Disease index

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

MedicineMeetingOutcomeConsumer 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.