Medication info

DICABAM Tablet 12.5mg (Carvedilol)

Prescription medicationTabletOralExpired
Ingredient · strength
Carvedilol›12.5mg / 1 tablet
Manufacturer / importer
Mothers Pharmaceutical Co., Ltd.
Appearance
Reddish-brown round tablet
Packaging
90 tablets (10 tablets/PTP×9) - 90 tablets/PTP [90 tablets (10 tablets/PTP×9)]
Approval status
Expired

MFDS item code 201905651 · Approved 2019.08.12

This product's status changed to Expired on 2024.08.12. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Adjunctive treatment of congestive heart failure; treatment of essential hypertension and chronic stable angina
Who takes it
Adults
Adult dose
Do not increase the dose or discontinue treatment without a doctor's instructions. 1. Essential hypertension 1) Adults (1) Administer carvedilol 12.5 mg orally once daily for the first 2 days, then administer 25 mg orally once daily. (2) The usual dose is 25 mg orally once daily for 2 weeks. If a dose increase is needed, increase to 25 mg 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. However, if the effect is insufficient after 2 weeks of treatment, the dose may be increased. 2. Chronic stable angina 1) Administer 12.5 mg of this drug twice daily for the first 2 days, then administer 25 mg twice daily. 2) The usual dose is 25 mg twice daily for 2 weeks. If a dose increase is needed (excluding older adults), it may be increased to 50 mg twice daily. 3. Congestive heart failure Before starting treatment with this drug, the standard treatment regimen already being used (the conventional treatment regimen for chronic heart failure, generally including an ACE inhibitor, a diuretic, and a digitalis preparation) should be stable. Fluid retention should also be minimized before starting treatment with this drug. 1) The usual initial dose is 3.125 mg of this drug twice daily for 2 weeks. If the patient tolerates this treatment well, increase to 6.25 mg twice daily for 2 weeks, then increase to 12.5 mg twice daily for 2 weeks, and then increase to 25 mg twice daily. 2) After taking each dose for at least 2 weeks, increase the dose gradually to the highest dose the patient can tolerate. 3) The effective minimum dose is 6.25 mg twice daily. The maximum dose is 25 mg twice daily in patients weighing 85 kg or less, and 50 mg twice daily in patients weighing more than 85 kg. 4) To control the rate of absorption, administration with meals in the morning and evening is recommended. Taking this drug with meals slows the rate of absorption and may reduce the incidence of orthostatic hypotension.

Ingredients

Manufacturer
Mothers Pharmaceutical Co., Ltd.

Efficacy & effects

Adjunctive treatment of congestive heart failure; treatment of essential hypertension and chronic stable angina

  • Essential hypertension
  • chronic stable angina
  • congestive heart failure
View approved original text

This medication is used for cardiovascular diseases such as essential hypertension, chronic stable angina, and congestive heart failure. It is particularly effective as an adjunctive therapy with diuretics, digoxin, ACE inhibitors, and other vasodilators. It helps to regulate blood pressure and improve heart function, alleviating symptoms. It should be used appropriately according to the patient's condition to contribute to health improvement.

How to take

Adult dose

Do not increase the dose or discontinue treatment without a doctor's instructions. 1. Essential hypertension 1) Adults (1) Administer carvedilol 12.5 mg orally once daily for the first 2 days, then administer 25 mg orally once daily. (2) The usual dose is 25 mg orally once daily for 2 weeks. If a dose increase is needed, increase to 25 mg 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. However, if the effect is insufficient after 2 weeks of treatment, the dose may be increased. 2. Chronic stable angina 1) Administer 12.5 mg of this drug twice daily for the first 2 days, then administer 25 mg twice daily. 2) The usual dose is 25 mg twice daily for 2 weeks. If a dose increase is needed (excluding older adults), it may be increased to 50 mg twice daily. 3. Congestive heart failure Before starting treatment with this drug, the standard treatment regimen already being used (the conventional treatment regimen for chronic heart failure, generally including an ACE inhibitor, a diuretic, and a digitalis preparation) should be stable. Fluid retention should also be minimized before starting treatment with this drug. 1) The usual initial dose is 3.125 mg of this drug twice daily for 2 weeks. If the patient tolerates this treatment well, increase to 6.25 mg twice daily for 2 weeks, then increase to 12.5 mg twice daily for 2 weeks, and then increase to 25 mg twice daily. 2) After taking each dose for at least 2 weeks, increase the dose gradually to the highest dose the patient can tolerate. 3) The effective minimum dose is 6.25 mg twice daily. The maximum dose is 25 mg twice daily in patients weighing 85 kg or less, and 50 mg twice daily in patients weighing more than 85 kg. 4) To control the rate of absorption, administration with meals in the morning and evening is recommended. Taking this drug with meals slows the rate of absorption and may reduce the incidence of orthostatic hypotension.

