Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Norethindrone acetate
Drug ID BADD_D01586
Description Not Available
Indications and Usage Not Available
Marketing Status Not Available
ATC Code Not Available
DrugBank ID Not Available
KEGG ID D00953
MeSH ID D000077563
PubChem ID 5832
TTD Drug ID Not Available
NDC Product Code 60870-0236; 68462-304; 73774-009; 0555-0211; 16571-658; 64918-1404; 51285-424; 0378-7291; 50742-267
UNII 9S44LIC7OJ
Synonyms Norethindrone Acetate | Norethisterone Acetate | Estr-4-en-3-one, 17-(acetyloxy)-17-ethynyl-, (17beta)- | Norethindrone Acetate, (17alpha)-(+-)-isomer | Aygestin | Norlutate | Norethindrone Acetate, (17alpha)-isomer
Chemical Information
Molecular Formula C22H28O3
CAS Registry Number 51-98-9
SMILES CC(=O)OC1(CCC2C1(CCC3C2CCC4=CC(=O)CCC34)C)C#C
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)
Deep vein thrombosis24.01.02.003---
Affect lability19.04.01.001---
Haemorrhage24.07.01.002---
Postmenopausal haemorrhage21.02.01.002; 24.07.03.002---
Endometrial thickening21.07.01.013---
Blood bilirubin abnormal13.03.04.016---
Adverse event08.06.01.010---
Appetite disorder14.03.01.004; 19.09.01.002---
Embolism24.01.01.009--
Libido disorder19.08.03.004; 21.03.02.006---
Retinal vascular thrombosis06.10.01.004; 24.01.07.001---
Abnormal withdrawal bleeding08.06.02.001; 21.01.01.008---
Intermenstrual bleeding21.01.01.015---
Superficial vein thrombosis24.01.02.016---
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