Viewing nowCombinationEska HCT Tablets 5/20/12.5 mg
Olmesartan Medoxomil 20mg · Amlodipine Besylate 6.944mg +1 more
Tablet · Prescription medication · Combination
Samik Pharmaceutical Co., Ltd.

MFDS item code 201900270 · Approved 2019.01.18 · Insurance code 644004040
Improvement in blood pressure control of essential hypertension
The combination therapy of Amlodipine and Olmesartan Medoxomil is used in patients with essential hypertension who have difficulty in controlling blood pressure with existing treatment. This medication helps dilate blood vessels and lower blood pressure, thereby reducing the risk of cardiovascular disease. Thus, it is effective for preventing complications associated with essential hypertension and improving blood pressure management.
This medication should be taken once daily at 1 tablet with or without food, preferably at the same time each day (e.g., morning). The maximum dosage is Amlodipine/Olmesartan Medoxomil/Hydrochlorothiazide at 10/40/25 mg. Considering the blood pressure response, doses should be adjusted at intervals of more than 2 weeks. The recommended dosages are as follows: - 5/20/12.5 mg: Amlodipine
The safety and efficacy of this medication in patients under 18 years have not been established; therefore, administration is not recommended.
This medication can cause serious harm to the fetus and newborn during the second and third trimesters of pregnancy; therefore, it should be discontinued immediately upon confirmation of pregnancy. People with allergies or hypersensitivity to any component of this medication or similar drugs should not take this medication. Patients with severe hypotension, heart valve problems, unstable heart failure after acute myocardial infarction, or severe kidney or liver dysfunction should not use this medication. Patients with low blood volume or low salt may experience hypotension at the beginning of treatment with this medication; therefore, caution is needed and their condition should be monitored closely. Patients with impaired kidney function or those who have received kidney transplants, as well as patients with renovascular hypertension, should also exercise caution as changes in kidney function may occur while using this medication. Patients with impaired liver function or progressive liver disease should be aware of the risks of hepatic coma when using this medication. Patients with aortic or mitral stenosis, or obstructive heart disease should pay particular attention while taking this medication. Patients with systemic lupus erythematosus or those allergic to the components of this medication, as well as patients who have been using diuretics for long periods, should also use caution. Since this medication lowers blood pressure, there is potential for interactions with other medications when used concurrently for hypertension treatment, so consultation with a healthcare professional is advised. During the use of this medication, dizziness or drowsiness may occur, so it is advisable to avoid driving or operating dangerous machinery. The skin may become more sensitive to sunlight; therefore, it is important to take precautions against UV exposure, and if any skin reactions occur, it is essential to consult a healthcare professional immediately. This medication can be used in the elderly; however, starting with a lower dosage is recommended considering the decline in liver or kidney function. In case of overdose, symptoms such as hypotension, palpitations, and bradycardia may occur; thus, patients should visit a hospital for appropriate treatment if symptoms manifest. The safety and efficacy of this medication have not been established in children, so it is advisable not to use it in this population. If breastfeeding, it is recommended to discontinue either breastfeeding or the medication, as this drug may transfer into breast milk and potentially cause adverse reactions in the infant.
Urticaria, severe swelling (edema), anaphylactic reaction, angioedema, Quincke's edema, severe allergic reactions, severe rash with fever, blisters, skin peeling, pain in oral/eye mucosa, severe skin reactions, shortness of breath, pulmonary edema, acute respiratory distress syndrome (ARDS), difficulty breathing, respiratory issues, jaundice, hepatitis, cholestatic jaundice, severe liver abnormalities, sudden and very severe headache, seizures,
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to prevent air or moisture from entering, preferably at room temperature between 1°C and 30°C. Storing it this way will help maintain the drug's effectiveness.
White-orange round film-coated tablets
30 tablets (10 tablets/Alu-Alu × 3)
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Samik Pharmaceutical Co., Ltd.
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CombinationOlmesartan Medoxomil 20mg · Amlodipine Besylate 6.944mg +1 more
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HanKook Daiichi Sankyo Co., Ltd.
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
Prescription medication · Combination
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.