GNH USA

Europe — EMA

Ivabradina Tarbis

GNH USA supplies Ivabradina Tarbis (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 Tarbis, is a If channel inhibitor presented as an oral tablet for oral use. It reduces heart rate and is used to manage chronic stable angina and heart failure with reduced ejection fraction in adult patients.

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

What is Ivabradine Hydrochloride used for?

Ivabradine acts on the cardiac If current to lower heart rate, benefiting conditions where heart‑rate control improves outcomes.

- Chronic stable angina: decreases frequency of angina episodes by lowering myocardial oxygen demand. - Heart failure with reduced ejection fraction: improves symptoms and reduces hospitalisations by maintaining target heart rate. - Inadequate heart‑rate control despite optimal therapy: provides additional rate reduction when beta‑blockers are insufficient or not tolerated.

What are the side effects of Ivabradine Hydrochloride?

Ivabradine may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects: - Visual disturbances (phosphenes): transient luminous phenomena. - Bradycardia: heart rate slower than intended. - Headache: mild to moderate intensity. - Dizziness or vertigo. - Fatigue or weakness. - Blurred vision.

Serious or Rare Side Effects: - Symptomatic bradycardia requiring medical attention. - Atrial fibrillation or other arrhythmias. - Severe hypotension. - Symptomatic heart block. - Acute coronary syndrome (rare). - Allergic skin reactions.

What precautions apply to Ivabradine Hydrochloride?

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

- Heart‑rate monitoring: ensure resting rate remains above 50 bpm. - Hepatic impairment: use with caution in moderate to severe liver disease. - Sick sinus syndrome or AV block: contraindicated unless a pacemaker is present. - Concomitant bradycardic agents: avoid or adjust dose when combined with beta‑blockers or calcium‑channel blockers. - Pregnancy and lactation: safety not established; use only if benefit outweighs risk. - Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

What does Ivabradine Hydrochloride interact with?

Ivabradine can interact with several drug classes, influencing its efficacy or safety.

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

Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): may require dose adjustment. - Diuretics and antihypertensives: monitor blood pressure and electrolytes. - St. John’s wort (CYP3A4 inducer): may reduce ivabradine effectiveness.

Frequently asked questions

What conditions is Ivabradina Tarbis used for?+
Ivabradina Tarbis contains ivabradine, which is prescribed to lower heart rate in adults with chronic stable angina and in patients with heart failure with reduced ejection fraction. By reducing the heart rate, it helps relieve angina symptoms 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 pacemaker of the heart. Inhibition of this current slows the spontaneous depolarisation of pacemaker cells, leading to a reduction in heart rate without affecting myocardial contractility or blood pressure.
What is the usual dose of Ivabradina Tarbis?+
The dose of ivabradine 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 Tarbis safe during pregnancy or breastfeeding?+
Safety data for ivabradine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.
How do I order Ivabradina Tarbis from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com with 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 necessary import documentation.
How does ivabradine compare with beta‑blockers?+
Both ivabradine and beta‑blockers lower heart rate, but ivabradine does so by selectively inhibiting the If current without affecting contractility or blood pressure. Beta‑blockers act on adrenergic receptors and also reduce contractile force, which may be advantageous or limiting depending on the patient’s comorbidities.
What are the recommended storage conditions for Ivabradina Tarbis?+
Ivabradina Tarbis should be stored at room temperature, below 25 °C, in the original packaging to protect it from moisture and light. Keep the tablets away from excessive heat and humidity to maintain stability.
How is Ivabradina Tarbis administered?+
The medication is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with a glass of water and not crushed or chewed, unless otherwise instructed by a healthcare professional.
What are the most serious risks associated with ivabradine?+
Serious risks include symptomatic bradycardia, atrial fibrillation, severe hypotension, and heart block. Patients should be monitored for signs of excessive slowing of the heart rate, palpitations, dizziness, or fainting, and medical attention should be sought promptly if these occur.
Who should not use Ivabradina Tarbis?+
Ivabradina Tarbis is contraindicated in patients with severe hepatic impairment, sick sinus syndrome, second‑ or third‑degree atrioventricular block without a pacemaker, and in those who are already on strong CYP3A4 inhibitors. It should also be avoided in patients 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 Hydrochloride
Route
Oral Use
Manufacturer
Tarbis Farma, S.L.
Origin
EU

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