Amoclar 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, amoxicillin/potassium clavulanate should be taken in two divided doses of 25 mg/3.6 mg per kg of body weight daily. For severe infections such as otitis media, sinusitis, lower respiratory infections such as bronchopneumonia, and urinary tract infections, it should be taken in two divided doses of 45 mg/6.4 mg per kg of body weight daily. Potential...

Child dose

The 7:1 syrup is not suitable for children under 2 months of age and also not suitable for pediatric patients with renal failure.

This medication contains the artificial sweetener aspartame, which is broken down into phenylalanine in the body. Therefore, it should not be used in patients with phenylketonuria, a genetic disorder. This drug is a beta-lactam antibiotic, and patients who have had allergic reactions to this ingredient or to penicillin should avoid taking it. Patients with infectious mononucleosis or lymphocytic leukemia should also be cautious, as the use of this medication may increase the risk of rash. Patients with impaired liver or kidney function should use this drug cautiously, adjusting the dosing interval particularly in cases of severe kidney impairment. Also, patients with allergic predispositions, gastrointestinal diseases, and the elderly should be monitored carefully. Gastrointestinal symptoms such as diarrhea, vomiting, and abdominal pain may occur after taking this medication, and in severe cases, serious illnesses such as pseudomembranous colitis or acute pancreatitis may develop. If any abnormal symptoms appear, discontinue use immediately and consult a doctor. Rarely, hypersensitivity reactions such as liver function abnormalities, skin rashes, hives, and dyspnea may occur; if these symptoms appear, discontinue medication immediately. This drug may also affect blood components, potentially leading to leukopenia or thrombocytopenia during blood tests, so regular monitoring is needed during long-term use. Pregnant or breastfeeding women should consult a doctor before using this medication, particularly avoiding use during the first three months of pregnancy. In children and the elderly, body functions may be weaker, so dosing and intervals should be adjusted and carefully monitored. This medication may interact with other drugs; be sure to inform medical personnel, especially when taking anticoagulants, other antibiotics, allopurinol, etc. In case of overdose, symptoms such as vomiting, diarrhea, rash, and drowsiness may occur, and in severe cases, renal failure or seizures may develop, so immediate medical attention is required. This medication should be stored under refrigeration after preparation and should be consumed within 7 days for safety. Also, shake well before use.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blistering, peeling skin, pain in mouth/eye mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory distress associated with cough and fever, jaundice (yellowing of skin or eyes), profound malaise, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, urination problems.

Mild side effects

• Diarrhea
• dyspepsia
• stomatitis
• gastritis
• glossitis
• nausea
• vomiting
• loss of appetite
• abdominal pain
• abdominal fullness

This medication may be sensitive to air and moisture, so it should be stored in a tightly sealed container. A cool place at a temperature between 1 to 25 degrees Celsius is suitable for storage. Storing it this way will help maintain the effectiveness of the drug for a longer period.

Appearance

A whitish powder with a peculiar smell, used as a syrup that is dissolved before use.

Package unit

50 mL/bottle