Viewing nowRemipide Tablet (Levamisole)
Rebamipide 100mg
Tablet · Prescription medication
CMG Pharmaceutical Co., Ltd.

MFDS item code 200402879 · Notified 2004.08.13 · Insurance code 648600290
Improvement of gastric ulcer and gastric mucosal lesions (erosion, bleeding, etc.)
This medication is used in the treatment of gastric ulcers and also helps improve gastric mucosal lesions such as erosion, bleeding, redness, and edema during acute exacerbations of acute and chronic gastritis. Therefore, it is effective in protecting the gastric mucosa and alleviating gastrointestinal symptoms.
Administer 100 mg of Rebamipide orally 3 times a day. In the case of gastric ulcers, it is administered before breakfast, in the evening, and at bedtime.
This medication should not be used in patients who have had hypersensitivity reactions to its components. Additionally, it contains lactose, so individuals with galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption should not take it. Rarely, severe allergic reactions similar to shock or anaphylaxis may occur, so if any abnormal symptoms occur during use, treatment should be stopped immediately, and medical attention should be sought. Regular observation is necessary as there may be a decrease in white blood cells or platelets or liver function issues, and medication should be discontinued if abnormalities are observed. Allergic reactions such as hives, rash, and itching may occur, and neurological symptoms such as dizziness, drowsiness, or numbness may also be experienced. Gastrointestinal symptoms may include dry mouth, constipation, abdominal distension, diarrhea, nausea, vomiting, heartburn, abdominal pain, belching, and dysgeusia. If liver enzyme levels rise or fever and rash occur, medication should be stopped, and medical attention should be sought. Blood tests may reveal decreased white blood cells or platelets or other blood abnormalities, so caution is advised. Other symptoms may include breast pain, palpitations, fever, flushing of the face, tongue numbness, cough, shortness of breath, hair loss, menstrual irregularities, edema, etc. Women who are pregnant or may become pregnant should be cautious, as the safety of this medication is not clearly established; it should only be taken if deemed absolutely necessary. Breastfeeding women are advised to avoid this medication as it may pass into breast milk. Safety for children, neonates, and low-birth-weight infants has not been adequately established, so caution should be exercised. In elderly patients, physiological functions may decline, so special attention should be paid to gastrointestinal symptoms and other adverse reactions. Finally, this medication should be kept out of the reach of children, and transferring it to another container could pose a risk of accidents or quality deterioration, so caution is advised.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light; it should be stored in a container that does not allow light to pass through. Additionally, to maintain the effectiveness of the medication, it is recommended to store it at room temperature between 1 degree and 30 degrees.
White, round film-coated tablet
For domestic use: 600 tablets per bottle, 30 tablets per bottle For export: 100 tablets (10 tablets/PTP packaging x 10)
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.
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For anything that needs medical judgment, consult a doctor or pharmacist.
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.