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 approved
ATC Code A16AX06
DrugBank ID DB00419
KEGG ID D05032
MeSH ID C059896
PubChem ID 51634
TTD Drug ID D0HR8Z
NDC Product Code 49187-0827; 76339-178; 42799-709; 43975-310; 65571-0014; 42799-708; 71794-959; 42973-166; 10148-201; 66215-201; 50137-4237; 66005-0045; 51991-959
UNII ADN3S497AZ
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
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal distension07.01.04.0010.006469%
Abdominal pain07.01.05.0020.021562%
Abdominal pain upper07.01.05.003--
Acute respiratory failure14.01.04.004; 22.02.06.0010.006469%-
Administration site reaction08.02.04.011; 12.07.04.011---
Aggression19.05.01.0010.012937%-
Amnesia17.03.02.001; 19.20.01.0010.006469%
Anger19.04.02.0010.004312%-
Apathy19.04.04.0020.008625%-
Aphasia17.02.03.001; 19.21.01.0010.010781%
Apraxia17.02.03.002; 19.21.01.0020.004312%-
Aspiration22.02.07.0070.006469%
Asthenia08.01.01.0010.023718%-
Ataxia08.01.02.004; 17.02.02.0010.023718%
Back pain15.03.04.005--
Bladder cancer16.08.01.001; 20.03.04.001---
Cardiac arrest02.03.04.0010.006469%
Cardio-respiratory arrest02.03.04.002; 22.02.06.0070.006469%-
Cataplexy15.05.04.010; 17.15.01.003; 19.02.02.0030.018112%-
Cerebellar atrophy17.11.01.0080.004312%-
Cerebellar syndrome17.02.02.0020.004312%-
Cerebral atrophy17.11.01.0010.008625%-
Chills08.01.09.001; 15.05.03.016--
Choking22.12.03.0030.004312%-
Coagulopathy01.01.02.001---
Condition aggravated08.01.03.0040.075466%-
Constipation07.02.02.0010.015956%
Coordination abnormal17.02.02.0040.004312%-
Crohn's disease07.08.01.015; 10.02.01.0050.006469%-
Crying08.01.03.005; 12.02.11.001; 17.02.05.013; 19.04.02.0020.006469%-
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