Product image of Halibrell (Ranolazine) supplied by GNH India

Halibrell

Active Ingredient:
Ranolazine
Origin:
EU

Halibrell (Ranolazine)

Halibrell is a prescription medication that contains the active ingredient ranolazine. It is supplied as an oral dosage form, with the specific strength not disclosed in the available data. Classified as an anti‑anginal agent, Halibrell belongs to the therapeutic class for chronic stable angina and is marketed in the European Union. The drug works by modulating cardiac sodium currents and improving myocardial relaxation during episodes of chest pain.

Manufacturer / TM Owner

Sandoz Pharmaceuticals D.D.

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Indications & Clinical Uses

Halibrell (ranolazine) is indicated for the management of chronic stable angina in patients for whom other anti‑anginal therapies are insufficient or not tolerated.

  • Reduces the frequency of angina attacks.
  • Improves exercise tolerance in patients with stable angina.
  • Can be used as adjunct therapy with beta‑blockers, calcium‑channel blockers, or nitrates.
  • May be considered when conventional therapy does not adequately control symptoms.
  • Provides an alternative mechanism of action targeting myocardial sodium overload.
  • May be prescribed for patients with documented coronary artery disease experiencing angina.

Side Effects

The safety profile of Halibrell reflects the typical adverse events reported for ranolazine, ranging from mild to potentially serious.

Common

  • Dizziness or light‑headedness, especially when standing quickly.
  • Nausea, vomiting, or abdominal discomfort that may affect appetite.
  • Constipation or diarrhea, sometimes accompanied by gas or bloating.
  • Headache or fatigue, which can be intermittent during treatment.

Serious

  • Prolongation of the QT interval on electrocardiogram, increasing risk of cardiac rhythm disturbances.
  • Severe arrhythmias such as ventricular tachycardia or torsades de pointes.
  • Marked hypotension or syncope, particularly in patients with pre‑existing low blood pressure.

Precautions & Warnings

Before initiating Halibrell, clinicians should evaluate several patient‑specific factors to minimize risks and ensure appropriate use.

  • Assess baseline electrocardiogram for QT interval lengthening.
  • Review history of liver disease, as ranolazine is metabolized hepatically.
  • Use caution in patients with severe renal impairment; dose adjustment may be required.
  • Avoid use in individuals with known hypersensitivity to ranolazine or its excipients.
  • Monitor for signs of hypotension, especially when combined with other anti‑anginal agents.
  • Consider pregnancy and lactation status; safety data are limited.
  • Evaluate concomitant use of drugs that affect CYP3A4 metabolism.

Avoid Interactions

Halibrell can interact with other medications through shared metabolic pathways or additive cardiac effects.

Avoid

  • Strong CYP3A4 inhibitors such as ketoconazole, clarithromycin, or ritonavir, which can raise ranolazine levels.
  • Other drugs known to prolong the QT interval (e.g., certain anti‑psychotics, macrolide antibiotics).

Use with caution

  • Moderate CYP3A4 inhibitors (e.g., diltiazem, verapamil) may require dose adjustment.
  • CYP2D6 substrates (e.g., metoprolol, tricyclic antidepressants) as ranolazine can increase their plasma concentrations.
  • Concurrent use of other anti‑anginal agents (beta‑blockers, nitrates) may enhance hypotensive effects.
  • Diuretics that affect electrolyte balance, potentially influencing cardiac repolarization.

Frequently Asked Questions

Halibrell inhibits the late inward sodium current in cardiac myocytes, reducing intracellular sodium and calcium overload, which improves myocardial relaxation and coronary perfusion.

Yes, Halibrell is marketed in the EU as a prescription medication for chronic stable angina.

Halibrell may be used together with beta‑blockers, but clinicians should monitor blood pressure and heart rate for additive hypotensive effects.

Common side effects include dizziness, nausea, abdominal discomfort, constipation or diarrhea, headache, and fatigue.

Ranolazine can prolong the QT interval; patients with existing QT prolongation or those taking other QT‑prolonging drugs should be monitored closely.

Because ranolazine is metabolized in the liver, baseline liver function tests are recommended before initiating therapy.

Patients with severe renal impairment may require dose adjustment, and renal function should be evaluated prior to prescribing.

Safety data for ranolazine during pregnancy and lactation are limited; it should be used only if the potential benefit justifies the potential risk.

Strong CYP3A4 inhibitors such as ketoconazole, clarithromycin, and ritonavir, as well as other QT‑prolonging agents, should be avoided.

Store the medication at room temperature, away from excess heat and moisture, and keep it out of reach of children.

Baseline and periodic ECGs are advisable to monitor the QT interval, especially in patients with cardiac risk factors.

Ranolazine can be taken with or without food; however, taking it with meals may reduce gastrointestinal discomfort for some patients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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