Nebivolol
Brand names: Nebilet
Nebivolol is a highly beta-1-selective beta-blocker with additional nitric-oxide-mediated vasodilation, used for hypertension and as an adjunct for stable mild-to-moderate heart failure in older patients.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
US labelling (FDA)
Reference — US labelling, may differ from UKCan be taken with and without food. Individualize to the needs of the patient and monitor during up-titration. ( 2 ) Hypertension: Most patients start at 5 mg once daily. Dose can be increased at 2-week intervals up to 40 mg. ( 2.1 ) 2.1 Hypertension The dose of nebivolol tablets must be individualized to the needs of the patient. For most patients, the recommended starting dose is 5 mg once daily, with or without food, as monotherapy or in combination with other agents. For patients requiring further reduction in blood pressure, the dose can be increased at 2-week intervals up to 40 mg. A more frequent dosing regimen is unlikely to be beneficial. Renal Impairment In patients with severe …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2024-10-31. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Clinical monograph
How it works
It selectively blocks beta-1 adrenoceptors, reducing heart rate, myocardial contractility and renin release; it also promotes endothelial nitric oxide release, producing peripheral vasodilation.
Prescribing in practice
- Avoid in asthma and other reversible obstructive airways disease, and in marked bradycardia, second- or third-degree heart block, sick sinus syndrome and decompensated heart failure.
- Do not stop abruptly, particularly in ischaemic heart disease, as this risks rebound angina or arrhythmia; withdraw gradually.
- May mask the warning signs of hypoglycaemia, such as tachycardia, in patients with diabetes.
Monitoring
Monitor heart rate and blood pressure; in heart failure assess clinical status closely after initiation and dose changes, watching for fluid retention or worsening symptoms.
Counselling the patient
- Do not stop the tablets suddenly without medical advice.
- It may cause tiredness, headache or dizziness, especially when starting.
- If you have diabetes, be aware it can hide the usual warning signs of a low blood sugar.
Evidence & guidelines
Guideline-recommended option for hypertension and for heart failure in older people (NICE NG136; NICE NG106).
Reference: NICE NG136/NG106; ESC; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Acute Heart Failure · ESC 2021 Heart Failure Guidelines; NICE NG106
- NSTEMI / Unstable Angina · ESC 2020 NSTEMI Guidelines; NICE NG185
- New-Onset Atrial Fibrillation · ESC 2020 AF Guidelines; NICE NG196
- Hypertensive Emergency · ESC/ESH 2018 Hypertension Guidelines; NICE NG136
- Bradycardia Management · Resuscitation Council UK ABCDE; ESC 2021 Pacing Guidelines
- Ventricular Tachycardia / Fibrillation · Resuscitation Council UK ACLS; ESC 2022 Ventricular Arrhythmia Guidelines