Benpra Tablet (Rabeprazole Sodium)

Adult dose

Gastric ulcer, duodenal ulcer: 10 mg orally once daily; if symptoms allow, it can be administered up to 20 mg orally once daily. Erosive or ulcerative gastroesophageal reflux disease: 10 mg or 20 mg orally once daily for 4 to 8 weeks; if not resolved after 8 weeks of treatment, it may be administered again as 10 mg or 20 mg orally twice daily for an additional 8 weeks (Note: 20 mg administered twice daily only for patients with severe mucosal damage).

This medication should not be used in patients who are allergic or have experienced hypersensitivity reactions to specific components. Caution is particularly needed in cases of allergy to penicillin or macrolide antibiotics, especially when used in combination during Helicobacter pylori eradication therapy. Additionally, it is safest for women who are pregnant or breastfeeding not to use this medication. Patients with liver dysfunction, elderly individuals, or those with a history of drug hypersensitivity should use this medication cautiously. This drug contains specific dyes, so caution is needed if allergic to those components. If symptoms of allergy such as rash or itching occur, discontinue use immediately. Regular blood tests and liver function tests should be performed, and if any abnormal signs are detected, the medication should be discontinued and a doctor consulted. Various side effects may occur in multiple areas such as the heart, gastrointestinal tract, nervous system, respiratory system, and skin, so careful observation is required if symptoms occur. Long-term use may increase the risk of osteoporosis and fractures, so consulting a doctor for appropriate measures is advisable if needed. This medication suppresses gastric acid secretion, which may affect the absorption or efficacy of certain drugs, so consulting a specialist is recommended when used in conjunction with other medications. Pregnant or breastfeeding women should not use this medication, and for safety, it should be kept out of reach of children. It is important to swallow the tablets whole without chewing or crushing. Caution is required when driving or operating machinery during use, as drowsiness or decreased concentration may occur. If long-term use is required, dosage and duration should be adjusted according to regular check-ups and the doctor's instructions.

Serious side effects

Urticaria, swelling, chest tightness, dyspnea, severe allergic reactions, fulminant hepatitis, jaundice, acute interstitial nephritis, liver dysfunction, jaundice, severe skin reactions (toxic epidermal necrolysis, Stevens-Johnson syndrome), sudden death, coma, seizures, confusion, vision disturbances, paralysis, severe neurological symptoms, thrombocytopenia, agranulocytosis, hemolytic anemia, pancytopenia, severe edema associated with elevated blood pressure, sudden and very

Mild side effects

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

This medication may be sensitive to air and moisture, so it must be stored in a tightly sealed container. It is best to maintain a storage temperature between 1 degree and 30 degrees Celsius at room temperature. This will help maintain the efficacy and safety of the medication for an extended period.

Appearance

Light yellow round enteric-coated tablet

Package unit

28 tablets (14 tablets/PTP × 2)