CEFIMEX Capsule

ក្រុមហ៊ុនផលិតឱសថ:

 

FYNK Pharmaceuticals, Pakistan

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

    Cefixime 400mg

  • ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់

    INDICATIONS:

    Cefimex is an orally active cephalosporine antibiotic, which has marked in vitro bactericidal activity against a wide variety of Gram positive & Gram negative organisms. It is indicated for the treatment of the following acute infections when caused by susceptible micro-organisms Upper respiratory tract infections (URTI): e.g. Otitis media, sinusitis, pharyngitis & tonsillitis Lower respiratory tract infections (LRTI) e.g. bronchitis, urinary tract infections (UTI): e.g. cystitis, cystourethritis, uncomplicated pyelonephritis & uncomplicated gonorrhoea (cervical/urethral, rectal and pharyngeal).

    DOSAGE & ADMINISTRATION:

    Absorption of Cefimex is not significantly modified by the presence of food. The usual course of treatment is 5-14days. Adults & children over 12 years. The recommended adult dosage is 400mg daily administered as a single dose.

  • ហាមប្រើ

    Patients with known hypersensitivity to Cephalosporin antibiotics.

  • ផលរំខាន

    Cefimex is generally well tolerated. The majority of adverse reactions observed in clinical trials were mild and self-limiting in nature.

  • អន្តរប្រតិកម្ម

    No significant drug interactions have been reported to data. A false positive reaction for glucose in the urine may occur with Benedicts or solutions or with copper sulphate test tablets, but not with test based on enzymatic glucose oxidase reactions. A false positive direct Coombs test has been reported during treatment with cephalosporin antibiotics, therefore it should be recognized that a positive Coombs test may be due to the drug.

  • ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន

    Reproduction studies have been performed in mice and rats at does up to 400 times the human dose and reveated no evidence of impaired fertility or harm to the fetus due to Cefixime Trihydrate in the rabbit, at doses upto 4 times the human dose. There are no evidences of a teratogenic effect, there was a high incidence of abortion and maternal death which is an expected consequence of the known sensitivity of rabbits to antibiotic induced changes in the population of the microflora of the intestine. There are no adequate and well-controlled studies in pregnant women. Cefimex should therefore not be used in pregnancy or in nursing mothers unless considered essential by the physician.

  • ការប្រុងប្រយ័ត្នជាពិសេស

    Cefimex should be given with caution to patients who have shown hypersensitivity to other drugs Cephalosporins would be given with caution to penicillin-sensitives, as there is more some evidence of partial cross-allergenicity between the penicillins and the cephalosporins. Patients have severe reactions (including anaphylaxis) to both classes of drugs. If an allergic effect occurs with Cefimex the drug should be discontinued and the patient treated with appropriate agents, if necessary.

    Cefimex should be administered with caution in patients with markedly impaired renal function (see dosage in renal impairment). Treatment with broad spectrum antibiotics alter the normal flora of the colon and may permit overgrowth of clostridia. Studies indicate that a toxin produced by clostridium difficile is a primary cause of antibiotic-associated diarrhoea. Pseudomembranous colitis is associates with the use of broad-spectrum antibiotics including macrolides, semi-synthetic penicillins lincosamides and cephalosporins. It is therefore important to consider its diagnosis on patients who develop diarrhoea is association with the use of antibiotics Symptoms of pseudomembranous colitis may occur.

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

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