Precautions

This medication is often contraindicated in specific patients. For example, individuals allergic to this medication or its components, those with severely impaired cardiac function, those with bradycardia, those with pulmonary-related cardiac diseases, those with severe metabolic disorders due to diabetes, and those with respiratory diseases such as asthma or chronic obstructive pulmonary disease may be at risk when taking this medication. Additionally, pregnant or breastfeeding women and those with severely impaired liver or kidney function should avoid this medication. When using this medication, special caution should be exercised in patients with diabetes, those with severe allergic reactions, the elderly, those with low blood pressure, and those with heart disease. During treatment, symptoms such as dizziness, fatigue, and headaches may occur, and in rare cases, heart rate may slow down or blood pressure may drop too low. If cardiac function worsens or symptoms such as severe swelling or shortness of breath occur, medical consultation should be sought immediately. This medication can affect liver and kidney function; therefore, regular check-ups are required. Do not suddenly discontinue this medication, especially in patients with heart disease; the dosage should be reduced gradually. This medication may interact with other drugs, so it is essential to inform your doctor or pharmacist about any medications currently being taken. Moreover, caution is warranted when taking this medication with alcohol or grapefruit juice. This medication has not been established as safe or effective in children or adolescents and is not recommended. Elderly patients may experience increased drug concentration due to decreased liver function, and should start with lower doses due to the risk of excessive hypotension resulting in stroke. In cases of overdose, severe hypotension, arrhythmias, and shortness of breath may occur, and immediate medical attention is necessary for appropriate treatment. Finally, this medication may discolor when exposed to light, so it should be stored in a light-blocking container and kept out of reach of children.

Side effects

  • Dizziness
  • headache
  • fatigue
  • weakness
  • hallucinations
  • confusion
  • depression
  • sleep disturbances
  • nightmares
  • psychosis
Show 54 more
  • severe bradycardia
  • shock
  • complete atrioventricular block
  • heart failure
  • cardiac arrest
  • hypotension
  • loss of consciousness
  • decreased pulse rate
  • cold extremities
  • edema
  • cardiac arrest
  • worsening of renal function
  • renal failure
  • increased airway resistance
  • nausea
  • diarrhea
  • abdominal pain
  • vomiting
  • constipation
  • urticaria
  • itching
  • lichenoid reactions
  • sweating
  • allergic rash
  • changes in serum aminotransferases
  • thrombocytopenia
  • leukopenia
  • hypoglycemia
  • thyroid hyperfunction masking
  • bradycardia
  • hypotension
  • shortness of breath
  • hypertension in angina
  • hepatic dysfunction
  • jaundice
  • limb pain
  • decreased tear production
  • sensory disturbances
  • visual disturbances
  • eye irritation
  • dry mouth
  • urinary disorders
  • sexual dysfunction
  • allergic reactions
  • toxic epidermal necrolysis
  • Stevens-Johnson syndrome
  • blood pressure lowering
  • myocardial weakness
  • cardiac arrest
  • dyspnea
  • bronchospasm
  • vomiting
  • consciousness disturbance
  • generalized seizures

Not everyone experiences these, and they can vary from person to person.

Storage

This medication may be sensitive to light, so it should be stored in a light-protective container. Additionally, it is best to store the medication at room temperatures between 1 degree and 30 degrees Celsius. This helps to maintain the medication's effectiveness and allows for safe usage.

Appearance and packaging

Appearance

Reddish-brown round tablet

Package unit

90 tablets (10 tablets/PTP×9) - 90 tablets/PTP [90 tablets (10 tablets/PTP×9)]

Same-ingredient medicines

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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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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.