Viewing nowLerogen (Levocetirizine Hydrochloride)
Levocetirizine Hydrochloride 5mg
Tablet · Prescription medication
Nexpharm Korea Co., Ltd.

MFDS item code 202001353 · Notified 2020.02.26 · Insurance code 662504370
Relief of symptoms of allergic rhinitis and chronic urticaria
This medication alleviates symptoms of seasonal or perennial allergic rhinitis and is effective for chronic idiopathic urticaria. Additionally, it is utilized in conjunction with hydrocortisone topical preparations for the treatment of dermatitis and eczema accompanied by itching. It is used to assist in improving the quality of life for patients through symptom relief.
Adults and children over 6 years: Administer 1 tablet (Levocetirizine Hydrochloride 5mg) once daily orally, regardless of meals. Adjust dosage according to kidney function. - Normal kidney function (eGFR ≥ 90): 1 tablet once a day - Mild renal impairment (eGFR 60 -< 90): 1 tablet once a day - Moderate renal impairment (eGFR 30 -< 60): 1 tablet every other day
Children over 6 years: Administer 1 tablet (Levocetirizine Hydrochloride 5mg) once daily orally, regardless of meals. Adjust dosing appropriately based on age and symptoms.
This medication should not be used by patients with allergies to specific components or those hypersensitive to hydroxyzine or piperazine derivatives. Patients with end-stage renal disease or those undergoing dialysis should not be administered this medication. It should not be used in infants under 1 year of age, and children under 6 years should be given the liquid form instead of the tablet form. This tablet contains lactose; therefore, patients with lactose intolerance or specific genetic lactose metabolism disorders should avoid taking it. Patients with impaired kidney or liver function, as well as the elderly, should use this medication with caution as blood concentrations may increase. Side effects related to the nervous system such as drowsiness, headache, and dizziness may occur when taking this medication, as well as hypersensitivity reactions like gastrointestinal symptoms or skin rashes. Care is necessary for activities requiring concentration such as driving or operating machinery after taking this medication, and it should be avoided in combination with alcohol or central nervous system depressants. Patients at risk of urinary retention or those with epilepsy need special attention when using this medication. Pregnant or breastfeeding women must consult a doctor before using this medication, as the effects on the fetus or newborn have not been fully elucidated. Dosage adjustments are required for children and the elderly, particularly reducing the dose for the elderly due to decreased kidney function. If undergoing allergy testing, it is advisable to discontinue this medication 3-5 days prior to testing. In cases of overdose, symptoms such as drowsiness or agitation may occur, and there is no specific antidote; treatment should be symptomatic, and blood dialysis is ineffective in eliminating this medication.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container protected from light. Additionally, it is important to maintain storage at a temperature between 1 to 30 degrees Celsius to preserve the medication's efficacy.
White or pale yellow oval film-coated tablets
30 tablets/bottle, 300 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Tablet · Prescription medication
Nexpharm Korea Co., Ltd.

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Tablet · Prescription medication
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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.