Viewing nowAnguk Carvedilol Tablet 12.5 mg
Carvedilol 12.5mg
Tablet · Prescription medication
Anguk Pharmaceutical Co., Ltd.

MFDS item code 200702195 · Notified 2007.02.20 · Insurance code 650201480
Treatment of essential hypertension; adjunctive treatment of congestive heart failure; treatment of chronic stable angina
This medication is used for the treatment of essential hypertension, chronic stable angina, and congestive heart failure. It is particularly helpful in reducing the burden on the heart caused by hypertension, improving heart function, and is expected to have a supplemental therapeutic effect when prescribed in combination with diuretics, digitalis preparations, ACE inhibitors, or other vasodilators. Therefore, it is a good choice for effectively controlling blood pressure and alleviating symptoms of heart disease.
Do not increase the dose or stop taking this medicine without your doctor's instructions. 1. Essential hypertension 1) Adults (1) For the first 2 days, administer 12.5 mg of carvedilol orally once daily, then administer 25 mg orally once daily. (2) The usual dosage is 25 mg orally once daily for 2 weeks. If an increase is needed, increase to 25 mg per dose twice daily. The maximum dose per administration is 25 mg, and the maximum daily dose is 50 mg. 2) Older adults In some older adults, 12.5 mg once daily may be sufficient to produce an adequate effect. However, the dose may be increased if the effect is insufficient after 2 weeks of administration. 2. Chronic stable angina 1) For the first 2 days, administer 12.5 mg of this medicine per dose twice daily orally, then administer 25 mg per dose twice daily orally. 2) The usual dosage is 25 mg per dose twice daily for 2 weeks. If an increase is needed (excluding older adults), the dose may be increased to 50 mg per dose twice daily. 3. Congestive heart failure Before starting treatment with this medicine, the patient's existing standard treatment regimen (conventional treatment for chronic heart failure with an ACE inhibitor, a diuretic, and usually a digitalis preparation) must be stable. Fluid retention should also be minimized before starting treatment with this medicine. 1) The usual initial dosage is 3.125 mg of this medicine per dose twice daily orally for 2 weeks. If the patient tolerates this treatment well, increase the dose to 6.25 mg per dose twice daily for 2 weeks, then to 12.5 mg per dose twice daily for 2 weeks, and then to 25 mg per dose twice daily. 2) After taking each dose for at least 2 weeks, gradually increase the dose to the highest dose the patient can tolerate. 3) The minimum effective dose is 6.25 mg per dose twice daily. The maximum dose is 25 mg per dose twice daily for patients weighing 85 kg or less, and 50 mg per dose twice daily for patients weighing more than 85 kg. 4) To control the rate of absorption, it is recommended that the medicine be taken with meals in the morning and evening. Taking it with meals slows the rate of absorption and may reduce the incidence of orthostatic hypotension.
This medication should not be used in certain patients. For example, individuals allergic to this drug or its components, patients with cardiogenic shock, patients with heart conduction problems, patients with cor pulmonale, and those with metabolic abnormalities due to diabetes should not take this medication. Additionally, individuals with respiratory diseases such as asthma or chronic obstructive pulmonary disease, as well as pregnant or nursing women, should not use this medication. There are also patients who should use this medication with caution. Patients with diabetes, a history of severe allergic reactions or sensitivity to beta-blockers, those with hypotension or impaired kidney function, the elderly, and patients with acute heart disease should exercise caution when using this medication. Mild symptoms such as dizziness, headache, and fatigue may occur while taking this medication, and in rare cases, severe heart problems or psychiatric-related side effects may appear. Heart rate may slow significantly or blood pressure may drop sharply, so regular heart function tests should be conducted, and if any abnormal symptoms occur, consult a doctor immediately. For prolonged use, heart function, blood pressure, liver, and kidney functions should be regularly checked, and sudden discontinuation of the medication may exacerbate heart symptoms, so dosages should be gradually reduced according to a doctor's instructions. This medication may interact with various drugs, so if taking other medications, patients must inform their doctor or pharmacist, especially when taking blood pressure medications, diabetes medications, heart medications, or sedatives. Pregnant or nursing women should not take this medication, and safety in children and adolescents has not been established. Elderly patients may experience prolonged retention of the medication in their bodies due to decreased liver function; therefore, starting with a lower dosage and careful monitoring of their condition is advisable. In cases of overdose, serious heart problems, difficulty breathing, or altered consciousness may occur, necessitating immediate contact with healthcare professionals for appropriate treatment. This medication may discolor when exposed to light, so it should be stored in light-resistant containers and kept out of reach of children.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light, so it should be stored in a special container that does not allow light in. Additionally, it is best to keep the medication at room temperature between 1°C and 30°C, avoiding extremely hot or cold places.
brownish-red round tablet
100 tablets/PTP
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.