Storabec 20mg (Rabeprazole Sodium)

Adult dose

For gastric ulcers and duodenal ulcers: 10 mg orally once daily. Depending on symptoms, 20 mg may be administered orally once daily. For erosive or ulcerative gastroesophageal reflux disease: 10 mg or 20 mg orally once daily for 4 to 8 weeks. If untreated, an additional 8 weeks of 10 mg or 20 mg may be administered orally twice daily. For symptomatic relief in gastroesophageal reflux disease: 10 mg orally once daily.

This medication should not be used in certain patients. For instance, patients allergic to this medication or its components, patients with hypersensitivity to certain antibiotics, pregnant or breastfeeding women, and patients taking certain antiviral drugs should avoid administration. Patients with poor liver function or elderly patients, as well as those with a history of drug hypersensitivity, should use this medication with caution. As this medication can cause various side effects, if skin rashes, itching, blood abnormalities, liver function abnormalities, heart issues, gastrointestinal symptoms, neurological issues, respiratory difficulties, muscle or joint pain, skin abnormalities, or urinary tract issues occur during use, the medication should be discontinued immediately and a doctor consulted. It is particularly advisable to undergo regular blood tests and liver function tests, and seek appropriate measures should any abnormal symptoms arise. Prolonged use of this medication may increase the risk of osteoporosis-related fractures. Additionally, there is a possibility of hypomagnesemia developing with long-term use, so magnesium levels should be checked regularly and supplementation may be necessary as needed. This medication suppresses gastric acid secretion and may slightly increase the risk of bacterial infection in the gastrointestinal tract, therefore it is important to inform a doctor immediately if diarrhea persists. Caution is advised when driving or operating machinery due to the potential for drowsiness. This medication can interact with other drugs, particularly anticoagulants, antiviral agents, and antibiotics, so it is essential to consult a doctor when used in combination. Pregnant or breastfeeding women should not use this medication and elderly patients should use it with caution due to an increased risk of side effects associated with liver dysfunction. It is advisable not to use this medication in children as safety has not been established. When taking this medication, do not chew or crush the tablets; they should be swallowed whole, and stored out of reach of children. Long-term use of this medication may lead to impaired absorption of vitamin B12, requiring periodic monitoring. Furthermore, this medication may worsen certain autoimmune diseases, so if symptoms such as skin rashes or joint pain occur, a specialist should be consulted. In the case of an overdose, there is no specific antidote, and appropriate treatment should be given based on symptoms; this medication is not removed by hemodialysis.

Serious side effects

• Urticaria
• severe swelling (edema)
• chest tightness
• difficulty breathing
• fever
• severe rash accompanied by high fever
• blisters
• skin peeling
• oral/eyelid mucous membrane pain
• fulminant hepatitis

Mild side effects

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

This medication should be stored in a tightly sealed container to protect it from air and moisture. The storage temperature should be maintained at room temperature between 1°C and 30°C. Proper storage will help maintain the drug's effectiveness and safety for a longer time.

Appearance

Light yellow round enteric-coated tablets

Package unit

28 tablets/pack [28T (14T/PTP x 2 EA)]