Product image of Nebilet (Nebivolol) supplied by GNH India

Nebilet

Active Ingredient:
Nebivolol
Origin:
EU

Nebilet (Nebivolol)

Nebivolol, the active ingredient in Nebilet, is a beta‑adrenergic blocking agent presented as an oral dosage form for oral administration. It selectively antagonizes β1‑adrenergic receptors, reducing heart rate and myocardial contractility while enhancing nitric‑oxide‑mediated vasodilation, thereby lowering elevated blood pressure in adult patients diagnosed with hypertension.

GNH India supplies Nebilet as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to quality‑assured medicines across global markets.

Manufacturer / TM Owner

Berlin-Chemie Ag

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Indications & Clinical Uses

Nebilet (nebivolol) is used to treat conditions within the cardiovascular disease pathway, primarily hypertension.

  • Hypertension: lowers blood pressure and reduces cardiovascular risk in adult patients.
  • Heart failure: improves left‑ventricular function and alleviates symptoms in patients with chronic heart failure.

How It Works

  • Nebivolol acts as a selective β1‑adrenergic receptor antagonist, decreasing heart rate and myocardial contractility. In addition, it stimulates endothelial nitric‑oxide synthase, increasing nitric‑oxide release which causes vasodilation. The combined effect reduces systemic vascular resistance and arterial pressure, providing antihypertensive activity.

Side Effects

Nebivolol may cause a range of adverse reactions, some of which are more frequently observed than others.

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: unusual tiredness or lack of energy.
  • Bradycardia: slower than normal heart rate.
  • Nausea: feeling of stomach upset.
  • Peripheral edema: mild swelling of the ankles or feet.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Hypotension: dangerously low blood pressure.
  • Heart block: impairment of electrical conduction in the heart.
  • Bronchospasm: narrowing of airways, especially in asthmatic patients.
  • Allergic reactions: rash, itching, or swelling of the face and throat.
  • Liver enzyme elevation: abnormal liver function tests.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Monitor blood pressure: ensure adequate control and avoid excessive lowering.
  • Assess heart rate: watch for bradycardia, especially in patients with conduction disorders.
  • Use caution in asthma or chronic obstructive pulmonary disease: β‑blockade may exacerbate bronchospasm.
  • Avoid abrupt discontinuation: taper dose to prevent rebound hypertension.
  • Adjust dose in renal or hepatic impairment: consider reduced dosing in severe dysfunction.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with several drug classes, influencing its efficacy and safety.

Major Interactions (Avoid)

  • Combined with other β‑blockers: may cause excessive bradycardia or hypotension.
  • Co‑administration with non‑dihydropyridine calcium‑channel blockers (e.g., verapamil, diltiazem): increases risk of heart block.
  • Potent CYP2D6 inhibitors (e.g., paroxetine, quinidine): raise nebivolol plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance antihypertensive effect, requiring blood pressure monitoring.
  • ACE inhibitors or ARBs: additive blood pressure lowering, watch for hypotension.
  • Anti‑arrhythmic agents (e.g., amiodarone): may affect cardiac conduction.

Frequently Asked Questions

Nebilet contains nebivolol, a beta‑blocker indicated for the treatment of hypertension in adult patients. It helps lower elevated blood pressure and may also be used in certain cases of chronic heart failure to improve cardiac function.

Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and myocardial contractility. It also stimulates endothelial nitric‑oxide synthase, increasing nitric‑oxide release that causes vasodilation, together resulting in lowered systemic blood pressure.

The dose of Nebilet is individualized by the prescribing clinician based on the patient’s blood pressure, age, renal and hepatic function, and response to therapy. The prescriber determines the appropriate starting dose and any subsequent titration.

Safety of nebivolol in pregnancy and lactation has not been fully established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified health professional.

To order Nebilet, 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.

Nebilet (nebivolol) differs from traditional β‑blockers by also enhancing nitric‑oxide‑mediated vasodilation, which may improve tolerability and metabolic profile. Compared with ACE inhibitors or calcium‑channel blockers, it primarily reduces heart rate and contractility, offering an alternative mechanism for patients who need a β‑blocker.

Nebilet should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date printed on the label.

Nebilet is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water and follow the dosing schedule provided by the healthcare professional.

Serious risks include severe bradycardia, marked hypotension, heart block, bronchospasm in patients with reactive airway disease, and rare allergic reactions. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, swelling, or difficulty breathing.

Nebilet is contraindicated in patients with known hypersensitivity to nebivolol, those with severe bradycardia, second‑ or third‑degree atrioventricular block, cardiogenic shock, or uncontrolled heart failure. Caution is also advised in individuals with severe asthma or chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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