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

Nebivolol Cf

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Cf (Nebivolol)

Nebivolol, the active ingredient in Nebivolol Cf, is a beta blocker presented as an oral tablet for oral use. It is used to lower high blood pressure in adult patients.

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

Manufacturer / TM Owner

Centrafarm B.V.

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic antagonist used in the management of elevated blood pressure and related cardiovascular conditions.

  • Hypertension: lowers systolic and diastolic blood pressure in adults.
  • Isolated systolic hypertension: reduces elevated systolic pressure while preserving diastolic values.
  • Essential hypertension: improves vascular tone and overall blood pressure control.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility, which lowers cardiac output. In addition, it stimulates endothelial nitric oxide release, causing vasodilation and further decreasing peripheral resistance, thereby contributing to blood pressure reduction.

Side Effects

Nebivolol may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: general tiredness or lack of energy.
  • Nasal congestion: blocked or runny nose.
  • Bradycardia: slower than normal heart rate.
  • Nausea: feeling of stomach upset.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Symptomatic hypotension: significant drop in blood pressure causing faintness.
  • Atrioventricular block: impaired electrical conduction in the heart.
  • Bronchospasm: narrowing of airways, especially in patients with asthma.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Heart failure exacerbation: worsening of existing cardiac insufficiency.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Cardiovascular assessment: monitor heart rate and blood pressure regularly.
  • Renal impairment: evaluate kidney function and adjust therapy if needed.
  • Hepatic disease: use with caution in patients with liver dysfunction.
  • Concomitant beta‑blockers: avoid duplicate therapy to prevent excessive β‑blockade.
  • Pregnancy: safety not established; weigh risks and benefits.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Other beta‑blockers: additive β‑blockade may cause severe bradycardia.
  • Calcium‑channel blockers (verapamil, diltiazem): increase risk of heart block and low heart rate.
  • Clonidine: abrupt discontinuation can cause rebound hypertension.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor for excessive hypotension.
  • Diuretics: watch for electrolyte disturbances and volume depletion.
  • SSRIs or other antidepressants: may affect heart rate and blood pressure control.

Frequently Asked Questions

Nebivolol Cf contains the beta‑blocker nebivolol and is prescribed to treat hypertension, helping to lower elevated systolic and diastolic blood pressure in adult patients.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility, while also stimulating nitric‑oxide release from the endothelium, which causes vasodilation and further decreases peripheral vascular resistance.

The dose of nebivolol is individualized by the prescribing clinician based on the patient’s blood pressure, age, renal and hepatic function, and response to therapy. No fixed regimen is provided here.

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 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 required import documentation.

Nebivolol combines β1‑selective blockade with nitric‑oxide‑mediated vasodilation, offering blood‑pressure reduction with a lower incidence of metabolic side effects compared with non‑selective beta‑blockers. It is often considered when a patient needs both heart‑rate control and vasodilation.

Nebivolol Cf should be stored at ambient temperature, preferably below 25 °C, in its original container, protected from moisture and direct sunlight to maintain product stability.

Nebivolol Cf is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a glass of water.

Serious risks include severe bradycardia, symptomatic hypotension, atrioventricular block, bronchospasm in susceptible individuals, and rare allergic reactions. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, or difficulty breathing.

Nebivolol is contraindicated in patients with known hypersensitivity to nebivolol or any component of the formulation, those with severe bradycardia, second‑ or third‑degree heart block without a pacemaker, and patients in cardiogenic shock.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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