Medication info
Stafinjisokjeong (Felodipine)

Stafinjisokjeong (Felodipine)

Prescription medicationTabletOral
Ingredient · strength
Felodipine›5mg / 1 tablet
Manufacturer / importer
Hana Pharmaceutical Co., Ltd.
Appearance
Pale pink round film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 200202093 · Approved 2002.04.10

Summary

Main use
Treatment of hypertension and stable angina
Who takes it
Adults · Children
Adult dose
Swallow this medicine whole with water. Do not split, 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 the maximum daily dose of 20㎎. This medicine may be administered concomitantly with a β-blocker or diuretic, and may be administered as monotherapy when other antihypertensive agents are inappropriate. Adjust the dose according to the patient's therapeutic response. 2. Stable angina The initial dose is 5㎎ once daily and may be increased to 10㎎ as needed. This medicine may be administered concomitantly when an adequate response is not achieved with a β-blocker. Adjust the dose according to the patient's therapeutic response. 3. Elderly patients Administer with caution while monitoring the patient's condition, considering an initial dose of 2.5㎎ once daily. 4. Patients with renal impairment Renal impairment does not affect felodipine plasma concentrations. Dose adjustment is not necessary, but administer with caution to patients with severe renal impairment (GFR<30ml/min). 5. Patients with hepatic impairment Felodipine plasma concentrations may be increased in patients with hepatic impairment, and a therapeutic response may occur at a lower dose. Therefore, administer with caution to patients with hepatic impairment, considering an initial dose of 2.5mg once daily; do not administer to patients with severe hepatic impairment.
Child dose
The safety and efficacy of this medication in children have not been established.

Ingredients

Manufacturer
Hana Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of hypertension and stable angina

  • Hypertension
  • stable angina
View approved original text

This medication is mainly used for the treatment of hypertension and stable angina. It helps to control blood pressure within normal range, reducing the burden on the cardiovascular system and the risk of complications. It also aids in relieving chest pain and improving blood flow in patients with stable angina. Regular use of this medication is effective for controlling blood pressure and improving heart function.

How to take

Adult dose

Swallow this medicine whole with water. Do not split, 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 the maximum daily dose of 20㎎. This medicine may be administered concomitantly with a β-blocker or diuretic, and may be administered as monotherapy when other antihypertensive agents are inappropriate. Adjust the dose according to the patient's therapeutic response. 2. Stable angina The initial dose is 5㎎ once daily and may be increased to 10㎎ as needed. This medicine may be administered concomitantly when an adequate response is not achieved with a β-blocker. Adjust the dose according to the patient's therapeutic response. 3. Elderly patients Administer with caution while monitoring the patient's condition, considering an initial dose of 2.5㎎ once daily. 4. Patients with renal impairment Renal impairment does not affect felodipine plasma concentrations. Dose adjustment is not necessary, but administer with caution to patients with severe renal impairment (GFR<30ml/min). 5. Patients with hepatic impairment Felodipine plasma concentrations may be increased in patients with hepatic impairment, and a therapeutic response may occur at a lower dose. Therefore, administer with caution to patients with hepatic impairment, considering an initial dose of 2.5mg once daily; do not administer to patients with severe hepatic impairment.

Child dose

The safety and efficacy of this medication in children have not been established.

Precautions

This medication should not be used in women who are pregnant or may become pregnant. It should not be administered to patients with severely impaired cardiac function or those with acute myocardial infarction or unstable angina. Patients with severe liver or kidney dysfunction and certain heart valve diseases should also exercise caution. Patients with genetic issues such as lactose intolerance should avoid using this medication due to the lactose content. Caution is required when administering this medication to the elderly, patients with heart failure, hypotension, or liver dysfunction, and their condition should be closely monitored. When starting treatment or increasing the dosage, symptoms such as facial flushing, headache, and palpitations may occur. Cardiac-related side effects such as chest tightness or shortness of breath may rarely occur. Neurological symptoms such as headache, dizziness, drowsiness, and fatigue may also appear, so caution is needed. Gastrointestinal symptoms may include nausea, constipation, and abdominal pain. If there are dental health issues, symptoms of gingivitis or gingival hyperplasia may occur, so attention to oral hygiene is important. Liver and kidney functions may also be affected, requiring regular check-ups. Skin reactions such as rash, itching, and urticaria may also occur, and if symptoms become severe, discontinuation of the medication is necessary. Other endocrine side effects such as myalgia or arthralgia, and occasionally increased blood glucose have been reported. This medication may interact with other drugs, so it's essential to consult with a doctor or pharmacist when taken with blood pressure medications, antibiotics, antifungals, anticonvulsants, etc. Avoid taking with grapefruit juice, as it may enhance the drug's effect. The safety of this medication during pregnancy or breastfeeding has not been established, so it should be avoided or discussed with a specialist. It is not advisable for children as safety has not been confirmed. In case of overdose, serious cardiovascular side effects and toxicity symptoms can occur, requiring immediate emergency treatment. Sudden discontinuation of this medication can worsen symptoms, so dosage should be gradually reduced following a doctor's instructions. Dizziness or fatigue may occur when taking this medication, so caution is advised when driving or operating machinery. This medication is best taken in the morning on an empty stomach or after a light meal.

Side effects

  • Facial flushing
  • headache
  • palpitations
  • dizziness
  • fatigue
  • tachycardia
  • feeling of suffocation
  • chest tightness
  • ankle swelling
  • tachycardia causing angina
Show 80 more
  • hypotension
  • extrasystole
  • heaviness in the head
  • lightheadedness
  • staggering
  • lethargy
  • drowsiness
  • anxiety
  • sensory disturbances
  • syncope
  • nausea
  • constipation
  • discomfort in the stomach
  • heartburn
  • abdominal pain
  • loss of appetite
  • diarrhea
  • thirst
  • vomiting
  • gingival hypertrophy
  • gingivitis
  • elevated AST
  • elevated ALT
  • elevated ALP
  • elevated LDH
  • elevated BUN
  • elevated creatinine
  • anemia
  • rash
  • itching
  • exfoliative dermatitis
  • skin erythema
  • urticaria
  • photosensitivity reaction
  • vascular edema
  • leukocyte lytic vasculitis
  • myalgia
  • arthralgia
  • hyperglycemia
  • weight gain
  • peripheral edema
  • leg cramps
  • shoulder stiffness
  • weakness
  • hand tremor
  • cough
  • throat irritation
  • sweating
  • tears
  • conjunctival injection
  • paresthesia
  • elevated CPK
  • elevated total cholesterol
  • elevated triglycerides
  • decreased serum potassium
  • gynecomastia
  • erectile dysfunction
  • sexual dysfunction
  • increased urination
  • angioedema
  • fever
  • confusion
  • sleep disturbances
  • hypothermia
  • nausea
  • vomiting
  • bradycardia
  • atrioventricular block
  • atrioventricular dissociation
  • ventricular extrasystole
  • deficient contraction
  • impaired consciousness
  • coma
  • convulsions
  • respiratory distress
  • pulmonary edema
  • apnea
  • adult respiratory distress syndrome
  • acidosis
  • hypocalcemia

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

Storage

This medication is sensitive to light, so it should be stored in a tightly sealed container that blocks light. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius. Proper storage will help maintain the effectiveness and safety of the medication.

Appearance and packaging

Appearance

Pale pink round film-coated tablet

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.

Questions about this medicine

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

Related searches

Search tags

Suggested searches

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.