Product image of Nebicur (Nebivolol Hydrochloride) supplied by GNH India

Nebicur

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebicur (Nebivolol Hydrochloride)

Nebivolol Hydrochloride, the active ingredient in Nebicur, is a beta blocker presented as an oral tablet for oral use. It is used to treat hypertension and heart failure in adult patients.
GNH India supplies Nebicur as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bennett Pharmaceuticals Sa

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Indications & Clinical Uses

  • Nebivolol Hydrochloride is a selective β1‑adrenergic blocker indicated for conditions that involve elevated blood pressure or impaired cardiac function.
  • Hypertension: lowers systolic and diastolic pressure by reducing cardiac output and peripheral vascular resistance.
  • Heart failure: improves left‑ventricular ejection fraction and reduces symptoms in patients with reduced‑ejection‑fraction heart failure.

How It Works

  • Nebivolol Hydrochloride selectively antagonises β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility. In addition, it stimulates endothelial nitric oxide synthase, leading to nitric‑oxide‑mediated vasodilation, which further contributes to blood‑pressure reduction without significant β2‑receptor blockade.

Side Effects

Nebivolol Hydrochloride may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or general tiredness.
  • Nausea or mild gastrointestinal upset.
  • Nasal congestion or rhinorrhoea.

Serious or Rare Side Effects

  • Severe bradycardia or heart block.
  • Marked hypotension leading to syncope.
  • Bronchospasm in patients with asthma or COPD.
  • Allergic reactions such as rash, angioedema, or anaphylaxis.
  • Hepatic enzyme elevations or liver injury.
  • Worsening heart failure symptoms.

Precautions & Warnings

  • Before initiating Nebivolol Hydrochloride, clinicians should consider several safety aspects.
  • Monitor blood pressure: verify adequate control and avoid excessive hypotension.
  • Assess cardiac function: evaluate baseline heart rate and conduction abnormalities.
  • Use caution in asthma/COPD: β‑blockade may precipitate bronchospasm.
  • Review concomitant beta‑blockers: avoid additive negative‑chronotropic effects.
  • Adjust in renal/hepatic impairment: dose may need modification in severe dysfunction.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol Hydrochloride can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Other beta‑blockers: additive bradycardia and AV‑node depression.
  • Non‑dihydropyridine calcium‑channel blockers (verapamil, diltiazem): increased risk of heart block.
  • Potent CYP2D6 inhibitors (paroxetine, fluoxetine, quinidine): may raise nebivolol plasma levels.
  • Clonidine abrupt withdrawal: can cause rebound hypertension.
  • Antihypertensive agents that cause profound vasodilation (e.g., nitroglycerin): risk of severe hypotension.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance orthostatic hypotension.
  • Antidiabetic drugs: beta‑blockade can mask hypoglycaemia symptoms.
  • NSAIDs: may reduce antihypertensive efficacy.
  • Antidepressants (serotonergic agents): monitor for additive dizziness.
  • Digoxin: monitor for bradycardia when combined.

Frequently Asked Questions

Nebicur contains nebivolol hydrochloride, a selective β1‑blocker that is prescribed to lower high blood pressure (hypertension) and to improve symptoms and cardiac function in patients with heart failure with reduced ejection fraction.

Nebivolol blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility, while simultaneously stimulating nitric‑oxide release from the endothelium, causing vasodilation. This dual action reduces systemic vascular resistance and lowers blood pressure.

The specific dose of Nebicur is determined by the prescribing clinician based on the patient’s medical condition, age, renal function and response to therapy. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Safety data for nebivolol 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.

To request Nebicur, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Nebicur (nebivolol) differs from many beta‑blockers by adding nitric‑oxide‑mediated vasodilation, which can result in better blood‑pressure control and a more favourable metabolic profile compared with non‑vasodilating β‑blockers such as atenolol or metoprolol.

Nebicur should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, heat and direct sunlight to maintain its stability.

Nebicur is taken orally, usually once daily, with or without food, as directed by the prescribing physician. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse events can include severe bradycardia, symptomatic hypotension, bronchospasm in patients with reactive airway disease, and rare cases of liver injury or heart block. Patients should seek immediate medical attention if they experience fainting, severe dizziness, difficulty breathing or chest pain.

Nebicur is contraindicated in patients with known hypersensitivity to nebivolol or any excipients, those with severe bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and individuals with uncompensated heart failure or severe hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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