הממלכה המאוחדת - אנגלית - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - fesoterodine fumarate - modified-release tablet - 4mg

הממלכה המאוחדת - אנגלית - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - fesoterodine fumarate - modified-release tablet - 8mg

הממלכה המאוחדת - אנגלית - MHRA (Medicines & Healthcare Products Regulatory Agency)

dr reddy's laboratories (uk) ltd - fesoterodine fumarate - modified-release tablet - 4mg

הממלכה המאוחדת - אנגלית - MHRA (Medicines & Healthcare Products Regulatory Agency)

dr reddy's laboratories (uk) ltd - fesoterodine fumarate - modified-release tablet - 8mg

יפן - אנגלית - すりの適正使用協議会 RAD-AR Council, Japan

pfizer pharmaceuticals inc. - fesoterodine fumarate - pale blue tablet, major axis: 13 mm, minor axis: 6.5 mm, thickness: 4.8 mm

יפן - אנגלית - すりの適正使用協議会 RAD-AR Council, Japan

pfizer pharmaceuticals inc. - fesoterodine fumarate - blue tablet, major axis: 13 mm, minor axis: 6.5 mm, thickness: 4.8 mm

בלגיה - אנגלית - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

teva pharma belgium sa-nv - desfesoterodine succinate 3,5 mg - eq. desfesoterodine 2,6 mg - prolonged-release tablet - 3,5 mg - desfesoterodine succinate 3.5 mg - desfesoterodine

בלגיה - אנגלית - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

teva pharma belgium sa-nv - desfesoterodine succinate 7 mg - eq. desfesoterodine 5,2 mg - prolonged-release tablet - 7 mg - desfesoterodine succinate 7 mg - desfesoterodine

ארצות הברית - אנגלית - NLM (National Library of Medicine)

cardinal health - tolterodine tartrate (unii: 5t619tqr3r) (tolterodine - unii:whe7a56u7k) - tolterodine tartrate 2 mg - detrol la capsules is indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency [see clinical studies (14) ]. detrol la is contraindicated in patients with urinary retention, gastric retention, or uncontrolled narrow-angle glaucoma. detrol la is also contraindicated in patients with known hypersensitivity to the drug or its ingredients, or to fesoterodine fumarate extended-release tablets which, like detrol la, are metabolized to 5-hydroxymethyl tolterodine [see warnings and precautions (5.2) (5.3), (5.4) ]. pregnancy category c. at approximately 9–12 times the clinical exposure to the pharmacologically active components of detrol® la, no anomalies or malformations were observed in mice (based on the auc of tolterodine and its 5-hmt metabolite at a dose of 20 mg/kg/day). at 14–18 times the exposure (doses of 30 to 40 mg/kg/day) in mice, tolterodine has been shown to be embryolethal and reduce fetal weight, and increase the incidence of fetal abno

ארצות הברית - אנגלית - NLM (National Library of Medicine)

remedyrepack inc. - tolterodine tartrate (unii: 5t619tqr3r) (tolterodine - unii:whe7a56u7k) - tolterodine tablets are indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency. tolterodine tablets are contraindicated in patients with urinary retention, gastric retention, or uncontrolled narrow-angle glaucoma. tolterodine tablets are also contraindicated in patients who have demonstrated hypersensitivity to the drug or its ingredients, or to fesoterodine fumarate extended-release tablets which, like tolterodine tablets, are metabolized to 5-hydroxymethyl tolterodine.