Eurocef Capsule 500 mg (Cefadroxil Hydrate)

Adult dose

1) Urinary tract infections: For uncomplicated lower urinary tract infections (such as cystitis), administer 1-2 g (potency) of cefadroxil orally in 1-2 divided doses per day. For other urinary tract infections, administer 2 g (potency) in two divided doses per day. 2) Skin and soft tissue infections: Administer 1 g (potency) orally in 1-2 divided doses per day. 3) Pharyngitis, tonsillitis: For pharyngitis and tonsillitis caused by beta-hemolytic streptococcal infections, administer 1 g (potency) daily in 1-2 divided doses for 10 days.

Child dose

1) Urinary tract infections, skin, and soft tissue infections: Administer 30 mg (potency) per kg body weight, orally in two divided doses per day. 2) Pharyngitis, tonsillitis: Administer 30 mg (potency) per kg body weight, orally in 1-2 divided doses per day.

This medication should not be used in patients who have previously experienced a severe allergic reaction or shock due to this drug. It is also safe to avoid administration in patients with a history of allergy to cephalosporin antibiotics and in those with infectious mononucleosis. Caution should be exercised when administering this drug to individuals with a history of allergies, particularly those who have had hypersensitivity reactions to penicillin antibiotics. Attention is also required for individuals with a family history prone to allergies such as asthma, rashes, or hives. Patients with severely impaired kidney function, those who have difficulty swallowing, elderly individuals, and those with poor overall health should be monitored closely when using this medication. Due to the risk of bleeding from vitamin K deficiency, it is necessary to carefully check the patient's condition. Patients with gastrointestinal diseases, particularly those with a history of colitis, should use this medication with caution. Rarely, this drug may cause severe shock or various allergic reactions; if any abnormal symptoms occur, administration should be immediately halted, and appropriate medical treatment sought. Regular tests are required as changes in blood cell counts or liver and kidney function may occur. Gastrointestinal symptoms such as diarrhea, nausea, and abdominal pain may occur, and if severe colitis symptoms appear, the medication should be stopped immediately. Respiratory symptoms may include interstitial pneumonia or pulmonary infiltration, requiring prompt treatment if related symptoms manifest. Oral inflammation or candidiasis, central nervous system symptoms (dizziness, drowsiness, headache, etc.), and skin reactions (including Stevens-Johnson syndrome) have also been reported, warranting careful observation. Long-term use may result in symptoms of vitamin deficiency and bleeding tendency; blood tests should be carried out if necessary to check the condition. To prevent the emergence of resistant strains, it is crucial to use this medication for an appropriate duration determined by susceptibility testing. If an allergic reaction is suspected, administration should be immediately halted, and appropriate treatment, such as oxygen supply, intravenous fluids, antihistamines, or corticosteroids, should be provided. In patients with impaired kidney function, dosage adjustment is necessary, and caution should be exercised as neurological symptoms such as seizures may occur. The risk of renal dysfunction may increase when used in combination with other nephrotoxic agents or diuretics, thus careful administration is required. Women who are pregnant or may become pregnant should only use this medication if the benefits of treatment outweigh the risks, as its safety has not been established. Nursing mothers should also use this medication cautiously. Elderly individuals are at a higher risk of adverse reactions due to decreased bodily functions, thus careful observation while adjusting dosage and administration intervals is crucial. This medication may affect some clinical test results, and it is advisable to inform the healthcare personnel during tests. Lastly, this medication may rarely cause photosensitivity reactions, so caution should be exercised to avoid excessive sun exposure.

Serious side effects

Hives, shock (severe allergic reaction), anaphylaxis, severe colitis with bloody stools, shortness of breath, interstitial pneumonia, eosinophilic pulmonary infiltration, Stevens-Johnson syndrome, respiratory abnormalities accompanied by fever and cough, acute renal failure, seizures

Mild side effects

Rash, erythema, facial swelling, angioedema, mucosal vesicles, itching, fever, thrombocytopenia, granulocytopenia, agranulocytosis, eosinophilia, cholestasis, elevated AST, ALT, ALP, diarrhea, nausea, vomiting, stomach pain, loss of appetite, stomach discomfort, dizziness, weakness, drowsiness, irritability, headache, symptoms of vitamin K deficiency (hypoprothrombinemia, bleeding tendency), vitamin B group deficiency, genital itching, genital candidiasis,

This medication should be stored in a tightly sealed container to protect it from air and moisture. This will help maintain the effectiveness of the medication for an extended period.

Appearance

A hard capsule containing a white to yellowish crystalline powder: upper part: reddish-brown, lower part: white.

Package unit

30 capsules/bottle, 100 capsules/bottle