Viewing nowAltirizine Tablets (Levocetirizine Hydrochloride)
Levocetirizine Hydrochloride 5mg
Tablet · Prescription medication
Hubist Pharmaceuticals Co., Ltd.

MFDS item code 201403886 · Notified 2014.08.20 · Insurance code 628800100
Relief of symptoms of allergic rhinitis and chronic urticaria
This medication helps relieve the symptoms of seasonal and perennial allergic rhinitis and chronic idiopathic urticaria. It can also be used to improve symptoms when applied with hydrocortisone topical preparation for dermatitis and eczema associated with itching. It is used to reduce discomfort from allergies and skin conditions.
Adults and children over 6 years: take 1 tablet (5 mg of levocetirizine hydrochloride) orally once daily, regardless of meals. Adjust according to age and symptoms. For patients with renal impairment, adjust dosage based on renal function (estimated glomerular filtration rate [eGFR]). - Normal renal function (≥ 90 mL/min): 1 tablet once daily. - Mild renal impairment (60 -< 90 mL/min): 1 tablet once daily.
This medication should not be used in patients who are allergic to specific components or have hypersensitivity to hydroxysine or piperazine derivatives. Patients with end-stage renal disease or those undergoing hemodialysis should not take this medication. It should not be administered to infants under 1 year, and children under 6 years should receive it in liquid form rather than as tablets. This tablet contains lactose, so patients with lactose intolerance or related genetic disorders should not use this medication. Patients with renal or liver function impairment, as well as the elderly, should take this medication cautiously, as its concentration may increase. Drowsiness, fatigue, headache, dizziness, and other central nervous system symptoms may occur during treatment, so caution is advised when driving or operating machinery. Gastrointestinal symptoms such as nausea, abdominal pain, and diarrhea may also occur. Rare side effects such as heart palpitations, blood abnormalities, allergic reactions, and blurred vision have been reported. Drowsiness or lethargy may occur after taking this medication, so caution is required, and taking it with alcohol or central nervous system depressants may exacerbate these symptoms. Patients with urinary excretion disorders or epilepsy should use this medication cautiously as their condition may worsen. Pregnant women should take this medication according to their doctor’s instructions due to limited safety data, and breastfeeding women should be cautious as this medication may be secreted in breast milk and could cause adverse reactions in the infant. Children and the elderly may require dose adjustments due to decreased kidney function which could lead to increased drug concentrations. This medication may affect the results of allergy tests; it is advisable to discontinue it before testing. In case of overdose, symptoms such as drowsiness, agitation, and restlessness may occur, and as there is no specific antidote, treatment should be symptomatic. This medication is difficult to remove by hemodialysis.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container that can block light, at a temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the drug's effectiveness for a longer period.
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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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.