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)
Pyrexia08.05.02.0030.160207%
Rash23.03.13.001--Not Available
Respiratory disorder22.02.07.0020.064083%Not Available
Respiratory distress22.02.01.0120.042722%Not Available
Respiratory failure22.02.06.002; 14.01.04.0030.025076%
Salivary hypersecretion07.06.01.0090.042722%Not Available
Seizure17.12.03.0010.694231%
Sensory loss17.02.07.007--Not Available
Sepsis11.01.11.0030.022290%
Skin lesion23.03.03.0100.021361%Not Available
Sleep disorder19.02.04.0010.021361%Not Available
Sneezing22.02.05.0110.021361%
Somnolence19.02.05.003; 17.02.04.0060.064083%
Speech disorder19.19.02.002; 17.02.08.003; 22.02.05.0340.021361%Not Available
Splenomegaly01.09.02.0010.064083%Not Available
Thrombocytopenia01.08.01.0020.213609%Not Available
Tonic convulsion17.12.03.0110.032041%Not Available
Transient ischaemic attack24.04.06.005; 17.08.04.0010.021361%
Tremor17.01.06.0020.320414%
Upper respiratory tract infection22.07.03.011; 11.01.13.0090.008359%
Urinary incontinence20.02.02.010; 17.05.01.0080.008359%
Urinary tract infection20.08.02.001; 11.01.14.0040.053402%
Vertigo17.02.12.002; 04.04.01.003--
Viral infection11.05.04.0010.032041%Not Available
Visual impairment06.02.06.008--Not Available
Vitamin B12 deficiency14.12.02.004--Not Available
Vomiting07.01.07.0030.128166%
Weight decreased13.15.01.0050.384497%
Weight increased13.15.01.006--
Yellow skin23.03.03.042; 09.01.01.009; 08.01.03.0460.021361%Not Available
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