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Metabolics  Metabolics

"Foods for special medical purposes" (FSMP) are dietetic products designated for individuals with special dietary requirements, for example due to a specific disease. These special dietetic products can be distinguished into nutritionally complete and nutritionally incomplete foods, according to their dietary intention. Nutritionally incomplete foods, in contrast to nutritionally complete foods, have to be consumed in addition to regular nutrition in order to meet the complete dietary needs of the patient.

A number of metabolic diseases can be controlled and managed by use of foods for special medical purposes. The composition of these products and their benefit for the patient must be scientifically proven. For some indications they are the only therapeutic option (e.g. PKU) and thus are to be used under medical supervision.



 XPhe overview

 XPhe-System...

Phe-free amino acid mixtures for the dietary management of Phenylketonuria  (PKU) and Hyperphenylalaninemia (HPA).
Available in different dosage forms - as a powder, liquid, as tablets or as a fruit bar.

 

 
 

 Zero-Systems...

amino acid mixtures for the dietary management of rare metabolic disorders , e.g. Maple Syrup Urine Disease (MSUD), Homocystinuria, Methyl Malonic Aciduria or Propionic Aciduria, Glutaric Aciduria Type I, and Tyrosinemia.
Available in different dosage forms - as a powder or as tablets.


XPhe Übersicht

plus8-System...

Amino acid mixture for the dietary management of Urea Cycle Disorders, such as e.g. Argininemia, Argininosuccinic Aciduria, OTC-Deficiency, Citrullinemia, Hyperammonemia, Hyperornithinemia.
Available in different dosage forms - as a powder or as tablets.



 single amino acids


Single amino acids...

Single amino acids for the dietary management of urea cycle disorders or other metabolic disorders where supplementation with a single amino acid is indicated.

 SineLys K


SineLys K...

Amino acid mixture for the dietary management of disorders in lysine-metabolism. Suitable for use within the scope of an add-on dietary management in Pyridoxine-Dependent Epilepsy in children 1 to 6 years of age. Not a replacement for the vitamin B6 treatment.

 


   
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