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

Nebivolol Hydrochloride Amarox

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Hydrochloride Amarox (Nebivolol Hydrochloride)

Nebivolol Hydrochloride, the active ingredient in Nebivolol Hydrochloride Amarox, is a beta‑adrenergic blocker presented as an oral tablet for oral use. It treats hypertension in adult patients by lowering elevated blood pressure.

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

Manufacturer / TM Owner

Amarox Pharma Gmbh

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Indications & Clinical Uses

Nebivolol Hydrochloride is a selective β1‑blocker used in the management of high‑blood‑pressure disorders.

  • Primary hypertension: reduces systolic and diastolic pressure in patients with essential hypertension.
  • Essential hypertension: provides long‑term blood‑pressure control in adults.
  • Isolated systolic hypertension: helps lower elevated systolic readings in elderly patients.

How It Works

  • Nebivolol Hydrochloride selectively antagonizes β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and myocardial contractility. Concurrently, it stimulates endothelial nitric oxide synthase, enhancing nitric oxide release and causing vasodilation. The combined effect reduces systemic vascular resistance and arterial pressure, contributing to its antihypertensive action.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness: often related to blood‑pressure lowering.
  • Fatigue: general tiredness or reduced energy.
  • Nausea: occasional stomach upset.
  • 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.
  • Allergic reaction: rash, itching, or swelling of face and throat.
  • Hepatic injury: abnormal liver function tests.
  • Heart block: impaired electrical conduction in the heart.
  • Acute bronchospasm: difficulty breathing, especially in asthmatic patients.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety factors.

  • Renal impairment: monitor kidney function and adjust therapy as needed.
  • Asthma or chronic obstructive pulmonary disease: use with caution as β‑blockade may worsen bronchospasm.
  • Diabetes mellitus: may mask hypoglycaemia symptoms; monitor blood glucose closely.
  • Concomitant use of other antihypertensives: risk of additive blood‑pressure lowering.
  • Pregnancy: safety not established; avoid unless benefits outweigh risks.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol Hydrochloride can interact with several drug classes, influencing its safety profile.

Major Interactions (Avoid)

  • Non‑selective beta‑blockers: additive bradycardia and hypotension.
  • Calcium‑channel blockers (verapamil, diltiazem): increased risk of AV‑block.
  • Clonidine: abrupt discontinuation may cause rebound hypertension.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may enhance hypotensive effect.
  • Diuretics: can increase risk of electrolyte disturbances.
  • SSRIs or other antidepressants: may affect heart‑rate regulation.

Frequently Asked Questions

Nebivolol Hydrochloride Amarox is prescribed to lower high blood pressure in adults. By reducing systemic vascular resistance and heart rate, it helps achieve target blood‑pressure levels and lowers the risk of cardiovascular complications associated with hypertension.

Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and contractility. It also stimulates endothelial nitric oxide production, causing vasodilation. The combined actions lower cardiac output and peripheral resistance, resulting in reduced arterial pressure.

The specific dose and titration schedule are determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Nebivolol in pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

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 β1‑selective blocker with additional nitric‑oxide‑mediated vasodilation, which can offer better tolerability regarding metabolic effects compared with non‑selective beta‑blockers. Compared with ACE inhibitors or calcium‑channel blockers, it provides a distinct mechanism and may be chosen based on patient comorbidities and response.

Store the tablets at ambient temperature, preferably below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Nebivolol Hydrochloride Amarox is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless otherwise directed by a healthcare professional.

Serious adverse events include severe bradycardia, symptomatic hypotension, heart block, and rare allergic reactions such as angio‑edema. Patients should seek immediate medical attention if they experience fainting, very slow heart rate, chest pain, or signs of an allergic reaction.

Nebivolol is contraindicated in patients with severe sinus bradycardia, second‑ or third‑degree AV block without a pacemaker, cardiogenic shock, or known hypersensitivity to the drug. Caution is also advised for individuals with uncontrolled asthma or severe chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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