مشخصات محصول
شیر متابولیک پودر 500 گرم
MILK 500 g POWDER
مشخصات محصول
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نام عمومی انگلیسیMILK 500 g POWDER
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نام برند انگلیسیXPHEN TYR MAXAMAIDER®
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نام عمومی فارسیشیر متابولیک پودر 500 گرم
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نام برند فارسیایکس فن ترای ماکسامیدر®
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سازندهNutricia HCP
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کد eRxeRx105291
نقد و بررسی
شیر متابولیک پودر 500 گرم
MILK 500 g POWDER
A powder free from phenylalanine and tyrosine-free but containing a balanced mixture of the other essential and nonessential amino acids, carbohydrates, vitamins, minerals and trace elements
• 0.62kcal/ml (1 to 5 dilution)
• 25g protein equivalent per 100g powder
• Fat-free • Unflavoured
The quantity of feed should be determined by a clinician or dietitian only and is dependent on the age, bodyweight and medical condition of the patient • Each level scoop of XPHEN TYR Maxamaid contains approximately 35g of powder • The recommended feed dilution is 1 to 5 i.e. 100g XPHEN TYR Maxamaid plus 500ml water. A lower concentration may initially be required until recommended concentration is tolerated
• 0.62kcal/ml (1 to 5 dilution)
• 25g protein equivalent per 100g powder
• Fat-free • Unflavoured
The quantity of feed should be determined by a clinician or dietitian only and is dependent on the age, bodyweight and medical condition of the patient • Each level scoop of XPHEN TYR Maxamaid contains approximately 35g of powder • The recommended feed dilution is 1 to 5 i.e. 100g XPHEN TYR Maxamaid plus 500ml water. A lower concentration may initially be required until recommended concentration is tolerated
• Not suitable for metabolic disorders other than tyrosinaemia or as a supplement for individuals who do not have tyrosinaemia
• Use under strict medical supervision
• Use under strict medical supervision
• Diet must be supplemented with natural protein, fluid and other nutrients in medically prescribed quantities to supply the phenylalanine, tyrosine and general nutritional requirements of the patient
• Not intended for use as a sole source of nutrition
• Not intended for use as a sole source of nutrition
For the dietary management of proven tyrosinaemia