Viewing nowCandeamor Tablets 8 mg (Candesartan Cilexetil)
Candesartan Cilexetil 8mg
Tablet · Prescription medication
Jong Kun Dang Co., Ltd.

MFDS item code 200807205 · Notified 2008.06.27 · Insurance code 643304840
Improvement of essential hypertension and heart failure (left ventricular dysfunction)
This medication helps control blood pressure in patients with essential hypertension, reducing the risk of cardiovascular complications. Additionally, in heart failure patients with impaired left ventricular systolic function, this drug is used as an adjunct treatment, especially when monotherapy with ACE inhibitors is insufficient or intolerable, improving cardiac function. This medication helps alleviate heart failure symptoms and enhance the patient's daily living abilities. Therefore, it is effectively used for the treatment of both essential hypertension and heart failure.
Essential hypertension in adults: The recommended starting and maintenance dose of Candesartan Cilexetil is 8 to 16 mg taken orally once daily. If blood pressure remains insufficiently controlled after 4 weeks of treatment with 16 mg once daily, the dose may be increased to a maximum of 32 mg once daily. For patients with intravascular volume depletion, renal impairment, or liver impairment, the initial dose should be adjusted accordingly. Heart failure in adults: The initial dose is recommended to be 4 mg taken once daily. The dose may be doubled at intervals of at least 2 weeks, and depending on the patient's tolerance, it may be increased to a maximum of 32 mg once daily.
Pediatric: The safety and efficacy of this medication in adolescents and children under 18 years have not been established.
This medication can cause serious harm to the fetus and newborn when administered during pregnancy, especially in the second and third trimesters, so it should be discontinued immediately upon confirmation of pregnancy. This medication should not be used by individuals with a known allergy to this drug or its components, pregnant or nursing women, patients with severe liver dysfunction, or those with hereditary angioedema. Elderly patients, patients with hyperkalemia, liver dysfunction, cardiovascular diseases, and impaired renal function should use this medication with caution and require regular monitoring. During treatment, side effects may occur, such as dizziness, back pain, and respiratory infections, and serious side effects, though rare, such as blood abnormalities, liver function abnormalities, skin rashes, and renal dysfunction may also arise, necessitating immediate consultation with a physician if unusual symptoms occur. Heart failure patients, kidney transplant patients, and patients on dialysis need to closely monitor blood pressure and renal function while using this medication, and it is safer to start with a lower initial dose and gradually increase it. The blood pressure-lowering effects may be enhanced when used with other antihypertensive medications, so it is advised to consult with a physician or pharmacist regarding interactions with other medicines being taken. Women who are capable of becoming pregnant should confirm their pregnancy status before taking this medication and should take precautions not to become pregnant during treatment, while it is advisable to avoid using this medication while breastfeeding. The safety and efficacy of this medication in children and adolescents have not been adequately established, therefore its use in individuals under 18 years of age is not recommended. In the case of overdose, hypotension, dizziness, and rapid heart rate may occur, and in such cases, immediate medical attention is required. This medication should be stored out of the reach of children, and it is safer not to transfer it to another container. Caution is required when driving or operating machinery as dizziness or drowsiness may occur.
Hives, severe swelling (edema), shock, fainting, loss of consciousness, difficulty breathing, cold sweat, pallor, severe allergic reactions, severe rash with high fever, blisters, skin peeling, painful mucous membranes of the mouth/eyes, severe skin reactions, shortness of breath or difficulty breathing, asthma attacks, respiratory issues accompanied by cough and fever, jaundice (yellowing of skin or eyes), generalized malaise, liver abnormalities (jaundice), sudden
Dizziness, back pain, respiratory infection (upper respiratory tract infection, pharyngitis, rhinitis), fatigue, peripheral edema, chest pain, headache, bronchitis, cough, sinusitis, nausea, abdominal pain, diarrhea, vomiting, arthralgia, proteinuria, weakness, fever, sensory disturbances, indigestion, gastroenteritis, tachycardia, palpitations, increased creatine kinase, hyperglycemia, hypertriglyceridemia, hyperuricemia, myalgia, nasal hemorrhage, anxiety, depression, drowsiness, dyspnea, rash, sweating
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to air and moisture, so it should be stored in a tightly sealed container. It is best to maintain a storage temperature between 1 and 30 degrees Celsius.
Bright pink, biconvex round tablets
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.