Roxol Tablet (Ambroxol Hydrochloride)

Adult dose

Ambroxol hydrochloride 30 mg should be taken three times a day for each dose. For continued treatment, 30 mg should be taken twice a day for each dose.

This medicine should not be taken by individuals who are allergic to this medicine or its components. It should also not be taken by those with severe kidney or liver dysfunction. This medicine may contain sorbitol, so caution is advised for those with fructose intolerance. Additionally, since it contains lactose, patients with genetic disorders like galactose intolerance, lactase deficiency, or glucose-galactose malabsorption should not take it. Those with kidney problems or peptic ulcers must consult a doctor or pharmacist before taking this medicine. During pregnancy, especially within the first three months, this medicine is not recommended, and caution is needed as it can cross the placenta. Nursing women should also avoid this medicine as it may be passed to breast milk. Elderly individuals, who may have diminished bodily functions, should be cautious and may need dosage adjustments. If a rash, itching, or abnormalities around the skin, mouth, or mucous membranes of the eyes 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 also occur, so caution is advised. If allergic reactions such as hives, difficulty breathing, or facial swelling occur, the medicine should be stopped immediately and medical advice sought. Neurological symptoms like changes in tongue sensation or taste, and arm numbness may also occur, so caution is needed. Taking this medicine with certain antibiotics may increase the concentration of antibiotics in the bronchi or phlegm, so it is advisable to consult a professional when taking them together. No specific symptoms have been reported for overdose, but if any adverse reactions occur, medical personnel should be informed immediately and treatment should be based on the symptoms. There are no reported effects on driving or operating machinery, but individual differences may exist, so caution is advised. This medicine should be kept out of the reach of children and stored in a cool, dry place away from direct sunlight. It should be stored in its original container, as transferring it to another container may result in misuse or degradation of quality.

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, anaphylactic reactions accompanied by fever and chills (including anaphylactic shock), Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell's syndrome), difficulty breathing, and arm numbness.

Mild side effects

Nausea, vomiting, diarrhea, dyspepsia, abdominal pain, heartburn, dry mouth, gastric discomfort, bloating, constipation, loss of appetite, hives, skin rash, abnormal tongue sensation, changes in taste, oral numbness, arm numbness, purulent rhinitis accompanied by increased leukocytes, itching, facial swelling, and fever with chills.

Drug interactions

This medicine should be taken with caution when used with antibiotics such as erythromycin, cephalexin, oxytetracycline, amoxicillin, cefoxitin, and doxycycline; consultation with a doctor or pharmacist is advised.

This medicine should be stored in a sealed container to avoid exposure to air or moisture. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius.

Appearance

This medicine is a white round tablet.

Package unit

1000 tablets (bottle)