GNH USA

Europe — EMA

Ivabradina Tarbis Farma

GNH USA supplies Ivabradina Tarbis Farma (Ivabradine), a If channel inhibitor for chronic heart failure and stable angina pectoris. Request pricing supply.

Ivabradine

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What is Ivabradine?

Ivabradine, the active ingredient in Ivabradina Tarbis Farma, is a If channel inhibitor presented as an oral formulation for oral use. It reduces heart rate by selectively inhibiting the funny current in the sino‑atrial node and is indicated for chronic heart failure and stable angina pectoris in adult patients.

GNH USA supplies Ivabradina Tarbis Farma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory documentation for global distribution.

What is Ivabradine used for?

Ivabradine is used to manage conditions related to cardiac workload and heart rate. - Chronic heart failure with reduced ejection fraction: helps achieve target heart rate and may reduce hospitalization when added to guideline‑directed therapy. - Stable angina pectoris: relieves chest pain by lowering heart rate and myocardial oxygen demand. - Inadequate heart‑rate control despite beta‑blocker therapy: provides additional rate reduction without affecting contractility.

What are the side effects of Ivabradine?

Ivabradine may be associated with several adverse reactions, which are categorized by frequency and severity.

Common Side Effects: - Visual disturbances (phosphenes): transient luminous phenomena. - Bradycardia: heart rate below prescribed range. - Headache: mild to moderate intensity. - Dizziness: may occur on standing.

Serious or Rare Side Effects: - Atrial fibrillation: new onset arrhythmia. - Severe bradycardia requiring medical intervention. - Allergic reactions: rash, angioedema, or anaphylaxis.

What precautions apply to Ivabradine?

When prescribing ivabradine, clinicians should consider several precautionary measures to ensure safe use. - Cardiac monitoring: assess heart rate and rhythm before and during therapy. - Concomitant beta‑blockers: avoid excessive bradycardia when combined. - Severe hepatic impairment: use with caution or avoid. - Pregnancy and lactation: safety not established; weigh benefits against risks. - Visual disturbances: discontinue if persistent luminous phenomena occur. - Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture.

What does Ivabradine interact with?

Ivabradine can interact with other medicines, influencing its plasma levels or cardiac effects.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase ivabradine exposure, risk of bradycardia. - Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): reduce efficacy, may require dose adjustment. - Concomitant ivabradine with other heart‑rate lowering agents (beta‑blockers, digoxin) at high doses: risk of severe bradycardia.

Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., diltiazem, verapamil): may modestly raise ivabradine levels. - Antihypertensives: additive effect on blood pressure. - QT‑prolonging drugs: monitor cardiac rhythm.

Frequently asked questions

What is Ivabradina Tarbis Farma used for?+
Ivabradina Tarbis Farma contains ivabradine, which is prescribed to lower heart rate in adults with chronic heart failure with reduced ejection fraction and in patients who experience stable angina pectoris. By reducing the heart rate, it helps lessen symptoms and may decrease the risk of hospitalization in heart‑failure patients.
How does ivabradine work?+
Ivabradine selectively blocks the funny (If) current in the sino‑atrial node by binding to HCN channels. This inhibition slows the spontaneous depolarisation of pacemaker cells, leading to a lower heart rate while preserving myocardial contractility and blood pressure.
What is the usual dose of Ivabradina Tarbis Farma?+
The dose of ivabradine is individualized by the prescribing clinician based on the patient’s heart‑rate, clinical condition, and concomitant therapies. The prescriber determines the appropriate strength, frequency, and any necessary titration, following local labeling and guideline recommendations.
Is Ivabradina Tarbis Farma safe in pregnancy or breastfeeding?+
Safety data for ivabradine during 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. Clinicians should discuss individual risk factors with the patient and consider alternative therapies when possible.
How do I order Ivabradina Tarbis Farma 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 the necessary import documentation.
How does ivabradine compare with the main alternative drug class?+
The primary alternative for heart‑rate reduction in heart failure and angina is the beta‑blocker class. Unlike beta‑blockers, ivabradine lowers heart rate without affecting contractility or blood pressure, making it useful when beta‑blockers are contraindicated, not tolerated, or insufficient to achieve target heart rates.
How should Ivabradina Tarbis Farma be stored and handled?+
Store the product at ambient temperature, preferably below 25 °C. Keep it in the original container, protect it from moisture and direct sunlight, and ensure the packaging remains sealed until use. Do not store in a refrigerator or freezer.
How is Ivabradina Tarbis Farma given or administered?+
Ivabradina Tarbis Farma is taken orally, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed. Dosing times are typically spaced evenly (e.g., twice daily) as directed by the prescriber, and the medication should be taken with or without food according to label instructions.
What are the most serious risks to watch for while taking ivabradine?+
The most serious adverse events include symptomatic bradycardia, atrial fibrillation, and severe allergic reactions such as rash, angioedema, or anaphylaxis. Patients should be instructed to report any new or worsening chest discomfort, fainting, palpitations, or visual disturbances promptly.
Who should not use Ivabradina Tarbis Farma?+
Ivabradine is contraindicated in patients with severe hepatic impairment, acute decompensated heart failure, sick sinus syndrome, or a resting heart rate below 50 bpm. It should also be avoided in individuals with known hypersensitivity to ivabradine or any of the tablet’s excipients.
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
Tarbis Farma, S.L.
Origin
EU

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