Itocan 50 mg (Itopride Hydrochloride)

Adult dose

○ Adults: Administer 50 mg of itopride hydrochloride orally 3 times daily before meals. Reduce the dose appropriately according to symptoms.

This medication should not be used in patients who have had allergic reactions to this drug or its components. In patients with gastrointestinal problems such as bleeding, obstruction, or perforation, this medication should not be administered as it may stimulate gastrointestinal motility and worsen their condition. This drug contains lactose, so it should not be used in patients with lactose intolerance or certain genetic metabolic disorders. During the course of taking this drug, serious allergic reactions such as shock or anaphylaxis may occur, so symptoms should be closely monitored. Liver function may be affected, so liver enzyme levels should be checked periodically, and if abnormalities are detected, the medication should be discontinued immediately. Gastrointestinal symptoms such as nausea, diarrhea, constipation, and abdominal pain may appear, so medical consultation should be sought if these symptoms occur. Neurological symptoms such as headache, anxiety, sleep disorders, and dizziness may occur, so caution is needed. If endocrine symptoms such as gynecomastia or increased prolactin levels occur, the medication should be stopped, and appropriate measures should be taken. Blood tests may show decreased platelet or white blood cell counts, so regular testing is necessary, and if abnormalities are found, administration should be stopped. Kidney function indicators may increase, so kidney status should also be monitored. Rarely, allergic reactions such as skin rash, itching, or redness may occur, so the drug should be stopped if symptoms appear. Movement disorders such as tremors may occur, and if these symptoms are observed, the medication should be discontinued and medical consultation sought. Chest or back pain and fatigue may occur, so caution should be exercised if these symptoms develop. This medication enhances acetylcholine action, so this should be considered during use, and it should not be used long-term if gastrointestinal symptoms do not improve. When taken with anticholinergics, the efficacy of this medication may be reduced, so careful adjustment of dosing intervals is necessary. Pregnant women or women who may become pregnant should only use this medication when the benefits are judged to outweigh the risks, as its safety has not been established. Breastfeeding women should avoid this medication if possible, since it may be excreted in breast milk, and if unavoidable, breastfeeding should be stopped. Safety in children has not been sufficiently confirmed, so caution is needed when using it in this population. Elderly patients may experience adverse reactions more easily due to decreased physiological function, so symptoms should be monitored closely, and dosage adjustments or discontinuation should be considered as needed. This medication should be stored out of reach of children, and transferring it to another container should be avoided as it may lead to accidents or degradation of quality.

• Shock
• anaphylactic-like symptoms
• hypotension
• dyspnea
• laryngeal edema
• urticaria
• pallor
• sweating
• liver dysfunction
• jaundice

This medication may be sensitive to air or moisture, so it must be stored in a tightly sealed container. It is important to maintain the storage temperature between 1 degree and 30 degrees Celsius to preserve the effectiveness of the medication for as long as possible.

Appearance

White round film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle