Allercure Tablets (epinastine hydrochloride)

Adult dose

Asthma, urticaria, eczema/dermatitis, pruritus, prurigo (itchy eruptions), and ordinary psoriasis accompanied by pruritus Adults: Administer 20 mg of epinastine hydrochloride orally once daily. Adjust the dose appropriately according to symptoms. Allergic rhinitis Adults: Administer 10～20 mg of this drug orally once daily. Adjust the dose appropriately according to symptoms.

This medication should not be used in patients who have an allergic reaction to this drug or its components. Additionally, this medication contains lactose, so it should not be administered to patients with genetic disorders that prevent lactose digestion. Patients with liver disease or a history of liver disease should exercise caution when using this medication, as it may worsen liver conditions. If symptoms of allergy such as rash, urticaria, swelling of the face or extremities occur during treatment, use should be discontinued immediately and medical consultation should be sought. Neurotic symptoms such as drowsiness, headache, dizziness, and insomnia may occasionally occur, so caution is necessary if these symptoms arise. Gastrointestinal symptoms such as indigestion, nausea, abdominal pain, diarrhea, or constipation may occur, and if symptoms are severe, a doctor should be consulted. Due to potential abnormal liver function or jaundice symptoms, it is important to regularly check liver health. Rarely, this drug may affect kidney function, possibly leading to proteinuria, so kidney health should be closely monitored. Urinary symptoms such as increased urinary frequency, hematuria, and urinary retention may occur, and any unusual symptoms should be reported to medical personnel. Rarely, symptoms such as rapid heartbeat or respiratory difficulties like nasal congestion may occur. There may be blood-related adverse reactions, such as thrombocytopenia or leukocytosis, so regular blood tests are needed to monitor condition. Rare adverse reactions such as gynecomastia, menstrual irregularities, and changes in taste may occur, so any unusual changes in the body should be reported. This medication is not intended for immediate relief of asthma attacks, so it should be thoroughly explained to asthma patients regarding its intended use and effects. If patients using long-term steroid treatment take this medication, the tapering of steroids should be done gradually with medical supervision. This drug may cause drowsiness; therefore, caution is required when driving or operating machinery. If there is no effect, do not use it long-term, and seasonal allergy patients should start taking it before symptoms begin. There is a low possibility of drug interactions, but caution may be necessary in cases of concurrent use, so consultation with medical personnel is advised. Pregnant women or those who may become pregnant should only use this medication when absolutely necessary due to uncertain effects on the fetus. Lactating women should avoid using this medication if possible, or discontinue breastfeeding, as it may be excreted in breast milk. Safety in children, infants, and minors has not been fully established, so caution is needed in usage. Elderly patients may have impaired liver and kidney function; thus, regular monitoring for adverse reactions is required, and dosage adjustments may be necessary. In case of overdose, there is a risk of cardiac arrhythmia, so immediate treatment at a medical institution is required, and emergency measures such as gastric lavage or induction of micturition may be necessary. This medication should be stored out of reach of children, and care should be taken not to transfer it to another container, as this may degrade its quality. Taking this drug on an empty stomach may increase blood concentration, so it is advisable to follow the instructions of medical personnel regarding the time and method of administration.

Allergic reactions (rash, hives, reddening), itching, swelling (face, limbs, etc.), erythema with itching, drowsiness, fatigue, headache, dizziness, insomnia, nightmares, numbness, feeling of heaviness in the head, nausea, upper abdominal discomfort, dry mouth, abdominal pain, loss of appetite, vomiting, heaviness in the stomach, feeling of fullness, diarrhea, constipation, dry lips, abdominal bloating, stomatitis, liver dysfunction (increased AST, ALT, γ-GTP, ALP, LDH), jaundice, hepatitis, worsening of symptoms, proteinuria, frequent urination, hematuria, urinary retention, palpitations, shortness of breath, difficulty in expectoration, nasal congestion, thrombocytopenia, leukocytosis, gynecomastia, breast enlargement, menstrual irregularities, flushing, bitter taste, decreased taste sensation, chest pain

This medication should be stored in a sealed container to prevent air and moisture from entering, and it is best kept at room temperature between 1 and 30 degrees Celsius. By storing it this way, the medication's efficacy can be maintained and deterioration can be prevented.

Appearance

White or pale yellow round film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle