inborn errors of amino acid metabolism
Metabolic · 2020–2021
4decisions
2medicines
0carried consumer input
0individual submissions
No submission for this condition has carried consumer input, including the 4 made since the comments facility came into use.
Every decision
| Medicine | Meeting | Outcome | Consumer input |
|---|---|---|---|
| amino acid formula with vitamins and minerals (multiple formulations) Nutritional management of inborn errors of amino acid metabolism (homocystinuria, phenylketonuria, tyrosinaemia, and maple syrup urine disease) in patients… | Jul 2021 | Recommended | unclear |
| amino acid formula with vitamins and minerals (multiple formulations) Nutritional support for patients from three years of age with disorders of protein metabolism including homocystinuria, phenylketonuria, tyrosinemia, and maple… | Jul 2021 | Recommended | unclear |
| amino acid formula with vitamins and minerals (multiple formulations) Nutritional supplementation for patients from three years of age with disorders of protein metabolism (homocystinuria, phenylketonuria, maple syrup urine… | Jul 2021 | Recommended | unclear |
| amino acid formula (multiple formulations for PKU, tyrosinaemia, GA1, MMA/PA, HCU, MSUD) Dietary management of proven inborn errors of amino acid metabolism: Phenylketonuria (PKU), Tyrosinaemia (TYR), Glutaric Aciduria Type 1 (GA1), Methylmalonic… | Jul 2020 | Recommended with restriction | none received |
Conditions are classified by a language model from the indication text of each submission, so an individual label here can be wrong. Consumer input is read from the document's own consumer comments section: 0 of 4 decisions since 2014 carried some. Silence means no comment reached the committee through that facility, not that nobody was affected. More on how this was built.