Medication info
Detrusitol SR Capsule 4mg (Tolterodine L-tartrate)

Detrusitol SR Capsule 4mg (Tolterodine L-tartrate)

Prescription medicationOral
Ingredient · strength
Tolterodine-L-Tartrate›4mg / 1 capsule
Manufacturer / importer
Viatris
Appearance
A blue capsule with white granules inside.
Packaging
30 capsules/bottle
Approval status
Active

MFDS item code 200008568 · Approved 2006.09.11 · Insurance code 073400080

Summary

Main use
Treatment of overactive bladder (e.g., urinary urgency, frequency)
Who takes it
Adults
Adult dose
Adults: Administer 4 mg of tolterodine L-tartrate orally once daily. Patients with renal impairment, hepatic impairment, or receiving ketoconazole or another potent CYP3A4 inhibitor: Administer 2 mg of this medicine once daily. If adverse reactions occur, the dose may be reduced from 4 mg to 2 mg once daily. This medicine may be taken with or without food. Swallow the dosage form whole; do not crush or split it.

Ingredients

Importer
Viatris

Efficacy & effects

Treatment of overactive bladder (e.g., urinary urgency, frequency)

  • Urinary urgency
  • frequency
  • urgency incontinence
View approved original text

This medication is used to treat symptoms of overactive bladder, such as urinary urgency, frequency, and urgency incontinence. These symptoms include a sudden strong urge to urinate or urinating frequently. The drug alleviates symptoms by regulating excessive contractions of the bladder muscles, improving the quality of life for patients. Regular use of this medication stabilizes symptoms and makes daily life more comfortable. Therefore, it effectively improves symptoms of overactive bladder.

How to take

Adult dose

Adults: Administer 4 mg of tolterodine L-tartrate orally once daily. Patients with renal impairment, hepatic impairment, or receiving ketoconazole or another potent CYP3A4 inhibitor: Administer 2 mg of this medicine once daily. If adverse reactions occur, the dose may be reduced from 4 mg to 2 mg once daily. This medicine may be taken with or without food. Swallow the dosage form whole; do not crush or split it.

Precautions

This medication should not be used in patients with urinary retention symptoms or gastrointestinal motility disorders. It should also not be administered to patients with uncontrolled angle-closure glaucoma, severe myasthenia gravis, severe ulcerative colitis, or toxic megacolon. Use with caution in patients who are at risk of urinary retention or have controlled angle-closure glaucoma, gastrointestinal obstructive diseases, or renal and liver function impairments. Be cautious of potential drug interactions when taking this medication together with certain antibiotics, antifungals, immunosuppressants, etc. While using this medication, side effects such as dry mouth, dyspepsia, and decreased tear production may occur, and rarely symptoms such as dizziness, headache, and difficulty urinating may arise. There is a risk of heart problems associated with QT interval prolongation, so patients with heart disease or electrolyte abnormalities must consider this factor. Caution is required when driving or operating machinery, as these activities may be affected. Pregnant or breastfeeding women are advised not to take this medication, and women of childbearing age should use appropriate contraception. The safety and efficacy of this medication in children have not been adequately confirmed, so its use is not recommended. In cases of overdose, symptoms such as visual disturbances, difficulty urinating, and severe agitation may occur, necessitating immediate medical attention and appropriate treatment. Keep out of reach of children and avoid transferring the medication to other containers.

Side effects

  • dry mouth
  • indigestion
  • decreased tear production
  • bronchitis
  • allergic reactions
  • confusion
  • drowsiness
  • dizziness
  • headache
  • hyperexcitability
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  • anxiety disorders
  • sensory disturbances
  • constipation
  • abdominal pain
  • bowel obstruction
  • vomiting
  • gastroesophageal reflux
  • urinary retention
  • dysuria
  • urinary pain
  • chest pain
  • weight gain
  • fatigue
  • ocular dryness
  • visual disturbances
  • skin flushing
  • xerosis
  • diarrhea
  • sinusitis
  • arthralgia
  • anaphylactic-like reactions
  • hallucinations
  • disorientation
  • memory impairment
  • tachycardia
  • palpitations
  • angioedema
  • peripheral edema
  • urinary blockage
  • abdominal pain
  • drowsiness
  • ocular dryness
  • hyperexcitability
  • vomiting
  • dysuria
  • edema
  • visual disturbances
  • diarrhea
  • dizziness
  • fatigue
  • gastric ulcer
  • abdominal distension
  • facial edema
  • sensory disturbances
  • insomnia
  • confusion
  • facial flushing
  • xerosis
  • duodenal ulcer
  • apathy
  • weakness
  • pruritus
  • skin hypersensitivity
  • abnormal γ-GTP
  • vision adjustment disorder

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

Storage

This medication may be sensitive to air and moisture, so it must be stored in a tightly sealed container. Additionally, it is recommended to store the medication at room temperature, specifically below 25 degrees Celsius. This will help maintain the medication's effectiveness and safety for a longer period.

Appearance and packaging

Appearance

A blue capsule with white granules inside.

Package unit

30 capsules/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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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.