Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Exemestane
Drug ID BADD_D00861
Description Exemestane is an oral steroidal aromatase inhibitor used in the adjuvant treatment of hormonally-responsive (also called hormone-receptor-positive, estrogen-responsive) breast cancer in postmenopausal women. It irreversibly binds to the active site of the enzyme resulting in permanent inhibition.
Indications and Usage For the treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy.
Marketing Status Prescription
ATC Code L02BG06
DrugBank ID DB00990
KEGG ID D00963
MeSH ID C056516
PubChem ID 60198
TTD Drug ID D0D2VS
NDC Product Code 62157-091; 51991-005; 59057-007; 73377-132; 64918-0621; 50090-5193; 52128-134; 63629-2056; 59057-008; 69097-316; 0009-7663; 62756-981; 68382-383; 64181-0005; 0832-0595; 44278-025; 0378-5001; 65427-030; 71921-190; 46439-8746; 49386-026; 65162-240; 53104-7666; 47781-108; 59762-2858; 0054-0080; 65129-1217; 70771-1374; 64918-0622; 65089-0046
Synonyms exemestane | examestane | 6-methyleneandrosta-1,4-diene-3,17-dione | FCE 24304 | FCE-24304 | Aromasil | Aromasin | Aromasine
Chemical Information
Molecular Formula C20H24O2
CAS Registry Number 107868-30-4
SMILES CC12CCC3C(C1CCC2=O)CC(=C)C4=CC(=O)C=CC34C
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Cardiovascular disorderAdenylate kinase isoenzyme 1P00568Not Available9456245; 10473018; 14623544; 10514021; 10388095; 9556789; 15814851; 14513432; 11850229; 14687601; 15083379
OsteoporosisAdenylate kinase isoenzyme 1P00568Not Available9456245; 10473018; 14623544; 10514021; 10388095; 9556789; 15814851; 14513432; 11850229; 14687601; 15083379
Urogenital disorderAdenylate kinase isoenzyme 1P00568Not Available9456245; 10473018; 14623544; 10514021; 10388095; 9556789; 15814851; 14513432; 11850229; 14687601; 15083379
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Diarrhoea07.02.01.001--
Discomfort08.01.08.0030.007189%Not Available
Disturbance in attention17.03.03.001; 19.21.02.0020.011982%
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.004--
Drug hypersensitivity10.01.01.0010.045530%Not Available
Dry eye06.08.02.0010.007189%
Dyspepsia07.01.02.001--
Dysphagia07.01.06.0030.033548%
Dysphonia17.02.08.004; 22.02.05.005; 19.19.03.002--
Dyspnoea22.02.01.004; 02.01.03.0020.055115%
Embolism venous24.01.01.003--Not Available
Emotional disorder19.04.02.0050.007189%Not Available
Endometrial adenocarcinoma21.07.02.011; 16.12.02.0030.004793%Not Available
Endometrial hyperplasia21.07.01.002--Not Available
Erythema23.03.06.0010.014378%Not Available
Erythema multiforme23.03.01.003; 10.01.03.0150.004793%
Fatigue08.01.01.0020.067097%
Febrile neutropenia08.05.02.004; 01.02.03.0020.004793%
Feeling abnormal08.01.09.014--Not Available
Foot fracture15.08.03.012; 12.04.01.0120.004793%Not Available
Fracture15.08.02.001; 12.04.02.0010.007189%
Fungal infection11.03.05.0010.004793%Not Available
Gait disturbance17.02.05.016; 08.01.02.0020.028756%
Gamma-glutamyltransferase increased13.03.01.0110.009585%
Gastric ulcer07.04.03.002--
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal pain07.01.05.005--
Gingival bleeding24.07.02.010; 07.09.07.0010.007189%Not Available
Glycosylated haemoglobin increased13.02.02.0050.004793%Not Available
Haematuria24.07.01.047; 20.02.01.0060.007189%
The 3th Page    First    Pre   3 4 5 6 7    Next   Last    Total 10 Pages