Second-lineAldomet
Methyldopa
Central α2-adrenergic agonist
Oldest, most-studied antihypertensive — safe but sedating.
Oral
First-line for
- Chronic HTN pre-pregnancy (continue if controlled)
- Second-line when Labetalol & Nifedipine unsuitable
Mechanism
Converted to α-methylnoradrenaline → stimulates central α2 receptors → ↓ sympathetic outflow → ↓ SVR & BP.
“DOPA-D” — Methyldopa cautions
- D — Depression (avoid in PND history)
- O — Orthostatic hypotension
- P — Positive Coombs test (haemolysis)
- A — Abnormal LFTs / hepatitis
- D — Drowsiness / sedation
Dosing
- Start
- 250 mg BD–TDS
- Titration
- Increase every 2 days
- Max
- 3 g/day in divided doses
Contraindications
- AbsoluteActive liver disease, prior methyldopa-induced hepatitis
- AbsolutePhaeochromocytoma
- AbsoluteCurrent or past depression (RCOG — avoid postpartum)
Side effects
- Sedation, depression
- Dry mouth
- Postural hypotension
- Haemolytic anaemia (+ve Coombs)
- Hepatitis (rare)
Fetal & maternal notes
- • Excellent safety record — used for >50 years.
- • No teratogenicity, no FGR signal.
- • STOP within 48 h postpartum — risk of postnatal depression.
Key interactions
MAOIs
AvoidHypertensive crisis — avoid
Iron salts
Caution↓ methyldopa absorption
Lithium
Caution↑ lithium toxicity
Clinical pearls
- 💡 Always swap to alternative within 2 days postpartum.
- 💡 Check LFTs and FBC at baseline, 6 and 12 weeks.
Content last reviewed: REPLACE_ME (e.g. 2026-07)
Spotted something out of date? See our disclaimer or use Report an Error above.