Product image of Nebivolol Teva-Ratiopharm (Nebivolol Hydrochloride) supplied by GNH India

Nebivolol Teva-Ratiopharm

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Teva-Ratiopharm (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Teva‑Ratiopharm, is a beta‑blocker presented as an oral tablet for oral use. It is used to treat hypertension and may be prescribed for certain patients with heart failure.

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

Manufacturer / TM Owner

Teva Pharma S.L.U.,

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Indications & Clinical Uses

  • Nebivolol is a selective β1‑adrenergic antagonist used in cardiovascular therapy.
  • Hypertension: lowers elevated blood pressure in adult patients.
  • Heart failure: improves cardiac function and reduces symptoms in patients with chronic heart failure.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in the heart, decreasing heart rate and myocardial contractility, which reduces cardiac output and blood pressure. In addition, it stimulates endothelial nitric‑oxide synthase, causing nitric‑oxide‑mediated vasodilation that further contributes 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 intensity.
  • Dizziness or light‑headedness: especially on standing.
  • Fatigue or tiredness: general lack of energy.
  • Nasal congestion: feeling of a blocked nose.
  • Gastrointestinal discomfort: nausea or abdominal pain.
  • Bradycardia: slower than normal heart rate.

Serious or Rare Side Effects

  • Severe bradycardia: may require medical attention.
  • Hypotension: dangerously low blood pressure.
  • Bronchospasm: difficulty breathing, especially in asthmatic patients.
  • Heart block: impaired electrical conduction of the heart.
  • Acute heart failure exacerbation: worsening of heart failure symptoms.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.

Precautions & Warnings

  • Before initiating therapy with Nebivolol, consider the following safety measures.
  • Cardiovascular assessment: evaluate heart rate and blood pressure baseline.
  • Asthma or chronic obstructive pulmonary disease: use with caution due to potential bronchospasm.
  • Diabetes mellitus: monitor blood glucose as beta‑blockade may mask hypoglycaemia symptoms.
  • Severe liver impairment: dose adjustment may be required.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit evaluation.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Combined use with other β‑blockers: risk of excessive bradycardia and hypotension.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, quinidine): may increase nebivolol plasma levels.
  • Calcium channel blockers (verapamil, diltiazem): additive negative inotropic and AV‑node effects.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents (ACE inhibitors, diuretics): monitor for additive blood pressure lowering.
  • Antidiabetic drugs (insulin, sulfonylureas): observe for masked hypoglycaemia signs.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive effect.

Frequently Asked Questions

Nebivolol Teva‑Ratiopharm is a prescription medication that belongs to the beta‑blocker class. It is primarily used to lower high blood pressure (hypertension) and may also be prescribed for patients with chronic heart failure to improve cardiac function.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility, which lowers cardiac output and blood pressure. Additionally, it enhances nitric‑oxide release from the endothelium, causing vasodilation that further contributes to blood pressure reduction.

The dosage of nebivolol is individualized by a qualified prescriber based on the patient’s clinical condition, age, renal and hepatic function, and response to therapy. Patients should follow the dosing instructions provided by their healthcare professional.

Nebivolol should be used during pregnancy or while breastfeeding only if the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers will assess the risk‑benefit ratio before prescribing it to pregnant or nursing women.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and import documentation.

Nebivolol differs from many beta‑blockers by also promoting nitric‑oxide‑mediated vasodilation, which can result in better blood pressure control with fewer metabolic side effects. Compared with non‑beta‑blocker antihypertensives, it offers a combined heart‑rate‑lowering and vasodilatory effect.

Nebivolol tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and keep out of reach of children.

Nebivolol 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; do not crush or chew unless specifically instructed.

Serious risks include severe bradycardia, marked hypotension, bronchospasm in patients with asthma or COPD, and worsening heart failure. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, swelling, 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. A healthcare provider will evaluate suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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