TD-Rabec Tablet 10 mg (Rabeprazole Sodium)

Adult dose

For gastric ulcers and duodenal ulcers: Administer 10 mg orally once a day. Depending on symptoms, it may be increased to 20 mg once daily, with treatment duration of up to 8 weeks for gastric ulcers and 6 weeks for duodenal ulcers. For erosive or ulcerative gastroesophageal reflux disease: Administer 10 mg or 20 mg orally once daily for 4-8 weeks. If untreated, it can be prescribed for an additional 8 weeks at a dosage of 10 mg or 20 mg orally twice daily.

This medication should not be administered to patients with certain allergic reactions. For example, it should not be used in patients who are hypersensitive to this drug or its components, or to benzimidazole derivatives. Moreover, when used in combination with amoxicillin or clarithromycin for the eradication of Helicobacter pylori, it can be risky for those allergic to these antibiotics to take this medication. Pregnant or nursing women should also avoid this drug, as it may affect the fetus or newborn. Patients with impaired liver function or elderly individuals should use this medication with caution, and those with a history of drug hypersensitivity may also require special attention. If rash, itching, or other allergic symptoms occur while taking this medication, it should be discontinued immediately. Routine blood tests are recommended as this medication may cause changes in red or white blood cell counts. Regular liver function tests should also be conducted, and immediate consultation with a doctor should occur if symptoms of hepatitis or jaundice arise. Beware of possible side effects related to the heart or blood pressure, indigestion, diarrhea, nausea, abdominal pain, and other associated symptoms. Neurological symptoms can include headache, dizziness, and insomnia; in severe cases, confusion or seizures may occur, so reporting any unusual symptoms is necessary. Respiratory problems or skin rashes, hair loss have also been reported, so consult with healthcare professionals if these symptoms manifest. Long-term use may increase the risk of fractures related to osteoporosis, so caution is advised during prolonged use. Furthermore, as this medication suppresses gastric acid secretion, there may be a slight increase in the risk of gastrointestinal bacterial infections. Exercise caution when driving or operating machinery, as drowsiness may occur. This medication may interact with other drugs, so inform your healthcare provider of any other medications you are currently taking. In case of overdose, there is no specific antidote; treatment and supportive therapy based on symptoms are required. This drug should be swallowed whole and not chewed or crushed, and stored out of reach of children. It is crucial to consult healthcare professionals immediately if any adverse symptoms arise during use of this medication.

Serious side effects

Hives, severe swelling (edema), chest tightness, shortness of breath, cold sweat, pallor, severe rash with fever, blistering, peeling skin, pain in mouth/eye mucosa, difficulty breathing or shortness of breath, asthma attack, respiratory abnormalities accompanied by cough and fever, jaundice, profound lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, urination problems

Mild side effects

• Rash
• itching
• decreased red blood cells
• decreased white blood cells
• increased eosinophils
• increased neutrophils
• decreased lymphocytes
• anemia
• petechial hemorrhage
• lymphadenopathy

This medication must be stored in a tightly closed container to prevent exposure to air or moisture. It is best to maintain storage temperatures between 1 degree and 30 degrees Celsius.

Appearance

Pale yellow round enteric-coated tablet

Package unit

28 tablets/box [(14 tablets/Alu-Alu x 2)]