ARBI-SD Tablet

Adult dose

This medication is administered once daily at a dose of 1 tablet, irrespective of meals. Dosage adjustments should be made every 2 to 4 weeks based on the patient's blood pressure response. For elderly patients, start at the lowest dose and carefully adjust based on the patient’s kidney function, heart function, comorbidities, and other concomitant medications.

Child dose

Safety and efficacy in pediatric patients have not been established.

This medication can cause serious harm or death to the fetus or newborn if taken during the second or third trimester of pregnancy, so treatment should be discontinued immediately upon confirmation of pregnancy. Patients with allergies to this medication’s ingredients, those with specific kidney and liver diseases, pregnant or breastfeeding women, and those with certain electrolyte imbalances or other specific conditions should not take this medication. Patients with decreased blood volume or impaired kidney function may experience hypotension or kidney function deterioration while taking this medication, so they should be monitored closely. This medication can cause electrolyte imbalances, particularly changes in potassium, sodium, magnesium, and calcium levels, so regular blood tests are necessary. During treatment, symptoms such as dizziness or headaches may occur; in severe cases, consult a healthcare provider. Interactions may occur when taken with other medications, so inform your healthcare provider of any drugs currently being taken. This medication may cause the skin to become sensitive to sunlight, so limit sun exposure and appropriate skin protection is necessary. Breastfeeding women should consult a physician before taking this medication, as it can pass into breast milk and affect the infant. In elderly patients or children, the safety and efficacy of this medication have not been fully established, so exercise special caution. In case of overdose, symptoms such as hypotension, electrolyte imbalance, and dehydration may occur; seek appropriate treatment immediately.

Serious side effects

Hives, severe swelling (edema), angioedema, anaphylactic reactions, severe allergic reactions, severe rash with high fever, blistering, peeling skin, pain in oral or ocular mucosa, severe skin reactions, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, respiratory problems, jaundice (yellowing of skin or eyes), liver abnormalities, sudden and severe headaches, lightning headache, seizures, loss of consciousness

Mild side effects

Nausea, metabolic abnormalities (hyperuricemia, hyperglycemia, hyperlipidemia), dizziness, upper respiratory tract infections, headaches, urinary tract infections, chest pain, back pain, peripheral edema, lightheadedness, abdominal pain, dyspepsia, gastroenteritis, diarrhea, elevated AST, elevated GGT, elevated ALT, elevated creatine phosphokinase, arthritis, arthralgia, myalgia, cough, hematuria, hair loss, itching, hives, vomiting, increased serum creatinine, palpitations, anemia,

Store this medication in a tightly closed container to avoid exposure to air and moisture, and it is recommended to keep it at room temperature between 1 to 25 degrees Celsius. This storage method helps maintain the medication's efficacy and prevents deterioration.

Appearance

Round film-coated tablet with reddish-yellow color

Package unit

30 tablets/bottle