Fenimentin Duo Syrup [Amoxicillin-Clavulanate Potassium (7:1)]

Adult dose

For mild to moderate infections such as recurrent tonsillitis, upper respiratory infections, lower respiratory infections, urinary tract infections, and skin and soft tissue infections, the dosage is 25 mg/3.6 mg of amoxicillin/clavulanate potassium per kg of body weight, divided into two doses per day. For severe infections such as otitis media, sinusitis, and lower respiratory infections like bronchopneumonia, the dosage is 45 mg/6.4 mg of amoxicillin/clavulanate potassium per kg of body weight, divided into two doses per day.

Child dose

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

This medication contains the artificial sweetener aspartame, so it should not be used by patients with phenylketonuria who need to limit phenylalanine intake. Patients allergic to any of the ingredients or beta-lactam antibiotics may experience severe hypersensitivity reactions upon administration and should avoid it. Patients with viral infections such as infectious mononucleosis or lymphocytic leukemia should be cautious as using this medication may increase the risk of rash. Patients with impaired liver or kidney function should be cautious as the side effects of this medication may be exacerbated, and it should be used carefully under medical supervision. Gastrointestinal side effects such as diarrhea, abdominal pain, and vomiting may occur with this medication, and are especially likely in young children; prompt consultation with medical personnel is necessary if symptoms are severe. Liver dysfunction symptoms can rarely occur, making regular liver function tests important during prolonged use. Severe skin reactions such as rashes, itching, and in severe cases, stevens-johnson syndrome can occur, thus medication use should be ceased immediately and medical attention sought if such symptoms arise. This medication can affect the blood, and symptoms such as anemia or thrombocytopenia can occur rarely; notify your healthcare provider if unusual symptoms appear. Pregnant or breastfeeding women must consult with a doctor before using this medication, and it is advisable to avoid use, particularly in early pregnancy. Safety for very young infants or premature infants is not established, thus caution is necessary for this age group. This medication may interact with other drugs, so it's essential to inform your doctor or pharmacist about any other medications being taken. In the case of overdose, gastrointestinal disorder, allergic reactions, or kidney problems may occur, so it's crucial to adhere to the prescribed dosage and visit a healthcare facility if any unusual symptoms appear. After preparation, refrigerate and use within 7 days, avoiding direct sunlight and storing it in a dry place.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions; severe rashes, blisters, skin peeling, oral/ocular mucosal pain, severe skin abnormal reactions; difficulty breathing or shortness of breath, asthma attacks, cough with fever accompanying respiratory abnormalities; yellowing of the skin or eyes (jaundice), profound general malaise, liver abnormalities (jaundice); sudden and severe headache, thunderclap headache

Mild side effects

• Diarrhea
• pseudomembranous colitis
• indigestion
• stomatitis
• gastritis
• glossitis
• nausea
• vomiting
• loss of appetite
• abdominal pain

This medication should be stored in a sealed container to protect it from air and moisture. Additionally, it is recommended to store it in a cool and dry place below 25 degrees Celsius.

Appearance

A whitish powder with a peculiar odor, used as a syrup that dissolves when needed

Package unit

50 milliliters/bottle, 500 milliliters/bottle