When to Discontinue Mirabegron (Myrbetriq)
Mirabegron should be discontinued immediately if severe uncontrolled hypertension develops (systolic ≥180 mmHg and/or diastolic ≥110 mmHg), if angioedema occurs, or if the patient develops worsening voiding symptoms or urinary retention, particularly in those with bladder outlet obstruction or concurrent antimuscarinic use. 1
Absolute Indications for Discontinuation
Cardiovascular Contraindications
- Stop immediately if severe uncontrolled hypertension develops (systolic BP ≥180 mmHg and/or diastolic BP ≥110 mmHg), as mirabegron is contraindicated in this setting 1
- Discontinue if dose-dependent blood pressure increases occur that cannot be managed with antihypertensive therapy, as mirabegron can cause mean increases of approximately 3.5/1.5 mmHg in systolic/diastolic BP 1
- In the small subset of patients (6.5%) who experience blood pressure elevation despite well-controlled baseline hypertension, stop mirabegron once increased BP is noted rather than adding additional antihypertensive agents 2
Hypersensitivity and Angioedema
- Discontinue immediately if angioedema of the face, lips, tongue, and/or larynx occurs, as this may be life-threatening, particularly with upper airway involvement 1
- Stop if any hypersensitivity reaction to mirabegron or tablet inactive ingredients develops 1
Urinary Retention and Voiding Dysfunction
- Patients should discontinue medication if worsening voiding symptoms or urinary stream is noted after initiation, as recommended by the European Association of Urology for men with lower urinary tract symptoms 3
- Stop if urinary retention develops, particularly in patients with bladder outlet obstruction or those taking concurrent muscarinic antagonist medications 1
- Monitor post-void residual volume regularly and discontinue if clinically significant increases occur 3
Relative Indications for Discontinuation
Recurrent Urinary Tract Infections
- If a patient develops recurrent UTIs (≥3 episodes within 12 months) while on mirabegron, discontinue the medication and evaluate for underlying anatomical abnormalities or complicated UTI risk factors 3
- The most frequent adverse events with mirabegron include UTIs, and if these become recurrent, the medication should be stopped to allow proper evaluation 3, 1
- Consider that recurrent UTIs may indicate underlying bladder dysfunction, high post-void residuals, or other structural abnormalities that warrant imaging and further workup before continuing any OAB therapy 3
Treatment Failure
- Discontinue if inadequate symptom control persists after 4-8 weeks at the 50 mg dose, as this represents the maximum recommended dose and further escalation is not indicated 4
- Consider stopping if no meaningful improvement in OAB symptoms (frequency, urgency, incontinence episodes) is observed by week 4-8, as efficacy should be evident by this timeframe 1
Intolerable Adverse Effects
- Stop if patients develop intolerable headache, nasopharyngitis, or other common adverse effects that significantly impact quality of life 3
- Discontinue if patients experience rare but serious skin reactions or kidney stones 5
Special Population Considerations
Drug Interactions Requiring Discontinuation
- Stop mirabegron if patients require initiation of narrow therapeutic index CYP2D6 substrates (thioridazine, flecainide, propafenone) that cannot be adequately monitored, as mirabegron is a moderate CYP2D6 inhibitor 1
- Consider discontinuation if patients develop cardiac arrhythmias, especially tachycardia, particularly when combined with antimuscarinic drugs due to additive cardiac effects 5
Pregnancy and Lactation
- Discontinue if pregnancy is confirmed or suspected, as there is lack of clinical safety data in pregnant women 5
Surgical Considerations
- Stop mirabegron if patients require cataract surgery and are on concurrent alpha-1 blockers due to increased risk of intraoperative floppy iris syndrome 3
Common Pitfalls to Avoid
- Do not continue mirabegron indefinitely without periodic blood pressure monitoring, especially during initial treatment, as dose-dependent BP increases may develop insidiously 1
- Do not assume UTIs are unrelated to OAB therapy—recurrent infections warrant medication discontinuation and comprehensive urologic evaluation 3
- Do not add additional antihypertensive medications to manage mirabegron-induced hypertension—instead, discontinue mirabegron as the primary intervention 2
- Do not overlook worsening voiding symptoms as a reason to stop therapy, particularly in men with baseline lower urinary tract symptoms or elevated post-void residuals 3