AXOL Tablet

ក្រុមហ៊ុនផលិតឱសថ:

 

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

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

  • ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់

    Mucolytic agent used in the treatment of respiratory tract disorders associated with viscid mucus.

    Dosage and Administration:

    For adults: 1 tablet, thrice daily.

    For long-term treatment, 1 tablet, twice daily.

    To be taken with water after meals.

  • ហាមប្រើ

    It is contraindicated in patients who have shown hypersensitivity to this drug.

  • ផលរំខាន

    Gastric discomfort, gastralgia, diarrhoea, nausea, vomiting, constipation and dyspepsia. Other side effects such as skin rash, pruritus and erythema have also been reported.

  • ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន

    The benefits of the drug in pregnant women during first trimester should be weighed against a possible risk to the fetus.

  • ការប្រុងប្រយ័ត្នជាពិសេស

    The benefits of the drug in pregnant women during first trimester should be weighed against a possible risk to the fetus.

  • សកម្មភាពឱសថ

    Ambroxol, a metabolite of Bromhexine, is a mucolytic agent capable of increasing sputum volume and reducing its viscosity, improving breathing and reducing cough with no influence on gastric acid secretion.

    1. Axol Tablet is a “mucus-modifier”. Its active compound is Ambroxol. Several human studies showed that Ambroxol affects the secret motor activity of serous glands, facilitates the repair of bronchial epithelium, and accelerated mucociliary transport and clearance.

    2. Ambroxol, a metabolite of Bromhexine, has been found to stimulate the synthesis of lung surfactant, as the surfactant may play a role in airway mucus transport acting as a lubricant.

    3. In several studies, Ambroxol also produced statistically significant symptomatic improvement, measured as difficulty in expectoration, coughing, presence of dyspnea and the auscultatory sign as compared to controls.

    4. Absorption after oral administration of Ambroxol was found to be fast and complete. Elimination half-life in the blood was estimated as 20-25 hours in men. In man and rabbit, radioactive-labelled substance was excreted almost completely in to the urine.

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

ប្រភពព័ត៌មាន៖

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