Product image of Nebivolol Unifarma (Nebivolol) supplied by GNH India

Nebivolol Unifarma

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Unifarma (Nebivolol)

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

Manufacturer / TM Owner

Unifarma

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic blocker used in cardiovascular disease management.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Heart failure: improves left‑ventricular ejection fraction and reduces symptoms of fluid overload.
  • Left ventricular systolic dysfunction: decreases mortality and hospitalisation rates in patients with reduced ejection fraction.

How It Works

  • Nebivolol selectively antagonises β1‑adrenergic receptors in cardiac tissue, reducing 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‑blockade.

Side Effects

Nebivolol may cause a range of adverse reactions.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or tiredness.
  • Nasal congestion or rhinorrhoea.
  • Bradycardia: heart rate below 60 bpm.
  • Nausea or mild gastrointestinal upset.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Marked hypotension with syncope.
  • Acute bronchospasm in patients with reactive airway disease.
  • Allergic reactions such as rash, pruritus, or angio‑edema.
  • Hepatic enzyme elevations.
  • Cardiogenic shock in severe heart failure.

Precautions & Warnings

Nebivolol should be used with careful clinical monitoring.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Heart rate assessment: observe for bradycardia, especially in patients with conduction disorders.
  • Asthma or COPD: use with caution due to potential bronchoconstriction.
  • Discontinuation: avoid abrupt cessation; taper under physician guidance to prevent rebound hypertension.
  • Renal/hepatic impairment: dose adjustment may be required based on organ function.
  • Pregnancy and lactation: safety not established; weigh benefits against risks.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with several drug classes, requiring vigilance.

Major Interactions (Avoid)

  • Co‑administration with other beta‑blockers: may cause excessive bradycardia or AV block.
  • Calcium‑channel blockers (verapamil, diltiazem): increase risk of severe bradycardia and hypotension.
  • Potent CYP2D6 inhibitors (paroxetine, fluoxetine): raise nebivolol plasma concentrations.

Moderate Interactions (Monitor Closely):\n- Non‑selective beta‑agonists (albuterol): may reduce bronchodilator efficacy.

  • Diuretics (thiazides, loop diuretics): additive hypotensive effect, monitor electrolytes.
  • ACE inhibitors or ARBs: combined effect on blood pressure may require dose titration.

Frequently Asked Questions

Nebivolol Unifarma is prescribed to lower high blood pressure (hypertension) and to improve symptoms and outcomes in patients with chronic heart failure, particularly those with reduced left‑ventricular ejection fraction.

Nebivolol blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractile force, while also stimulating nitric‑oxide release from the endothelium, which relaxes blood vessels and further reduces arterial pressure.

The appropriate dose of nebivolol is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and any co‑existing health issues. Dosage adjustments are made during follow‑up visits.

Safety data for nebivolol in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the possible risk to the fetus or infant, and the decision must be made by a qualified health professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying 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.

Nebivolol is a highly selective β1‑blocker with additional nitric‑oxide‑mediated vasodilation, which may result in fewer metabolic side effects and better tolerability compared with non‑selective beta‑blockers such as propranolol or atenolol.

Store the tablets at ambient temperature, below 25 °C, in the original blister pack or container. Keep them away from moisture, heat and direct sunlight to maintain product stability.

Nebivolol Unifarma 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 instructed otherwise.

Serious adverse events include severe bradycardia, marked hypotension, heart block, and bronchospasm in patients with reactive airway disease. Prompt medical attention is required if symptoms such as fainting, extreme fatigue, or breathing difficulty occur.

Nebivolol is contraindicated in patients with known hypersensitivity to the drug, severe bradycardia, second‑ or third‑degree atrioventricular block, uncompensated heart failure, or those taking certain interacting medications without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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