GNH USA

Europe — EMA

Ivabradina Aurovitas

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

Ivabradine Hydrochloride

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What is Ivabradine Hydrochloride?

Ivabradine, the active ingredient in Ivabradina Aurovitas, is a If channel inhibitor presented as an oral tablet for oral use. It lowers heart rate and is indicated for chronic stable angina and heart failure with reduced ejection fraction in adult patients.

GNH USA supplies Ivabradina Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Ivabradine Hydrochloride used for?

Ivabradina Aurovitas acts on the cardiac If current to manage conditions where heart‑rate reduction is therapeutic.

- Chronic stable angina: decreases frequency of angina attacks by lowering myocardial oxygen demand. - Heart failure with reduced ejection fraction: improves symptoms and reduces hospitalization risk through heart‑rate control. - Ischemic heart disease: alleviates chest pain by reducing cardiac workload.

What are the side effects of Ivabradine Hydrochloride?

Adverse reactions may vary in frequency and severity.

Common Side Effects: - Visual disturbances (phosphenes): transient luminous phenomena. - Bradycardia: heart rate below 50 bpm. - Headache. - Dizziness. - Fatigue. - Nausea.

Serious or Rare Side Effects: - Symptomatic bradycardia requiring medical intervention. - Atrial fibrillation or other arrhythmias. - Severe hypotension. - Persistent visual impairment. - Hepatic dysfunction. - Allergic reactions including rash or angioedema.

What precautions apply to Ivabradine Hydrochloride?

Before initiating therapy, clinicians should evaluate patient‑specific risk factors. - Cardiac monitoring: obtain baseline heart rate and ECG. - Concomitant beta‑blockers: assess for excessive bradycardia. - Severe hepatic impairment: use with caution or avoid. - Pregnancy: safety not established; avoid unless benefit outweighs risk. - CYP3A4 inhibitors: monitor for increased exposure. - Store at below 25°C: keep in original packaging, protect from moisture and light.

What does Ivabradine Hydrochloride interact with?

Ivabradina Aurovitas may interact with several drug classes.

Major Interactions (Avoid):\n- Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise ivabradine levels. - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy. - Other bradycardic agents (beta‑blockers, digoxin, amiodarone): risk of severe bradycardia. - Concomitant ivabradine with verapamil or diltiazem: can cause marked heart‑rate reduction.

Moderate Interactions (Monitor Closely): - Calcium channel blockers (verapamil, diltiazem): may modestly increase ivabradine exposure. - Antidepressants (fluoxetine, paroxetine): potential CYP3A4 inhibition. - Antihypertensives (ACE inhibitors, ARBs): monitor blood pressure and heart rate. - Diuretics: watch for electrolyte shifts that could affect cardiac conduction.

Frequently asked questions

What conditions is Ivabradina Aurovitas used for?+
Ivabradina Aurovitas is prescribed to lower heart rate in adults with chronic stable angina and in patients with heart failure that has a 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 to lower heart rate?+
Ivabradine selectively blocks the funny (If) current in the sinoatrial node, the heart’s natural pacemaker. Inhibiting this current slows the spontaneous depolarisation of pacemaker cells, resulting in a lower heart rate without decreasing the strength of cardiac contraction or blood pressure.
What is the usual dose of Ivabradina Aurovitas?+
The dose of Ivabradina Aurovitas is determined by the prescribing clinician based on the patient’s clinical condition, heart‑rate response, and tolerance. Dosage adjustments are made according to therapeutic goals and any concomitant medications, following local prescribing guidelines.
Is Ivabradina Aurovitas safe during pregnancy or breastfeeding?+
Safety data for ivabradine in pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.
How do I order Ivabradina Aurovitas from GNH USA?+
To place an order, 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 (including any cold‑chain requirements) and necessary import documentation.
How does Ivabradina Aurovitas compare with beta‑blockers?+
Both ivabradine and beta‑blockers lower heart rate, but ivabradine does so by selectively inhibiting the If current without affecting myocardial contractility or blood pressure. Beta‑blockers act on adrenergic receptors and can reduce contractile force and blood pressure, which may be undesirable in some patients. Ivabradine is often considered when beta‑blockers are contraindicated or not tolerated.
What are the storage requirements for Ivabradina Aurovitas?+
Store Ivabradina Aurovitas at temperatures below 25 °C in its original container. Protect the tablets from moisture, direct sunlight and excessive heat to maintain stability and potency throughout the shelf‑life.
How is Ivabradina Aurovitas administered?+
Ivabradina Aurovitas is taken orally, usually with a glass of water. The tablet should be swallowed whole and not split, crushed, or chewed, unless the prescribing information specifically allows it. Dosing times are generally spaced evenly to maintain consistent heart‑rate control.
What are the most serious risks associated with Ivabradina Aurovitas?+
The most serious adverse events include symptomatic bradycardia, atrial fibrillation, severe hypotension, persistent visual disturbances, and rare cases of hepatic dysfunction or severe allergic reactions. Patients should be monitored for these events, especially when initiating therapy or adjusting doses.
Who should not use Ivabradina Aurovitas?+
Ivabradina Aurovitas should be avoided in patients with severe hepatic impairment, uncontrolled hypotension, acute decompensated heart failure, or those with a resting heart rate below 50 bpm before treatment. It is also contraindicated in individuals taking strong CYP3A4 inhibitors without appropriate dose adjustment.
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 Hydrochloride
Route
Oral Use
Manufacturer
Aurovitas Spain,s.A.U.
Origin
EU

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