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Prescribing Information
TOVIAZ® (fesoterodine fumarate) extended-release tablets
How Supplied
Return to the TOVIAZ Product Center

TOVIAZ® (fesoterodine fumarate) extended-release tablets 4 mg are light blue, oval, biconvex, film-coated and engraved with “FS” on one side. They are supplied as follows:
Bottles of 30NDC 0069-0242-30
Bottles of 90NDC 0069-0242-68
Unit Dose Package of 100NDC 0069-0242-41

TOVIAZ® (fesoterodine fumarate) extended-release tablets 8 mg are blue, oval, biconvex, film-coated and engraved with “FT” on one side. They are supplied as follows:
Bottles of 30NDC 0069-0244-30
Bottles of 90NDC 0069-0244-68
Unit Dose Package of 100NDC 0069-0244-41

Storage

Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from moisture.

Manufactured by:
SCHWARZ PHARMA PRODUKTIONS-GmbH
08056 Zwickau, Germany

Distributed by:
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LAB-0381-3.0
Revised November 2008

TOVIAZ Safety Information

TOVIAZ® (fesoterodine fumarate) is indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency.

IMPORTANT SAFETY INFORMATION

TOVIAZ is contraindicated in patients with urinary retention, gastric retention, or uncontrolled narrow-angle glaucoma, and in patients with known hypersensitivity to the drug or its ingredients.

TOVIAZ tablets should be used with caution in patients with clinically significant bladder outlet obstruction, decreased gastrointestinal motility, controlled narrow-angle glaucoma, or myasthenia gravis. TOVIAZ is not recommended for use in patients with severe hepatic impairment.

The recommended starting dose of TOVIAZ is 4 mg once daily. Based upon individual response and tolerability, the dose may be increased to 8 mg once daily. Doses greater than 4 mg are not recommended in patients with severe renal insufficiency or in patients taking a potent CYP3A4 inhibitor; in patients taking a weak or moderate CYP3A4 inhibitor, careful assessment at 4 mg is advised prior to increasing to 8 mg.

The most frequently reported adverse events (≥4%) for TOVIAZ were: dry mouth (placebo, 7%; TOVIAZ 4 mg, 19%; TOVIAZ 8 mg, 35%) and constipation (placebo, 2%; TOVIAZ 4 mg, 4%; TOVIAZ 8 mg, 6%).

Download the Full U.S. Prescribing and Patient Information.

 

Please see full prescribing information.

TOVIAZ® (fesoterodine fumarate)

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