When would you stop Myrbetriq (mirabegron) in a patient with a history of overactive bladder and recurrent urinary tract infections?

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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

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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