Aroksol Tablet (Ambroxol Hydrochloride)

Adult dose

As Ambroxol Hydrochloride, the dose is 30 mg taken three times a day. For continuous treatment, the dose is 30 mg taken twice a day.

This medication should not be taken by anyone allergic to this medication or any of its components. It should also not be taken by individuals with severe kidney dysfunction. Patients with very poor liver function should not use this medication. Since this medication contains sorbitol, individuals with a genetic disorder that prevents fructose digestion should not take it. Additionally, this medication contains lactose, so patients with galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption should avoid it. Before taking this medication, individuals with weakened kidney function should consult a doctor or pharmacist. Patients with peptic ulcers should also consult a specialist before taking this medication. Pregnant women are advised not to take this medication, especially during the first three months of pregnancy, as it can cross the placenta. Breastfeeding women are advised against using this medication as it can be transferred through breast milk. Elderly patients may have diminished bodily functions, so careful dosage adjustments and monitoring are necessary. If any unusual symptoms such as severe skin damage, rash, itching, fever, or cough occur during treatment, the medication should be stopped immediately and a specialist consulted. Gastrointestinal symptoms such as nausea, vomiting, diarrhea, indigestion, abdominal pain, heartburn, and dry mouth may occur. Hypersensitivity reactions such as urticaria, skin rash, difficulty breathing, facial swelling, chills, and fever may occur rarely. Neurological symptoms such as purulent rhinitis, altered sensation of the tongue, taste changes, and arm paresthesia have also been reported. This medication may increase antibiotic concentrations in sputum and broncho secretion when taken with certain antibiotics. No specific symptoms have been reported in case of overdose, but appropriate treatment should be provided for any adverse reactions. The effects of this medication on driving and operating machinery are unknown, but caution is advised. This medication should be stored out of the reach of children and in a place that is cool, dry, and away from direct sunlight, preferably in its original container to prevent misuse or degradation of quality.

Serious side effects

Severe allergic reactions (anaphylactic reactions, angioedema, difficulty breathing), severe skin reactions (Stevens-Johnson syndrome, toxic epidermal necrolysis), respiratory issues (difficulty breathing), severe swelling (facial swelling)

Mild side effects

• Nausea
• vomiting
• diarrhea
• indigestion
• abdominal pain
• heartburn
• dry mouth
• discomfort in the stomach
• abdominal bloating
• constipation

Drug interactions

This medication should be discussed with a doctor or pharmacist when taken with antibiotics such as erythromycin, cephalexin, oxytetracycline, amoxicillin, cefuroxime, or doxycycline.

This medication should be stored in a sealed container to prevent exposure to air and moisture. It is best kept at room temperature between 1 and 30 degrees Celsius.

Appearance

White round tablets

Package unit

500 tablets/bottle