Medication info
Lafralite Tablet 10 mg (Rabeprazole Sodium)

Lafralite Tablet 10 mg (Rabeprazole Sodium)

Prescription medicationTablet경구
Ingredient · strength
Rabeprazole Sodium›10mg / 1 tablet
Manufacturer / importer
(주)라이트팜텍
Appearance
Light yellow round enteric-coated tablet
Packaging
28 tablets/box [28 tablets (14 tablets/Alu Alu packaging x 2)]
Approval status
Active

MFDS item code 201901579 · Approved 2019.03.15 · Insurance code 690300610

Summary

Main use
Treatment of gastric and duodenal ulcers, relief of symptoms of gastroesophageal reflux disease, and maintenance therapy effects
Who takes it
Adults
Adult dose
For gastric and duodenal ulcers: typically, 10 mg should be administered orally once daily, with a possibility to increase up 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 orally once daily for 4 to 8 weeks; if symptoms are not treated, an additional 8-week course of 10 mg or 20 mg can be given twice daily orally.

Ingredients

Manufacturer
(주)라이트팜텍

Efficacy & effects

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

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

This medication is used for the treatment of ulcers in the stomach and duodenum and is effective for the relief of symptoms of gastroesophageal reflux disease and long-term maintenance therapy. It is also used in combination with antibiotics to treat gastrointestinal ulcers infected with Helicobacter pylori and is applied in the treatment of Zollinger-Ellison syndrome. In summary, it is used for the treatment of various gastrointestinal disorders and relief of symptoms.

How to take

Adult dose

For gastric and duodenal ulcers: typically, 10 mg should be administered orally once daily, with a possibility to increase up 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 orally once daily for 4 to 8 weeks; if symptoms are not treated, an additional 8-week course of 10 mg or 20 mg can be given twice daily orally.

Precautions

This medication should not be used in patients with allergies to specific medications or ingredients. For example, those who have had hypersensitivity reactions to this drug or benzimidazole derivatives should avoid taking it. Additionally, when used in combination with certain antibiotics like amoxicillin or clarithromycin for the eradication of Helicobacter pylori, this drug should not be administered if there is an allergy to those antibiotics. Patients on specific heart-related medications or antiviral agents, as well as pregnant or breastfeeding women, should not use this medication. Patients with impaired liver function, elderly individuals, and those with a history of drug allergies should be particularly cautious when using this drug and should take it carefully under a doctor's direction. While taking the medication, a variety of side effects such as skin rash, itching, blood abnormalities, liver dysfunction, cardiovascular problems, gastrointestinal issues, and neurological symptoms may occur; therefore, if these symptoms arise, immediate consultation with healthcare personnel is necessary. This drug strongly suppresses gastric acid secretion, so prolonged use may increase the risk of fractures due to osteoporosis. Therefore, regular check-ups are recommended during long-term use. Furthermore, as this drug lowers gastric acidity, there may be a slightly increased risk of bacterial infections in the gastrointestinal tract. If diarrhea persists or worsens, it should be reported to a physician. Caution is advised when driving or operating machinery, as drowsiness or dizziness may occur. This medication may interact with other drugs, so if taking other medications, it is essential to inform healthcare personnel. Special caution is needed when used in conjunction with warfarin, methotrexate, antibiotics, and antiviral agents. Use of this drug during pregnancy or breastfeeding is not recommended, and its safety in children has not been established. When taking this medication, it should be swallowed whole and not chewed or crushed, and it should be stored out of reach of children. There is no specific antidote for overdose, so treatment should be based on symptoms, and any adjustments to the medication should be made under a doctor's direction. Long-term use of this drug may cause vitamin B12 absorption disorders, so supplementation may be necessary. Finally, this drug should be used with caution, and it is vital to consult healthcare personnel immediately if any unusual symptoms occur.

Storage

This medication should be stored in a tightly sealed container to protect it from air and moisture, ideally at room temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the efficacy of the drug for a longer period.

Appearance and packaging

Appearance

Light yellow round enteric-coated tablet

Package unit

28 tablets/box [28 tablets (14 tablets/Alu Alu 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.

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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.