Medication info
Rabevica Tablet 20/700 mg (Rabeprazole Sodium, Sodium Bicarbonate)

Rabevica Tablet 20/700 mg (Rabeprazole Sodium, Sodium Bicarbonate)

Prescription medicationTablet경구
Ingredient · strength
Rabeprazole Sodium›20mg / 1 tabletSodium Bicarbonate›700mg / 1 tablet
Manufacturer / importer
대웅바이오(주)
Appearance
Light pink oval film-coated tablets
Packaging
28 tablets/bottle
Approval status
Active

MFDS item code 202402101 · Approved 2024.08.30 · Insurance code 694004330

Summary

Main use
Treatment of gastric ulcers, duodenal ulcers, and alleviation of symptoms of gastroesophageal reflux disease
Who takes it
Adults · Children
Adult dose
1) Gastric ulcer, duodenal ulcer: Generally, for adults, 10/700 mg is administered orally once daily. Depending on symptoms, 20/700 mg may be administered orally once daily. Usually, treatment is continued for up to 8 weeks for gastric ulcers and 6 weeks for duodenal ulcers. 2) Erosive or ulcerative gastroesophageal reflux disease: Administer 10/700 mg or 20/700 mg orally once daily for 4 to 8 weeks. Proton pump inhibitors.
Child dose
Safety in pediatric patients has not been established.

Ingredients

Manufacturer
대웅바이오(주)

Efficacy & effects

Treatment of gastric ulcers, duodenal ulcers, and alleviation of symptoms of gastroesophageal reflux disease

  • Gastric ulcers
  • duodenal ulcers
  • erosive gastroesophageal reflux disease
  • ulcerative gastroesophageal reflux disease
View approved original text

This medication is used for the treatment of gastrointestinal ulcers such as gastric and duodenal ulcers. It also alleviates symptoms of erosive or ulcerative gastroesophageal reflux disease and is effective for long-term maintenance therapy of gastroesophageal reflux disease. Therefore, it helps manage gastrointestinal-related ulcers and gastroesophageal reflux disease.

How to take

Adult dose

1) Gastric ulcer, duodenal ulcer: Generally, for adults, 10/700 mg is administered orally once daily. Depending on symptoms, 20/700 mg may be administered orally once daily. Usually, treatment is continued for up to 8 weeks for gastric ulcers and 6 weeks for duodenal ulcers. 2) Erosive or ulcerative gastroesophageal reflux disease: Administer 10/700 mg or 20/700 mg orally once daily for 4 to 8 weeks. Proton pump inhibitors.

Child dose

Safety in pediatric patients has not been established.

Precautions

This medication should not be used in patients with allergies to certain components or who have experienced hypersensitivity reactions. It is advisable not to administer this medication to pregnant or breastfeeding women. Patients with compromised liver or kidney function, elderly patients, and those with heart or lung issues should exercise special caution when using this medication. As this medication contains sodium, it should be administered with caution to patients who need to restrict sodium intake. If symptoms of an allergic reaction such as skin rash, itching, or hives occur while taking this medication, stop taking it immediately and consult healthcare professionals. Regular blood tests or liver function tests are recommended to monitor for abnormalities. This medication may slightly increase the risk of gastrointestinal infections by suppressing gastric acid secretion; therefore, inform healthcare providers if diarrhea persists. Caution is needed when driving or operating machinery, as drowsiness or dizziness may occur. Since this medication can interact with other drugs, especially anticoagulants, antivirals, and antifungals, it is essential to inform healthcare providers if you are taking these medications. Long-term use of this medication may increase the risk of bone fractures, so it should only be used at the minimal effective dose and duration as prescribed by a physician. In case of overdose, seek immediate medical attention for appropriate treatment. Keep out of reach of children and do not transfer to another container for safety.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, fever, systemic lupus erythematosus, cutaneous lupus erythematosus, toxic epidermal necrolysis (Lyell syndrome), Stevens-Johnson syndrome, angioedema, hypotension, asthma, liver abnormalities (jaundice), fulminant hepatitis, liver dysfunction, jaundice, severe allergic reactions, hypertension with severe edema, acute interstitial nephritis, severe rash accompanied by high fever, blisters, skin

Mild side effects

  • Rash
  • itching
  • decrease in red blood cells
  • decrease in white blood cells
  • increase in white blood cells
  • increase in eosinophils
  • increase in neutrophils
  • decrease in lymphocytes
  • anemia
  • petechiae
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  • lymphadenopathy
  • hypochromic anemia
  • pancytopenia
  • agranulocytosis
  • thrombocytopenia
  • hemolytic anemia
  • elevated ALT
  • elevated AST
  • elevated ALP
  • elevated γ-GTP
  • elevated LDH
  • abdominal pain
  • abdominal distension
  • dyspepsia
  • belching
  • nausea
  • diarrhea
  • constipation
  • rectal bleeding
  • bloody stools
  • anorexia
  • gallstone disease

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

Storage

Store this medication in a sealed container to protect it from air and moisture. The recommended storage temperature is between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

Light pink oval film-coated tablets

Package unit

28 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.