Daitus Tablet (Ambroxol Hydrochloride)

Adult dose

Take 30 mg of Ambroxol Hydrochloride three times a day. For continued treatment, take 30 mg twice a day.

Do not take this medicine if you have had an allergic reaction to this medicine or its components. Patients with severe renal impairment or severe liver impairment should refrain from taking this medication. Additionally, individuals with a genetic issue that affects the breakdown of fructose should not take this medication due to its constituents. This medication contains lactose, hence individuals with a genetic inability to digest galactose or lactose should also avoid it. Patients with mild renal impairment or those with peptic ulcers must consult a doctor or pharmacist before taking this medication. It is not recommended for pregnant women, especially within the first three months of pregnancy, as it may cross the placenta and requires caution. Breastfeeding women are also advised to avoid this medication as it may be transmitted through breast milk. Elderly individuals may have decreased bodily functions, so they should adjust the dosage or consult with a physician. This medication contains yellow dye components; individuals with allergies to these components should take it with caution. If symptoms such as skin rash, severe itching, inflammation around the mouth, eyes, or lips appear, discontinue use immediately and consult a healthcare provider. Gastrointestinal symptoms such as nausea, vomiting, diarrhea, abdominal pain, or indigestion may occur; consult a physician if symptoms are severe. Allergic reactions such as hives, angioedema, and breathing difficulties may occur; if these symptoms develop, discontinue use immediately. This medication can increase the concentration of antibiotics in mucus secreted in the bronchi or lungs when taken with certain antibiotics. No specific symptoms have been reported in cases of overdose, but if any abnormal symptoms occur, seek medical advice immediately and receive appropriate treatment according to the symptoms. There are no reports that this medication affects driving or operating machinery, but caution is advised as it may vary by individual. Keep this medication out of the reach of children and store it in a cool, dry place away from direct sunlight. Medicines should be stored in their original containers, as transferring them to another container may lead to quality deterioration or misuse.

Serious side effects

Hives, angioedema, anaphylaxis (including anaphylactic shock), breathing difficulties, mucocutaneous syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome)

Mild side effects

Nausea, vomiting, diarrhea, indigestion, abdominal pain, heartburn, dry mouth, discomfort in the upper stomach, bloating in the abdomen, constipation, loss of appetite, abnormal taste sensations, oral numbness, numbness in the arms, purulent rhinitis associated with leukocytosis, skin rash, itching, facial swelling, and fever that includes chills.

Drug interactions

Consult a physician or pharmacist when this medication is taken with antibiotics such as erythromycin, cephalexin, oxytetracycline, amoxicillin, cefuroxime, and doxycycline.

This medication should be stored in a tightly sealed container to prevent air and moisture from entering. This ensures the efficacy is maintained longer and prevents spoilage.

Appearance

Round tablet, pale yellow in color

Package unit

500 tablets/bottle