Medication info
Pariba Tablet 10 mg (Rabeprazole Sodium)

Pariba Tablet 10 mg (Rabeprazole Sodium)

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

MFDS item code 201305968 · Approved 2013.03.04 · Insurance code 654304710

Summary

Main use
Relief of symptoms of gastric ulcer and gastroesophageal reflux disease, and treatment effect on Helicobacter pylori infection
Who takes it
Adults
Adult dose
For gastric ulcer, duodenal ulcer: usually 10 mg orally once a day, can be administered up to 20 mg once a day according to symptoms. Maximum treatment duration is 8 weeks for gastric ulcer and 6 weeks for duodenal ulcer. For erosive or ulcerative gastroesophageal reflux disease: 10 mg or 20 mg orally once a day for 4-8 weeks. If symptoms are absent after 8 weeks of treatment, an additional 8 weeks of 10 mg or 20 mg may be provided.

Ingredients

Manufacturer
오스틴제약(주)

Efficacy & effects

Relief of symptoms of gastric ulcer and gastroesophageal reflux disease, and treatment effect on Helicobacter pylori infection

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

This medication is used for the treatment of gastric ulcers and duodenal ulcers, aiding in the relief of symptoms of erosive or ulcerative gastroesophageal reflux disease. It is also used for long-term maintenance therapy of gastroesophageal reflux disease and is treated in combination with antibiotics for patients with gastrointestinal ulcers accompanied by Helicobacter pylori infection. It is effective for the treatment of Zollinger-Ellison syndrome. It is widely used for various gastrointestinal disease treatments.

How to take

Adult dose

For gastric ulcer, duodenal ulcer: usually 10 mg orally once a day, can be administered up to 20 mg once a day according to symptoms. Maximum treatment duration is 8 weeks for gastric ulcer and 6 weeks for duodenal ulcer. For erosive or ulcerative gastroesophageal reflux disease: 10 mg or 20 mg orally once a day for 4-8 weeks. If symptoms are absent after 8 weeks of treatment, an additional 8 weeks of 10 mg or 20 mg may be provided.

Precautions

This medication should not be used in patients who are allergic to specific drugs or ingredients. Pregnant or breastfeeding women should not take this medication. Caution is necessary when administering to patients with liver dysfunction or the elderly. Since this medication may cause allergic reactions such as skin rash and itching, it should be discontinued immediately if symptoms appear. Regular blood tests and liver function tests are recommended, and immediate consultation with a doctor is required if abnormal symptoms occur. Abnormal reactions may appear in various areas such as the heart, gastrointestinal system, and nervous system, so symptoms should be carefully monitored. Prolonged use may increase the risk of fractures related to osteoporosis, so caution is needed. Additionally, this medication reduces gastric acid secretion, which may affect the absorption of some drugs; therefore, if taking other medications, consult a specialist. Caution is advised as drowsiness may occur while driving or operating machinery. Low magnesium levels may occur, so regular blood tests are necessary when taking for an extended period or in conjunction with related medications. This medication should be swallowed whole and not chewed or crushed. Keep out of reach of children and avoid transferring to other containers.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, pallor, severe rash with fever, blisters, skin peeling, pain in the oral/eye mucosa, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough + fever, yellowing of the skin or eyes (jaundice), severe lethargy throughout the body, sudden and very severe headache, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, significant decrease in urine output

Mild side effects

  • Rash
  • itching
  • decreased red blood cells
  • decreased white blood cells
  • increased white blood cells
  • increased eosinophils
  • increased neutrophils
  • decreased lymphocytes
  • anemia
  • petechiae
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  • lymphadenopathy
  • hypopigmented anemia
  • pancytopenia
  • agranulocytosis
  • thrombocytopenia
  • hemolytic anemia
  • increased ALT
  • increased AST
  • increased ALP
  • increased γ-GTP
  • increased LDH
  • increased total bilirubin
  • hypertension
  • myocardial infarction
  • ECG abnormalities
  • migraine
  • fainting
  • angina
  • heart blockade
  • palpitations

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

Storage

This medication should be stored in a tightly closed container to prevent exposure to air or moisture, and it is important to maintain a storage temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the effectiveness of the medication for a longer time.

Appearance and packaging

Appearance

Pale yellow round enteric-coated tablet

Package unit

28 tablets (14 tablets/AluAlu 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.