Medication info
Bukwang Itopride Tablet 50 mg (Itopride Hydrochloride)

Bukwang Itopride Tablet 50 mg (Itopride Hydrochloride)

Prescription medicationTabletOral
Ingredient · strength
Itopride Hydrochloride›50mg / 1 tablet
Manufacturer / importer
Bukwang Pharmaceutical Co., Ltd.
Appearance
White round film-coated tablet
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 200908355 · Notified 2009.11.27

Summary

Main use
Relief of functional dyspepsia symptoms (including abdominal distension, upper abdominal pain, and nausea)
Who takes it
Adults
Adult dose
○ Adults: Administer itopride hydrochloride 50 mg orally 3 times daily before meals. The dose may be appropriately reduced according to symptoms.

Ingredients

Manufacturer
Bukwang Pharmaceutical Co., Ltd.

Efficacy & effects

Relief of functional dyspepsia symptoms (including abdominal distension, upper abdominal pain, and nausea)

  • Abdominal distension
  • epigastric pain
  • loss of appetite
  • heartburn
  • nausea
  • vomiting
View approved original text

This medication is used to improve gastrointestinal symptoms associated with functional dyspepsia, including abdominal distension, epigastric pain, loss of appetite, heartburn, nausea, and vomiting.

How to take

Adult dose

○ Adults: Administer itopride hydrochloride 50 mg orally 3 times daily before meals. The dose may be appropriately reduced according to symptoms.

Precautions

This medication should not be used by individuals who have experienced allergic reactions to this medication or its ingredients. It should not be administered to patients with gastrointestinal bleeding, mechanical obstruction, or perforation, as stimulating gastrointestinal motility can be harmful. This medication contains lactose, so it should not be used in patients with lactose intolerance or certain genetic metabolic disorders. During treatment with this medication, severe allergic reactions such as shock or anaphylaxis may occur, so symptoms should be carefully monitored. Liver function impairment or jaundice symptoms may appear, so liver-related tests should be conducted regularly, and if abnormalities are found, medication should be stopped immediately. Gastrointestinal symptoms such as nausea, diarrhea, constipation, abdominal pain, and increased salivation may occur, so caution is necessary. Psychoneurological symptoms such as headaches, anxiety, sleep issues, and dizziness may arise, so the condition should be well monitored. Gynecomastia or elevated prolactin levels may occur, so if any abnormal signs appear, the medication should be discontinued and appropriate measures taken. Thrombocytopenia or leukopenia may occur, so regular blood tests should be conducted to monitor the condition. Kidney function impairment may lead to elevated blood urea nitrogen (BUN) and creatinine levels, requiring kidney function monitoring. Elevation of liver enzymes (AST, ALT, γ-GTP, ALP) may occur, so liver health should be regularly assessed. Rare instances of hypersensitivity like rashes, redness, and itching may occur, necessitating careful observation of skin conditions. There may be issues with motor control, so consult a physician immediately if any unusual symptoms arise. Chest or back pain and fatigue may frequently occur, so any changes in body condition should be reported. This medication enhances acetylcholine action, so this should be considered during use, and long-term use is not recommended if gastrointestinal symptoms do not improve. When taken with anticholinergics, this medication's effectiveness may be reduced, so dosing intervals should be adjusted or caution exercised. Women who are pregnant or may become pregnant should only use this medication when absolutely necessary, as safety has not been established; nursing mothers should avoid this medication or stop breastfeeding. Safety for children has not been sufficiently verified, so it should be used cautiously. Elderly individuals may experience adverse reactions more easily due to decreased bodily functions, so symptoms should be closely monitored during administration, and dose adjustments or discontinuation should be considered if necessary. This medication should be kept out of reach of children and should not be transferred to another container as this may affect quality.

Side effects

  • Shock
  • anaphylaxis-like symptoms
  • hypotension
  • dyspnea
  • laryngeal edema
  • urticaria
  • pallor
  • diaphoresis
  • liver dysfunction
  • jaundice
Show 29 more
  • nausea
  • diarrhea
  • constipation
  • abdominal pain
  • increased salivation
  • headache
  • anxiety
  • sleep disturbances
  • dizziness
  • gynecomastia
  • increased prolactin
  • thrombocytopenia
  • leukopenia
  • increased BUN
  • increased creatinine
  • elevated AST
  • elevated ALT
  • elevated γ-GTP
  • elevated ALP
  • rash
  • erythema
  • pruritus
  • tremor
  • chest pain
  • back pain
  • fatigue
  • heartburn
  • thirst
  • abdominal distension

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. Also, it is best to store it at room temperature, maintaining a temperature between 1 and 30 degrees Celsius. Storing it this way helps to maintain the medication's efficacy for a longer period.

Appearance and packaging

Appearance

White round film-coated tablet

Package unit

30 tablets/bottle, 500 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.