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

    Avoid

    Hypertensive 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Spotted something out of date?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.

For educational use only

Not medical advice. Verify dosing against the BNF and your local trust guidelines before prescribing.