Felodipine Tablet (Felodipine)
Felodipine 5mg
Prescription medication
Korea Union Pharmaceutical Co., Ltd.
MFDS item code 200401590 · Notified 2004.12.06
This product's status changed to Expired on 2024.07.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Treatment of hypertension and stable angina
This medication is used for hypertension and stable angina.
Swallow this medicine whole with water. Do not divide, chew, or crush it. 1. Hypertension The initial dose of felodipine is 5㎎ once daily, and the maintenance dose is 5-10㎎ daily, administered orally in the morning. Do not exceed 20㎎ per day. This medicine may be administered concomitantly with a β-blocker or diuretic, and may be administered as monotherapy when other antihypertensive agents are unsuitable. Adjust the dose according to the patient's response to treatment. 2. Stable angina Administer an initial dose of 5㎎ once daily; the dose may be increased to 10㎎ as needed. This medicine may be administered concomitantly when a β-blocker does not provide a sufficient effect. Adjust the dose according to the patient's response to treatment. 3. Elderly patients Administer with caution while monitoring the patient's condition; consider an initial dose of 2.5㎎ daily. 4. Patients with renal impairment Renal impairment does not affect the plasma concentration of felodipine. Dose adjustment is not necessary, but administer with caution to patients with severe renal impairment (GFR<30ml/min). 5. Patients with hepatic impairment The plasma concentration of felodipine may increase in patients with hepatic impairment, and they may respond to treatment at lower doses. Therefore, administer with caution to patients with hepatic impairment; consider an initial dose of 2.5mg daily. Do not administer to patients with severe hepatic impairment.
Safety and efficacy in pediatric patients have not been established.
This medication should not be used in women who are pregnant or may become pregnant. It should also not be administered to patients with severely impaired heart function, acute myocardial infarction, or unstable angina. Patients with severe liver or kidney function impairment, as well as those with specific genetic lactose metabolism issues, should not use this medication. Careful use is required in elderly patients or patients with excessively low blood pressure or liver function problems. Initial doses or dose increases can cause symptoms such as flushing, headache, palpitations, dizziness, and fatigue. These symptoms are usually temporary and can vary with dosage. If blood pressure drops too low or heart rhythm becomes irregular, consult a physician immediately. Additionally, this medication contains certain colorants and lactose, so caution is needed for those with allergies or lactose intolerance. Sudden discontinuation of this medication may worsen symptoms, so the dosage should be gradually reduced according to a physician's instructions. In cases of excessively low blood pressure, the medication should be reduced or stopped, and appropriate treatment should be received. It is recommended to take this medication in the morning on an empty stomach or after a light meal. When taking it with other antihypertensive medications or specific antibiotics, antifungals, or anticonvulsants, interactions may occur, so it is essential to consult with a physician or pharmacist. In particular, taking it with grapefruit juice may excessively increase the effect of the medication, so it should be avoided. It is safest for pregnant or breastfeeding women not to use this medication, and if necessary, breastfeeding should be stopped. Safety for children has not been established, therefore it should not be used in pediatric patients. Elderly patients should start at a lower dose and be closely monitored. In cases of overdose, severe symptoms such as decreased blood pressure, arrhythmia, and decreased consciousness may occur, and emergency treatment should be received immediately. Dizziness or fatigue may occur during the use of this medication, so caution should be exercised while driving or operating machinery.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a closed container that can block light, preferably at room temperature between 1 and 30 degrees Celsius. This storage condition helps maintain the effectiveness of the medication.
Round, pale pink film-coated tablet
30 tablets/bottle, 300 tablets/bottle, 500 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.