What is the usual dose of cabergoline?

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Usual Dose of Cabergoline

The standard initial dose of cabergoline is 0.25 mg twice weekly, with gradual titration up to 1-2 mg per week for most patients with hyperprolactinemia. 1

Initial Dosing

  • Start with 0.25 mg twice weekly (0.5 mg total per week) for initiation of therapy 1, 2
  • This low starting dose minimizes gastrointestinal intolerance and postural hypotension 2

Dose Titration

  • Increase by 0.25 mg twice weekly (0.5 mg total per week increments) based on serum prolactin levels 1
  • Do not increase dosage more rapidly than every 4 weeks to allow adequate assessment of response at each dose level 1
  • The typical therapeutic range is 1-2 mg per week for most patients with prolactinomas 2, 1

Standard Maintenance Dosing

  • For microprolactinomas or idiopathic hyperprolactinemia: 0.5-1 mg per week is often sufficient 3
  • For macroprolactinomas: 1-2 mg per week is typically required 3
  • The FDA-approved maximum is 1 mg twice weekly (2 mg total per week) 1

Higher Doses for Resistant Cases

  • For dopamine agonist resistance: graduated dose increments up to 3.5 mg per week can be offered 2
  • In exceptional cases: doses up to 7 mg per week may be used, though evidence for additional benefit above 3.5 mg/week is limited 2
  • Resistance is defined as failure to normalize prolactin and/or achieve <50% tumor reduction after 3-6 months at maximally tolerated doses (at least 2 mg/week) 2

Cardiac Monitoring Requirements

  • Baseline echocardiogram should be obtained before initiating treatment 1, 4
  • For doses >2 mg per week: annual echocardiography with cardiac auscultation is required 4, 2
  • For doses ≤2 mg per week: echocardiographic surveillance every 5 years 4, 2

Dose Reduction and Discontinuation

  • After serum prolactin normalizes for 6 months, cabergoline may be discontinued with periodic monitoring 1
  • Once adequate control is achieved, the dose can often be reduced by 50% while maintaining efficacy 3

Important Caveats

  • Small nocturnal dose increments help reduce gastrointestinal side effects 2
  • Psychological side effects (mood changes, impulse control disorders) are dose-independent and may occur at any dose 2
  • The durability of efficacy beyond 24 months has not been established by the FDA 1

References

Guideline

Cabergoline Dosage and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cabergoline in the treatment of hyperprolactinemia: a study in 455 patients.

The Journal of clinical endocrinology and metabolism, 1999

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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