شیر متابولیک پودر 500 گرم
MILK 500 g POWDER
- نام عمومی انگلیسی: MILK 500 g POWDER
- نام برند انگلیسی: COMIDA-TYRO B FORMULA®
- نام عمومی فارسی: شیر متابولیک پودر 500 گرم
- نام برند فارسی: کومیدا TYRO فرمول B®
- سازنده: comidamed
+ موارد بیشتر
- بستن
کد :eRx105327
قیمت : 10,500 تومان
مشخصات محصول
شیر متابولیک پودر 500 گرم
MILK 500 g POWDER
مشخصات محصول
-
نام عمومی انگلیسیMILK 500 g POWDER
-
نام برند انگلیسیCOMIDA-TYRO B FORMULA®
-
نام عمومی فارسیشیر متابولیک پودر 500 گرم
-
نام برند فارسیکومیدا TYRO فرمول B®
-
سازندهcomidamed
-
کد eRxeRx105327
نقد و بررسی
شیر متابولیک پودر 500 گرم
MILK 500 g POWDER
comida-TYRo B formula is an amino acid mixture free from phenylalanine and tyrosine. Its amino acid profile is based to that of comida-TYRo B ensuring supply of high quality protein. comida-TYRo B formula is supplemented with vitamins, minerals and trace elements according to current international recommendations. The source of carbohydrates is maltodextrin, the fat blend from vegetable oils contains the essential fatty acids linoleic acid and αlinolenic acid in accordance with international recommendations.
must be used under medical supervision-
not suitable as sole source of nutrition-
not to be used by individuals without Tyrosinaemia Type I, II and III -
for toddlers and children over 1 year of age with Tyrosinaemia Type I, II and III-
not suitable for parenteral use-
not suitable as sole source of nutrition-
not to be used by individuals without Tyrosinaemia Type I, II and III -
for toddlers and children over 1 year of age with Tyrosinaemia Type I, II and III-
not suitable for parenteral use-
The daily amount of comida-TYRo B formula needed to supplement the daily protein requirements depends on age, body weight and individual tolerance for these amino acids. The dose of comida-TYRo B formula is to be determined by a physician and must be adjusted regularly.
comida-TYRo B formula is to be used in the dietary treatment of toddlers and children over 1 year of age with Tyrosinaemia Type I (Fumarylacetoacetase-deficiency), Tyrosinaemia Type II (Tyrosine-Aminotransferase-deficiency) and Tyrosinaemia Type III (4- Hydroxyphenyl-pyruvate dioxygenase deficiency).
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