AERIUS Tablet

ក្រុមហ៊ុនផលិតឱសថ:

 

Schering-Plough Labo N.V., Belgium

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

  • ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់

    For the rapid relief of symptoms associated with allergic rhinitis, such as sneezing, nasal discharge and itching, congestion/stuffiness, as well as ocular itching, tearing and redness, itching or palate and coughing.

    AERIUS are also indicated for the relief of symptoms associated with urticaria such as the relief of itching and the size and number of hives.

    Posology and Method of administration

    Adults (including geriatric patients) and children 12 years of age and older:

    1 tablet once a day regardless of mealtime for the relief of symptoms associated with allergic rhinitis (including intermittent and persistent allergic rhinitis) and urticaria. For oral use.

    Children 6 months-11 years of age: Take AERIUS syrup.

    Intermittent allergic rhinitis (presence of symptoms for less than 4 days per week or for less than 4 weeks) should be managed in accordance with the evaluation of patient’s disease history and the treatment could be discontinued after symptoms are resolved and reinitiated upon their reappearance.

    In persistent allergic rhinitis (presence of symptoms for 4 days or more per week and for more than 4 weeks), continued treatment may be proposed to the patients during allergen exposure periods.

  • ហាមប្រើ

    In patients who are hypersensitive to this medication or to any of its ingredients, or to loratadine.

  • ផលរំខាន

    In infants and toddlers aged 6-23 months, the most frequent adverse events reported in excess of placebo were diarrhoea (3.7%), fever (2.3%) and insomnia (2.3%)

    In clinical trials in a range of indications including allergic rhinitis and chronic idiopathic urticaria, at the recommended dose of 5mg daily, undesirable effects with these tablets were reported in 3% of patients in excess of those treated with placebo. The most frequent adverse events reported in excess off placebo were fatigue (1.2%), dry mouth (0.8%) and headache (0.6%).

    Very rare cases of hypersensitivity reactions, including anaphylaxis and rash, have been reported during the marketing of desloratadine. In addition, cases of tachycardia, palpitations, seizures, psychomotor hyperactivity, somnolence, elevated liver enzymes and bilirubin, and hepatitis have been reported very rarely.

  • អន្តរប្រតិកម្ម

    No clinically relevant interactions with desloratadine were observed in clinical trials in which azithromycin, erythromycin, ketoconazole, fluoxetine or cimetidine was co-administered.

    There was no effect of food or grapefruit juice on the disposition of desloratadine.

  • ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន

    Pregnancy

    This medicine is not be used during pregnancy unless the potential benefits outweigh the risks.

    (See the package insert about the details.)

    Lactation

    Desloratadine passes into breast milk, therefore, breastfeeding is not recommended in lactating women taking desloratadine.

    Desloratadine showed no mutagenic effects in in vitro and in vivo mutagenicity studies.

  • ការប្រុងប្រយ័ត្នជាពិសេស

    Efficacy and safety of this tablet in children under 12years of age have not been established.

  • សកម្មភាពឱសថ

    After oral administration, desloratadine selectively blocks peripheral histamine H1-receptors because the drug is effectively excluded from entry to the central nervous system (CNS).

    (See the package insert about the details.)

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

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