CLAMOXYL Powder for suspension

ក្រុមហ៊ុនផលិតឱសថ:

 

GlaxoSmithKline, France

  • សារធាតុសកម្ម
  • ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់
  • ហាមប្រើ
  • ផលរំខាន
  • អន្តរប្រតិកម្ម
  • ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន
  • ការប្រុងប្រយ័ត្នជាពិសេស
  • សកម្មភាពឱសថ
  • បរិយាយប័ណ្ណឱសថ 
  • សារធាតុសកម្ម

    1. CLAMOXYL Powder for suspension 125mg/5mL:

    Amoxicillin 125mg/5mL

    2. CLAMOXYL Powder for suspension 250mg/5mL:

    Amoxicillin 250mg/5mL

    3. CLAMOXYL Powder for suspension 500mg/5mL:

    Amoxicillin 500mg/5mL

  • ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់

    - indicated for the treatment of infections caused by sensitive bacteria

    - indicated in adults, for the treatment of certain gastric or duodenal ulcers.

    Dosage

    Dosage varies depending on the disease being treated.

    - For adults: from 1g to 6g per 24 hours

    -For children: from 25mg/kg to 150mg/kg per 24 hours.

    Particular case of some tonsillitis's treatment:

    -For adults: 2g twice a day

    -For children over 30 months of age: 50mg/kg/day twice a day, during 6 days

    The does should be adjusted in the case of renal impairment

    Oral use

    This medicine can be taken at any time, before, during or after meals

    Generally two to three does per day

  • ហាមប្រើ

    - Allergy to antibacterial agents from betalactam antibiotic family (penicillins or cephalosporins ) or to the other ingredients.

    - Phenylketonuria (hereditary disease detected at birth), due to the presence of aspartam.

    This medicine should not generally be used in combination with methotrexate (an immunosuppressant)

  • ផលរំខាន

    Side effects

    Uncommon:

    -nausea, diarrhoea,

    - skin eruption,

    - Mucocutaneous candidiasis (infection due to certain microscopic fungi).

    Very uncommon:

    - vomiting,

    - urticaria, itching

    Very rare:

    -leukopenia (more or less marked decrease in white blood cells), neutropenia (decrease in white blood cells: neutrophils), agranulocytosis (marked decrease in agranulocytosis), thrombocytopenia (decrease in platelets), reversible haemolytic anaemia (red blood cells destruction),

    - severe allergic reactions, including angioneurotic oedema, anaphylaxis, serum disease (skin eruption with fever and articulation pains) and hypersensitivity vasculitis (inflammation of smallest vessels) ,

    - convulsions,

    - pseudomembranous colitis (intestine inflammation with diarrhoea and/or abdominal pains), haemorrhagic colitis (intestine inflammation with diarrhoea and/or bleeding),

    - hepatitis (liver inflammation), jaundice,

    - skin reactions such as multiform erythema, Stevens-Johnson syndrome, Lyell syndrome (toxic epidermal necrolysis), bullous and exfoliative dermatitis (skin inflammation with bullous),

    - acute generalized exanthematous pustulosis (red blotch generalized to the entire body with pustule followed by fever).

    Unknown frequency

    - allergies of varying severity: Quincke’s oedema (sudden swelling of the face or the neck), respiratory distress, urticaria,

    - eosinophilia (rise of certain white blood cells),

    - superficial dental coloration reported in children with oral suspension, generally reversible after teeth brushing,

    - dizziness,

    - interstitial nephritis (inflammation of the kidney), crystalluria (crystal found in urine),

    - a moderate and passing rise in AST and/r ALT.

  • អន្តរប្រតិកម្ម

    Methotrexate

  • ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន

    Pregnancy

    If necessary, this medicine can be taken during pregnancy.

    Breastfeeding

    Breast-feeding is possible while taking this medicine. If the baby suffers problems such as diarrhea, skin rash, candidiasis (infection caused by certain microscopic fungi),inform your doctor immediately.

  • ការប្រុងប្រយ័ត្នជាពិសេស

    Inform your doctor in the case of known renal impairment.

    Drink plentiful amounts of liquid during treatment.

    This medicine can falsify certain test results : Coombs test, blood sugar and total serum proteins, test for glucose in the urine. Inform your doctor that you are taking amoxicillin if these tests are prescribed for you.

    Convulsions may occur in patients with impaired renal function, in those receiving high doses or in patient with history of convulsion, treated for epilepsy or with brain disease.

    Patient under strict sodium restrictive diet must be informed that this medicine contains 5mg of sodium per measuring spoon.

  • សកម្មភាពឱសថ

    Beta-lactam group of antibiotics

*ព័ត៌មានឱសថត្រូវបានរៀបរៀងដោយ អ៊ីម៉ាតុគឹ មេឌីក (ខេមបូឌា) ដោយផ្អែកលើប្រភពព័ត៌មានខាងក្រោម។ សម្រាប់ព័ត៌មានលម្អិត សូមស្វែងរកនៅក្នុងក្រដាសព័ត៌មាននៃឱសថនីមួយៗ ឬ សាកសួរទៅកាន់ក្រុមហ៊ុនឱសថឬតំណាងចែកចាយនៃឱសថនីមួយៗ។

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