Eden Ambroxol Hydrochloride Tablet (Ambroxol Hydrochloride)

Adult dose

Administer orally 30 mg of ambroxol hydrochloride three times a day. For continuous treatment, administer 30 mg two times a day. This medicine can be taken regardless of meals. Dose may be adjusted according to age and symptoms.

This medicine should not be taken by individuals allergic to this medicine or its components. Individuals with severe renal impairment should also not take this medicine. Additionally, those with severe hepatic impairment should not use this medicine. This medicine contains lactose, so those with lactose intolerance or certain genetic issues should avoid taking it. Individuals with renal problems should consult a doctor or pharmacist before taking this medicine. It is also advisable for individuals with peptic ulcers to consult a specialist before taking. Pregnant women, especially during the first three months of pregnancy, are recommended to avoid this medicine, and consultation is required in the later stages of pregnancy. Breastfeeding women should avoid this medicine as it may be transmitted through breast milk. Elderly patients should adjust doses or use cautiously due to potential decline in bodily functions. If symptoms such as skin rash, itching, fever, or sore throat occur while taking this medicine, it should be discontinued immediately, and a professional should be consulted. Gastrointestinal symptoms such as nausea, vomiting, diarrhea, abdominal pain, and heartburn may occur, so caution is needed. Hypersensitivity reactions such as urticaria, skin rash, facial swelling, and breathing difficulties may occur; if symptoms arise, it should be stopped immediately and consultation is necessary. Rarely, respiratory symptoms such as nasal inflammation or increased white blood cells have been reported. Changes in tongue sensation, taste alteration, and paresthesia in limbs may also occur rarely. This medicine may increase antibiotic concentrations in bronchial secretions and phlegm when taken with certain antibiotics. No specific symptoms of overdose have been reported; however, appropriate treatment should be received if symptoms occur. The effects on driving or operating machinery are unknown. This medicine should be kept out of the reach of children and stored in a tightly sealed container, avoiding direct sunlight and keeping in a cool, dry place. Additionally, it should be stored in its original container to prevent misuse or quality degradation.

Serious side effects

Severe skin reactions such as urticaria, severe swelling (angioedema), chest tightness, difficulty breathing, anaphylactic reactions (including anaphylactic shock), and serious skin damage such as mucocutaneous syndrome (Stevens-Johnson syndrome) or toxic epidermal necrolysis (Lyell syndrome)

Mild side effects

Nausea, vomiting, diarrhea, dyspepsia, abdominal pain, heartburn, dry mouth, gastric discomfort, abdominal distention, constipation, loss of appetite, urticaria, skin rash, itching, facial swelling, purulent rhinitis associated with increased white blood cells, changes in tongue sensation, taste alteration, oral paresthesia, paresthesia in arms, chills, mild fever

Drug interactions

Consult a doctor or pharmacist if taking this medicine with antibiotics such as erythromycin, cephalexin, oxytetracycline, amoxicillin, cefuroxime, or doxycycline.

This medicine should be stored in a sealed container to prevent air or moisture from entering and is best kept at room temperature between 1 and 30 degrees Celsius. Storing this way helps maintain the medicine's effectiveness and prevents degradation.

Appearance

White round tablets

Package unit

10 tablets/PTP, 500 tablets/bottle