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

Medications and Drugs for Treatment of Inborn Errors of Metabolism

Discover top medications for 'treating Inborn Errors of Metabolism'? This page compiles essential information on generic and brand-name drugs specifically used for Inborn Errors of Metabolism treatment.Here, you can explore dosages, prices, side effects, and administration recommendations to find a treatment that suits your needs.

The FAQ drug section on some common drugs addresses questions, offering insights into prescribed Inborn Errors of Metabolism medications and management strategies. Always check with your healthcare provider to confirm the suitability of any treatment option discussed here.

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

Brand 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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