BetmigaTM (mirabegron) is indicated for symptomatic treatment of urgency, increased micturition frequency and/or urgency incontinence as may occur in adult patients with overactive bladder (OAB) syndrome and for treatment of neurogenic detrusor overactivity (NDO) in paediatric patients aged 3 to <18 years.1
OAB in men is often linked to other urological conditions, such as benign prostatic enlargement or obstruction, neurogenic bladder or complications from prostate cancer treatment3
Men with LUTS often present with a combination of symptoms4
Post-micturition symptoms in combination with other symptoms are included in the percentages. Figure adapted from Sexton CC, et al. 2009.4
References
1.BETMIGA (mirabegron) prolonged-release tablets. Summary of Product Characteristics 2. Zhang L. et al. Int Urogynecology J. 2025;36:1547–1566 3. Blaivas, JG. et al. J Urol. 2009;182(6):2814-7 4. Sexton CC et al. EpiLUTS. BJU International. 2009 Apr;103:12–23. 5. Kakizaki H et al. European urology focus. 2020 Jul 1;6(4):729–37. 6. Kaplan SA et al. (PLUS). 2020 Jan 2;203(6):1163–71.
Adverse events should be reported. For Ireland, Healthcare professionals are asked to report any suspected adverse reactions via: HPRA Pharmacovigilance, Website: www.hpra.ieor Astellas Pharma Co. Ltd. Tel:+353 1 467 1555, E-mail: irishdrugsafety@astellas.com.
MAT-IE-BET-2026-00017 Sep 2026