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.