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Cardioselective beta-blocker (β1 + β2 partial agonist) Pregnancy: Safety in human pregnancy not established; should not be used during pregnancy unless there is no safer alternative. Beta-blockers may reduce placental perfusion (risk of intrauterine death, immature/premature delivery) and cause neonatal hypoglycaemia, bradycardia and respiratory distress. Not recommended in breast-feeding mothers.

Celiprolol hydrochloride

Brand names: Celectol

Celiprolol is a cardioselective beta-blocker with partial beta-2 agonist and weak vasodilator activity, used in the management of hypertension.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 200 mg once daily (initial dose)
Route: Oral
Frequency: once daily
Max: 400 mg once daily
Initial dose 200 mg once daily, taken on rising with a glass of water, one hour before or two hours after meals. If response is inadequate, the dose may be increased to 400 mg once daily after 2 to 4 weeks. It may take several weeks for the full antihypertensive effect. Do not discontinue abruptly — reduce gradually over 7–10 days (over 1–2 weeks in ischaemic heart disease) to avoid acute worsening. Celiprolol therapy must be reported to the anaesthetist before general anaesthesia. Children: not recommended.

Dose adjustments

Renal

Reduce the dose by half in patients with creatinine clearance 15–40 ml/min (monitor heart rate; reconsider treatment if bradycardia <50–55 bpm at rest). Not recommended if creatinine clearance is less than 15 ml/min.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to celiprolol hydrochloride or to any of the excipients
  • Second or third degree heart block
  • Severe bradycardia (<45–50 beats per minute)
  • Sick sinus syndrome (including sinoatrial block)
  • Untreated phaeochromocytoma (only after alpha-receptor blockade)
  • Metabolic acidosis
  • Hypotension (systolic blood pressure less than 100 mmHg)
  • Severe peripheral arterial circulatory disturbances; late stages of peripheral arterial occlusive disease and Raynaud's syndrome
  • Uncontrolled heart failure; cardiogenic shock
  • Severe renal impairment (creatinine clearance less than 15 ml/min)
  • Acute episode of asthma, severe bronchial asthma and severe chronic obstructive pulmonary disease
  • Concomitant theophylline

Side effects

  • Headache and dizziness, somnolence, tremor (common)
  • Depression (common)
  • Significant decrease in blood pressure including orthostatic hypotension (common)
  • Hot flush (common)
  • Nausea, vomiting, abdominal pain and discomfort, dry mouth (common)

Interactions

  • Theophylline — celiprolol should not be prescribed for patients being treated with theophylline
  • Anaesthetic agents (e.g. ether, cyclopropane, trichloroethylene) — special care; report celiprolol therapy to the anaesthetist before general anaesthesia
  • Other antihypertensive agents (particularly diuretics) — increased blood pressure monitoring recommended when combined

Clinical monograph

How it works

It selectively blocks beta-1 adrenoceptors to reduce heart rate and cardiac output while exerting partial beta-2 agonism that contributes to peripheral vasodilatation.

Prescribing in practice

  • As with other beta-blockers, avoid abrupt withdrawal, which can precipitate rebound angina, arrhythmia or myocardial infarction; taper gradually.
  • Use with caution in patients with a history of obstructive airways disease, and avoid in unstable or uncontrolled heart failure.
  • Absorption is reduced when taken with food, so consistent timing in relation to meals is advised; consult current prescribing references.

Monitoring

Monitor blood pressure and heart rate, with clinical assessment for signs of heart failure or bronchospasm.

Counselling the patient

  • Do not stop this medicine suddenly without medical advice.
  • Report breathlessness, wheeze, marked dizziness or a very slow pulse.
  • Take it consistently with respect to meals as advised.

Evidence & guidelines

Beta-blockers are an established option in the management of hypertension within NICE guidance, generally after other first-line agents.

Reference: NICE NG136; RCP / EDS guidance; ESC HT; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.