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🇪🇺EU · EMAAuthorisedATC: G04BD12

Betmiga(Mirabegron)

Urinary Bladder, Overactive

Marketing Authorisation Holder: Astellas Pharma Europe B.V.

EMA Authorisation: 20/12/2012

INN: mirabegron

Indication

Overactive bladder in adults  Betmiga prolonged-release tablets are indicated for symptomatic treatment of urgency, increased micturition frequency and/or urgency incontinence as may occur in adult patients with overactive bladder (OAB) syndrome.  Neurogenic detrusor overactivity in the paediatric population  Betmiga prolonged release tablets are indicated for treatment of neurogenic detrusor overactivity (NDO) in paediatric patients aged 3 to less than 18 years.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.