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Medindia » Drugs » Drugs by Conditions » Drugs for Inborn Errors of Metabolism

Drugs for Treatment of Inborn Errors of Metabolism

Are you searching for medications to treat 'Inborn Errors of Metabolism'? Welcome to this page which serves as an archive for medications that are relevant to the treatment of Inborn Errors of Metabolism. The page includes both the generic and brand names and can serve as an invaluable resource for healthcare professionals and individuals who wish to get an insight on different medication options.

Click on a medication below to view details including brand names, prices, dosages, side effects, and administration guidelines.

A FAQ section has been added for each medication, addressing popular customer inquiries that provides a deeper insight into its use for Inborn Errors of Metabolism management.

We recommend consulting your doctor to verify the information presented on this page or for any additional clarifications.

Inborn Errors of Metabolism

Inborn errors of metabolism are genetic disorders that hamper the body’s metabolism resulting in severe clinical manifestations.

Brand Names and Generic Names of Drugs for Treatment of Inborn Errors of Metabolism

Glutathione

Glutathione has antioxidant properties and is used to prevent adverse effects to anticancer drugs

Trade Names :
Hepafresh | M-GAM | M-GAM
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Pegvaliase-pqpz

Pegvaliase-pqpz is a phenylalanine-metabolizing enzyme prescribed for treating adult patients suffering from phenylketonuria (a rare inherited disorder); it acts by decreasing the high concentrations of phenylalanine in the blood

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Suggested Readings on Inborn Errors of Metabolism

Galactosemia - Genetic Disorder of Sugar Galactose

Galactosemia - Genetic Disorder of Sugar Galactose

Galactosemia is one of many genetically inherited diseases and it affects one’s ability to process galactose. Learn about the symptoms, diagnosis and treatment for galactosemia.

Mucopolysaccharidosis | Inborn Metabolic Diseases - Types, Symptoms, Diagnosis, Treatment

Mucopolysaccharidosis | Inborn Metabolic Diseases - Types, Symptoms, Diagnosis, Treatment

Mucopolysaccharidosis (MPS) are a group of inborn metabolic disorders due to the absence or malfunctioning of specific enzymes required to process molecules called glycosaminoglycans.

Metabolic Defects - Phenylketonuria

Metabolic Defects - Phenylketonuria

Encyclopedia section of medindia gives information regarding Phenylketonuria type of Metabolic defect

Alkaptonuria (Black Urine Disease) - Causes, Symptoms, Diagnosis, Treatment and Prognosis

Alkaptonuria (Black Urine Disease) - Causes, Symptoms, Diagnosis, Treatment and Prognosis

Alkaptonuria or black urine disease is an inherited disorder where a chemical called homogentisic acid accumulates in the tissues and body fluids staining them dark brown. The spine and large joints (hip, knee) are affected leading to pain and stiffness.

Homocystinuria | Amino Acid Metabolism Disorder - Causes, Symptoms, Diagnosis and Treatment

Homocystinuria | Amino Acid Metabolism Disorder - Causes, Symptoms, Diagnosis and Treatment

Homocystinuria is a rare inherited condition characterized by increased levels of the amino acid homocysteine in the blood and urine. Early diagnosis and treatment is important to avoid serious complications later

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