Ambrect Tablet (Ambroxol Hydrochloride)

Adult dose

Ambroxol Hydrochloride as 30 mg per dose, taken three times a day. For continuous treatment, take 30 mg per dose, two times a day.

This medication should not be taken by individuals who have had allergic reactions to this medication or its components. Patients with severely impaired kidney function and severely compromised liver function should not take this medication. This medication may contain sorbitol, so individuals with a genetic predisposition to fructose intolerance should avoid taking it. Additionally, this medication contains lactose and should not be given to patients with genetic issues such as galactose intolerance, lactose deficiency, or glucose-galactose malabsorption. Patients with kidney issues, those with peptic ulcers, pregnant women, particularly in the first trimester, should consult a physician or pharmacist before taking this medication. This medication crosses the placenta during pregnancy, so its use during pregnancy is not recommended, and breastfeeding women should also avoid it as it can transfer through breast milk. Elderly patients may have reduced bodily functions, so care should be taken with dosage adjustments when taking this medication. If symptoms such as rash, itching, fever, or mucosal damage occur while taking this medication, discontinue its use immediately and consult a specialist. Gastrointestinal symptoms such as nausea, vomiting, diarrhea, dyspepsia, abdominal pain, heartburn, and dry mouth may occur, so caution is advised. Allergic symptoms such as hives, skin rash, facial swelling, difficulty breathing, angioedema, or anaphylactic reactions may also occur, so any abnormal signs should be reported to medical personnel immediately. Respiratory issues may include purulent rhinitis, and rare neurological symptoms such as altered taste or sensation in the tongue and arm numbness have also been reported. This medication may increase antibiotic concentrations in bronchial secretions and phlegm when taken with certain antibiotics, so caution is advised when taken together. No specific symptoms of overdose have been reported; however, treatment tailored to the symptoms should be provided if adverse reactions occur. There are no reports of this medication affecting driving or operating machinery, but caution may be needed. For storage, keep this medication out of children's reach, avoid direct sunlight, and store in a cool, dry place, tightly closed. Do not transfer the medication from its original container to another container for storage, as this may cause misuse or degradation of quality; always keep it in its original container.

Serious side effects

Hives, severe swelling (angioedema), tightness in the chest, difficulty breathing (dyspnea), anaphylactic reaction (including anaphylactic shock), skin and mucosal reaction syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell's syndrome)

Mild side effects

Nausea, vomiting, diarrhea, dyspepsia, abdominal pain, heartburn, dry mouth, discomfort in the stomach, bloating, constipation, loss of appetite, purulent rhinitis accompanied by an increased white blood cell count, altered taste in the tongue, changes in taste, numbness in the mouth, numbness in the arms, skin rash, itching, facial swelling, chills including fever.

Drug interactions

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

This medication should be stored in a sealed container to prevent air and moisture from entering, and should be kept in a cool room away from direct sunlight.

Appearance

White round tablets (Export version: white round tablets)

Package unit

500 tablets/bottle