Nulrabec 10mg (Rabeprazole Sodium)

Adult dose

Gastric ulcer, duodenal ulcer: Typically, 10 mg is administered orally once a day, which can be increased to 20 mg once daily depending on symptoms. Treatment duration is up to 8 weeks for gastric ulcers and up to 6 weeks for duodenal ulcers. Erosive or ulcerative gastroesophageal reflux disease: Administer 10 mg or 20 mg once daily for 4 to 8 weeks. If symptoms persist after 8 weeks, 10 mg or 20 mg can be taken orally twice daily for an additional 8 weeks (for severe lesions).

This medication should not be used in patients who have had allergies or hypersensitive reactions to any of its ingredients. This medication should not be administered to pregnant or breastfeeding women. Patients with liver dysfunction or the elderly should exercise caution when using this medication. If symptoms such as rash or itching occur during treatment, use should be stopped immediately. It is important to have regular blood tests and liver function tests to check for abnormalities. This medication can cause adverse reactions in various areas such as the heart, gastrointestinal tract, nervous system, and skin, so consult a healthcare professional if symptoms occur. Long-term use may increase the risk of fractures and should be approached with care. This medication may interact with other medications, so it is essential to inform healthcare providers about any drugs currently being taken. Caution is needed when driving or operating machinery as drowsiness may occur. There is no specific antidote for overdose, so appropriate treatment should be administered based on symptoms. This medication should be swallowed whole without chewing or breaking the tablets. Keep the medication in a safe place out of reach of children. Long-term use may affect the absorption of vitamin B12, so supplementation may be necessary. This medication suppresses gastric acid secretion, which may slightly increase the risk of gastrointestinal infections. If skin rash or autoimmune symptoms such as systemic lupus erythematosus appear during the use of this medication, notify your healthcare provider immediately. You may need to temporarily stop taking this medication before certain tests, so consult with your healthcare provider if tests are planned.

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, fulminant hepatitis, liver dysfunction, jaundice, angina, ventricular tachycardia, thrombotic venous inflammation, supraventricular tachycardia, deep vein thrombosis, pulmonary embolism, ventricular tachycardia, angioedema, skin necrolysis (Lyell syndrome), mucocutaneous eruption syndrome (Stevens-Johnson syndrome), severe skin adverse reactions, acute interstitial nephritis (potential progression to renal failure), severe allergic reactions, dyspnea

Mild side effects

• Rash
• itching
• decreased red blood cells
• decreased white blood cells
• increased white blood cells
• increased eosinophils
• increased neutrophils
• decreased lymphocytes
• anemia
• purpura

This medication is susceptible to air and moisture, so it must be stored in a sealed container. The recommended storage temperature is between 1 and 30 degrees Celsius at room temperature. Storing the medication this way will help maintain its effectiveness.

Appearance

Pale yellow round enteric-coated tablet

Package unit

28 tablets (14 tablets/Alu-Alu pack x 2)