Medication info
Candeamor Tablets 8 mg (Candesartan Cilexetil)

Candeamor Tablets 8 mg (Candesartan Cilexetil)

Prescription medicationTablet경구
Ingredient · strength
Candesartan Cilexetil›8mg / 1 tablet
Manufacturer / importer
(주)종근당
Appearance
Bright pink, biconvex round tablets
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 200807205 · Notified 2008.06.27 · Insurance code 643304840

Summary

Main use
Improvement of essential hypertension and heart failure (left ventricular dysfunction)
Who takes it
Adults · Children
Adult dose
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.
Child dose
Pediatric: The safety and efficacy of this medication in adolescents and children under 18 years have not been established.

Ingredients

Manufacturer
(주)종근당

Efficacy & effects

Improvement of essential hypertension and heart failure (left ventricular dysfunction)

  • Essential hypertension
  • heart failure
  • left ventricular systolic dysfunction
  • decreased left ventricular ejection fraction
View approved original text

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.

How to take

Adult dose

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.

Child dose

Pediatric: The safety and efficacy of this medication in adolescents and children under 18 years have not been established.

Precautions

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.

Side effects and when to seek care immediately

Serious side effects

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

Mild side effects

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.

Storage

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.

Appearance and packaging

Appearance

Bright pink, biconvex round tablets

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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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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.