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

Nebivolol Accord

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Accord (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Accord, is a beta blocker presented as an oral dosage form for oral use. It treats hypertension in adult patients by lowering elevated blood pressure.

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

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

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

  • Hypertension: reduces systolic and diastolic blood pressure in patients with essential hypertension.
  • Heart failure with reduced ejection fraction: improves cardiac output and may reduce hospitalization risk.
  • Left ventricular hypertrophy: may slow progression of structural heart changes associated with high blood pressure.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility, which lowers cardiac output and blood pressure. In addition, it stimulates endothelial nitric oxide release, causing vasodilation and further contributing to antihypertensive effects without significant β2 blockade.

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 after standing.
  • Fatigue or tiredness.
  • Bradycardia: slower than normal heart rate.
  • Nausea or mild gastrointestinal upset.
  • Nasal congestion.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Acute bronchospasm in patients with asthma or COPD.
  • Allergic reactions such as rash, itching, or angioedema.
  • Hepatic dysfunction or elevated liver enzymes.
  • Marked hypotension leading to syncope.
  • Cardiovascular collapse in overdose.

Precautions & Warnings

Before initiating Nebivolol therapy, clinicians should consider several safety measures.

  • Monitor blood pressure: ensure adequate control and avoid excessive drops.
  • Assess cardiac function: evaluate heart rate and ECG for bradyarrhythmias.
  • Use caution in asthma or chronic obstructive pulmonary disease: risk of bronchospasm.
  • Avoid abrupt discontinuation: taper dose to prevent rebound hypertension.
  • Adjust dose in renal impairment: consider reduced clearance.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Other beta‑blockers: additive bradycardia and hypotension.
  • Calcium channel blockers (verapamil, diltiazem): increased risk of AV block.
  • Strong CYP2D6 inhibitors (paroxetine, fluoxetine): elevated Nebivolol plasma levels.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect.
  • Diuretics: potential for excessive blood pressure reduction.
  • ACE inhibitors or ARBs: monitor for additive hypotensive effect.
  • Clonidine: risk of rebound hypertension if stopped abruptly.

Frequently Asked Questions

Nebivolol Accord contains the beta‑blocker nebivolol and is prescribed to lower high blood pressure in adults. It may also be used in certain cases of heart failure to improve cardiac function, as determined by a healthcare professional.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractile force. It also enhances nitric oxide release from the endothelium, causing blood vessels to relax and further decreasing blood pressure.

The appropriate dose of Nebivolol Accord is set by the prescribing clinician based on the patient’s condition, response, and other medical factors. Dosage may be adjusted during treatment to achieve target blood pressure.

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 under close medical supervision.

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 necessary import documentation.

Nebivolol is a highly selective β1‑blocker with additional nitric‑oxide‑mediated vasodilation, which may result in fewer metabolic side effects compared with non‑selective beta‑blockers. Its dual action can provide effective blood pressure control while preserving peripheral circulation.

Nebivolol Accord should be stored at ambient temperature, below 25 °C, in its original container. Keep the product away from moisture, heat and direct sunlight to maintain stability.

Nebivolol Accord is taken orally, usually once daily with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless instructed otherwise.

Serious risks include severe bradycardia, heart block, marked hypotension, bronchospasm in patients with asthma or COPD, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience fainting, severe shortness of breath, or swelling of the face or throat.

Nebivolol should be avoided in patients with severe bradycardia, second‑ or third‑degree AV block without a pacemaker, uncontrolled asthma, or known hypersensitivity to nebivolol or any excipients. It is also contraindicated in patients taking certain interacting medications without proper monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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