This study is a Post-Marketing Surveillance study in Korea to evaluate the safety and efficacy of botulinum toxin Type A to treat urinary incontinence in patients with neurogenic detrusor overactivity (NDO) or overactive bladder (OAB) not adequately controlled by anticholinergic drugs.
Inclusion Criteria:
-Patients with urinary incontinence due to NDO or OAB treated with BOTOX® as per local standard of care in clinical practice.
Exclusion Criteria:
-None.