Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Mifepristone
Drug ID BADD_D01463
Description Mifepristone is a progestational and glucocorticoid hormone antagonist. Its inhibition of progesterone induces bleeding during the luteal phase and in early pregnancy by releasing endogenous prostaglandins from the endometrium or decidua. As a glucocorticoid receptor antagonist, the drug has been used to treat hypercortisolism in patients with nonpituitary cushing syndrome. The two marketed forms of mifepristone are Mifeprex® (mifepristone 200mg) and Korlym™ (mifepristone 300mg). Currently under investigation for use in psychotic depression (phase 3 trials).
Indications and Usage For the medical termination of intrauterine pregnancy through 49 days' pregnancy. Also indicated to control hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing's syndrome who have type 2 diabetes mellitus or glucose intolerance and are not candidates for surgery or have had unsuccessful surgery.
Marketing Status approved; investigational
ATC Code G03XB01
DrugBank ID DB00834
KEGG ID D00585
MeSH ID D015735
PubChem ID 55245
TTD Drug ID D0Z4EI
NDC Product Code 44132-005; 44132-013; 65089-0043; 43393-001; 51508-011; 76346-073; 66499-0056; 69989-0003; 60722-3002
UNII 320T6RNW1F
Synonyms Mifepristone | ZK-98296 | ZK 98296 | ZK98296 | R-38486 | R 38486 | RU-486 | RU 486 | RU486 | R38486 | RU-38486 | RU 38486 | RU38486 | Mifegyne | Mifégyne | Mifeprex
Chemical Information
Molecular Formula C29H35NO2
CAS Registry Number 84371-65-3
SMILES CC#CC1(CCC2C1(CC(C3=C4CCC(=O)C=C4CCC23)C5=CC=C(C=C5)N(C)C)C)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 pain07.01.05.002--
Abortion incomplete18.01.01.0030.005771%Not Available
Adrenal insufficiency14.11.01.004; 05.01.02.0010.000485%
Amenorrhoea21.01.02.001; 05.05.01.0020.001007%
Anaemia01.03.02.0010.001708%
Angioedema22.04.02.008; 23.04.01.001; 10.01.05.009--Not Available
Anxiety19.06.02.0020.000701%
Arthralgia15.01.02.0010.000701%
Asthenia08.01.01.0010.000485%Not Available
Back pain15.03.04.005--
Blood potassium decreased13.11.01.010--Not Available
Blood thyroid stimulating hormone increased13.10.03.006--
Blood triglycerides increased13.12.03.001--Not Available
Body temperature increased13.15.01.001--Not Available
Chills08.01.09.001; 15.05.03.016--
Constipation07.02.02.001--
Death08.04.01.0010.000989%
Depression19.15.01.0010.000611%
Dermatitis23.03.04.002--Not Available
Dermatitis exfoliative23.03.07.001; 10.01.01.004--
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.0030.002103%
Drug interaction08.06.03.0010.001312%Not Available
Dry mouth07.06.01.002--
Dyspnoea02.11.05.003; 22.02.01.0040.001097%
Ectopic ACTH syndrome05.08.02.003; 16.32.02.002--Not Available
Endometrial cancer21.07.02.002; 16.12.02.001--Not Available
Endometrial hyperplasia21.07.01.0020.000396%Not Available
Endometrial hypertrophy21.07.01.003--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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