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RUTH IS A 75-YEAR-OLD LONG-TERM CARE (LTC) RESIDENT STRUGGLING WITH UNTREATED OVERACTIVE BLADDER (OAB)

Impact of untreated OAB symptoms on Ruth's daily activities in the last 3+ months

  • Leakage episodes and skin irritation due to prolonged leakage exposure despite daily briefing
  • Frequent nighttime falls trying to get to the restroom
  • Family concerns about more frequent urinary tract infections and sacral wounds
  • Dysphagia impacts her ability to swallow medications
  • Unable to identify and report OAB symptoms due to dementia
patient image

Not an actual patient.

Comorbidities

  • Prediabetes
  • Hypertension
  • Dyslipidemia
  • Back pain
  • Osteoporosis
  • Depression
  • Atrial fibrillation
  • Gastroesophageal reflux disease (GERD)

Current medications

  • Metformin
  • Lisinopril
  • Simvastatin
  • Omeprazole
  • Alendronate
  • Venlafaxine
  • Metoprolol
  • Apixaban
  • Tramadol

Want to see how GEMTESA may be able to help your LTC residents?

 

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

GEMTESA is contraindicated in patients with known hypersensitivity to vibegron or any components of the product.

WARNINGS AND PRECAUTIONS

Urinary Retention

Urinary retention has been reported in patients taking GEMTESA. The risk of urinary retention may be increased in patients with bladder outlet obstruction and also in patients taking muscarinic antagonist medications for the treatment of OAB. Monitor patients for signs and symptoms of urinary retention, particularly in patients with bladder outlet obstruction and patients taking muscarinic antagonist medications for the treatment of OAB. Discontinue GEMTESA in patients who develop urinary retention.

ADVERSE REACTIONS

Most common adverse reactions (2%) reported with GEMTESA were headache, urinary tract infection, nasopharyngitis, diarrhea, nausea, and upper respiratory tract infection.

 

INDICATIONS AND USAGE

GEMTESA® is a beta-3 adrenergic agonist indicated for the treatment of overactive bladder (OAB) with symptoms of urge urinary incontinence, urgency, and urinary frequency in adults.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

GEMTESA is contraindicated in patients with known hypersensitivity to vibegron or any components of the product.

WARNINGS AND PRECAUTIONS

Urinary Retention

Urinary retention has been reported in patients taking GEMTESA. The risk of urinary retention may be increased in patients with bladder outlet obstruction and also in patients taking muscarinic antagonist medications for the treatment of OAB. Monitor patients for signs and symptoms of urinary retention, particularly in patients with bladder outlet obstruction and patients taking muscarinic antagonist medications for the treatment of OAB. Discontinue GEMTESA in patients who develop urinary retention.

ADVERSE REACTIONS

Most common adverse reactions (2%) reported with GEMTESA were headache, urinary tract infection, nasopharyngitis, diarrhea, nausea, and upper respiratory tract infection.

Please see full Prescribing Information.

You are encouraged to report side effects and product complaints associated with GEMTESA by calling 1-833-876-8268.

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GEMTESA, and the GEMTESA logo are trademarks of Urovant Sciences GmbH, registered in the U.S. and in other countries.

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