Hyoscine Butylbromide 10 mg (Solipecan Subsuccinate)
Solifenacin Succinate 10mg
Tablet · Prescription medication
Huons Co., Ltd.
MFDS item code 201600696 · Approved 2016.02.03
This product's status changed to Expired on 2026.02.03. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Treatment of symptoms of overactive bladder (such as frequent urination and urinary urgency)
Used to treat the major symptoms of overactive bladder such as urgency incontinence, frequent urination, and urinary urgency.
The usual recommended dose for adults (including elderly patients) is 5mg once daily. If necessary, the dose may be increased to a maximum of 10mg once daily. This medicine may be taken with or without food and should be swallowed whole with water. Dosage adjustment is required for the following patients. 1. Patients with renal impairment No dose adjustment is necessary in patients with mild or moderate renal impairment (creatinine clearance>30ml/min). Use with caution in patients with severe renal impairment (creatinine clearance≤30ml/min), and do not exceed 5mg once daily 2. Patients with hepatic impairment No dose adjustment is necessary in patients with mild hepatic impairment. Use with caution in patients with moderate hepatic impairment (Child-Pugh class B), and do not exceed 5mg once daily. 3. Patients receiving potent cytochrome P450 3A4 (CYP3A4) inhibitors For patients receiving ketoconazole or another potent CYP3A4 inhibitor (e.g., ritonavir, nelfinavir, itraconazole), limit the maximum daily dose to 5mg.
This medication should not be used in patients with certain medical conditions. For example, it should not be administered to patients with urinary retention symptoms where urination is not efficient, severe gastrointestinal issues, myasthenia gravis, glaucoma with eye troubles, patients allergic to this medication or its components, patients undergoing hemodialysis, patients with severe liver or kidney damage, and patients with specific genetic metabolic disorders. Additionally, caution should be exercised when used in patients at risk for urinary retention or with risks of gastrointestinal obstruction or reduced gastrointestinal motility, as well as in patients with moderately impaired liver or kidney function. Dose adjustments may be required when used in conjunction with certain medications. Common side effects that may occur while using this medication include dry mouth and constipation, and may also lead to dry eyes or blurred vision. Rarely, severe side effects such as gastrointestinal obstruction, severe allergic reactions, angioedema, and anaphylaxis have been reported. This medication may cause issues related to heart rhythm, thus caution is necessary in patients with heart diseases. If symptoms of angioedema or anaphylaxis occur, the medication should be stopped immediately and appropriate treatment sought. Before starting this medication, other causes of urinary issues should be investigated, and appropriate antibiotic treatment is required if a urinary tract infection is present. Caution is advised during driving or operating machinery as symptoms such as drowsiness or blurred vision may occur. Caution is required when using this medication alongside other anticholinergic drugs as the effects may strengthen or increase side effects, and it may reduce the effectiveness of certain gastrointestinal motility drugs. Moreover, dose adjustments may be necessary when used with other medications that affect the enzymes responsible for metabolizing this drug. Safety has not been established for pregnant women, thus use should be avoided when possible, and during lactation, it is recommended not to use this medication as it may pass into breast milk. Use in children is not recommended as safety and effectiveness have not been established. Symptoms may include headache, dizziness, drowsiness, and blurred vision in case of overdose, and medical attention should be sought immediately. Treatment for overdose may include administering charcoal, gastric lavage, and potentially specialized treatment based on symptoms.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container, protected from air and moisture, at room temperature between 1 and 30 degrees Celsius. Storing it in this manner helps maintain the medication's efficacy and prevent degradation.
Light pink round film-coated tablets
100 tablets (10 tablets/PTP * 10), 30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Solifenacin Succinate 10mg
Tablet · Prescription medication
Huons Co., Ltd.

Solifenacin Succinate 10mg
Tablet · Prescription medication
Astellas Pharma Korea, Inc.

Solifenacin Succinate 5mg
Tablet · Prescription medication
Korea Astellas Pharma Co., Ltd.

Solifenacin Succinate 10mg
Tablet · Prescription medication
Withus Pharmaceutical Co., Ltd.

Solifenacin Succinate 5mg
Tablet · Prescription medication
Withus Pharmaceutical Co., Ltd.

Solifenacin Succinate 10mg
Tablet · Prescription medication
Mothers Pharmaceutical Co., Ltd.

Solifenacin Succinate 10mg
Tablet · Prescription medication
Aju Pharmaceutical Co., Ltd.

Solifenacin Succinate 10mg
Tablet · Prescription medication
Korea Hyutecs Pharmaceutical Co., Ltd.
Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
No questions yet.
For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.