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Our resource library covers a variety of topics including access, prior authorizations, and patient education

Cigna and Express Scripts Medicare® Flashcard

Find out about GEMTESA Part D coverage at ESI/Cigna for 2022.

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GEMTESA Get Set Tracker

Patients can explore lifestyle tips to help manage OAB, worksheets to identify personal and treatment goals, and track progress with GEMTESA.

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GEMTESA Patient Brochure

Patients can learn about OAB, prevalence, lifestyle tips, and how GEMTESA may help reduce the symptoms of OAB.

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GEMTESA Prior Authorization Checklist

Prepare for prior authorizations with this checklist and find out more about access resources from Patient Connect Support.

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Low-income Subsidy Information

Get the facts on the Medicare Extra Help Program for people with limited income/resources.

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Pharmacy-initiated Prior Authorization Requests Information

Find additional details about completing a pharmacy-initiated prior authorization request.

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Prior Authorizations and Medical Exceptions Information

See insights and support when additional steps are needed to obtain GEMTESA.

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TRICARE® Formulary Card

Explore the position of GEMTESA on the TRICARE Uniform formulary and learn about the requirements for beneficiaries.

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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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is a trademark of Sumitomo Pharma Co., Ltd., used under license. SUMITOMO PHARMA is a trademark of Sumitomo Pharma Co., Ltd., used under license. SUMITOMO is a registered trademark of Sumitomo Chemical Co., Ltd., used under license. Sumitomo Pharma America, Inc. is a U.S. subsidiary of Sumitomo Pharma Co., Ltd.

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

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