Clamoxil Duo Dry Syrup (Amoxicillin. Potassium Clavulanate (7:1))

Adult dose

For recurrent tonsillitis and other upper respiratory infections, lower respiratory infections, urinary tract infections, and mild to moderate skin and soft tissue infections, take 25 mg/3.6 mg per kg of body weight divided into two doses. For severe infections such as otitis media, sinusitis, and bronchial pneumonia, take 45 mg/6.4 mg per kg of body weight divided into two doses. To minimize potential gastrointestinal intolerance, take it at the beginning of a meal.

Child dose

The 7 : 1 syrup is not suitable for children under 2 months. Pediatric patients with renal failure are not suitable for the 7 : 1 syrup.

This medication contains the artificial sweetener aspartame and should not be used in patients with phenylketonuria. It is important to avoid exceeding the daily allowable intake of aspartame. It should not be administered to patients with a history of hypersensitivity to its components or beta-lactam antibiotics, patients with infectious mononucleosis or lymphocytic leukemia, and those with a history of liver dysfunction. Patients with impaired liver function or severe kidney impairment, allergic individuals, those who have difficulty in oral intake, elderly patients, and those with gastrointestinal disorders should use it with caution. If any adverse reactions such as diarrhea, abdominal pain, rash, or breathing difficulties occur during treatment, discontinue immediately and consult a doctor. It is particularly important to be cautious of the rare occurrence of pseudomembranous colitis, liver dysfunction, or severe allergic reactions. For long-term use, to avoid the emergence of resistant bacteria, only administer for the necessary duration and regularly monitor kidney and liver function. This medication may interact with other drugs, so inform and consult a doctor or pharmacist if you are taking other medications. Avoid use during the first three months of pregnancy, and carefully administer under a doctor's judgment during pregnancy or breastfeeding. Caution is required for young children, especially infants under 2 months, as safety has not been established. Elderly patients should monitor dosage and intervals due to the risk of bleeding related to kidney function decline and vitamin K deficiency. When taking the medication, shake it well, refrigerate after preparation, and use within 7 days. In case of overdose, gastrointestinal symptoms, renal failure, convulsions, and hypersensitivity shock may occur, requiring immediate medical attention.

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions, severe rashes with high fever, blisters, skin peeling, pain in mucous membranes of the mouth/eyes, severe skin reactions, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, liver dysfunction (jaundice), sudden and severe headaches, lightning headache, seizures

Mild side effects

• Diarrhea
• pseudomembranous colitis
• dyspepsia
• stomatitis
• gastritis
• glossitis
• black hairy tongue
• nausea
• vomiting
• loss of appetite

Store this medication in a tightly closed container to prevent exposure to air and moisture. It is advisable to maintain storage temperatures between 1 degree and 25 degrees.

Appearance

A whitish powder with a peculiar smell, used as a syrup to be dissolved before use.

Package unit

50 mL/bottle