Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Miglustat
Drug ID BADD_D01465
Description Miglustat, commonly marketed under the trade name Zavesca, is a drug used to treat Gaucher disease. It inhibits the enzyme glucosylceramide synthase, an essential enzyme for the synthesis of most glycosphingolipids. It is only used for patients who cannot be treated with enzyme replacement therapy with imiglucerase. Miglustat is now the first and only approved therapy for patients with Niemann-Pick disease type C (NP-C). It has recently been approved for treatment of progressive neurological symptoms in adult and pediatric patients in the European Union, Brazil, and South Korea. Miglustat was first developed as an anti-HIV agent in the 1990s. However, clinical experience with miglustat showed that therapeutic levels of the drug could not be achieved in patients without a high incidence of adverse effect.
Indications and Usage For the treatment of adult patients with mild to moderate type 1 (nonneuropathic) Gaucher's disease for whom enzyme replacement therapy is not a therapeutic option (e.g. due to constraints such as allergy, hypersensitivity, or poor venous access). Now approved in some countries for the treatment of progressive neurological symptoms in adult and pediatric patients with Niemann-Pick disease type C (NP-C).
Marketing Status Prescription
ATC Code A16AX06
DrugBank ID DB00419
KEGG ID D05032
MeSH ID C059896
PubChem ID 51634
TTD Drug ID D0HR8Z
NDC Product Code 66215-201; 49187-0827; 66005-0045; 10148-201; 42799-708; 65571-0014; 51991-959; 43975-310; 42973-166; 50137-4237; 76339-178
Synonyms miglustat | N-(n-butyl)deoxy-nojirimycin | n-butyl deoxynojirimycin | n-butyldeoxynojirimycin | butyldeoxynojirimycin | N-(n-butyl)deoxynojirimycin | SC 48334 | SC-48334 | Zavesca | OGT 918 | OGT-918
Chemical Information
Molecular Formula C10H21NO4
CAS Registry Number 72599-27-0
SMILES CCCCN1CC(C(C(C1CO)O)O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Eye swelling06.08.03.0030.021361%Not Available
Fatigue08.01.01.002--
Feeling abnormal08.01.09.014--Not Available
Feeling jittery08.01.09.016--Not Available
Flatulence07.01.04.0020.064083%
Gait disturbance17.02.05.016; 08.01.02.0020.096124%
Gastroenteritis11.01.07.004; 07.19.03.0010.021361%Not Available
Gastrointestinal disorder07.11.01.0010.138846%Not Available
Gastrointestinal pain07.01.05.005--
Generalised tonic-clonic seizure17.12.01.0020.011145%Not Available
Haematochezia07.12.02.003; 24.07.02.0120.021361%Not Available
Haematuria24.07.01.047; 20.02.01.0060.032041%
Haemoglobin13.01.05.018--Not Available
Haemoglobin decreased13.01.05.0030.053402%Not Available
Hallucination19.10.02.0020.021361%
Headache17.14.01.001--
Hepatic neoplasm16.07.03.001; 09.04.03.0010.021361%Not Available
Hepatomegaly09.01.05.0010.042722%Not Available
Hypoaesthesia17.02.06.023--Not Available
Hypotonia17.05.02.002; 15.05.04.0080.021361%Not Available
Hypoxia22.02.02.0030.032041%
Infection11.01.08.0020.013931%Not Available
Influenza22.07.02.001; 11.05.03.0010.053402%Not Available
Influenza like illness08.01.03.010--
Insomnia19.02.01.002; 17.15.03.0020.053402%
Intestinal obstruction07.13.01.0020.021361%Not Available
Lacrimation increased06.08.02.0040.021361%
Lactose intolerance14.02.02.001; 07.17.01.0030.021361%Not Available
Lethargy17.02.04.003; 08.01.01.008; 19.04.04.0040.021361%
Libido decreased21.03.02.005; 19.08.03.001--
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