Medication info
Lafrate 20 mg (Rabeprazole Sodium)

Lafrate 20 mg (Rabeprazole Sodium)

Prescription medicationTablet경구
Ingredient · strength
Rabeprazole Sodium›20mg / 1 tablet
Manufacturer / importer
(주)라이트팜텍
Appearance
Pale yellow round enteric coated tablet
Packaging
28 tablets/box [14 tablets/Alu Alu packaging x 2]
Approval status
Active

MFDS item code 201903700 · Approved 2019.06.03

Summary

Main use
Treatment of gastric ulcers and gastroesophageal reflux disease (symptom relief, long-term maintenance)
Who takes it
Adults
Adult dose
For gastric ulcers and duodenal ulcers: Typically, 10 mg of Rabeprazole Sodium is administered orally once daily for adults. Depending on symptoms, 20 mg may be taken orally once daily. It should be administered 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 mg or 20 mg once daily for 4 to 8 weeks. If not resolved after 8 weeks of treatment, further

Ingredients

Manufacturer
(주)라이트팜텍

Efficacy & effects

Treatment of gastric ulcers and gastroesophageal reflux disease (symptom relief, long-term maintenance)

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

This medication helps treat gastrointestinal ulcers such as gastric ulcers and duodenal ulcers, as well as relieve the symptoms of erosive and ulcerative gastroesophageal reflux disease. It is also used for long-term maintenance therapy of gastroesophageal reflux disease and is combined with antibiotics when treating patients with gastrointestinal ulcers infected with Helicobacter pylori. Additionally, it is effective in treating conditions of excessive stomach acid secretion, such as Zollinger-Ellison syndrome. Overall, it is used to improve and treat symptoms related to gastrointestinal ulcers and reflux-related diseases.

How to take

Adult dose

For gastric ulcers and duodenal ulcers: Typically, 10 mg of Rabeprazole Sodium is administered orally once daily for adults. Depending on symptoms, 20 mg may be taken orally once daily. It should be administered 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 mg or 20 mg once daily for 4 to 8 weeks. If not resolved after 8 weeks of treatment, further

Precautions

This medication should not be administered to individuals who are allergic to specific ingredients or have had hypersensitivity reactions to benzimidazole derivatives. Patients who are allergic to penicillin-based or macrolide antibiotics should exercise caution when using this medication in conjunction with those antibiotics. It is also safer not to use this medication for individuals taking specific heart-related medications or antiviral agents, as well as for pregnant or nursing women. Patients with poor liver function or elderly individuals should use this medication more cautiously, and those with a history of drug allergies should also take care. This medication may cause adverse reactions such as rashes, itching, or other reactions in various areas including blood, liver, heart, digestive system, and nervous system, so if any abnormal symptoms occur, immediate consultation with a healthcare provider is advised. Regular monitoring of liver and blood tests is important during long-term use, as the risk of fractures may increase, thus caution is needed for prolonged administration. As this medication suppresses stomach acid secretion, there may be a slight increase in the risk of gastrointestinal bacterial infections, so if abnormal symptoms like diarrhea persist, diagnosis and treatment are necessary. Caution should be taken while driving or operating machinery as drowsiness may occur, and interactions with other medications may be present; therefore, it is essential to inform healthcare providers of any other medications being taken. Pregnant or nursing women should not use this medication, and elderly patients may experience more side effects due to decreased liver function, so treatment may be discontinued if symptoms occur. Safety for children has not been established, and there is limited experience in usage. In case of overdose, there are no specific antidotes, and appropriate treatment should be given based on symptoms; this medication should be swallowed whole and not chewed or crushed. When storing, keep this medication in a closed container away from children, and it is advisable not to transfer it to another container. Long-term use of this medication may cause vitamin B12 absorption disorders, so nutritional status should be monitored if necessary. Furthermore, this medication may affect the results of neuroendocrine tumor tests, so it may be necessary to discontinue it for a certain period before testing. Kidney diseases such as acute nephritis may arise, so if there are any abnormal symptoms related to kidney function, immediate consultation with healthcare providers is necessary.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, fulminant hepatitis, liver dysfunction, jaundice, angina, pulmonary embolism, thrombophlebitis, ventricular tachycardia, supraventricular tachycardia, myocardial infarction, conscious confusion, seizures, severe skin adverse reactions (toxic epidermal necrolysis, Stevens-Johnson syndrome), severe allergic reactions (anaphylaxis, shock), respiratory problems (dyspnea, asthma, apnea, respiratory depression), liver abnormalities (hepatic encephalopathy, jaundice)

Mild side effects

  • Rash
  • itching
  • reduced red blood cells
  • reduced white blood cells
  • increased white blood cells
  • increased eosinophils
  • increased neutrophils
  • reduced lymphocytes
  • anemia
  • petechiae
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  • lymphadenopathy
  • hypochromic anemia
  • pancytopenia
  • agranulocytosis
  • thrombocytopenia
  • hemolytic anemia
  • increased ALT
  • increased AST
  • increased ALP
  • increased γ-GTP
  • increased LDH
  • increased total bilirubin
  • hypertension
  • myocardial infarction
  • electrocardiogram abnormalities
  • migraine
  • syncope
  • angina
  • heart block
  • palpitations

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

Storage

This medication may be sensitive to air or moisture, so it should be stored in a sealed container. It is recommended to maintain a storage temperature between 1 degree and 30 degrees Celsius at room temperature to preserve its efficacy for a longer duration.

Appearance and packaging

Appearance

Pale yellow round enteric coated tablet

Package unit

28 tablets/box [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.

Questions about this medicine

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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.