Vesicare (solifenacin succinate) tablets Information for Healthcare Professionals
Information for Consumers
 
 
 
WHAT IS OAB? TREATING OAB ABOUT VESIcare PATIENTS ON VESIcare PROFESSIONAL RESOURCES
Compliance Side Effects Dosing Tolerability  
Patients on VESIcare
Compliance
81% of patients remained on VESIcare throughout a 40-week, open-label extension study.17

Completion and Discontinuation Rates in a 40-week, Open-label, Safety Study
Completion and discontinuance rates (%)

Patients who completed two 12-week, double-blind, placebo-controlled, randomized studies had the option to enter a 40-week, open-label extension study with flexible dosing of VESIcare. 91% (1637/1802) of eligible patients chose to enter the 40-week safety study17.
Patients received VESIcare 5 mg once daily for the first 4 weeks of the 40-week extension study. At subsequent visits, based on efficacy and tolerability, patients were offered the option to adjust the dose between 5 mg and 10 mg. 81% of patients remained on VESIcare throughout an open-label extension study.

To help ensure patient compliance with a treatment course that includes VESIcare, you might consider telling your patients the following:

  • VESIcare improves incontinence, urgency, and frequency.15 No OAB medication—VESIcare included—is indicated for nocturia.
  • All OAB medications, including VESIcare, take time to work. Symptom improvement might be seen in as little as two weeks, or it might take more time.21
  • Once symptoms improve, patients should continue to take one VESIcare dose once daily, to ensure that the improvements persist.

Treating OAB takes time. It is important that your patients know this from the beginning of treatment, so that they continue to follow the course of treatment that you prescribe even if, after a few days, they have noticed no significant improvement in symptoms.

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Learn more about VESIcare with an interactive online experience. Click here.
Patient Resources
VESIcare can help you and your patients address overactive bladder together. The Fresh Approach Kit includes a bladder checklist, a bladder diary, and a list of questions for patients to ask physicians. Download Fresh Approach Kit.

The Vantage ProgramSM provides valuable information and exclusive savings for your patients. Click here to learn more.

Important Safety Information

VESIcare tablets are indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. The recommended dose of VESIcare is 5 mg once daily. If the 5-mg dose is well tolerated, the dose may be increased to 10 mg once daily.

As with other anticholinergic agents, VESIcare is contraindicated in patients with urinary retention, gastric retention, uncontrolled narrow-angle glaucoma, and in patients with hypersensitivity to the product.

As with other anticholinergic agents, VESIcare should be administered with caution to patients with bladder outflow obstruction, decreased gastrointestinal motility, controlled narrow-angle glaucoma, or reduced renal or hepatic function. Doses of VESIcare higher than 5 mg are not recommended in patients with severe renal impairment, moderate hepatic impairment, or when administered with ketoconazole or other potent CYP3A4 inhibitors. Use of VESIcare in patients with severe hepatic impairment is not recommended.

In placebo-controlled studies, the most common adverse events reported by patients were dry mouth (10.9%, 27.6%, 4.2%), constipation (5.4%, 13.4%, 2.9%), blurred vision (3.8%, 4.8%, 1.8%), and dyspepsia (1.4%, 3.9%, 1.0%) with VESIcare 5 mg, 10 mg, and placebo, respectively.

The overall rate of serious adverse events was 2%. For the 10-mg dose, three intestinal serious adverse events were reported (one fecal impaction, one colonic obstruction, and one intestinal obstruction). For the 5-mg dose, one case of angioneurotic edema was reported.

Complete Prescribing Information for VESIcare

Astellas
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