TREN Capsule

ក្រុមហ៊ុនផលិតឱសថ:

 

Y.S.P. INDUSTRIES (M) SDN. BHD., Malaysia

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

  • ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់

    Treatment of haemorrhage, or threatened haemorrhage associated with excessive fibrinolysis. It is also used in the management of haemophiliacs undergoing dental extractions, and in the prophylaxis of hereditary angioedema.

    Dosage and Administration

    The usual adult dose is 4-6 capsules to be taken 2-3 times daily. The dosage should be adjusted according to patient’s age and symptoms.

  • ហាមប្រើ

    1. Patients with a history or risk of thrombosis should not be given Tranexamic acid, unless at the same time it is possible to give treatment with anticoagulants.

    2. The preparation should not be given to patients with acquired disturbances of color vision. If disturbances of color vision arise during the course of treatment, the administration of the preparation should be discontinued.

  • ផលរំខាន

    Anorexia, hypnosia, pruritus, erythema, skin rash, and heartburn. Gastrointestinal disturbances (nausea, vomiting, diarrhoea) may occur.

  • អន្តរប្រតិកម្ម

    1. Concurrent use of oral contraceptives or estrogen-containing medication with tranexamic acid may increase the potential for thrombus formation.

    2. Concurrent use of Factor Ⅸcomplex with tranexamic acid may increase risk of thrombotic complication in perisurgical management of hemophilic patients. Some hematologists recommended that tranexamic acid not to be administered within 8 hours of these clotting factors concentrate.

  • ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន

    Tranexamic acid crosses the placenta. However, healthy infants have been born to women who received Tranexamic acid during pregnancy for the treatment of fibrinolytic bleeding or bleeding associated with abruptio placentae. (FDA Pregnancy Category B).

    Tranexamic acid is distributed into breast milk; concentrations reach approximately 1% of the maternal plasma concentration. Therefore risk-benefit of the use of tranexamic acid in nursing mother should be considered.

  • ការប្រុងប្រយ័ត្នជាពិសេស

    1. Tranexamic acid should be given in reduced doses to patient with impaired renal function.

    2. Tranexamic acid therapy is not indicated in hematuria caused by diseases of the renal parenchyma. Intravascular precipitation of fibrin frequently occurs in these conditions and may aggravate the disease.

    3. The risk of clotting may be increased in those with underlying thrombotic states.

  • សកម្មភាពឱសថ

    Tranexamic acid produces an antifibrinolytic effect by competitively inhibiting the activation of plasminogen to plasmin. It is also a weak noncompetitive inhibitor of plasmin. These properties make possible its clinical use as an antifibrinolytic in the treatment of both general and local fibrinolytic haemorrhages. It has an action mechanism similar to, but about 10 times more patient in vitro than that of epsilon aminocaproic acid.

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

ប្រភពព័ត៌មាន៖

- ក្រដាសព័ត៌មាននៃឱសថសម្រាប់អ្នកជំនាញវេជ្ជសាស្ត្រដែលប្រើប្រាស់នៅប្រទេសជប៉ុន (Pharmaceutical and Medical Devices Agency, Pmda): https://www.pmda.go.jp

- ព័ត៌មានសង្ខេបនៃឱសថសម្រាប់អ្នកជំងឺដែលប្រើប្រាស់នៅប្រទេសជប៉ុន: http://www.rad-ar.or.jp