Cabergoline Dosage for Lactation Inhibition in Adult Females
For lactation inhibition in adult females, a single oral dose of 1 mg cabergoline is recommended, which can be administered either as a single dose or divided as 0.25 mg twice daily for 2 days to minimize side effects. 1, 2
Dosing Regimens
- Single dose administration: 1 mg cabergoline as a single oral dose within 24-27 hours after delivery 2
- Divided dose administration: 0.25 mg twice daily for 2 days (total 1 mg) to minimize adverse events while maintaining efficacy 1, 3
Efficacy
- Cabergoline successfully inhibits lactation in approximately 78-94% of women 1, 4
- The prolactin-lowering effect begins rapidly and persists for up to 14-21 days after a single dose 5, 2
- Cabergoline demonstrates superior efficacy compared to alternative treatments:
Advantages Over Other Treatments
- Simpler administration: Single dose vs. bromocriptine's 14-day regimen 2
- Longer duration of action: Prolactin-lowering effects persist for up to 21 days 5
- Lower rebound rate: Significantly fewer cases of rebound breast symptoms compared to bromocriptine (3.7% vs 16.9%) 2
- Better tolerability: Although side effects occur in about 31% of patients, they are generally mild 1
Side Effects and Monitoring
- Common side effects include nausea, vomiting, headache, and dizziness 5
- While cabergoline has more adverse effects than pyridoxine (31% vs 9%), these are typically mild and well-tolerated 1
- Caution should be exercised in patients with hypertensive disorders, fibrotic, cardiac, or hepatic diseases, as cabergoline may be contraindicated in these conditions 1
Clinical Considerations
- Cabergoline is considered the drug of choice for lactation inhibition due to its efficacy, convenience, and tolerability profile 5, 2
- For women with contraindications to cabergoline, pyridoxine (200 mg three times daily for 7 days) may be considered as an alternative, though it has lower efficacy 1
- The timing of administration is important - cabergoline should be given within 27 hours after delivery for optimal results in preventing lactation 2
Special Populations
- Limited data exists on cabergoline's teratogenic potential in humans, with 10 congenital abnormalities reported in 199 cabergoline-associated pregnancies 5
- Due to limited experience with cabergoline in pregnancy, it should not be considered first-line therapy for treating infertility associated with hyperprolactinemia 5