Itrid Tablets (Itopride Hydrochloride)

Adult dose

○ Adults: Administer 50 mg of itopride hydrochloride orally per dose 3 times daily before meals. Adjust the dose as appropriate according to symptoms.

This medicine should not be used in patients who are allergic to this medicine or any of its components or who have experienced hypersensitivity reactions. It should also not be administered to patients with gastrointestinal problems such as gastrointestinal bleeding, mechanical bowel obstruction, or perforation, as this medicine may stimulate gastrointestinal motility and worsen their condition. This medicine contains lactose, and it should not be used in patients with genetic metabolic disorders such as lactose intolerance, galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption. Serious allergic reactions, such as shock or anaphylaxis, may occur during the course of treatment; if any symptoms appear, the administration should be stopped immediately and medical personnel should be informed. Liver dysfunction or symptoms of jaundice may occur, so regular liver function tests should be conducted, and administration should be discontinued if abnormalities are found. Gastrointestinal symptoms such as nausea, diarrhea, constipation, abdominal pain, and increased salivation may occur; if symptoms are severe, consultation with a doctor is recommended. Central nervous system symptoms such as headache, anxiety, sleep disturbances, and dizziness may occur, so caution is necessary. Endocrine abnormalities such as gynecomastia and increased prolactin levels may occur; if any abnormal symptoms appear, medical personnel should be informed immediately. Hematological abnormalities such as thrombocytopenia or leukopenia may occur, so monitoring through blood tests is recommended. Kidney function abnormalities may occur, so regular kidney function tests are advisable. Rarely, allergic reactions such as rash, redness, or itching may occur; if any skin abnormalities develop, administration should be stopped. Extrapyramidal symptoms such as tremors may occur, so consultation with medical personnel is necessary if abnormal movements are observed. Chest or back pain and fatigue may occur; if symptoms persist, consultation with a doctor is advised. This medicine enhances the action of acetylcholine, so this should be considered during use, and if no improvement in digestive symptoms is observed, long-term use is not recommended. When taken with anticholinergics, the efficacy of this medicine may be reduced, so caution is needed regarding the timing of administration. The safety of this medication during pregnancy has not been established, and it should only be administered if the therapeutic benefits outweigh the risks; during breastfeeding, it may be excreted in breast milk, so it's best to avoid administration or discontinue breastfeeding if possible. The safety of this medication in children has not been sufficiently established, so caution is advised. In elderly patients, decreased bodily function may make adverse reactions more likely, so symptoms should be closely monitored and dosages adjusted if necessary. Keep this medicine out of the reach of children, do not transfer it to other containers, and ensure quality is maintained.

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

This medication should be stored in a tightly sealed container to protect it from air and moisture. It is important to maintain a storage temperature between 1 and 30 degrees Celsius at room temperature. Proper storage will help maintain the medicine's efficacy and safety for a longer time.

Appearance

White round film-coated tablets

Package unit

30 tablets/bottle, 500 tablets/bottle