Medication info
RabeD Tablet (Rabeprazole Sodium)

RabeD Tablet (Rabeprazole Sodium)

Prescription medicationTablet경구
Ingredient · strength
Rabeprazole Sodium›10mg / 1 tablet
Manufacturer / importer
동국제약(주)
Appearance
Pale yellow, round enteric-coated tablet
Packaging
28 tablets (14 tablets/PTP packaging x 2)
Approval status
Active

MFDS item code 200610958 · Notified 2006.11.29 · Insurance code 653400400

Summary

Main use
Relief of symptoms of gastric ulcers and gastroesophageal reflux disease and treatment of Helicobacter pylori infection
Who takes it
Adults
Adult dose
For adults, Rabeprazole Sodium is generally administered orally once a day at a dose of 10 mg. Depending on the symptoms, a dose of 20 mg may be administered orally once a day. Generally, it is administered for up to 8 weeks for gastric ulcer and up to 6 weeks for duodenal ulcer. For erosive or ulcerative gastroesophageal reflux disease, 10 mg or 20 mg is administered orally once a day for 4 to 8 weeks. If not treated, an additional 8 weeks of 10 mg or 20 mg can be administered.

Ingredients

Manufacturer
동국제약(주)

Efficacy & effects

Relief of symptoms of gastric ulcers and gastroesophageal reflux disease and treatment of Helicobacter pylori infection

  • Gastric ulcer
  • duodenal ulcer
  • erosive gastroesophageal reflux disease
  • ulcerative gastroesophageal reflux disease
  • symptoms of gastroesophageal reflux disease
  • gastrointestinal ulcers
  • Zollinger-Ellison syndrome
View approved original text

This medication is effective for the treatment of gastrointestinal ulcers such as gastric ulcers and duodenal ulcers. Additionally, it is used for the relief of symptoms and long-term maintenance therapy of erosive or ulcerative gastroesophageal reflux disease. For patients with gastrointestinal ulcers caused by Helicobacter pylori infection, it is treated in combination with antibiotics. It is also effective for disorders associated with excessive gastric acid secretion, such as Zollinger-Ellison syndrome. Overall, it helps to treat diseases of the stomach and esophagus and improve symptoms.

How to take

Adult dose

For adults, Rabeprazole Sodium is generally administered orally once a day at a dose of 10 mg. Depending on the symptoms, a dose of 20 mg may be administered orally once a day. Generally, it is administered for up to 8 weeks for gastric ulcer and up to 6 weeks for duodenal ulcer. For erosive or ulcerative gastroesophageal reflux disease, 10 mg or 20 mg is administered orally once a day for 4 to 8 weeks. If not treated, an additional 8 weeks of 10 mg or 20 mg can be administered.

Precautions

This medication should not be used in patients with allergies to certain ingredients or medications. Women who are pregnant or breastfeeding should not take this medication. Patients with poor liver function or the elderly should use this medication with caution. If allergic reactions such as skin rash or itching occur while taking this medication, it should be discontinued immediately. Regular blood tests and liver function tests should be conducted, and if any abnormalities are found, the medication should be stopped. Prolonged use may increase the risk of osteoporosis and fractures, so caution is advised. This medication suppresses gastric acid secretion, which may slightly increase the risk of bacterial infection in the gastrointestinal tract. Drowsiness or dizziness may occur, so caution is required when driving or operating machinery. There may be interactions with other medications, particularly if used in combination with anticoagulants or antibiotics; consultation with a physician is necessary. This medication should be swallowed whole and not chewed or crushed. Keep out of reach of children and do not transfer to another container. If any abnormal symptoms occur while taking the medication, consult a healthcare professional immediately.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, yellowing of skin or eyes (jaundice), extreme lethargy, acute interstitial nephritis, acute hepatitis, jaundice, fulminant hepatitis, systemic allergic reactions (hypotension, dyspnea, facial swelling, etc.), severe edema or urinary abnormalities, severe allergic reactions, severe dermatological reactions, asthma attacks, respiratory abnormalities accompanied by cough and fever, serious

Mild side effects

  • Rash
  • hives
  • itching
  • erythrocytopenia
  • leukopenia
  • leukocytosis
  • eosinophilia
  • neutrophilia
  • lymphocytopenia
  • anemia
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  • petechial hemorrhage
  • lymphadenopathy
  • hypochromic anemia
  • pancytopenia
  • agranulocytosis
  • thrombocytopenia
  • hemolytic anemia
  • ALT elevation
  • AST elevation
  • ALP elevation
  • γ-GTP elevation
  • LDH elevation
  • total bilirubin elevation
  • hypertension
  • myocardial infarction
  • ECG abnormalities
  • migraine
  • syncope
  • angina
  • heart block

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

Storage

This medication may be sensitive to air or moisture, so it should be stored in a tightly closed container. It is best to maintain storage temperatures between 1 degree and 30 degrees Celsius to prolong the effectiveness and safety of the medication.

Appearance and packaging

Appearance

Pale yellow, round enteric-coated tablet

Package unit

28 tablets (14 tablets/PTP packaging x 2)

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.