Rabepra 20mg (Rabeprazole Sodium)
Rabeprazole Sodium 20mg
Tablet · Prescription medication
Alpha Pharmaceutical Co., Ltd.
MFDS item code 201902437 · Approved 2019.04.19
This product's status changed to Expired on 2024.04.19. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Relief of symptoms for gastric ulcers, duodenal ulcers, and gastroesophageal reflux disease, and efficacy in combination therapy with antibiotics
This medication is used to treat ulcers formed in the stomach and duodenum. It also relieves symptoms of erosive or ulcerative gastroesophageal reflux disease and aids in long-term treatment of gastroesophageal reflux disease. It is used in conjunction with antibiotics to treat gastrointestinal ulcers in patients infected with Helicobacter pylori. It is also effective for conditions that cause excessive gastric acid secretion, such as Zollinger-Ellison syndrome. It is used to treat and alleviate symptoms of various gastrointestinal diseases.
For gastric ulcers and duodenal ulcers: Administer 10 mg orally once daily for adults, with the possibility of increasing the dosage to 20 mg once daily depending on symptoms. The treatment duration is up to 8 weeks for gastric ulcers and up to 6 weeks for duodenal ulcers. For erosive or ulcerative gastroesophageal reflux disease: Administer 10 mg or 20 mg once daily for 4 to 8 weeks. If symptoms do not resolve after 8 weeks, consider administering 10 mg or 20 mg orally twice daily for an additional 8 weeks.
This medication should not be used in patients with allergies to specific ingredients or a history of hypersensitivity reactions. It is particularly contraindicated in patients allergic to penicillin-type or macrolide antibiotics, and in those taking certain heart-related medications. Pregnant or breastfeeding women should not use this medication. Patients with impaired liver function or the elderly should use this medication with caution, and those with a history of drug allergies should be closely monitored. If symptoms of allergy such as rash, hives, or itching occur while taking this medication, discontinue use immediately. Regular blood tests are recommended as changes in red or white blood cell counts may occur. Regular liver function tests should also be conducted, and if any liver function abnormalities or symptoms of jaundice appear, the medication should be discontinued. Caution is advised as symptoms related to the heart or changes in blood pressure, headaches, and neurogenic symptoms such as dizziness may occur. Gastrointestinal symptoms include diarrhea, abdominal pain, nausea, and vomiting, and if severe, immediate consultation with healthcare professionals is necessary. Respiratory symptoms may include cough and shortness of breath, and if symptoms are severe, the medication should be discontinued. Muscle pain, joint pain, skin rashes, and hair loss have also been reported, requiring careful observation if such symptoms arise. Long-term use of this medication may increase the risk of osteoporosis and fractures, so bone density testing is recommended if necessary. Regular monitoring of serum magnesium levels is needed as hypomagnesemia may occur with prolonged use. This medication inhibits gastric acid secretion, which may slightly increase the risk of bacterial infections in the gastrointestinal tract, so inform healthcare professionals if diarrhea persists. Caution is necessary while driving or operating machinery due to possible drowsiness or dizziness. There may be interactions with other medications, so consult a doctor or pharmacist if taking antibiotics, anticoagulants, antifungals, or antivirals. This medication should not be chewed or crushed and should be swallowed whole, stored out of reach of children. It is safest not to use this medication during pregnancy or breastfeeding, and care should be taken when administering to the elderly due to the potential for liver dysfunction. There is no specific antidote for overdose; treatment and supportive therapy should be administered according to symptoms.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweats, pallor, severe rash with fever, blisters, skin peeling, oral/ocular mucosal pain, difficulty or shortness of breath, asthma attacks, respiratory abnormalities accompanied by cough and fever, yellowing of skin or eyes (jaundice), profound lethargy, sudden and severe headaches, thunderclap headaches, seizures, confusion, vision changes, paralysis, urination
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to avoid exposure to air or moisture. It is recommended to maintain a storage temperature between 1 to 30 degrees Celsius. This will help maintain the effectiveness and safety of the medication.
Pale yellow round enteric-coated tablet
28 tablets (14 tablets/PTP packaging x 2), 28 tablets (14 tablets/Alu Alu packaging x 2)
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.