Viewing nowCombinationOlmesartan Medoxomil/Amlodipine Besylate/Hydrochlorothiazide Tablets 5/20/12.5 milligrams
Olmesartan Medoxomil 20mg · Amlodipine Besylate 6.944mg +1 more
Tablet · Prescription medication · Combination
Medica Korea Co., Ltd.

MFDS item code 202002972 · Approved 2020.04.24 · Insurance code 646005450
Improvement in blood pressure control for essential hypertension
This medication is used in combination therapy of Amlodipine and Olmesartan Medoxomil for patients with essential hypertension whose blood pressure is not adequately controlled. It efficiently lowers blood pressure and reduces the risk of cardiovascular complications. It aids in hypertension management and reduces strain on the heart and blood vessels, improving overall health.
The recommended dosage is one tablet once daily, taken with water regardless of meals. It is advisable to take it at the same time each day (e.g., in the morning). The maximum dosage is Amlodipine/Olmesartan Medoxomil/Hydrochlorothiazide at 10/40/25mg. Dosage escalation steps are as follows: 5/20/0mg → 5/20/12.5mg → 5/40/0mg → 5/40/12.5mg → 5/40/25mg.
Safety and efficacy for pediatric patients under 18 years have not been established, and the use of this medication is not recommended.
This medication can cause serious harm or death to the fetus and newborn if used during the second and third trimesters of pregnancy, so treatment must be discontinued immediately upon confirmation of pregnancy. Patients with allergies to any ingredients or related drugs, those who are pregnant or breastfeeding, or those with severe hypotension, heart valve problems, unstable heart failure after acute myocardial infarction, or severe kidney or liver impairment should not take this medication. Patients with reduced blood volume or renal function may experience hypotension initially when starting this medication. Their condition should be closely monitored, and appropriate measures taken as needed. This medication may affect kidney function, so patients dependent on renal function, kidney transplant recipients, or those with renal artery stenosis should exercise caution when using it. Patients with impaired liver function or liver disease are at risk for hepatic coma, and this medication is not recommended for those with severe liver impairment. During treatment, blood pressure may drop too low, causing dizziness or orthostatic hypotension, so caution is advised with activities such as heights or driving. This medication can cause electrolyte imbalances, so electrolyte levels should be regularly monitored through blood tests. Particular caution is necessary when taking this medication with potassium supplements or potassium-sparing diuretics, as potassium levels may increase. Numerous drug interactions may occur; consult a physician or pharmacist if taking other medications. Efficacy and safety for children and adolescents under 18 years have not been established, so its use is not recommended. In older adults, dosage should be adjusted with consideration for reduced renal and liver function, and caution should be exercised during use. In case of overdose, symptoms such as hypotension, palpitations, and bradycardia may occur, necessitating immediate treatment and monitoring in a hospital. This medication should be stored away from moisture, heat, and direct sunlight in a place inaccessible to children. Skin photosensitivity reactions may occur during treatment, so care should be taken to avoid excessive sun exposure. Women who are pregnant or planning to become pregnant should consult a physician before taking this medication, and breastfeeding mothers should either avoid it or consult a specialist.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in mucous membranes of mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, yellowing of skin or eyes (jaundice), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis.
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air and moisture, so it should be stored in a tightly sealed container. It is important to keep the storage temperature between 1°C and 30°C to maintain the medication's effectiveness and safety over time.
White-orange round film-coated tablet
30 tablets/Alu-Alu[(10 tablets/Alu-Alu × 3)]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Olmesartan Medoxomil · Amlodipine Besylate +1 more
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SYNEX Co., Ltd.
Olmesartan Medoxomil · Amlodipine Besylate +1 more
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Olmesartan Medoxomil · Amlodipine Besylate +1 more
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SYNEX Co., Ltd.
CombinationAmlodipine Besylate 6.944mg · Olmesartan Medoxomil 20mg +1 more
Tablet · Prescription medication · Combination
JW Pharmaceutical Corporation
Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.