy, the ramipril/amlodipine fixed‑dose provides complementary mechanisms—ACE inhibition and calcium‑channel blockade—offering more consistent blood‑pressure control and potentially reducing pill burden versus separate agents.

Store the tablets at room temperature, below 25 °C, in the original blister pack or container, protected from moisture and direct sunlight to maintain stability.

The tablets are taken orally, usually once daily, with or without food, as directed by the prescribing clinician; patients should swallow the tablet whole and not split or crush it unless instructed.

Serious adverse reactions can include angioedema, severe hypotension, and renal impairment; patients should seek immediate medical attention if they experience swelling of the face, lips or throat, dizziness, or a sudden drop in blood pressure.

Individuals with known hypersensitivity to ramipril, amlodipine or any component of the formulation, as well as patients with a history of angioedema related to ACE‑inhibitor therapy, should avoid using this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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