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 tablet for oral use. It is indicated for the management of hypertension in adult patients, helping to lower elevated blood pressure and reduce cardiovascular risk.

GNH India supplies Nebivolol Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality, regulatory compliance and reliable logistics for timely global delivery.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Nebivolol is a selective beta‑1 blocker used primarily in the cardiovascular therapeutic pathway to control blood pressure and support heart function.

  • Hypertension: lowers systolic and diastolic blood pressure in adult patients.
  • Chronic heart failure: improves ventricular function and may reduce mortality when added to standard therapy.
  • Age‑related systolic hypertension: provides better blood pressure control in older adults.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors, reducing heart rate and myocardial contractility, which decreases cardiac output. In addition, it stimulates endothelial nitric‑oxide synthase, leading to nitric‑oxide mediated vasodilation that further lowers peripheral vascular resistance and blood pressure.

Side Effects

Nebivolol is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate pain often transient.
  • Dizziness or light‑headedness: especially on standing.
  • Fatigue or tiredness: reduced energy levels.
  • Nausea or abdominal discomfort.
  • Bradycardia: slower than normal heart rate.
  • Peripheral edema: mild swelling of ankles or feet.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Symptomatic hypotension: sudden drop in blood pressure causing faintness.
  • Heart block or atrioventricular conduction disturbances.
  • Bronchospasm: difficulty breathing, particularly in patients with asthma.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Depression or mood changes: rare but reported.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety factors.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Cardiac assessment: evaluate heart rate and conduction abnormalities.
  • Respiratory caution: avoid use in patients with severe asthma or COPD.
  • Diabetes management: monitor glucose as beta‑blockers may mask hypoglycaemia symptoms.
  • Discontinuation: taper gradually to prevent rebound hypertension.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol may interact with other medicines, requiring careful management.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely):\n- Diuretics: may enhance antihypertensive effect, monitor electrolytes.

  • ACE inhibitors or ARBs: combined effect on blood pressure, watch for hypotension.
  • NSAIDs: may reduce antihypertensive efficacy.
  • Antidiabetic agents: possible masking of hypoglycaemia symptoms.

Frequently Asked Questions

Nebivolol Accord contains nebivolol hydrochloride, a beta‑blocker indicated for the treatment of hypertension in adult patients. It helps lower elevated blood pressure and may be used as part of a broader cardiovascular risk‑reduction strategy under a prescriber's guidance.

Nebivolol selectively blocks β1‑adrenergic receptors, reducing heart rate and contractility, which lowers cardiac output. It also enhances nitric‑oxide release from the endothelium, causing vasodilation and decreasing peripheral vascular resistance, together resulting in lower blood pressure.

The appropriate dose of Nebivolol Accord is determined by the prescribing clinician based on the individual’s blood pressure, comorbid conditions, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Nebivolol’s safety 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 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 selective β1‑blocker with additional nitric‑oxide‑mediated vasodilation, which can offer better tolerability for some patients compared with non‑selective beta‑blockers. Compared with ACE inhibitors or calcium‑channel blockers, its mechanism is distinct, and choice depends on individual patient profiles and comorbidities.

Nebivolol Accord tablets should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Nebivolol Accord is taken orally, usually once daily, with or without food as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious risks include severe bradycardia, symptomatic hypotension, heart block, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience fainting, extreme fatigue, difficulty breathing, or swelling of the face or throat.

Nebivolol Accord is contraindicated in patients with known hypersensitivity to nebivolol or any component of the formulation, in those with severe bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and in individuals with uncompensated heart failure or severe asthma/COPD unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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