Uroblock Tablet is prescribed for managing symptoms of overactive bladder (OAB) such as frequent urination, urgency, and urge incontinence in adults.
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Uroblock contains Mirabegron, the first β3-adrenoceptor agonist, which works by relaxing the bladder’s detrusor muscle during the storage phase of urination. It increases bladder capacity by raising cyclic AMP levels through β3-adrenoceptor activation. Mirabegron also influences the sensory nervous system, improving control over urinary urgency and frequency.
Adults (including elderly): The usual starting dose is 25 mg once daily, with or without food. Based on response and tolerance, the dose may be increased to 50 mg once daily.
Renal or hepatic impairment:
Administration:
Take the tablet once daily with water. Swallow whole — do not crush, chew, or split the tablet.
With enzyme inhibitors: Ketoconazole (strong CYP3A/P-gp inhibitor) can increase Uroblock exposure by up to 1.8 times. No dose adjustment is usually needed, but in patients with mild-to-moderate renal or hepatic impairment using strong CYP3A inhibitors (e.g., ketoconazole, ritonavir, clarithromycin), limit the dose to 25 mg daily.
With enzyme inducers: Rifampicin and other CYP3A or P-gp inducers may reduce Mirabegron levels; however, no dose adjustment is typically required.
CYP2D6 substrates: Mirabegron moderately inhibits CYP2D6, which may increase levels of drugs like metoprolol, desipramine, or tricyclic antidepressants. Use caution when co-administered with medicines having a narrow therapeutic index.
P-gp substrates: Mirabegron slightly increases digoxin concentration; start with the lowest digoxin dose and monitor serum levels.
Other interactions: No significant interactions observed with tamsulosin, solifenacin, warfarin, metformin, or combined oral contraceptives.
Hypersensitivity to Mirabegron or any excipients
Severe, uncontrolled hypertension (systolic ≥180 mmHg or diastolic ≥110 mmHg)
Common adverse effects include tachycardia (1.2%) and urinary tract infection (2.9%). Rarely, atrial fibrillation (0.2%) has been reported. Most side effects are mild and transient.
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