Resprazole Tablet 20 mg (Rabeprazole Sodium)

Adult dose

For gastric ulcers and duodenal ulcers: 10 mg is administered orally once a day. Depending on the symptoms, 20 mg may be administered orally once a day. Treatment duration is up to 8 weeks for gastric ulcers and up to 6 weeks for duodenal ulcers. For erosive or ulcerative gastroesophageal reflux disease: 10 mg or 20 mg is administered orally once a day for 4 to 8 weeks. If symptoms persist after 8 weeks, an additional 8 weeks of 10 mg or 20 mg may be given.

This medication should not be used in patients who are allergic to certain medications or ingredients or have had hypersensitivity reactions. Women who are pregnant or breastfeeding should not take this medication. Caution is required for patients with impaired liver function or the elderly. It is advisable to take this medication while undergoing regular blood tests and liver function tests. Long-term use may increase the risk of fractures. If allergic reactions such as rashes, itching, or difficulty breathing occur during use, discontinue immediately and inform healthcare personnel. This medication inhibits gastric acid secretion, which may increase the risk of bacterial infection in the gastrointestinal tract; consult a healthcare professional if diarrhea persists. Caution should be taken as drowsiness or dizziness may occur when driving or operating machinery. There may be interactions with other medications, so inform healthcare personnel of any other medications being taken. Do not chew or crush the tablets; swallow them whole, and keep them out of reach of children.

This medication should be stored in a tightly sealed container to protect it from air and moisture, and it is recommended to keep it at room temperature between 1 and 30 degrees Celsius. This storage method helps maintain the medication's effectiveness.

Appearance

Pale yellow round enteric-coated tablet

Package unit

28 tablets (14 tablets/Alu-alu X2)