Medication info
Eurocarina Sustained Release Tablet 4mg (Tolterodine L-Tartrate)

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

Prescription medicationTabletOral
Ingredient · strength
Tolterodine-L-Tartrate›4mg / 1 tablet
Manufacturer / importer
Donggu Bio Pharmaceutical Co., Ltd.
Appearance
White round film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 200600310 · Notified 2006.03.20

Summary

Main use
Treatment of overactive bladder (urgency, frequent urination, 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 taking ketoconazole or another potent CYP3A4 inhibitor: Administer 2 mg of this drug once daily. If adverse reactions occur, the dose may be reduced from 4 mg to 2 mg once daily. This drug may be taken with or without food. Swallow the dosage form whole; do not crush or split it.

Ingredients

Manufacturer
Donggu Bio Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of overactive bladder (urgency, frequent urination, etc.)

  • Urgency
  • frequency
  • urge incontinence
View approved original text

This medication is used to improve symptoms such as urgency, frequency, and urge incontinence caused by overactive bladder. It helps alleviate symptoms by controlling excessive contraction of the bladder and improving the quality of life for patients.

How to take

Adult dose

Adults: Administer 4 mg of tolterodine L-tartrate orally once daily. Patients with renal impairment, hepatic impairment, or taking ketoconazole or another potent CYP3A4 inhibitor: Administer 2 mg of this drug once daily. If adverse reactions occur, the dose may be reduced from 4 mg to 2 mg once daily. This drug 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 by patients with urinary retention symptoms. Patients with gastric atony symptoms should also not take this medication. Patients with uncontrolled narrow-angle glaucoma may be at risk when using this medication. Patients with allergic reactions to this medication or its ingredients should not take it. Patients with severe myasthenia gravis may experience worsening of symptoms and should avoid this medication. Patients with severe ulcerative colitis or toxic megacolon should also not use this medication. Patients with a risk of urinary retention due to bladder outlet obstruction or controlled narrow-angle glaucoma should use this medication cautiously. Caution is also advised for patients with gastrointestinal obstruction, or those with impaired kidney or liver function when taking this medication. Patients on certain antibiotics, antifungals, or immunosuppressants that inhibit CYP3A4 enzyme should be mindful of interactions with this medication. Patients with autonomic neuropathy, hiatal hernias, or those at risk for decreased gastrointestinal motility should be administered this medication cautiously. This medication may cause side effects such as dry mouth, dyspepsia, and reduced tearing. Adverse reactions such as bronchitis, allergic reactions, confusion, drowsiness, dizziness, headache, constipation, abdominal pain, vomiting, and urinary difficulty have been reported in clinical trials. Additionally, skin rash, chest pain, weight gain, fatigue, dry eyes, visual disturbances, and dry skin may occur. Caution should be taken as patients receiving treatment for dementia may experience worsening of symptoms. This medication may affect cardiac electrical activity, thus patients with heart disease or those taking specific medications should be careful. Caution is also required as reaction time may be delayed when driving or operating machinery. Taking this medication in conjunction with other antimuscarinic drugs may enhance its effects, and there may be interactions with some other medications. It is safest to avoid using this medication during pregnancy or while breastfeeding. Safety in children has not been established, so it is best not to use this medication in pediatric patients. In case of overdose, severe side effects such as vision disturbance or urinary difficulty may occur, and appropriate treatment should be sought immediately at a hospital. This medication should be kept out of reach of children and not transferred to another container.

Side effects

  • dry mouth
  • dyspepsia
  • decreased tears
  • bronchitis
  • allergic reactions
  • confusion
  • drowsiness
  • dizziness
  • headache
  • nervous hyperexcitability
Show 64 more
  • anxiety
  • sensory disturbances
  • 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
  • anaphylactoid reaction
  • hallucinations
  • impaired orientation
  • memory impairment
  • tachycardia
  • palpitations
  • angioedema
  • peripheral edema
  • urinary blockage
  • abdominal pain
  • drowsiness
  • dry eye syndrome
  • nervous hyperexcitability
  • vomiting
  • dysuria
  • edema
  • visual disturbances
  • diarrhea
  • dizziness
  • fatigue
  • gastric ulcer
  • abdominal distension
  • facial swelling
  • sensory disturbances
  • insomnia
  • confusion
  • facial flushing
  • dry skin
  • duodenal ulcer
  • apathy
  • weakness
  • itching
  • skin hypersensitivity
  • γ-GTP abnormalities
  • visual accommodation disorder
  • dysuria
  • hallucinations
  • severe agitation
  • agitation
  • seizures
  • respiratory failure
  • tachycardia
  • urinary retention
  • pupillary dilation

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

Storage

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

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

No questions yet.

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

Related searches

Search tags

Suggested searches

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.