Fabizol Tablet 10 mg (Rabeprazole Sodium)

Adult dose

For gastric ulcer and duodenal ulcer: Take 10 mg orally once daily, or 20 mg once daily depending on symptoms. Gastric ulcer can be treated for a maximum of 8 weeks; duodenal ulcer for a maximum of 6 weeks. For erosive or ulcerative gastroesophageal reflux disease: Take 10 mg or 20 mg once daily for 4 to 8 weeks. If not treated after 8 weeks, an additional 10 mg or 20 mg can be taken twice daily.

This medication should not be used by patients who have had allergic reactions to specific drugs or components. Caution is particularly needed for patients with hypersensitivity to penicillin or macrolide antibiotics, and those currently taking certain heart-related medications. Women who are pregnant or breastfeeding should not use this medication. Patients with impaired liver function, the elderly, and those with a history of hypersensitivity reactions should be given this medication with care. If symptoms like skin rash, itching, or hives develop after taking this medication, use should be stopped immediately. Regular blood tests may be necessary as there may be changes in red or white blood cell counts. Regular liver function tests should also be conducted, and if symptoms of hepatitis or jaundice appear, treatment should be discontinued. Abnormal heart symptoms or gastrointestinal issues, and central nervous system symptoms have also been reported, so consult a doctor if any unusual symptoms appear. Long-term use may increase the risk of osteoporosis and fractures; caution is particularly required, and there is also a risk of low magnesium levels, which may require supplementation and monitoring if necessary. This medication suppresses gastric acid secretion, which may slightly increase the risk of gastrointestinal bacterial infections, so inform a doctor if symptoms such as diarrhea persist. Caution is advised when driving or operating machinery as drowsiness may occur. This medication may interact with other drugs, so be sure to inform healthcare providers about any current medications, especially when combined with antibiotics or antiviral drugs. This medication should be swallowed whole and not chewed or crushed, and must be kept out of reach of children. Long-term use of this medication may lead to impaired absorption of vitamin B12, making periodic testing necessary. If pregnant or breastfeeding, this medication should not be taken, and if symptoms appear in elderly or patients with compromised liver function, treatment should be adjusted. In the case of overdose, no specific antidote is available, and appropriate treatment based on symptoms should be administered.

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, fulminant hepatitis, liver dysfunction, jaundice, rigidity, arrhythmia, seizure, coma, diarrhea, angioedema, severe edema accompanied by high blood pressure, severe allergic reaction, severe skin adverse reactions, respiratory problems, liver abnormalities (jaundice), severe neurological symptoms, severe swelling or urination issues, toxic epidermal necrolysis (Lyell syndrome), Stevens-Johnson syndrome (mucocutaneous reaction)

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 prevent exposure to air or moisture. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius to preserve the medication's efficacy and safety.

Appearance

Pale yellow round enteric coated tablet

Package unit

28 tablets (14 tablets/Alu Alu packaging x 2)