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

Nebivolol

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol, is a beta blocker presented as a tablet for oral use. It treats hypertension in adult patients by lowering blood pressure and improving vascular function.

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

Manufacturer / TM Owner

Noumed Life Sciences

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic blocker used in the management of arterial hypertension and related cardiovascular conditions.

  • Hypertension: lowers systolic and diastolic blood pressure in patients with essential hypertension.
  • Primary hypertension: improves vascular tone and reduces peripheral resistance.
  • Essential hypertension: helps prevent long‑term cardiovascular complications associated with high blood pressure.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility. In addition, it stimulates endothelial nitric oxide synthase, enhancing nitric oxide release and causing vasodilation, which together reduce peripheral vascular resistance and lower systemic blood pressure.

Side Effects

Nebivolol may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or tiredness.
  • Nausea or mild gastrointestinal upset.
  • Bradycardia: heart rate slower than normal.
  • Peripheral edema: swelling of the lower limbs.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Marked hypotension with risk of syncope.
  • Bronchospasm or worsening asthma symptoms.
  • Allergic reactions such as rash, pruritus, or angioedema.
  • Hepatic dysfunction or elevated liver enzymes.
  • Acute heart failure decompensation.

Precautions & Warnings

When prescribing or dispensing Nebivolol, consider the following safety measures.

  • Blood pressure monitoring: regularly assess to ensure therapeutic control.
  • Heart rate assessment: watch for excessive bradycardia.
  • Asthma or chronic obstructive pulmonary disease: use with caution due to potential bronchoconstriction.
  • Discontinuation: avoid abrupt cessation; taper under medical supervision.
  • Renal or hepatic impairment: dose adjustment may be required.
  • 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.
  • Calcium‑channel blockers (e.g., verapamil, diltiazem): may cause profound bradycardia or AV block.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): increase nebivolol plasma concentrations.

Moderate Interactions (Monitor Closely):\n- Diuretics: may enhance hypotensive effect.

  • ACE inhibitors or ARBs: combined use can lead to excessive blood pressure lowering.
  • NSAIDs: may reduce antihypertensive efficacy.
  • Antiarrhythmic agents (e.g., amiodarone): potential for conduction disturbances.
  • Antidiabetic drugs: monitor glucose as beta‑blockade may mask hypoglycaemia symptoms.

Frequently Asked Questions

Nebivolol is prescribed to lower high blood pressure in adults. It belongs to the beta‑blocker class and works by reducing heart rate and relaxing blood vessels, helping to prevent complications such as stroke or heart attack.

Nebivolol selectively blocks β1‑adrenergic receptors, decreasing cardiac output, while also stimulating nitric oxide release from the endothelium. This dual action leads to vasodilation and a reduction in peripheral vascular resistance, ultimately lowering blood pressure.

The specific dose of Nebivolol is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of Nebivolol in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To request Nebivolol, 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 offers a unique combination of β1‑blockade and nitric‑oxide‑mediated vasodilation, which may result in fewer metabolic side effects compared with non‑selective beta‑blockers. Its profile is often compared with agents such as atenolol or metoprolol, which lack the nitric‑oxide component.

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

Nebivolol 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 specifically instructed by a healthcare professional.

Serious adverse events can include severe bradycardia, marked hypotension, bronchospasm in patients with asthma, and rare cases of liver injury or heart block. Patients should seek immediate medical attention if they experience fainting, difficulty breathing, or rapid weight gain.

Nebivolol is contraindicated in patients with known hypersensitivity to the drug, severe bradycardia, second‑ or third‑degree atrioventricular block, or uncompensated heart failure. Caution is also advised for individuals with asthma, severe liver disease, or those taking interacting medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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