Omekel Duo Syrup (Amoxicillin Hydrate · Clavulanate Potassium (7:1))

Adult dose

For recurrent tonsillitis and other upper respiratory infections, lower respiratory infections, urinary infections, and skin/soft tissue infections of mild to moderate severity, administer 25 mg/3.6 mg per kg of body weight, divided into two doses daily. For severe infections such as otitis media, sinusitis, and bronchopneumonia, administer 45 mg/6.4 mg per kg of body weight, divided into two doses daily. To minimize potential gastrointestinal intolerance,

Child dose

The 7:1 syrup is not suitable for infants under 2 months or children with renal failure.

This drug contains aspartame, an artificial sweetener, and should not be used by patients with phenylketonuria. The daily allowable amount of aspartame included in this drug is restricted based on body weight, so only the minimum amount should be used. Patients who have previously had allergic reactions to this drug or have a history of hypersensitivity to beta-lactam antibiotics should not use this drug. Patients with concomitant viral diseases such as infectious mononucleosis or lymphocytic leukemia should also avoid this drug, as it increases the risk of rash. Patients with a history of jaundice or liver dysfunction due to this drug or penicillin-related medications should not use it due to the risk of recurrence. This drug contains lactose, and it should not be administered to patients with genetic conditions such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption. Patients with poor liver or kidney function need to use this drug with caution, and especially in cases of moderate to severe kidney dysfunction, the dosing interval or dosage needs adjustment. Patients with allergic predispositions or symptoms such as asthma, rash, or hives should use this drug with caution. Patients who have difficulty swallowing or the elderly, as well as those in poor general condition may experience vitamin K deficiency symptoms and should be monitored closely. Patients with gastrointestinal symptoms such as abdominal pain, diarrhea, or vomiting should also be cautious as drug absorption may not be adequate. If symptoms such as diarrhea, abdominal pain, or bloody stools occur while taking this drug, discontinue use immediately and consult a physician. Liver function abnormalities may also occur rarely, so it is advisable for males over 60 or those taking it for long periods to undergo liver function tests. If skin rash, itching, or severe skin reactions occur, discontinue use immediately and inform healthcare personnel. Blood tests revealing leukopenia, thrombocytopenia, and other blood abnormalities may occur rarely, necessitating regular check-ups. CNS symptoms such as anxiety, drowsiness, and seizures may occur rarely, so notify immediately if abnormal symptoms appear. Kidney function abnormalities or acute renal failure symptoms may develop, making it important to regularly check kidney function. This drug may affect the balance of intestinal bacteria, potentially leading to infections such as candidiasis, and patients should consult healthcare professionals if symptoms appear. Prolonged use may carry the risk of bleeding due to vitamin K deficiency, so caution is warranted, and vitamin supplementation may be necessary if required. It is advisable to avoid using this drug during the first three months of pregnancy and to use it cautiously during pregnancy or breastfeeding based on the physician's judgment. During breastfeeding, the medication may pass into breast milk, potentially causing diarrhea or skin rashes in the infant, warranting caution. The safety for premature infants or newborns under 2 months has not been established, so they should ideally not be used. Elderly patients may experience abnormal reactions more easily due to decreased bodily functions, so the dosage and administration interval should be adjusted and administered carefully. This drug may affect specific clinical test results, so it is important to inform the testing personnel about taking the medication. In cases of overdose, gastrointestinal disturbances, skin reactions, renal failure, seizures, etc. may occur, and immediate medical attention should be sought for appropriate treatment. Store this medication in a dry place below 25 degrees Celsius. After preparation, store it in the refrigerator and use it within 7 days for safety. To prevent antibiotic resistance, it is important to follow the physician's instructions regarding susceptibility testing and appropriate administration duration.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reaction, severe rash with high fever, blisters, skin peeling, pain in mouth/eye mucous membranes, severe skin adverse reactions, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough + fever, respiratory issues, yellowing of skin or eyes (jaundice), profound lethargy, liver abnormalities (jaundice), sudden and

Mild side effects

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

This medication should be stored in a tightly sealed container to protect it from air and moisture. The storage temperature should be in a cool place between 1 degree and 25 degrees Celsius.

Appearance

A whitish powder with a distinctive smell, a syrup that is dissolved for use.

Package unit

50mL (5.5057g)/bottle