Medication info
Ravagard Tablet 10/600 mg (Rabeprazole Sodium, Precipitated Calcium Carbonate)

Ravagard Tablet 10/600 mg (Rabeprazole Sodium, Precipitated Calcium Carbonate)

Prescription medicationTablet경구
Ingredient · strength
Rabeprazole Sodium›10mg / 1 tabletPrecipitated Calcium Carbonate›510mg / 1 tablet
Manufacturer / importer
(주)대웅제약
Appearance
Yellow round film-coated tablet
Packaging
28 tablets/bottle
Approval status
Active

MFDS item code 202400481 · Approved 2024.03.06 · Insurance code 641608140

Summary

Main use
Treatment of gastric and duodenal ulcers, alleviation of symptoms of gastroesophageal reflux disease, and maintenance therapy
Who takes it
Adults
Adult dose
Administer 10/600 mg orally once a day. Depending on the symptoms, 20/600 mg may be administered orally once a day. Generally, treatment lasts for up to 8 weeks for gastric ulcers and up to 6 weeks for duodenal ulcers. For erosive or ulcerative gastroesophageal reflux disease, administer 10/600 mg or 20/600 mg orally once daily for 4 to 8 weeks. If symptoms persist after administering a proton pump inhibitor (PPI) for 8 weeks, an additional 8

Ingredients

Manufacturer
(주)대웅제약

Efficacy & effects

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

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

This medication is used to treat gastric ulcers and duodenal ulcers. It is also effective for the treatment of erosive or ulcerative gastroesophageal reflux disease. It alleviates the symptoms of gastroesophageal reflux disease and can be used as a long-term maintenance therapy. This improves gastrointestinal health and stabilizes symptoms.

How to take

Adult dose

Administer 10/600 mg orally once a day. Depending on the symptoms, 20/600 mg may be administered orally once a day. Generally, treatment lasts for up to 8 weeks for gastric ulcers and up to 6 weeks for duodenal ulcers. For erosive or ulcerative gastroesophageal reflux disease, administer 10/600 mg or 20/600 mg orally once daily for 4 to 8 weeks. If symptoms persist after administering a proton pump inhibitor (PPI) for 8 weeks, an additional 8

Precautions

This medication should not be used if you have an allergy to certain ingredients or if you are pregnant or breastfeeding. It is also not safe for patients with severe kidney or liver dysfunction, hypercalcemia, or thyroid dysfunction. While using this medication, liver function and blood conditions should be regularly monitored, and if any abnormal symptoms arise, it should be stopped immediately. Rarely, allergic reactions such as skin rashes, hives, and itching may occur, so caution is necessary. Gastrointestinal symptoms such as abdominal pain, diarrhea, constipation, and nausea may occur, and if symptoms are severe, medical consultation is advised. As this medication inhibits gastric acid secretion, there is an increased risk of bone fractures with long-term use, so caution is necessary. Additionally, long-term use may lead to hypomagnesemia, so it is recommended to regularly check magnesium levels. Due to decreased gastric acidity, there may be a slightly increased risk of gastrointestinal bacterial infections, so if diarrhea persists, a hospital visit is necessary. Caution should be taken as drowsiness may occur while driving or operating machinery. There may be interactions with other medications, so if you are taking other medications, be sure to inform your healthcare provider. This medication should be swallowed whole and should not be chewed or crushed, and should be kept out of reach of children. It is best stored in a cool, dry place away from direct sunlight.

Side effects and when to seek care immediately

Serious side effects

  • Hives
  • severe swelling (edema)
  • chest tightness
  • shortness of breath
  • cold sweat
  • pallor
  • acute hepatitis
  • liver dysfunction
  • jaundice
  • angioedema
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  • anaphylactic reaction
  • shock
  • sudden death
  • coma
  • hyperammonemia
  • rhabdomyolysis
  • disorientation
  • delirium
  • hypomagnesemia
  • reduced platelets
  • reduced white blood cells
  • agranulocytosis
  • hemolytic anemia
  • pancytopenia
  • vesicular skin rash
  • systemic allergic reaction
  • severe edema
  • urinary disturbances

Mild side effects

  • Rash
  • itching
  • hives
  • reduced red blood cells
  • reduced white blood cells
  • increased white blood cells
  • increased eosinophils
  • increased neutrophils
  • reduced lymphocytes
  • anemia
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  • purpura
  • lymphadenopathy
  • hypopigmented anemia
  • pancytopenia
  • agranulocytosis
  • reduced platelets
  • hemolytic anemia
  • elevated ALT
  • elevated AST
  • elevated ALP
  • elevated γ-GTP
  • elevated LDH
  • elevated total bilirubin
  • hypertension
  • myocardial infarction
  • abnormal electrocardiogram
  • migraine
  • syncope
  • angina
  • heart block

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

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture. It is important to maintain the storage temperature between 1 to 30 degrees Celsius. Proper storage will help maintain the efficacy and safety of the medication for a longer time.

Appearance and packaging

Appearance

Yellow round film-coated tablet

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.