Lenipin Tablets (Lercanidipine Hydrochloride)
Lercanidipine Hydrochloride 10mg
Tablet · Prescription medication
Ally Pharmaceutical Co., Ltd.
MFDS item code 200500822 · Notified 2005.06.28
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.
Improvement of mild to moderate essential hypertension
This medication is used to treat mild to moderate essential hypertension.
Lercanidipine hydrochloride should be administered orally at a dose of 5 to 10 mg once daily at least 15 minutes before a meal. The dose may be increased up to 20 mg based on the patient's symptoms. Since the maximum blood pressure-lowering effect may be evident after 2 weeks, dosage adjustments should be gradual.
This medication should not be used in certain patients. For example, individuals who are allergic to this medication or similar components, those who are pregnant or nursing, as well as patients with severe heart, liver, or kidney issues should not take this medication. Additionally, this medication is not to be used by children or adolescents under the age of 18. Patients with genetic issues like lactose intolerance should also avoid this medication. When using this medication, particular caution should be exercised in patients with weakened heart function or slightly impaired kidney and liver function, as well as those with a history of angina. It is advisable to avoid alcohol as it may lead to significantly low blood pressure. During treatment, symptoms such as facial flushing, swelling of the hands and feet, rapid heartbeat, dizziness, headache, and digestive disturbances may occur. Regular tests may be necessary as there may be abnormalities in liver function. Abruptly stopping this medication can lead to worsening symptoms, so dosage should be gradually reduced when discontinuing. Furthermore, special care may be needed when driving or operating machinery. When taking this medication alongside other drugs, interactions may occur, so it is important to consult a doctor or pharmacist, especially when co-administering specific antifungals, antibiotics, anticonvulsants, or immunosuppressants. It is safer for women who are pregnant or may become pregnant, as well as women who are nursing, not to take this medication. Animal studies have reported potential effects on fetuses. In cases of overdose, severe hypotension or heart issues can occur, requiring immediate hospital visit, with treatment based on symptoms. Finally, this medication should be kept out of reach of children and it is advisable not to transfer it to other containers.
Facial flushing, peripheral edema, palpitations, tachycardia, headache, dizziness, weakness, fatigue, drowsiness, neuroses, digestive disturbances, nausea, vomiting, abdominal pain, diarrhea, polyuria, urinary frequency, gingival hyperplasia, rash, myalgia, tremors, insomnia, dry mouth, hand tingling, cough, abdominal bloating, erectile dysfunction, low blood pressure, arrhythmia, skin tingling, premature contractions, tongue stiffness, increased ventricular premature contractions, gastrointestinal disturbances
Not everyone experiences these, and they can vary from person to person.
This medication should be kept in a tightly sealed container to protect it from air and moisture. It is important to maintain the storage temperature between 1°C and 30°C. Doing so will help preserve the effectiveness of the medication and ensure safe use.
Yellow round film-coated tablets
30 tablets/bottle, 100 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.