Olmesartan Medoxomil Plus Tablet 20/12.5 mg

Adult dose

Take one tablet of this medication once daily, regardless of meals. The dosage should be adjusted every 2 to 4 weeks based on the patient's blood pressure response. Elderly patients should start at the lowest dose, adjusting carefully according to renal function, cardiac function, chronic conditions, and concomitant medications. It is administered to patients with mild to moderate renal impairment (creatinine clearance >30 mL/min), while it should not be given to patients with severe renal impairment.

Child dose

Safety and efficacy in pediatric patients have not been established.

This medication can cause serious harm to the fetus or newborn if taken during the second and third trimesters of pregnancy; therefore, it should be discontinued immediately upon confirmation of pregnancy. Patients with an allergy to any components of this medication or those with certain kidney or liver diseases, as well as pregnant or nursing women, should not take this medication. Patients with decreased blood volume or low salt levels should closely observe their condition before starting this medication and take immediate action if symptoms of low blood pressure occur. Patients with impaired kidney function or kidney transplant recipients should frequently check kidney function and electrolyte status via blood tests while taking this medication. Patients with liver disease or heart valve disease also need to exercise caution when using this medication. This medication may increase the risk of skin cancer, so one should avoid sun exposure and consult a physician immediately if there are any skin changes. Possible side effects include dizziness, headache, indigestion, and cough; severe side effects should be reported to healthcare professionals immediately. Be cautious of interactions when taken with other antihypertensive medications, potassium supplements, diuretics, etc., and especially avoid taking it together with lithium or non-steroidal anti-inflammatory drugs. Patients with diabetes may be affected in terms of blood sugar control; thus, blood sugar levels should be monitored frequently. Elderly patients and children may require dose adjustments and close supervision, as safety in pediatric patients has not been established. In the case of overdose, symptoms such as low blood pressure, electrolyte imbalance, and dehydration may occur, so immediate medical attention is necessary. If breastfeeding, this medication may be passed to breast milk and could cause adverse reactions in the baby; therefore, either breastfeeding or the medication should be discontinued. While taking this medication, regular blood tests and checks of physical condition should be performed, and immediate consultation with a physician is required if any abnormal symptoms occur.

Serious side effects

Hives, severe swelling (edema), angioedema, anaphylactic reaction, severe rash with fever, blisters, skin peeling, oral/ocular mucosal pain, difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough + fever, yellowing of the skin or eyes (jaundice), extreme lethargy, acute renal failure, jaundice, severe edema, hypertension, sudden and severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances

Mild side effects

• Nausea
• dizziness
• hyperuricemia
• upper respiratory infection
• headache
• urinary tract infection
• chest pain
• lower back pain
• peripheral edema
• lightheadedness

This medication should be stored in a tightly sealed container to protect it from air and moisture, preferably at a temperature between 1 to 25 degrees Celsius. Proper storage will help maintain the efficacy of the medication and prevent deterioration.

Appearance

A round film-coated tablet with a reddish-yellow color

Package unit

30 tablets per bottle, 300 tablets per bottle