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

Nivolon

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nivolon (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nivolon, is a beta blocker presented as an oral tablet for oral administration. It selectively blocks β1‑adrenergic receptors and also promotes nitric‑oxide‑mediated vasodilation, which together help to lower elevated blood pressure in adult patients diagnosed with hypertension. The medication is indicated for sustained blood‑pressure control and may be used as part of a comprehensive cardiovascular risk‑reduction strategy.

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

Manufacturer / TM Owner

Mylan S.P.A.

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Indications & Clinical Uses

  • Nivolon (nebivolol) is used to manage conditions within the cardiovascular disease pathway, primarily hypertension.
  • Hypertension: lowers elevated blood pressure in adults
  • Heart failure (reduced ejection fraction): improves cardiac output and reduces symptoms of fluid overload
  • Elderly patients with hypertension: provides effective blood‑pressure control with a favorable tolerability profile

How It Works

  • Nebivolol acts as a selective β1‑adrenergic receptor antagonist, reducing heart rate and myocardial contractility. In addition, it stimulates endothelial nitric‑oxide synthase, increasing nitric‑oxide release which causes vasodilation. The combined β1‑blockade and nitric‑oxide‑mediated vasorelaxation result in decreased systemic vascular resistance and lowered arterial pressure.

Side Effects

Nebivolol may be associated with a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Headache: mild to moderate headache reported.
  • Dizziness or light‑headedness.
  • Fatigue or tiredness.
  • Bradycardia: slower than normal heart rate.

Serious or Rare Side Effects

  • Severe bradycardia or heart block: may require medical attention.
  • Bronchospasm or worsening asthma symptoms.
  • Allergic reactions: rash, angioedema, or anaphylaxis.

Precautions & Warnings

When prescribing nebivolol, clinicians should consider several precautionary measures to ensure safe use.

  • Monitor blood pressure: check regularly after initiation or dose changes.
  • Assess heart rate: watch for bradycardia, especially in patients with conduction disorders.
  • Use caution in asthma or chronic obstructive pulmonary disease: β‑blockade may precipitate bronchospasm.
  • Avoid abrupt discontinuation: sudden stop can lead to rebound hypertension.
  • Pregnancy category B: discuss potential risks with prescriber before use in pregnant or breastfeeding women.
  • Store below 25°C: keep in the original container, protect from moisture and direct light.

Avoid Interactions

Nebivolol can interact with other medicines, and the significance of the interaction determines the management approach.

Major Interactions (Avoid)

  • Non‑selective beta‑blockers (e.g., propranolol): additive bradycardia and hypotension.
  • Calcium‑channel blockers verapamil or diltiazem: increased risk of AV‑block and severe bradycardia.
  • Clonidine: abrupt withdrawal after combined use may cause severe rebound hypertension.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may enhance hypotensive effect, requiring blood‑pressure monitoring.
  • Diuretics: additive blood‑pressure lowering, monitor electrolytes and volume status.
  • Antidiabetic agents (insulin, sulfonylureas): β‑blockade may mask hypoglycaemia symptoms, adjust monitoring.

Frequently Asked Questions

Nivolon contains nebivolol, a selective β1‑blocker that is prescribed primarily for the treatment of hypertension. By lowering elevated blood pressure, it helps reduce the risk of cardiovascular complications associated with high blood pressure.

Nebivolol blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility. It also stimulates endothelial nitric‑oxide release, causing vasodilation. The combined effect reduces systemic vascular resistance and lowers arterial pressure.

The appropriate dose of Nivolon is determined by the prescribing healthcare professional based on the patient’s condition, age, renal function and response to therapy. Dosage adjustments are made according to clinical judgment.

Nebivolol is classified as pregnancy category B, indicating that animal studies have not shown risk but there are limited human data. Use only if clearly needed and after discussion with a healthcare provider. Breastfeeding decisions should also be made with medical advice.

To request Nivolon, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Compared with non‑selective beta‑blockers, nebivolol offers additional nitric‑oxide‑mediated vasodilation, which may improve tolerability and metabolic profile. It is often chosen for patients who need heart‑rate control with a lower incidence of certain side effects such as cold extremities.

Nivolon should be stored below 25 °C in its original packaging, protected from moisture and direct light. Keep the tablets out of reach of children and do not use after the expiry date printed on the label.

Nivolon is taken orally, usually once daily with or without food, as directed by the prescribing clinician. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse reactions can include severe bradycardia, heart block, bronchospasm in patients with asthma or COPD, and rare allergic responses such as rash, angioedema or anaphylaxis. Prompt medical attention is required if any of these occur.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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