Rabeprazole Sodium 20 mg Tablets

Adult dose

Gastric ulcers, duodenal ulcers: The usual adult dose is 10 mg of rabeprazole sodium orally once daily. Depending on symptoms, 20 mg may be given once daily. The duration of treatment is up to 8 weeks for gastric ulcers and up to 6 weeks for duodenal ulcers. Erosive or ulcerative gastroesophageal reflux disease: 10 mg or 20 mg once daily for 4 to 8 weeks. If treatment is unsuccessful, an additional 8 weeks of 10 mg may be given.

This medication should not be used in patients with an allergy or history of hypersensitivity to certain components. Pregnant or breastfeeding women should also avoid using this medication. Patients with impaired liver function or the elderly should use this medication cautiously, and patients with a history of allergies should also take care. If symptoms of an allergic reaction, such as rash or itching, appear during treatment, use should be stopped immediately. Regular blood tests and liver function tests should be conducted, and if abnormalities are detected, appropriate measures should be discussed with a doctor. Adverse effects may occur in various systems including gastrointestinal, cardiovascular, neurological, respiratory, musculoskeletal, skin, eyes, and urinary tract; symptoms should be reported to healthcare professionals immediately if they arise. Long-term use may increase the risk of fractures, so caution is warranted, and regular monitoring of magnesium levels is recommended. This medication strongly suppresses gastric acid secretion, which may slightly increase the risk of gastrointestinal bacterial infections. Be cautious as drowsiness may occur when driving or operating machinery. Interactions with other medications may occur, especially when taken with antibiotics, antivirals, or blood coagulation medications, so consultation with a doctor or pharmacist is necessary. This medication should be swallowed whole and not chewed or crushed, and it should be kept out of reach of children. There is no specific antidote for overdose, but symptomatic treatment should be sought; recommended doses should not be exceeded. Long-term use of this medication may lead to vitamin B12 absorption disorders, so periodic testing is needed. Symptoms of autoimmune diseases such as erythema multiforme and lupus may develop, so if such symptoms are suspected, the medication should be discontinued immediately and a specialist consulted. This medication may impair kidney function; if kidney impairment symptoms arise, consult a healthcare professional immediately.

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, fulminant hepatitis, liver dysfunction, jaundice, hepatitis, hepatic encephalopathy, toxic epidermal necrolysis (Lyell syndrome), Stevens-Johnson syndrome, severe allergic reactions, dyspnea, asthma attacks, severe neurological symptoms (headache, seizures, altered consciousness, vision disturbances, paralysis), severe edema associated with elevated blood pressure, acute interstitial nephritis,

Mild side effects

• Rash
• urticaria
• itching
• erythrocytopenia
• leukopenia
• leukocytosis
• eosinophilia
• neutrophilia
• lymphocytopenia
• anemia

This medication may be sensitive to air and moisture and should be stored in a tightly sealed container. It is recommended to maintain a storage temperature between 1 and 30 degrees Celsius at room temperature. Doing so can help maintain the medication's effectiveness and safety for a longer period.

Appearance

Pale yellow circular enteric-coated tablet

Package unit

28 tablets (14 tablets/AluAlu packaging X 2)