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

Nebivolol Eg

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Eg (Nebivolol)

Nebivolol, the active ingredient in Nebivolol Eg, 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 Eg as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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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 in patients with essential hypertension.
  • Heart failure (reduced ejection fraction): improves ventricular function and reduces hospitalization risk.
  • Left ventricular systolic dysfunction: supports cardiac output and symptom control in chronic heart failure.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors, reducing heart rate and myocardial contractility. In addition, it stimulates endothelial nitric oxide release, causing vasodilation and further decreasing peripheral vascular resistance, which together lower arterial pressure and improve cardiac efficiency.

Side Effects

Nebivolol may cause adverse reactions that vary in frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain in the head region.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: reduced energy or feeling unusually tired.
  • Bradycardia: slower than normal heart rate.
  • Nausea: upset stomach with urge to vomit.
  • Peripheral edema: swelling of ankles or lower legs.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Atrioventricular block: impaired electrical conduction in the heart.
  • Bronchospasm: narrowing of airways, particularly in asthmatic patients.
  • Allergic reaction: rash, itching, swelling, or anaphylaxis.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Hypotension: dangerously low blood pressure causing faintness.

Precautions & Warnings

Nebivolol should be used with careful clinical monitoring.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Cardiac function assessment: evaluate heart rate and ECG, especially in patients with conduction disorders.
  • Asthma or COPD caution: use only if benefits outweigh risk of bronchospasm.
  • Concomitant beta‑blocker use: avoid duplicate therapy to prevent excessive β‑blockade.
  • Renal impairment adjustment: consider dose modification in severe renal dysfunction.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Nebivolol can interact with several drug classes, requiring clinical awareness.

Major Interactions (Avoid)

  • Other beta‑blockers: additive cardiac depression.
  • Calcium channel blockers (verapamil, diltiazem): may cause severe bradycardia or AV block.
  • Anti‑arrhythmic agents (e.g., amiodarone): increase risk of conduction abnormalities.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: enhanced hypotensive effect.
  • Diuretics: potential for excessive blood pressure drop.
  • NSAIDs: may blunt antihypertensive response.
  • Antidepressants (e.g., SSRIs): possible pharmacokinetic changes.

Frequently Asked Questions

Nebivolol Eg is prescribed for adults with essential hypertension and for patients with chronic heart failure, particularly when left ventricular systolic function is reduced. It helps lower blood pressure and improve cardiac output, reducing the risk of cardiovascular events.

Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and contractility. It also enhances nitric oxide release from the endothelium, causing vasodilation. The combined effect reduces peripheral resistance and arterial pressure, providing antihypertensive benefit.

The dosage of Nebivolol Eg is individualized by the prescribing clinician based on the patient’s blood pressure, heart‑failure status, renal function, and other medications. The prescriber determines the appropriate strength and titration schedule.

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

Nebivolol is a highly selective β1‑blocker with additional nitric‑oxide‑mediated vasodilation, which may result in fewer metabolic side effects compared with non‑selective beta‑blockers. Its profile can be advantageous in patients who need both heart‑rate control and improved vascular tone.

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

Nebivolol Eg is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless otherwise directed by a healthcare professional.

Serious risks include severe bradycardia, atrioventricular block, marked hypotension, bronchospasm in patients with reactive airway disease, and rare allergic reactions. Patients should be monitored for these events, especially when initiating therapy or adjusting doses.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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