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

Nebivolol Krka

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Krka (Nebivolol)

Nebivolol, the active ingredient in Nebivolol Krka, is a beta blocker presented as an oral tablet for oral use. It is used to treat hypertension in adult patients, helping to lower elevated blood pressure and reduce cardiovascular risk.

GNH India supplies Nebivolol Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Clients benefit from consistent batch release, regulatory support, and on‑time delivery across multiple regions.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic blocker used in the management of hypertension and related blood‑pressure disorders.

  • Essential hypertension: lowers systolic and diastolic pressure to achieve target blood‑pressure goals.
  • Isolated systolic hypertension: reduces elevated systolic readings, especially in older adults.
  • High blood pressure in elderly patients: provides effective control with a favorable heart‑rate profile.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors in cardiac tissue, decreasing heart‑rate and myocardial contractility, which reduces cardiac output. In addition, it stimulates endothelial nitric oxide synthase, leading to nitric oxide‑mediated vasodilation of peripheral vessels. The combined β1‑blockade and nitric‑oxide effect produce a net reduction in systemic vascular resistance and arterial pressure, contributing to its antihypertensive action.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness.
  • Fatigue or tiredness.
  • Bradycardia: slower than normal heart rate.
  • Nausea or gastrointestinal discomfort.
  • Nasal congestion.

Serious or Rare Side Effects

  • Severe bradycardia or heart block.
  • Acute bronchospasm, especially in asthmatic patients.
  • Allergic reactions such as rash, itching or angioedema.
  • Liver enzyme elevation or hepatitis.
  • Hypotension leading to fainting.
  • Cardiac failure exacerbation.

Precautions & Warnings

When prescribing Nebivolol, clinicians should observe several precautionary measures to ensure patient safety.

  • Monitor blood pressure: check regularly after initiation and dose adjustments.
  • Assess heart rate: watch for excessive bradycardia, especially in patients with conduction disorders.
  • Use caution in asthma or chronic obstructive pulmonary disease: β‑blockade may precipitate bronchospasm.
  • Avoid abrupt discontinuation: taper dose to prevent rebound hypertension.
  • Adjust dose in renal impairment: consider reduced clearance in severe kidney disease.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Other β‑blockers: additive cardiac depression.
  • Calcium channel blockers (verapamil, diltiazem): may cause marked bradycardia or AV block.
  • Clonidine: abrupt withdrawal can lead to severe hypertension.
  • Antiarrhythmic agents (e.g., amiodarone): increase risk of conduction disturbances.
  • MAO inhibitors: potential for hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect.
  • Diuretics: can enhance hypotensive response.
  • ACE inhibitors or ARBs: monitor for excessive blood‑pressure reduction.
  • Antidiabetic drugs: may mask hypoglycemia symptoms.
  • CYP2D6 inhibitors (e.g., fluoxetine): may increase nebivolol plasma levels.

Frequently Asked Questions

Nebivolol Krka contains the beta‑blocking agent nebivolol and is indicated for the treatment of hypertension. By lowering elevated blood pressure, it helps reduce the risk of cardiovascular events in adult patients.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility. It also stimulates nitric‑oxide release from the endothelium, causing peripheral vasodilation. The combined actions lower systemic vascular resistance and blood pressure.

The appropriate dose of Nebivolol Krka is determined by the prescribing clinician based on the patient’s clinical condition, blood‑pressure response, and any co‑existing medical issues. Dosage adjustments are made according to professional guidelines.

The safety of nebivolol in pregnancy and lactation has not been definitively established. 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 Nebivolol Krka 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 differs from many traditional beta‑blockers by adding nitric‑oxide‑mediated vasodilation, which can improve arterial compliance and cause fewer metabolic side effects. Compared with ACE inhibitors or calcium‑channel blockers, it offers a distinct mechanism, and clinicians may choose it based on patient‑specific factors such as heart‑rate control and tolerance.

Nebivolol Krka tablets should be stored at room temperature, below 25 °C, in the original packaging. Protect them from moisture, direct sunlight and extreme temperature fluctuations to maintain product stability.

Nebivolol Krka is taken orally, usually once daily, with or without food. Patients should follow the dosing schedule prescribed by their healthcare provider and not alter the timing or skip doses without medical advice.

Serious risks include severe bradycardia, heart block, acute bronchospasm in patients with asthma or COPD, and rare cases of liver injury or allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience symptoms like fainting, severe shortness of breath, or rash.

Nebivolol Krka is contraindicated in patients with known hypersensitivity to nebivolol or any excipients, those with severe bradycardia, second‑ or third‑degree AV block without a pacemaker, and individuals with uncompensated heart failure. It should also be used with caution in patients with asthma, COPD, or significant hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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