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Laxative Pregnancy: Limited pregnancy data indicate no malformative or foeto/neonatal toxicity; may be used during pregnancy if necessary. Can be used during breast-feeding.

Lactulose

Brand names: Duphalac, Lactugal

Lactulose, an osmotic laxative, used to treat constipation, which is common in pregnancy and the postnatal period, and is regarded as a suitable option in these settings.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Starting dose 15-45 ml daily (10-30 g lactulose); maintenance dose 15-30 ml daily (10-20 g lactulose)
Route: Oral (may be given diluted or undiluted)
Frequency: As a single daily dose or in 2-3 divided doses; titrate to clinical response
Same dosing as for constipation, relevant to constipation in pregnancy. Limited data in pregnant patients indicate neither malformative nor foeto/neonatal toxicity, and animal studies show no harmful effects on pregnancy or development — may be used during pregnancy if necessary. Can be used during breast-feeding. Titrate to response; drink 1.5-2 L fluid/day; reduce the dose if diarrhoea occurs. Paediatric bands (SPC): adolescents over 14 years as adults; children 7-14 years 15 ml daily (10 g); use the bottle presentation for children up to 6 years.

Dose adjustments

Renal

No special dosage recommendations in renal impairment (or in hepatic impairment).

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to the active substance or to any of the excipients
  • Galactosaemia
  • Acute inflammatory bowel disease (ulcerative colitis, Crohn's disease)
  • Gastrointestinal obstruction or subocclusive syndromes
  • Digestive perforation or risk of digestive perforation
  • Painful abdominal syndromes of undetermined cause

Side effects

  • Flatulence (very common; usually settles after a few days)
  • Abdominal pain (very common)
  • Nausea and vomiting (common)
  • Diarrhoea if dosed too high (may include electrolyte imbalance)
  • Not known: hypersensitivity reactions, rash, pruritus, urticaria

Interactions

  • May increase the potassium loss caused by other drugs (e.g. thiazides, corticosteroids, amphotericin B)
  • Cardiac glycosides — effect may be increased through lactulose-induced potassium deficiency
  • Colonic pH-dependent release drugs (e.g. 5-ASA / mesalazine) may be inactivated by the lower colonic pH

Clinical monograph

How it works

Lactulose is a non-absorbed disaccharide fermented by colonic bacteria into organic acids that draw water into the bowel by osmosis, softening stool and stimulating peristalsis.

Prescribing in practice

  • As it is not absorbed systemically it is considered suitable in pregnancy and breastfeeding, making it a reasonable first-line osmotic laxative in these groups.
  • Onset of effect is gradual over a day or more rather than immediate, so expectations should be set accordingly.
  • Flatulence, bloating and abdominal cramps are common, particularly when starting treatment.

Monitoring

Routine monitoring is not required; review the response and adjust the dose to produce a soft, comfortable stool.

Counselling the patient

  • It may take a day or two to work, so do not increase the dose too quickly.
  • Maintain a good fluid intake while taking it.
  • Some bloating and wind are common at first and usually settle.

Evidence & guidelines

General prescribing guidance supports lactulose as a suitable osmotic laxative in pregnancy and breastfeeding given its lack of systemic absorption.

Reference: RCOG (2022) Obstetric pharmacology; NICE CG190; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.