Paribenz 10mg (Rabeprazole Sodium)

Adult dose

For adults, take 10 mg of rabeprazole sodium orally once daily. Depending on symptoms, 20 mg may be taken orally once daily. For gastric ulcers, treatment can be continued for up to 8 weeks; for duodenal ulcers, up to 6 weeks. For erosive or ulcerative gastroesophageal reflux disease, 10 mg or 20 mg may be administered orally once daily for 4 to 8 weeks. If not treated after 8 weeks of PPI administration, an additional 8 weeks of 10

Child dose

Safety in children has not been established.

This medication should not be used in patients who have had an allergic reaction to this medication or its components. Patients allergic to penicillin-type antibiotics or macrolide antibiotics should exercise caution when using this medication in combination for Helicobacter pylori eradication therapy. Particularly, serious interactions can occur when used with certain medications, so it is essential to consult a healthcare professional. Women who are pregnant or breastfeeding are advised not to take this medication. Patients with poor liver function or the elderly should use this medication cautiously, as the likelihood of side effects may increase. If symptoms of hypersensitivity such as rash, hives, or itching occur while taking this medication, discontinue use immediately and consult a physician. Regular blood tests and liver function tests should be conducted, and medication should be stopped immediately if abnormal findings are noted. Patients with cardiovascular diseases need to be cautious as it may affect the heart and blood vessels. Gastrointestinal symptoms such as diarrhea, abdominal pain, or nausea may occur, and if severe, notify a healthcare professional immediately. CNS symptoms such as headache, dizziness, or insomnia may also occur, so be cautious. Respiratory symptoms or musculoskeletal pain have also been reported, so consult a physician if symptoms persist. Long-term use of this medication may increase the risk of fractures related to osteoporosis, so caution is required for prolonged use. Hypomagnesemia may occur; hence, it is necessary to periodically check magnesium levels in the blood during long-term use or when used with certain medications. Drowsiness may occur while driving or operating machinery, so caution is advised. Due to potential interactions with other drugs, inform your healthcare professional of any other medications you are taking. Do not chew or crush this medication; swallow it whole in its tablet form. Keep out of reach of children, and do not transfer to other containers. Report any suspected adverse symptoms that arise while taking this medication to a healthcare professional immediately, and regular check-ups and monitoring are necessary.

Serious side effects

Hives, severe swelling (edema), dry skin, toxic epidermal necrolysis (Lyell's syndrome), mucocutaneous syndrome (Stevens-Johnson syndrome), severe allergic reactions, fulminant hepatitis, liver dysfunction, jaundice, liver abnormalities (jaundice), severe edema, high blood pressure, cardiac-related ventricular tachycardia, ventricular tachycardia, pulmonary embolism, ventricular tachycardia, angioedema, difficulty breathing, asthma, respiratory distress, serious neurological symptoms (severe headache,

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 should be stored in a tightly sealed container to protect it from air and moisture. Additionally, it is best stored at room temperature, between 1 to 30 degrees Celsius, avoiding extremes of hot or cold.

Appearance

Pale yellow round enteric-coated tablets

Package unit

For domestic: 28 tablets (28 tablets/PTP X 1) For export: 28 tablets (14 tablets/PTP X 2)