GNH USA

Europe — EMA

Ivabradina Combix

GNH USA supplies Ivabradina Combix (Ivabradine), an If channel inhibitor for chronic stable angina and heart failure with reduced ejection fraction.

Ivabradine

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What is Ivabradine?

Ivabradine, the active ingredient in Ivabradina Combix, is an If channel inhibitor presented as an oral tablet for oral administration. It selectively reduces heart rate without affecting contractility, making it suitable for patients with chronic stable angina and heart failure with reduced ejection fraction.

GNH USA supplies Ivabradina Combix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, sourced from the European Union market and meeting EU quality standards.

What is Ivabradine used for?

Ivabradina Combix acts on the cardiac If current to manage specific cardiovascular conditions.

- Chronic stable angina: reduces the frequency of angina attacks by lowering heart rate. - Heart failure with reduced ejection fraction: improves symptoms and may lower hospitalization risk by decreasing myocardial oxygen demand. - Patients intolerant to beta‑blockers: provides heart‑rate control when beta‑blockers are contraindicated or not tolerated.

What are the side effects of Ivabradine?

Adverse reactions may occur with Ivabradina Combix and are reported in clinical use.

Common Side Effects: - Bradycardia: resting heart rate falls below the intended range. - Visual disturbances: luminous phenomena or phosphenes. - Headache. - Dizziness. - Fatigue. - Nausea.

Serious or Rare Side Effects: - Severe bradycardia requiring medical intervention. - Atrial fibrillation or other arrhythmias. - Symptomatic hypotension. - Visual loss or retinal abnormalities. - Heart block (second‑ or third‑degree). - Anaphylactic or severe allergic reactions.

What precautions apply to Ivabradine?

Before prescribing Ivabradina Combix, clinicians should consider several safety measures.

- Monitor heart rate: ensure resting heart rate remains above 50 bpm. - Avoid in severe hepatic impairment: dose adjustment may be required. - Caution in sick‑sinus syndrome or atrioventricular block: contraindicated in high‑grade block. - Review concomitant bradycardic agents: beta‑blockers or digoxin may amplify effects. - Adjust in renal impairment: use with caution in moderate to severe renal dysfunction. - Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture.

What does Ivabradine interact with?

Ivabradina Combix can interact with other medicines, influencing its safety and efficacy.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., clarithromycin, ketoconazole): may increase ivabradine plasma levels. - Other bradycardic agents (beta‑blockers, digoxin, diltiazem): risk of excessive heart‑rate reduction. - Certain antiarrhythmic drugs (e.g., amiodarone): can potentiate bradycardia.

Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): may modestly raise concentrations. - CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect. - Other anti‑anginal medications (nitrates, calcium‑channel blockers): monitor for additive hypotensive effects.

Frequently asked questions

What is Ivabradina Combix used for?+
Ivabradina Combix contains ivabradine, which is prescribed to lower heart rate in patients with chronic stable angina and in those with heart failure with reduced ejection fraction. By reducing the heart’s pacing activity, it helps relieve chest pain and improves functional capacity in heart‑failure patients.
How does ivabradine work?+
Ivabradine selectively blocks the funny (If) current in the sinoatrial node, the primary pacemaker of the heart. Inhibition of this current slows the spontaneous depolarisation of pacemaker cells, leading to a lower resting heart rate while preserving myocardial contractility and blood pressure.
What is the usual dose of Ivabradina Combix?+
The dose of Ivabradina Combix is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and tolerance. The prescriber determines the appropriate strength, frequency, and any necessary adjustments.
Is Ivabradina Combix safe during pregnancy or breastfeeding?+
Safety data for ivabradine in pregnancy and lactation are limited. It should only be used when the potential benefit justifies the potential risk to the fetus or infant, and decisions are made by the treating physician in consultation with the patient.
How do I order Ivabradina Combix from GNH USA?+
To request Ivabradina Combix, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does ivabradine compare with beta‑blockers?+
Both ivabradine and beta‑blockers lower heart rate, but ivabradine does so by directly inhibiting the If current without affecting beta‑adrenergic receptors. This means it does not influence blood pressure or contractility, making it useful when beta‑blockers are contraindicated, poorly tolerated, or insufficient alone.
How should Ivabradina Combix be stored and handled?+
Store Ivabradina Combix at ambient temperature, below 25 °C, in the original container to protect it from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.
How is Ivabradina Combix administered?+
Ivabradina Combix is taken orally, usually with a glass of water. It can be taken with or without food, but the dose should be taken at the same time each day to maintain consistent blood levels. Follow the prescribing clinician’s instructions.
What are the most serious risks associated with Ivabradina Combix?+
The most serious adverse events include severe bradycardia, atrial fibrillation or other arrhythmias, symptomatic hypotension, visual disturbances that may progress to vision loss, and high‑grade heart block. Patients should seek immediate medical attention if they experience fainting, severe dizziness, or sudden visual changes.
Who should not use Ivabradina Combix?+
Ivabradina Combix is contraindicated in patients with severe hypotension, sick‑sinus syndrome, second‑ or third‑degree atrioventricular block, acute myocardial infarction, or those taking strong CYP3A4 inhibitors that cannot be discontinued. It should also be avoided in individuals with known hypersensitivity to ivabradine.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Ivabradine
Route
Oral Use
Manufacturer
Laboratorios Combix, S.L.U.
Origin
EU

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