Medication info

Losiridine Sustained-Release Tablet 4 mg (Tolterodine L-Tartrate)

Prescription medicationTabletOralApproval withdrawn
Ingredient · strength
Tolterodine-L-Tartrate›4mg / 1 tablet
Manufacturer / importer
iWorld Pharmaceuticals Co., Ltd.
Appearance
White round film-coated tablet
Packaging
30 tablets/bottle
Approval status
Approval withdrawn

MFDS item code 201508026 · Approved 2015.11.30

This product's status changed to Approval withdrawn on 2024.05.31. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of overactive bladder (urgency, frequency, etc.)
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

Manufacturer
iWorld Pharmaceuticals Co., Ltd.

Efficacy & effects

Treatment of overactive bladder (urgency, frequency, etc.)

  • Urgency
  • frequency
  • urge incontinence
View approved original text

This medication is used to treat symptoms of overactive bladder such as urgency, frequency, and urge incontinence. These symptoms occur when the bladder contracts frequently, causing a sudden and strong urge to urinate. Through medication treatment, it helps control excessive contractions of the bladder muscles, alleviating symptoms. It aids in improving the patient's quality of life and reducing discomfort.

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 contains lactose, so individuals with genetic disorders that affect lactose metabolism should not take it. Patients with certain conditions such as urinary obstruction, gastrointestinal motility disorders, uncontrolled glaucoma, severe myasthenia gravis, severe ulcerative colitis, and toxic megacolon should also avoid this medication. Patients at risk of urinary obstruction or with controlled glaucoma, gastrointestinal obstruction, or impaired liver or kidney function should use this medication cautiously, especially if they are taking certain antibiotics, antifungals, or immunosuppressants. This medication may cause side effects such as dry mouth, dyspepsia, decreased tear production, and rarely allergic reactions, headaches, dizziness, constipation, urinary difficulties, fatigue, and various adverse reactions. There is a risk of cardiac problems associated with QT interval prolongation, so caution is advised for those with related conditions or taking medications that prolong the QT interval. This medication can affect concentration and reaction speed, so caution is needed when driving or operating machinery. Combining with other antimuscarinic medications may enhance effects, and concurrent use with drugs that inhibit certain metabolic enzymes may increase blood concentrations, so be mindful of drug interactions. Pregnant or breastfeeding women should not use this medication, and contraception is advised during pregnancy due to potential harm to the fetus. Safety and efficacy in pediatric patients have not been sufficiently established. In case of overdose, symptoms such as visual disturbances, urinary difficulties, and central nervous system abnormalities may occur, and immediate medical attention should be sought. This medication should be stored out of reach of children and not transferred to other containers to maintain quality.

Side effects

  • dry mouth
  • indigestion
  • decreased tear production
  • bronchitis
  • allergic reaction
  • confusion
  • drowsiness
  • dizziness
  • headache
  • hypersensitivity
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  • anxiety
  • sensory abnormalities
  • constipation
  • abdominal pain
  • intestinal pneumatosis
  • vomiting
  • gastroesophageal reflux
  • urinary retention
  • dysuria
  • painful urination
  • chest pain
  • weight gain
  • fatigue
  • dry eye syndrome
  • visual disturbances
  • skin flushing
  • dry skin
  • diarrhea
  • sinusitis
  • joint pain
  • anaphylactic-like reaction
  • hallucinations
  • disorientation
  • memory impairment
  • tachycardia
  • palpitations
  • angioedema
  • peripheral edema
  • urinary blockage
  • abdominal distension
  • facial swelling
  • insomnia
  • facial flushing
  • duodenal ulcer
  • apathy
  • weakness
  • itching
  • skin hypersensitivity
  • γ-GTP elevation
  • visual accommodation disorder

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

Storage

This medication may be sensitive to air or moisture, so it must be stored in a tightly sealed container. Additionally, it is best to store the medication at room temperature below 25 degrees Celsius. This helps maintain the medication's efficacy over time.

Appearance and packaging

Appearance

White round film-coated tablet

Package unit

30 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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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.