Uridisitol 2mg is an antimuscarinic medicine indicated for Overactive Bladder Syndrome (OAB) in adults. It helps control urinary urgency, urge incontinence, urinary frequency and nocturia and is clinically proven to improve bladder control and quality of life.
Product Description
Active Ingredient: Tolterodine tartrate 2 mg (film-coated tablet).
Pack Size: 30 tablets (3 × 10 blister strips).
Appearance: White, round, biconvex tablets, debossed "J" on one side and "158" on the other.
Storage: Store below 30°C in original package.
Shelf Life: 24 months.
Mechanism of Action & Clinical Effects
Competitive antagonist of muscarinic receptors (M2 and M3) in detrusor muscle; active 5-hydroxymethyl metabolite contributes to effect. Inhibits involuntary bladder contractions, increases functional bladder capacity, delays initial urge and reduces urgency episodes.
Dosage & Administration
Standard Dose: 2 mg twice daily (1 tablet BID).
Reduced Dose: 1 mg twice daily (use in renal impairment CrCl ≤30 mL/min, moderate hepatic impairment, elderly with comorbidities, or when combined with potent CYP3A4 inhibitors).
Administration: With or without food; follow prescriber instructions.
Indications (SFDA Approved)
Urinary Urgency: Sudden compelling desire to pass urine difficult to defer.
Urge Incontinence: Involuntary leakage accompanied by or immediately preceded by urgency.
Urinary Frequency: ≥8 voids/24h.
Nocturia: Waking ≥1 time/night to void with impact on sleep.
Contraindications & Precautions
Absolute contraindications: Hypersensitivity to tolterodine/excipients, urinary retention, uncontrolled narrow-angle glaucoma, myasthenia gravis, severe ulcerative colitis/toxic megacolon.
Use with caution: Bladder outflow obstruction, GI disorders, renal/hepatic impairment, autonomic neuropathy.
Pregnancy/Lactation: Not recommended — insufficient human data.
Use with caution: Other anticholinergics, QT-prolonging agents, muscarinic agonists (e.g., bethanechol).
Clinical Evidence & Guidelines
Proven efficacy in landmark trials and real-world studies: 50–70% reduction in incontinence, 2–3 fewer daily voids, onset within 1–2 weeks and high patient satisfaction (70–80%). Recommended by AUA/SUFU (2024), EAU, NICE and CUA as an evidence-based option for OAB management..
Uridisitol 2mg is an antimuscarinic medicine indicated for Overactive Bladder Syndrome (OAB) in adults. It helps control urinary urgency, urge incontinence, urinary frequency and nocturia and is clinically proven to improve bladder control and quality of life.
Product Description
Active Ingredient: Tolterodine tartrate 2 mg (film-coated tablet).
Pack Size: 30 tablets (3 × 10 blister strips).
Appearance: White, round, biconvex tablets, debossed "J" on one side and "158" on the other.
Storage: Store below 30°C in original package.
Shelf Life: 24 months.
Mechanism of Action & Clinical Effects
Competitive antagonist of muscarinic receptors (M2 and M3) in detrusor muscle; active 5-hydroxymethyl metabolite contributes to effect. Inhibits involuntary bladder contractions, increases functional bladder capacity, delays initial urge and reduces urgency episodes.
Dosage & Administration
Standard Dose: 2 mg twice daily (1 tablet BID).
Reduced Dose: 1 mg twice daily (use in renal impairment CrCl ≤30 mL/min, moderate hepatic impairment, elderly with comorbidities, or when combined with potent CYP3A4 inhibitors).
Administration: With or without food; follow prescriber instructions.
Indications (SFDA Approved)
Urinary Urgency: Sudden compelling desire to pass urine difficult to defer.
Urge Incontinence: Involuntary leakage accompanied by or immediately preceded by urgency.
Urinary Frequency: ≥8 voids/24h.
Nocturia: Waking ≥1 time/night to void with impact on sleep.
Contraindications & Precautions
Absolute contraindications: Hypersensitivity to tolterodine/excipients, urinary retention, uncontrolled narrow-angle glaucoma, myasthenia gravis, severe ulcerative colitis/toxic megacolon.
Use with caution: Bladder outflow obstruction, GI disorders, renal/hepatic impairment, autonomic neuropathy.
Pregnancy/Lactation: Not recommended — insufficient human data.
Use with caution: Other anticholinergics, QT-prolonging agents, muscarinic agonists (e.g., bethanechol).
Clinical Evidence & Guidelines
Proven efficacy in landmark trials and real-world studies: 50–70% reduction in incontinence, 2–3 fewer daily voids, onset within 1–2 weeks and high patient satisfaction (70–80%). Recommended by AUA/SUFU (2024), EAU, NICE and CUA as an evidence-based option for OAB management..