Beacra 625 mg (Amoxicillin Hydrate and Clavulanic Acid Potassium)

Adult dose

The dosage should be adjusted based on the patient's age, weight, kidney function, and severity of infection. Administer at the beginning of meals and take 250 mg/125 mg of amoxicillin/clavulanic acid potassium orally three times daily at 8-hour intervals. In cases of severe and respiratory infections, the dose may be increased to 500 mg/125 mg. In cases of renal impairment, the dosage should be adjusted based on creatinine clearance.

Child dose

Children aged 12 years or older or weighing 40 kg or more should take the same dose as adults: 250 mg/125 mg of amoxicillin/clavulanic acid potassium orally three times daily at 8-hour intervals for severe and respiratory infections.

This medication should not be used by patients with hypersensitivity to beta-lactam antibiotics or allergic reactions to penicillin-based drugs. Particularly, patients with infectious mononucleosis or lymphocytic leukemia have a higher risk of rash and should take caution. Patients with a history of liver dysfunction or jaundice should use this medication with caution. Liver dysfunction patients may experience worsening liver function; hence careful monitoring is needed. If renal function is moderately impaired or worse, dosage intervals should be adjusted. Patients with allergies, elderly individuals, or those with poor nutritional status may experience vitamin K deficiency symptoms and should take caution. For patients with gastrointestinal diseases experiencing severe vomiting or diarrhea, sufficient drug absorption may be compromised. This medication may cause gastrointestinal symptoms such as diarrhea, abdominal pain, nausea, and vomiting; if symptoms are severe, discontinue use immediately and consult a physician. Abnormal symptoms such as liver dysfunction, jaundice, skin rashes, and hypersensitivity reactions may occur; report any unusual symptoms to healthcare personnel immediately. Severe allergic reactions or anaphylactic shock may occur; hence careful observation is required after administration. Development of resistant bacteria may occur with prolonged use, so it is important to use only for the required duration. There may be interactions with other medications, so inform your healthcare provider about any medications you are taking. Avoid use in early pregnancy and consult a physician for careful use if pregnant or breastfeeding. Not recommended for children under 12 years or weighing less than 40 kg. Elderly patients have a higher risk of side effects due to reduced kidney and liver function, necessitating dosage and interval adjustments and careful monitoring. Regular testing of liver function, kidney function, and blood tests may be needed while taking this medication. In case of overdose, gastrointestinal symptoms and neurological symptoms may occur, so visit a medical facility immediately for appropriate treatment.

Serious side effects

• Hives
• severe swelling (edema)
• chest tightness
• difficulty breathing
• cold sweat
• pallor
• severe allergic reactions
• high fever with severe rash
• blisters
• sloughing skin

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 avoid moisture and kept at a cool temperature between 1 to 25 degrees. Storing it this way can help maintain the drug's efficacy for a longer period.

Appearance

White or almost white oval film-coated tablets

Package unit

40 tablets (4 tablets/PTP X 10)