GNH USA

Europe — EMA

Ivabradina Mylan Pharma

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

Ivabradine Oxalate

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What is Ivabradine Oxalate?

Ivabradine, the active ingredient in Ivabradina Mylan Pharma, is a If channel inhibitor presented as a tablet for oral use. It treats chronic stable angina pectoris and heart failure with reduced ejection fraction in appropriate adult patients.

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

What is Ivabradine Oxalate used for?

Ivabradina Mylan Pharma acts on the cardiac If current to lower heart rate in conditions where rate control improves outcomes.

Chronic stable angina pectoris: reduces the frequency of angina attacks by decreasing myocardial oxygen demand. Heart failure with reduced ejection fraction (NYHA class II‑III): improves symptoms and may lower hospitalization risk. Patients unable to tolerate beta‑blockers: provides heart‑rate reduction without affecting contractility or intracardiac conduction.

What are the side effects of Ivabradine Oxalate?

Adverse reactions may be observed with ivabradine therapy.

Common Side Effects: - Visual disturbances (phosphenes or luminous phenomena) - Bradycardia (resting heart rate <50 bpm) - Headache - Dizziness or light‑headedness - Fatigue - Nausea

Serious or Rare Side Effects: - Symptomatic bradyarrhythmias requiring medical intervention - Atrial fibrillation or other supraventricular tachyarrhythmias - Severe hypotension - Persistent visual loss or retinal disturbances - Allergic skin reactions (rash, pruritus)

What precautions apply to Ivabradine Oxalate?

Before prescribing Ivabradina Mylan Pharma, clinicians should consider several safety measures.

Assess baseline heart rate: ensure resting rate ≥60 bpm before initiation. Monitor ECG: watch for bradycardia or new arrhythmias during therapy. Caution in hepatic impairment: dose adjustment may be required. Avoid in severe hypotension or sick‑sinus syndrome. Contraindicated in patients with acute decompensated heart failure. Store at below 25°C: keep in the original pack, protect from moisture.

What does Ivabradine Oxalate interact with?

Ivabradina Mylan Pharma can interact with several drug classes.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase ivabradine exposure. - Concomitant bradycardic agents (beta‑blockers, digoxin, diltiazem, verapamil): risk of excessive heart‑rate reduction. - CYP3A4 inhibitors combined with diltiazem/verapamil: may cause severe bradycardia.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (rifampin, carbamazepine, phenytoin): may reduce efficacy. - Diuretics causing electrolyte shifts: monitor for arrhythmia risk. - Antihypertensive agents: observe for additive blood‑pressure lowering effects.

Frequently asked questions

What conditions is Ivabradina Mylan Pharma used for?+
Ivabradina Mylan Pharma is prescribed to lower heart rate in adults with chronic stable angina pectoris and in patients with heart failure with reduced ejection fraction (NYHA class II‑III). By reducing the heart rate, it helps relieve angina symptoms and may improve functional capacity in heart‑failure patients.
How does ivabradine work to lower heart rate?+
Ivabradine selectively blocks the funny (If) current in the sino‑atrial node, the pacemaker of the heart. This inhibition slows the spontaneous depolarisation of pacemaker cells, leading to a reduced resting and exercise heart rate while leaving contractility and conduction pathways largely unchanged.
What is the usual dose of Ivabradina Mylan Pharma?+
The exact dose of Ivabradina Mylan Pharma is determined by the prescribing clinician based on the patient’s heart‑rate, clinical status, and tolerance. Dosage adjustments are made according to therapeutic response and any adverse effects, following the product’s prescribing information.
Is Ivabradina Mylan Pharma safe during pregnancy or breastfeeding?+
Safety data for ivabradine in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies the potential risk to the fetus, and breastfeeding mothers should consult their healthcare provider before use.
How do I order Ivabradina Mylan Pharma from GNH USA?+
To request Ivabradina Mylan Pharma, 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 necessary import documentation.
How does ivabradine compare with beta‑blockers for heart‑rate control?+
Both ivabradine and beta‑blockers lower heart rate, but ivabradine acts specifically on the If channel without affecting myocardial contractility or blood pressure, whereas beta‑blockers also reduce contractility and have broader sympathetic effects. Ivabradine is often considered when beta‑blockers are contraindicated or not tolerated.
What are the storage requirements for Ivabradina Mylan Pharma tablets?+
Ivabradina Mylan Pharma tablets should be stored at temperatures below 25 °C, in the original container, protected from moisture and direct sunlight. Maintaining these conditions helps preserve tablet potency and stability throughout its shelf life.
How is Ivabradina Mylan Pharma administered?+
The medication is taken orally, usually with or without food, as directed by the prescribing physician. Tablets should be swallowed whole with a glass of water and not crushed or chewed, to ensure proper absorption and effect.
What are the most serious risks associated with ivabradine therapy?+
The most serious risks include symptomatic bradycardia, atrial fibrillation, severe hypotension, and rare visual disturbances that may affect vision. Patients should be monitored for these events, especially during dose titration or when combined with other heart‑rate‑lowering agents.
Who should not use Ivabradina Mylan Pharma?+
Ivabradina Mylan Pharma is contraindicated in patients with acute decompensated heart failure, severe hypotension, sick‑sinus syndrome, or a resting heart rate below 60 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 Oxalate
Route
Oral Use
Manufacturer
Mylan S.P.A.
Origin
EU

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