Dopamine Agonist (D2 Receptor) / Prolactin Inhibitor
Pregnancy: Can be continued in pregnancy if macroprolactinoma with high expansion risk — more pregnancy safety data than cabergoline. Stop at conception in microprolactinoma. Seek specialist advice.
Bromocriptine
Brand names: Parlodel
Adult dose
Dose: Hyperprolactinaemia: 1–1.25mg at bedtime initially; increase gradually every 2–4 weeks to 7.5–15mg daily in divided doses. Acromegaly (adjunct): 10–30mg daily in divided doses. Parkinson's disease: 1.25mg OD increasing to 10–40mg daily (specialist neurology dosing).
Route: Oral
Frequency: Two to three times daily (with meals)
Max: 30mg daily (hyperprolactinaemia); 40mg daily (Parkinson's — specialist)
Take with food at bedtime initially to reduce nausea and first-dose hypotension. Now largely superseded by cabergoline for hyperprolactinaemia due to twice-weekly dosing advantage and better tolerability. Still used in some cases of resistance, during pregnancy (more safety data than cabergoline), and in acromegaly as adjunct.
Paediatric dose
Route: Oral
Frequency: Two to three times daily
Max: Individualised
Seek specialist paediatric endocrinology opinion. Used in adolescent prolactinomas — cabergoline generally preferred where available.
Dose adjustments
Renal
No specific dose adjustment — use with caution in renal impairment.
Hepatic
Severe hepatic impairment: reduce dose — extensively hepatically metabolised.
Clinical pearls
- More safety data in pregnancy than cabergoline — some centres use bromocriptine preferentially in women with prolactinoma who are pregnant or planning pregnancy
- Postpartum: bromocriptine used historically for lactation suppression but withdrawn from this indication in most countries due to hypertension/stroke risk — use cabergoline 1mg single dose instead
- Nausea management: always start at lowest dose at bedtime; titrate very slowly over weeks — tolerance develops
- Acromegaly: bromocriptine reduces GH in ~10–20% of acromegaly patients (less effective than somatostatin analogues); used as adjunct
Contraindications
- Hypersensitivity to bromocriptine or ergot alkaloids
- Uncontrolled hypertension
- History of puerperal psychosis
- Cardiac valvulopathy (high-dose use)
- History of fibrotic disorders
Side effects
- Nausea and vomiting (very common)
- Dizziness, orthostatic hypotension
- Headache
- Nasal congestion
- Raynaud's phenomenon
- Impulse control disorders
- Retroperitoneal / pleuropulmonary fibrosis (high doses)
- Psychiatric symptoms (high doses — Parkinson's use)
Interactions
- Antipsychotics, metoclopramide — antagonise effect
- Antihypertensives — additive hypotension
- Erythromycin — increases bromocriptine levels
Monitoring
- Serum prolactin
- Blood pressure (particularly at initiation)
- MRI pituitary
- Visual fields (macroprolactinoma)
Reference: BNFc; BNF 90; Endocrine Society Prolactinoma Guidelines 2011. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- SMART Risk Score for Recurrent CVD · Cardiovascular Risk
- PCSK9 Inhibitor Eligibility Assessment · Lipid Management
- Immune-Related Adverse Events (irAE) -- GI Toxicity Colitis Grading · Oncology-Related GI
- irAE Hepatitis Grading (CTCAE) · Immunotherapy
- DIPSS — Dynamic International Prognostic Scoring System for Myelofibrosis · Cancer Prognosis
- BALL Score for Relapsed/Refractory CLL · Leukaemia
Pathways
- Diabetic Ketoacidosis (DKA) · JBDS 2013 / Joint British Diabetes Societies; NICE NG17
- Adult Hypoglycaemia (Treated Diabetes) · JBDS-IP (2023): Hospital Management of Hypoglycaemia
- Adrenal Crisis · Society for Endocrinology Emergency Guidance (2024)
- Type 2 Diabetes Management · NICE NG28 2022
- Hyperthyroidism Management · BTA / ETA 2018
- Adrenal Insufficiency · Society of Endocrinology / ESE 2016