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

Nebivolol Zentiva

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Zentiva (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Zentiva, is a beta blocker presented as a tablet for oral use. It treats hypertension in adult patients by lowering elevated blood pressure and improving cardiovascular outcomes.

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

Manufacturer / TM Owner

Zentiva Portugal, Lda

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic receptor blocker used in the management of cardiovascular conditions.

  • Essential hypertension: provides sustained reduction of high blood pressure.
  • Secondary hypertension: assists in controlling blood pressure when caused by another condition.
  • Isolated systolic hypertension: lowers systolic pressure to reduce cardiovascular risk.

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 release, causing vasodilation and further lowering peripheral vascular resistance, thereby contributing to blood pressure reduction.

Side Effects

Nebivolol may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: general feeling of tiredness.
  • Nausea: upset stomach or urge to vomit.
  • Bradycardia: slower than normal heart rate.
  • Peripheral edema: mild swelling of the ankles or feet.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Atrioventricular block: impaired electrical conduction in the heart.
  • Bronchospasm: tightening of airway muscles, especially in asthmatic patients.
  • Hypotension: dangerously low blood pressure.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Anaphylactic reaction: rare severe allergic response.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Blood pressure monitoring: ensure adequate control and avoid excessive lowering.
  • Heart rate assessment: watch for bradycardia, especially in patients with conduction disorders.
  • Asthma/COPD caution: use carefully in patients with reactive airway disease.
  • Discontinuation: avoid abrupt withdrawal to prevent rebound hypertension.
  • Renal impairment: adjust therapy based on renal function.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Non‑selective beta blockers: may cause additive bradycardia.
  • Calcium channel blockers (verapamil, diltiazem): increase nebivolol plasma levels.
  • Strong CYP2D6 inhibitors (paroxetine, fluoxetine): reduce metabolism, raising drug exposure.

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

  • ACE inhibitors or ARBs: combined use may lead to excessive blood pressure reduction.
  • Antidiabetic agents: nebivolol may mask hypoglycemia symptoms.

Frequently Asked Questions

Nebivolol Zentiva is prescribed to lower high blood pressure in adults. By reducing hypertension, it helps lower the risk of heart attack, stroke, and other cardiovascular complications.

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

The dose of Nebivolol Zentiva is individualized by the prescribing clinician based on the patient’s blood pressure, age, kidney function, and other medical factors. Patients should follow the prescriber’s instructions exactly.

Safety data for Nebivolol during 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 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 offers a dual mechanism—β1‑blockade plus nitric‑oxide‑mediated vasodilation—providing effective blood‑pressure control with a lower incidence of metabolic side effects compared with some older beta‑blockers. It is often chosen when patients need both heart‑rate reduction and vascular relaxation.

Store the tablets at ambient temperature, below 25 °C, in the original packaging. Keep them away from moisture, heat and direct sunlight to maintain stability.

Nebivolol Zentiva is taken orally, usually once daily with or without food, as directed by the prescriber. Swallow the tablet whole; do not crush or chew it.

Patients should be alert for severe bradycardia, symptomatic hypotension, heart block, bronchospasm, or signs of an allergic reaction such as rash, swelling or difficulty breathing. Any of these require immediate medical attention.

Nebivolol is contraindicated in patients with severe bradycardia, second‑ or third‑degree atrioventricular block, uncompensated heart failure, or known hypersensitivity to the drug. Caution is advised for individuals with asthma, chronic obstructive pulmonary disease, or significant liver impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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