Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Osilodrostat
Drug ID BADD_D02578
Description Osilodrostat is an inhibitor of 11β-hydroxylase (also referred to as CYP11B1), the enzyme that catalyzes the final step in the biosynthesis of endogenous cortisol.[L12123] It is used to lower circulating cortisol levels in the treatment of Cushing's disease, a disorder in which cortisol levels are chronically and supraphysiologically elevated. Cushing's disease is often the result of ACTH hypersecretion secondary to a pituitary tumor, and surgical resection of the tumour is generally the treatment of choice.[A191910] As an orally bioavailable drug therapy, osilodrostat provides a novel treatment option for patients in whom removal of the causative tumor is not an option or for whom previous pituitary surgery has not been curative. Osilodrostat is manufactured by Novartis under the brand name Isturisa.[L12123] It has undergone phase II clinical trials for the treatment of solid tumours, hypertension, and heart failure, but development for these indications was discontinued by Novartis in January 2013.[A191850] Osilodrostat was approved for use in the EU in January 2020 for the treatment of endogenous Cushing's syndrome (i.e. Cushing's disease),[A191850] and was granted FDA approval and Orphan Drug designation in the US in March 2020 for the same indication.[L12162]
Indications and Usage Osilodrostat is indicated for the treatment of adult patients with Cushing's disease for whom pituitary surgery is not an option or has not been curative.[L12123,A191850]
Marketing Status approved; investigational
ATC Code H02CA02
DrugBank ID DB11837
KEGG ID D11061
MeSH ID C553306
PubChem ID 44139752
TTD Drug ID D03AJU
NDC Product Code 55292-322; 55292-320; 55292-321
UNII 5YL4IQ1078
Synonyms Osilodrostat | benzonitrile, 4-((5R)-6,7-dihydro-5H-pyrrolo(1,2-c)imidazol-5-yl)-3-fluoro- | 4-((5R)-6,7-dihydro-5H-pyrrolo(1,2-c)imidazol-5-yl)-3-fluoro-benzonitrile | (+)-Osilodrostat | Isturisa | LCI699
Chemical Information
Molecular Formula C13H10FN3
CAS Registry Number 928134-65-0
SMILES C1CC2=CN=CN2C1C3=C(C=C(C=C3)C#N)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 pain07.01.05.0020.000075%
Adrenal insufficiency05.01.02.001; 14.11.01.0040.000240%
Asthenia08.01.01.0010.000075%-
Fatigue08.01.01.0020.000127%
Hypertension24.08.02.0010.000110%
Hypokalaemia14.05.03.0020.000034%
Hypotension24.06.03.0020.000075%
Malaise08.01.01.0030.000069%
Nausea07.01.07.0010.000254%
Orthostatic hypotension17.05.01.020; 24.06.03.0040.000034%-
Palpitations02.11.04.0120.000117%
Swelling face08.01.03.100; 10.01.05.018; 23.04.01.0180.000075%-
Vaginal haemorrhage21.08.01.001; 24.07.03.0050.000117%
Adverse event08.06.01.0100.000034%-
Disease progression08.01.03.0380.000034%
ACTH-producing pituitary tumour05.03.05.006; 16.24.07.0020.000034%-
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