Can cabergoline cause mood disorders?

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Cabergoline and Mood Disorders

Yes, cabergoline can cause mood disorders including depression, anxiety, mania, and other psychiatric symptoms as documented side effects. 1, 2, 3

Evidence for Cabergoline-Induced Mood Disorders

FDA-Documented Psychiatric Side Effects

  • Depression occurs in approximately 3% of patients taking cabergoline for hyperprolactinemic disorders 1
  • Other psychiatric adverse events documented in the FDA label include:
    • Anxiety (1%)
    • Insomnia (1%)
    • Nervousness (1%)
    • Impaired concentration (1%)
    • Somnolence (2%) 1

More Serious Psychiatric Adverse Events

  • Post-marketing surveillance has identified additional psychiatric concerns:
    • Impulse control/compulsive behavior symptoms
    • Hypersexuality
    • Increased libido
    • Pathological gambling
    • Aggression
    • Psychotic disorders 1

Case Reports and Clinical Evidence

  • The first documented case of cabergoline-induced mania was reported in 2016 3
  • Psychotic exacerbation has been observed in schizophrenic patients receiving cabergoline for antipsychotic-induced hyperprolactinemia 4
  • Dose-independent psychological intolerance (mood changes, depression, aggression, hypersexuality and impulse control disorder) has been reported in both adults and children/adolescents 2

Mechanism of Action and Risk Factors

Cabergoline is a potent dopamine D2 receptor agonist with a very long duration of action. This prolonged effect offers advantages for treatment but may complicate management of psychiatric side effects:

  • The long elimination half-life (up to 21 days after a single dose) means psychiatric side effects may persist even after discontinuation 3
  • Dopaminergic stimulation is a known risk factor for psychiatric symptoms, particularly in vulnerable individuals 3
  • The frequency of psychological adverse events may be higher in children and adolescents than in adults 2

Management Recommendations

Monitoring and Prevention

  • Before initiating cabergoline:
    • Screen for history of mood disorders, impulse control problems, or psychotic disorders
    • Consider lower starting doses in patients with psychiatric history
    • Start with small nocturnal dose increments to reduce adverse effects 2

If Mood Disorders Develop

  • For mild symptoms:

    • Consider dose reduction if clinically feasible
    • Monitor more frequently for symptom progression
  • For moderate to severe symptoms:

    • Consider discontinuation of cabergoline
    • Evaluate for alternative treatments for hyperprolactinemia
    • In prolactinoma patients with intolerable psychiatric side effects, surgical intervention may be warranted 2

Special Populations

  • Use with extreme caution in patients with:
    • Pre-existing psychiatric conditions
    • History of impulse control disorders
    • Concurrent medications that affect dopaminergic systems

Clinical Pearls

  • The psychiatric side effects of cabergoline are often dose-independent, meaning they can occur at any dosage level 2
  • Symptoms may emerge at any point during treatment, not just during initiation
  • Some patients who cannot tolerate cabergoline may be able to tolerate bromocriptine, though bromocriptine has a higher overall side effect profile 5
  • The risk-benefit ratio should be carefully considered in patients with or at risk for psychiatric disorders 3

In susceptible individuals, cabergoline can trigger significant mood disorders including depression, anxiety, mania, and psychosis, requiring careful patient selection, monitoring, and prompt intervention if psychiatric symptoms emerge.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Cabergoline-induced manic episode: case report.

Therapeutic advances in psychopharmacology, 2016

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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