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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Overactive-bladder pharmacotherapy

Obstetrics and gynaecology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Retention or serious medicine toxicity

New painful inability to void, severe abdominal distension, acute confusion, collapse, suspected angle-closure glaucoma, hypertensive crisis, arrhythmia, severe constipation with obstruction or hypersensitivity after an OAB medicine requires urgent assessment.

Action: Stop the suspected medicine when clinically appropriate, assess observations, cognition, abdomen, bladder residual, bowel function, blood pressure and ECG or eye symptoms as indicated, and obtain urgent medical, urological or ophthalmic care rather than waiting for a routine efficacy review.

Synopsis

Select and monitor antimuscarinic or beta-3-agonist treatment after appropriate behavioural care, using current UK doses, contraindications, interaction checks and structured review.

  • Use OAB medicine after bladder training has been offered and urgency or frequency remains troublesome; confirm infection, emptying and the diagnosis before escalation.
  • Explain that benefit varies, may take at least four weeks, and antimuscarinic dry mouth and constipation are common rather than evidence of an allergy.
  • Review frailty, cognition, glaucoma, gastric motility, bowel obstruction, myasthenia, residual urine, renal and hepatic function, blood pressure and total anticholinergic burden.
  • NICE advises the lowest-acquisition-cost suitable anticholinergic first; do not offer flavoxate, propantheline or imipramine for OAB or urinary incontinence.
  • Do not offer immediate-release oxybutynin to an older woman at higher risk of sudden physical or mental deterioration.
  • Mirabegron and vibegron are NICE options when antimuscarinics are unsuitable, insufficiently effective or cause unacceptable adverse effects, subject to their individual licences.
  • Review four weeks after every new medicine or dose change, sooner for adverse effects; review long-term treatment annually, or every six months when older than 75.
  • Stop ineffective treatment, switch within the pathway or refer after unsuccessful or intolerable medicine trials; retain bladder training and safety-netting.

Key red flags

Painful retention, rapidly rising residual, anuria or renal impairment after treatment requires urgent bladder and urological assessment.

A painful red eye, blurred vision or halos with an antimuscarinic raises concern for acute angle closure and needs emergency ophthalmic review.

Severe headache, chest pain, neurological symptoms or blood pressure at hypertensive-crisis levels while taking mirabegron requires immediate assessment.

New delirium, hallucinations, falls, severe constipation or heat intolerance may reflect clinically important anticholinergic toxicity.

Facial swelling, breathing difficulty, widespread rash or another serious hypersensitivity reaction requires emergency treatment.

Investigation priorities

01
Three-day bladder diaryFirst step

Confirm the storage pattern and establish baseline frequency, urgency, leakage and nocturia.

Management branches

Before prescribingConfirm indication and modifiers

Bladder training has not adequately controlled bothersome urgency or frequency.

  1. Recheck diary, urinalysis, emptying symptoms, fluid pattern, constipation, prolapse, neurological features and the person's treatment goal.
  2. Review cognition, frailty, falls, glaucoma, bowel disease, myasthenia, renal and hepatic function, blood pressure, pregnancy and every interacting medicine.
  3. Explain likely benefit, delayed onset, adverse effects and alternatives, then select the lowest-cost suitable anticholinergic or a NICE-indicated beta-3 agonist.

Key medicines

Oxybutynin immediate releaseStart 2.5 mg orally three times daily and titrate according to response and adverse effects up to 5 mg four times daily. In older or frail adults, start 2.5 mg twice daily and, if needed and tolerated, increase to 5 mg twice daily.Contraindicated in myasthenia gravis, narrow-angle glaucoma or a shallow anterior chamber, gastrointestinal obstruction or atony, severe ulcerative colitis or toxic megacolon, and bladder-outlet obstruction with retention risk. Review cognitive effects, constipation, heat intolerance, blurred vision and additive anticholinergic or CYP3A4 interactions.
SolifenacinTake 5 mg orally once daily; if needed and tolerated, increase to 10 mg once daily. Do not exceed 5 mg daily with creatinine clearance 30 mL/min or less, moderate hepatic impairment, or a potent CYP3A4 inhibitor.Contraindicated in urinary retention, severe gastrointestinal disease or toxic megacolon, myasthenia gravis, narrow-angle glaucoma risk, dialysis and severe hepatic impairment. Avoid a potent CYP3A4 inhibitor with severe renal or moderate hepatic impairment; consider QT-risk factors, constipation and cognitive or cumulative anticholinergic effects.
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Sources and review status8 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE NG123 medicines for overactive bladder
  • NICE TA290 mirabegron
  • NICE TA999 vibegron
  • Oxybutynin immediate-release UK product information
  • Solifenacin UK product information
  • Mirabegron UK product information
  • MHRA mirabegron severe-hypertension warning
  • Vibegron UK product information

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom