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

Nebivolol Generis

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Generis (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Generis, is a beta‑adrenergic blocker presented as an oral tablet for oral use. It is indicated for the management of high blood pressure and may be prescribed for certain cardiac conditions in adults.

GNH India supplies Nebivolol Generis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Generis Farmacêutica, S.A.

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Indications & Clinical Uses

Nebivolol is a selective β1‑blocker used primarily in the cardiovascular therapeutic area. It helps control blood pressure and supports heart function.

  • Hypertension: lowers systolic and diastolic blood pressure to target levels.
  • Heart failure with reduced ejection fraction: improves symptoms and may reduce mortality.
  • Left ventricular hypertrophy: attenuates cardiac remodeling associated with chronic pressure overload.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors, decreasing heart rate and myocardial contractility, which reduces cardiac output and peripheral resistance. In addition, it stimulates endothelial nitric‑oxide synthase, enhancing nitric‑oxide release and causing vasodilation that further contributes to blood pressure reduction.

Side Effects

Nebivolol may cause a range of adverse reactions, from mild to serious. Monitoring and patient education are essential.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or general weakness.
  • Nausea or mild gastrointestinal upset.
  • Bradycardia: heart rate slower than normal.
  • Peripheral edema: swelling of ankles or feet.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Marked hypotension leading to syncope.
  • Allergic reactions such as rash, pruritus, or angioedema.
  • Hepatic dysfunction or elevated liver enzymes.
  • Worsening of heart failure symptoms.
  • Depression or mood changes.

Precautions & Warnings

Before initiating Nebivolol, clinicians should assess several safety factors and advise patients accordingly.

  • Blood pressure monitoring: ensure target levels are achieved without excessive drop.
  • Heart rate assessment: avoid use in patients with baseline bradycardia.
  • Asthma or chronic obstructive pulmonary disease: use with caution due to potential bronchospasm.
  • Abrupt discontinuation: taper dose to prevent rebound hypertension.
  • Hepatic impairment: consider dose adjustment or close monitoring.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with several drug classes; awareness helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Other beta‑blockers: additive negative chronotropic effects.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, quinidine): increase nebivolol plasma concentrations.
  • Verapamil or diltiazem: may cause profound bradycardia or AV‑block.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may attenuate antihypertensive effect.
  • Diuretics: increase risk of orthostatic hypotension.
  • Antidiabetic agents: may mask hypoglycemia symptoms.
  • Calcium channel blockers (non‑verapamil): monitor for additive blood pressure lowering.
  • Antidepressants (e.g., SSRIs): observe for enhanced bradycardia.

Frequently Asked Questions

Nebivolol Generis contains the beta‑adrenergic blocker nebivolol and is used to treat hypertension. In some clinical settings it may also be prescribed for heart failure with reduced ejection fraction, helping to lower blood pressure and improve cardiac function.

Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and contractility, which lowers cardiac output. It also stimulates nitric‑oxide release from the endothelium, causing vasodilation and further decreasing peripheral vascular resistance.

The appropriate dose of Nebivolol Generis is determined by the prescribing clinician based on the patient’s condition, age, renal and hepatic 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 the treating physician.

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 vasodilatory properties, which may result in fewer metabolic side effects compared with non‑selective beta‑blockers. Its dual action can provide effective blood pressure control while preserving endothelial function.

Nebivolol Generis should be stored at room temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Nebivolol Generis is taken orally, usually once daily with or without food, as directed by the prescriber. Patients should swallow the tablet whole with a glass of water and follow any specific timing instructions provided by their healthcare professional.

Serious risks include severe bradycardia, heart block, marked hypotension, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience fainting, very slow heart rate, difficulty breathing, or swelling of the face or throat.

Nebivolol 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 in cardiogenic shock. Clinicians should also exercise caution in patients with uncontrolled asthma or severe hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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