Uni Epinephrine 20 mg (Epinastine Hydrochloride)

Adult dose

1. Asthma, urticaria, eczema/dermatitis, pruritus, prurigo, and common psoriasis accompanied by pruritus Adults: Administer 20 mg of epinastine hydrochloride orally once daily. Adjust the dose as appropriate according to symptoms. 2. Allergic rhinitis Adults: Administer 10～20 mg of this medicine orally once daily. Adjust the dose as appropriate according to symptoms.

This medicine must not be used by patients who are allergic to this medication or its components. Additionally, as it contains lactose, patients with genetic disorders that prevent them from digesting lactose should not take this medication. Patients with liver function problems or a history of liver disease should be cautious when using this medication as it may worsen liver condition. If allergic reactions such as rash, urticaria, swelling of the face or extremities, or severe itching occur during use, it is important to stop using this medication immediately and consult a medical professional. Neurological symptoms such as drowsiness, headache, dizziness, and insomnia may occasionally occur, so caution is advised when driving or operating machinery. Gastrointestinal symptoms such as nausea, abdominal pain, diarrhea, and constipation may occur, so report any unusual symptoms. Liver function abnormalities may appear, so regular liver function tests and monitoring of the condition are necessary. Rarely, kidney function abnormalities or urinary symptoms may also occur, thus caution is advised. Symptoms of rapid heartbeat may occur, and respiratory symptoms such as shortness of breath or nasal congestion may rarely arise. Blood abnormalities may also occur, so it is important to immediately report any unusual symptoms to healthcare personnel. This medication is not intended for the rapid relief of asthma attacks, and asthma patients should be aware of this. If there is no effect from long-term use, it is advisable to discontinue use. Women who are pregnant or may become pregnant should use this medication cautiously after consulting with a doctor, and breastfeeding women should avoid using it or discontinue breastfeeding if possible. Caution is advised in children, especially neonates and infants, as safety has not been sufficiently verified. Elderly patients may have impaired liver and kidney function, so dosage adjustments or drug holidays may be necessary if any unusual symptoms occur. In cases of overdose, there is a risk of cardiac arrhythmias, so appropriate treatment should be sought immediately.

Allergic reactions (rash, hives, redness), itching, swelling (face, extremities, etc.), erythema accompanied by itching, drowsiness, lethargy, headache, dizziness, insomnia, nightmares, numbness, feeling of heaviness in the head, nausea, gastric discomfort, dry mouth, abdominal pain, loss of appetite, vomiting, feeling of heaviness in the stomach, feeling of fullness, diarrhea, constipation, dry lips, abdominal distension, stomatitis, liver dysfunction, 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, diminished taste, chest pain

This medication should be stored in a tightly sealed container to protect it from air and moisture. It is advisable to maintain a storage temperature between 1°C and 30°C.

Appearance

White or yellowish round film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle