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)
Abdominal distension07.01.04.0010.042722%
Abdominal pain07.01.05.0020.096124%
Abdominal pain upper07.01.05.003--
Acute respiratory failure22.02.06.001; 14.01.04.0040.008359%Not Available
Administration site reaction12.07.04.011; 08.02.04.011--Not Available
Aggression19.05.01.0010.053402%Not Available
Alanine aminotransferase increased13.03.01.0030.021361%
Alopecia23.02.02.001--
Amnesia19.20.01.001; 17.03.02.0010.042722%
Anaemia01.03.02.0010.042722%
Anger19.04.02.0010.021361%Not Available
Anxiety19.06.02.002--
Apathy19.04.04.0020.053402%Not Available
Aphasia19.21.01.001; 17.02.03.0010.064083%
Apraxia19.21.01.002; 17.02.03.0020.021361%Not Available
Arthralgia15.01.02.001--
Aspartate aminotransferase increased13.03.01.0060.032041%
Aspiration22.02.07.0070.011145%
Asthenia08.01.01.0010.085444%Not Available
Ataxia17.02.02.001; 08.01.02.0040.030648%
Back pain15.03.04.005--
Bladder cancer20.03.04.001; 16.08.01.001--Not Available
Bronchitis11.01.09.001; 22.07.01.0010.005572%
C-reactive protein increased13.09.01.0070.021361%Not Available
Cardiac arrest02.03.04.0010.008359%
Cardio-respiratory arrest22.02.06.007; 02.03.04.0020.008359%Not Available
Cataplexy19.02.02.003; 17.15.01.003; 15.05.04.0100.053402%Not Available
Cerebellar atrophy17.11.01.0080.021361%Not Available
Cerebellar syndrome17.02.02.0020.021361%Not Available
Cerebral atrophy17.11.01.0010.042722%Not Available
The 1th Page    1 2 3 4 5    Next   Last    Total 7 Pages