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Antimuscarinic Pregnancy: Safety in pregnancy and lactation not established, though no definite evidence of adverse consequences if taken during early pregnancy; no significant quantities found in milk. Should not be used during pregnancy unless the expected benefit outweighs any possible risk to the foetus.

Hyoscine hydrobromide

Brand names: Joy-Rides, Kwells, Scopoderm

Hyoscine hydrobromide (scopolamine) is an antimuscarinic agent used for motion sickness and, in palliative care, for the management of excessive respiratory secretions.

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: One tablet
Route: Oral
Frequency: Take 20 minutes before the journey; may be repeated in 6-8 hours if necessary
Max: Not more than three doses in 24 hours
SPC for Boots Travel Calm Tablets (motion sickness). Adults and children over 12 years: one tablet. Elderly: the normal adult dose is still appropriate. Take 20 minutes before the journey; may be repeated in 6-8 hours if necessary; no more than three doses in 24 hours. Children by age band (fraction of a tablet): 7-12 years half a tablet; 3-7 years quarter of a tablet; not to be taken by children under 3 years. May cause drowsiness; avoid alcohol.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Prostatic enlargement
  • Paralytic ileus
  • Pyloric stenosis
  • Closed angle glaucoma

Side effects

  • Drowsiness, dryness of the mouth, thirst
  • Mydriasis, loss of accommodation, photophobia, increased intra-ocular pressure
  • Flushing, dry skin
  • Bradycardia followed by tachycardia, with palpitations and arrhythmias
  • Difficulty in micturition; constipation (reduced GI tone and motility); occasionally vomiting, giddiness, staggering; confusion and hallucinations reported in children

Interactions

  • Other drugs with anticholinergic properties (amantadine, some antihistamines, butyrophenones, phenothiazines, tricyclic antidepressants): may enhance the effects of hyoscine
  • Alcohol: should be avoided
  • Other drugs given orally: absorption may be affected by hyoscine-induced reduction in gastric motility

Clinical monograph

How it works

It is a competitive antagonist at muscarinic acetylcholine receptors and, being centrally penetrant, also acts within the central nervous system to reduce the vestibular and emetic responses underlying motion sickness.

Prescribing in practice

  • Antimuscarinic effects can precipitate or worsen angle-closure glaucoma, urinary retention and confusion, so use with caution in the elderly and in those at risk.
  • It commonly causes drowsiness, dry mouth and blurred vision, and may impair the ability to drive or operate machinery.
  • Distinguish hyoscine hydrobromide from hyoscine butylbromide, which is a peripherally acting antispasmodic with different uses, to avoid prescribing confusion.

Monitoring

Routine laboratory monitoring is not required; monitor clinically for antimuscarinic adverse effects, particularly in older or susceptible patients.

Counselling the patient

  • This medicine can make you drowsy and cause dry mouth and blurred vision; do not drive or operate machinery if affected.
  • Avoid alcohol, which can increase drowsiness.

Evidence & guidelines

Hyoscine hydrobromide is an established treatment for motion sickness and for the symptomatic control of respiratory secretions in palliative care.

Reference: Palliative care formulary; 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.