Vibegron
Brand names: Obgemsa
Vibegron is an oral beta-3 adrenergic receptor agonist used for the symptomatic treatment of overactive bladder, including urgency, urgency incontinence and frequency.
Adult dose
Dose auto-extracted from 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
- Known hypersensitivity to vibegron or any component of the product — hypersensitivity reactions, such as angioedema, have occurred
Side effects
- Headache
- Urinary tract infection
- Nasopharyngitis
- Diarrhoea and nausea
- Upper respiratory tract infection
- Urinary retention — a clinically significant adverse reaction; risk may be greater with bladder outlet obstruction or concurrent muscarinic antagonists; discontinue if it develops
- Angioedema of the face and/or larynx (may occur hours after the first or after multiple doses; may be life-threatening)
Interactions
- Digoxin — vibegron increases digoxin maximal concentration (Cmax) and systemic exposure (AUC); measure serum digoxin concentrations before initiating vibegron, monitor during therapy and use them to titrate the digoxin dose, and continue monitoring on discontinuation of vibegron, adjusting the digoxin dose as needed
Clinical monograph
How it works
It selectively stimulates beta-3 adrenoceptors in the detrusor muscle, promoting bladder smooth muscle relaxation during the storage phase to increase bladder capacity.
Prescribing in practice
- Avoid in patients with severe uncontrolled hypertension and monitor blood pressure, as beta-3 agonists can raise it.
- It offers an alternative to antimuscarinics, which may be useful where anticholinergic burden is a concern.
- Review response after an adequate treatment period and reassess if symptoms do not improve.
Monitoring
Monitor blood pressure before and periodically during treatment, particularly in patients with pre-existing hypertension.
Counselling the patient
- It helps reduce the sudden urge to pass urine and may take some weeks to reach full effect.
- Report any difficulty passing urine or new high blood pressure symptoms.
- Swallow tablets whole and take regularly as prescribed.
Evidence & guidelines
Use is supported by randomised controlled trials demonstrating reduced micturition frequency and urgency incontinence episodes in overactive bladder.
Reference: SmPC; 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.