Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Everolimus
Drug ID BADD_D00858
Description Everolimus is a derivative of Rapamycin (sirolimus), and works similarly to Rapamycin as an mTOR (mammalian target of rapamycin) inhibitor. It is currently used as an immunosuppressant to prevent rejection of organ transplants. In a similar fashion to other mTOR inhibitors Everolimus' effect is solely on the mTORC1 protein and not on the mTORC2 protein.
Indications and Usage Indicated in pediatric and adult patients with tuberous sclerosis complex (TSC) for the treatment of subependymal giant cell astrocytoma (SEGA) that requires therapeutic intervention but cannot be curatively resected.
Marketing Status Prescription
ATC Code L01EG02; L04AA18
DrugBank ID DB01590
KEGG ID D02714
MeSH ID D000068338
PubChem ID 6442177
TTD Drug ID D0K3QS
NDC Product Code 65727-064; 65129-1324; 0078-0626; 0078-0620; 0054-0482; 67877-719; 52076-6247; 0078-0594; 0054-0470; 49884-159; 0378-3097; 49884-158; 68254-6234; 65727-063; 49884-160; 70377-013; 71796-012; 49884-119; 0378-3098; 70225-1103; 52076-6253; 70377-010; 0078-0422; 0054-0497; 0078-0414; 0054-0471; 0378-0006; 0093-7767; 0078-0627; 52076-6234; 62227-013; 0093-7766; 0078-0628; 71052-559; 67877-720; 0378-0005; 65727-046; 49884-125; 0054-0472; 0054-0604; 0078-0566; 49884-283; 0378-0007; 67877-721; 67877-718; 51991-823; 0054-0481; 17404-1027; 0078-0417; 0078-0415; 0093-7768; 49884-127; 70377-011; 62227-018; 70377-012; 0054-0480; 62227-019; 51991-821; 51991-822; 0078-0567; 0378-3096; 51991-824
Synonyms Everolimus | SDZ RAD | RAD, SDZ | SDZ-RAD | 40-O-(2-hydroxyethyl)-rapamycin | RAD 001 | 001, RAD | RAD001 | Certican | Afinitor
Chemical Information
Molecular Formula C53H83NO14
CAS Registry Number 159351-69-6
SMILES CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O) C(C)CC4CCC(C(C4)OC)OCCO)C)C)O)OC)C)C)C)OC
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Blood glucose decreased13.02.02.0010.002919%Not Available
Blood glucose increased13.02.02.0020.035032%Not Available
Blood iron decreased13.11.01.0060.000476%Not Available
Blood lactate dehydrogenase increased13.04.02.0020.009853%
Blood luteinising hormone increased13.10.03.004--Not Available
Blood magnesium decreased13.11.01.0080.001825%Not Available
Blood potassium decreased13.11.01.0100.007663%Not Available
Blood potassium increased13.11.01.0110.002554%Not Available
Blood pressure abnormal13.14.03.001--Not Available
Blood pressure decreased13.14.03.002--Not Available
Blood pressure diastolic decreased13.14.03.0030.001460%Not Available
Blood pressure diastolic increased13.14.03.0040.000730%Not Available
Blood pressure fluctuation24.06.01.0020.001460%Not Available
Blood pressure increased13.14.03.0050.013137%Not Available
Blood pressure systolic increased13.14.03.0060.004014%Not Available
Blood sodium decreased13.11.01.0120.002919%Not Available
Blood testosterone decreased13.10.05.004--Not Available
Blood thyroid stimulating hormone decreased13.10.03.0110.000730%Not Available
Blood triglycerides abnormal13.12.03.0020.001095%Not Available
Blood triglycerides increased13.12.03.0010.007298%Not Available
Blood urea decreased13.13.01.0170.000730%Not Available
Blood urea increased13.13.01.0060.005109%Not Available
Blood uric acid increased13.02.04.0010.002189%Not Available
Body temperature decreased13.15.01.0100.002189%Not Available
Body temperature increased13.15.01.0010.002919%Not Available
Bone disorder15.02.04.004--Not Available
Bone pain15.02.01.0010.005839%
Breast cancer16.10.01.001; 21.05.01.0030.005521%Not Available
Breast cancer stage IV21.05.01.010; 16.10.01.0030.000190%Not Available
Breast mass21.05.04.0020.001460%Not Available
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