Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Lomitapide
Drug ID BADD_D01311
Description Lomitapide is a microsomal triglyceride transfer protein (MTP) inhibitor used in homozygous familial hypercholesterolemia (HoFH) patients. It is marketed under the name Juxtapid (R).
Indications and Usage Used in homozygous familial hypercholesterolemia (HoFH) patients to reduce low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), apolipoprotein B (apo B), and non-high-density lipoprotein cholesterol (non-HDL-C).
Marketing Status approved; investigational
ATC Code C10AX12
DrugBank ID DB08827
KEGG ID D09637
MeSH ID C473731
PubChem ID 9853053
TTD Drug ID D0H8VY
NDC Product Code Not Available
UNII 82KUB0583F
Synonyms BMS201038 | BMS-201038 | BMS 201038 | lomitapide | Juxtapid | AEGR 733 | AEGR733 | AEGR-733
Chemical Information
Molecular Formula C39H37F6N3O2
CAS Registry Number 182431-12-5
SMILES C1CN(CCC1NC(=O)C2=CC=CC=C2C3=CC=C(C=C3)C(F)(F)F)CCCCC4(C5=CC=CC=C5C6=CC=CC=C64)C (=O)NCC(F)(F)F
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 discomfort07.01.06.0010.002020%-
Abdominal distension07.01.04.0010.001000%
Abdominal pain07.01.05.0020.000808%
Abdominal pain lower07.01.05.0100.000043%-
Abdominal pain upper07.01.05.0030.002033%
Abdominal tenderness07.01.05.004---
Abnormal faeces07.01.03.0010.000084%-
Alanine aminotransferase increased13.03.04.005--
Anaemia01.03.02.001--
Angina pectoris02.02.02.002; 24.04.04.0020.000021%
Aortic stenosis24.04.01.0010.000021%-
Arrhythmia02.03.02.0010.000054%-
Arthralgia15.01.02.0010.000480%
Arthritis15.01.01.0010.000203%
Arthropathy15.01.01.0030.000069%-
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.0010.000366%-
Atrial fibrillation02.03.03.0020.000064%
Back disorder15.03.05.0030.000032%-
Back pain15.03.04.0050.000600%
Blister12.01.06.002; 23.03.01.001---
Blood bilirubin increased13.03.04.018--
Blood potassium decreased13.11.01.010---
Body temperature increased13.15.01.001---
Bone pain15.02.01.0010.000073%
Burning sensation08.01.09.029; 17.02.06.0010.000058%-
Cardiac failure congestive02.05.01.0020.000032%-
Carotene decreased13.02.05.005---
Chest pain02.02.02.011; 08.01.08.002; 22.12.02.0030.000606%-
Chills08.01.09.001; 15.05.03.0160.000146%
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ADReCS-Target
Drug Name ADR Term Target
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