Medication info

Solive Tablet 10 mg (Solifenacin Succinate)

Prescription medicationTabletOralExpired
Ingredient · strength
Solifenacin Succinate›10mg / 1 tablet
Manufacturer / importer
Hanpung Pharmaceutical Co., Ltd.
Appearance
Bright pink circular film-coated tablet
Packaging
100 tablets/PTP [10 tablets/PTP packaging x 10], 30 tablets/bottle, 100 tablets/bottle
Approval status
Expired

MFDS item code 201905900 · Approved 2019.08.21

This product's status changed to Expired on 2024.08.21. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of overactive bladder symptoms (such as urge urinary incontinence and frequent urination)
Who takes it
Adults
Adult dose
The usual recommended dose for adults (including elderly patients) is 5mg once daily. If necessary, the dose may be increased up to 10mg once daily. This drug may be taken irrespective of meals and should be swallowed whole with water. Dosage adjustment is required for the following patients. 1. Patients with renal impairment: No dose adjustment is required for patients with mild or moderate renal impairment (creatinine clearance>30ml/min). In patients with severe renal impairment (creatinine clearance≤30ml/min), administer with caution and do not exceed 5mg once daily. 2. Patients with hepatic impairment: No dose adjustment is required for patients with mild hepatic impairment. In patients with moderate hepatic impairment (Child-Pugh Class B), administer with caution and do not exceed 5mg once daily. 3. Patients receiving a strong cytochrome P450 3A4 (CYP3A4) inhibitor: For patients receiving ketoconazole or another strong CYP3A4 inhibitor (e.g., ritonavir, nelfinavir, itraconazole), limit the maximum daily dose to 5mg.

Ingredients

Manufacturer
Hanpung Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of overactive bladder symptoms (such as urge urinary incontinence and frequent urination)

  • Urgency incontinence
  • frequent urination
  • urge incontinence
  • symptoms of overactive bladder
View approved original text

This medication is used effectively to improve symptoms of overactive bladder such as urgency incontinence, frequent urination, and urge incontinence. These symptoms are characterized by the bladder contracting excessively, causing sudden and strong urges to urinate. The drug alleviates symptoms by suppressing the excessive contraction of the bladder muscles, reducing discomfort in the patient's daily life. Regular use is also beneficial in preventing the recurrence of symptoms. It is used for the improvement of symptoms of overactive bladder.

How to take

Adult dose

The usual recommended dose for adults (including elderly patients) is 5mg once daily. If necessary, the dose may be increased up to 10mg once daily. This drug may be taken irrespective of meals and should be swallowed whole with water. Dosage adjustment is required for the following patients. 1. Patients with renal impairment: No dose adjustment is required for patients with mild or moderate renal impairment (creatinine clearance>30ml/min). In patients with severe renal impairment (creatinine clearance≤30ml/min), administer with caution and do not exceed 5mg once daily. 2. Patients with hepatic impairment: No dose adjustment is required for patients with mild hepatic impairment. In patients with moderate hepatic impairment (Child-Pugh Class B), administer with caution and do not exceed 5mg once daily. 3. Patients receiving a strong cytochrome P450 3A4 (CYP3A4) inhibitor: For patients receiving ketoconazole or another strong CYP3A4 inhibitor (e.g., ritonavir, nelfinavir, itraconazole), limit the maximum daily dose to 5mg.

Precautions

This medication should not be used in patients with urinary retention, severe gastrointestinal disease, myasthenia gravis, or narrow-angle glaucoma. Additionally, patients who are allergic to any of the ingredients in this medication, those undergoing hemodialysis, and patients with severe liver or kidney disorders should avoid administration. Caution is advised in patients at risk of urinary retention or with gastrointestinal obstruction or decreased gastrointestinal motility, and dosage should be limited in patients with severe kidney or liver disorders. While taking this medication, side effects such as dry mouth, constipation, blurred vision, urinary retention, and dry eyes may occur, and caution is required. In particular, dry mouth and constipation may occur more frequently with higher doses. This medication may affect driving or operating machinery, so care should be taken if symptoms occur. Furthermore, this medication may interact with certain medicines; therefore, it is advisable to consult a physician before taking it with other anticholinergic medications or strong CYP3A4 inhibitors. Women who are pregnant or breastfeeding should exercise caution when using this medication, and it is advisable to avoid use during breastfeeding. Safety in children has not been established, so it should not be administered to children. In case of overdose, symptoms such as headache, dizziness, drowsiness, and blurred vision may occur, and in severe cases, professional treatment may be necessary. Before taking this medication, it is essential to inform healthcare professionals about any existing diseases or medications, and to consult a doctor immediately if unusual symptoms occur.

Side effects

  • Dry mouth
  • constipation
  • blurred vision
  • urinary retention
  • dry eyes
  • fecal impaction
  • colonic obstruction
  • intestinal obstruction
  • vascular neurogenic edema
  • nausea
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  • dyspepsia
  • upper abdominal pain
  • vomiting
  • urinary tract infection
  • influenza
  • pharyngitis
  • dizziness
  • depression
  • lower limb edema
  • fatigue
  • cough
  • hypertension
  • difficulty in urination
  • reduced urinary flow
  • bladder post-void residual
  • cystitis
  • nasopharyngitis
  • vomiting
  • gastroesophageal reflux disease
  • intestinal obstruction
  • peripheral edema
  • headache
  • hallucinations
  • drowsiness
  • delirium
  • kidney impairment
  • itching
  • rash
  • hives
  • angioedema
  • erythema multiforme
  • exfoliative dermatitis
  • atrial fibrillation
  • palpitations
  • tachycardia
  • polymorphic ventricular tachycardia
  • QT prolongation on ECG
  • abnormal liver function tests
  • decreased appetite
  • hyperkalemia
  • voice disorders
  • anaphylaxis reaction
  • glaucoma
  • muscle weakness
  • frequent urination
  • facial swelling
  • urinary disorders
  • urgency
  • neurogenic bladder
  • paresthesia
  • diarrhea
  • abdominal bloating
  • acute renal failure
  • nocturia
  • reduced urine volume
  • urinary stones
  • urinary incontinence
  • sensory abnormalities
  • difficulty walking
  • limb tremors
  • chest tightness
  • chest pain
  • periorbital edema
  • edema
  • benign prostatic hyperplasia
  • pruritus of the male genitalia
  • decreased erection
  • erectile dysfunction
  • abnormal orgasm
  • retrograde ejaculation
  • hematuria
  • pneumonia
  • keratosis
  • hair loss
  • sinking feeling
  • anxiety
  • decreased libido
  • back pain
  • vaginal bleeding
  • myocardial infarction
  • decreased cardiac output
  • syncope
  • hearing impairment
  • soft tissue infection
  • thirst
  • erectile dysfunction
  • headache
  • dry mouth
  • drowsiness

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture. It is recommended to maintain a storage temperature between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

Bright pink circular film-coated tablet

Package unit

100 tablets/PTP [10 tablets/PTP packaging x 10], 30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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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.