What is the typical dosing for Nebivolol (beta blocker) in treating hypertension?

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Nebivolol Dosing for Hypertension

The recommended starting dose of nebivolol for hypertension is 5 mg once daily, with titration up to 40 mg daily if needed for blood pressure control, with dose adjustments made at 2-week intervals. 1

Standard Dosing Protocol

  • Initial dose: 5 mg once daily (with or without food)
  • Titration: May increase dose at 2-week intervals
  • Maximum dose: 40 mg once daily
  • Administration: Can be taken as monotherapy or in combination with other antihypertensive agents

Special Population Dosing Adjustments

Renal Impairment

  • Severe renal impairment (CrCl <30 mL/min): Start with 2.5 mg once daily and titrate slowly as needed
  • Dialysis patients: Not studied, use with caution

Hepatic Impairment

  • Moderate hepatic impairment: Start with 2.5 mg once daily and titrate slowly
  • Severe hepatic impairment: Not recommended due to lack of studies

Elderly Patients

  • No dose adjustment necessary for elderly patients 1
  • However, clinical practice often suggests starting at lower doses (2.5 mg) in very elderly or frail patients

CYP2D6 Polymorphism

  • No dose adjustments necessary for CYP2D6 poor metabolizers
  • Clinical effects and safety profiles are similar between poor and extensive metabolizers 1

Efficacy and Clinical Considerations

Nebivolol is a highly selective beta-1 receptor antagonist with nitric oxide-mediated vasodilatory effects 2. This unique mechanism provides several advantages:

  • Effectively reduces blood pressure comparable to other beta-blockers (atenolol, metoprolol) and other antihypertensive classes 2
  • Response rates range from 58-81% after 4-52 weeks of treatment 2
  • Once-daily dosing provides 24-hour blood pressure control, including early morning blood pressure surges 2
  • Clinical trials have shown that the 5 mg dose is optimal for most patients, with minimal additional benefit at higher doses 3

Safety Profile

Nebivolol has a favorable side effect profile compared to other beta-blockers:

  • Most common adverse events are transient headache, dizziness, fatigue, and paresthesias 2
  • Lower incidence of erectile dysfunction and decreased libido compared to other beta-blockers 2
  • Does not significantly affect glucose or plasma lipid metabolism 2
  • No significant orthostatic hypotension reported in several studies 2

Monitoring Parameters

  • Blood pressure response (goal: reduction by at least 20/10 mmHg or to target <140/90 mmHg) 4
  • Heart rate (monitor for excessive bradycardia)
  • Signs of orthostatic hypotension, especially when initiating therapy
  • Achievement of target blood pressure within 3 months 4

Clinical Pearls

  • Nebivolol should not be abruptly discontinued due to risk of rebound hypertension 4
  • Consider combination therapy with thiazide diuretics for additive effects if monotherapy is insufficient 2
  • Nebivolol has protective effects on left ventricular function, making it a good choice for patients with hypertension and heart failure concerns 2
  • Unlike many other beta-blockers, nebivolol may be better tolerated in patients with mild reactive airway disease due to its high beta-1 selectivity

Nebivolol represents an effective option for treating hypertension with a favorable side effect profile compared to traditional beta-blockers, particularly regarding metabolic parameters and sexual function.

References

Research

Nebivolol: a new antihypertensive agent.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2008

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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