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)
Pelvic fluid collection21.07.04.011; 07.07.01.0090.000730%Not Available
Astrocytoma, low grade17.18.04.001; 16.09.04.0010.001460%Not Available
Procalcitonin increased13.09.01.0260.000730%Not Available
Apparent death08.01.03.0620.001095%Not Available
Pancreatic neuroendocrine tumour16.24.02.005; 07.21.09.009; 05.08.01.0140.001904%Not Available
Skin plaque23.03.03.0440.001095%Not Available
Oncologic complication16.32.03.0250.001047%Not Available
Pancreatic neuroendocrine tumour metastatic07.21.09.010; 05.08.01.015; 16.24.02.0060.001095%Not Available
Acute lung injury22.01.03.0100.000286%Not Available
Acquired gene mutation08.01.10.0020.000730%Not Available
Metastases to pelvis16.22.02.021; 21.07.04.0080.001460%Not Available
Exposed bone in jaw15.02.04.034--Not Available
Infectious pleural effusion22.05.01.004; 11.01.09.0110.000190%Not Available
Spinal pain17.10.01.020; 15.02.01.008; 08.01.08.0300.001825%Not Available
Eye colour change06.06.06.0080.000730%Not Available
Prerenal failure24.06.02.025; 20.01.03.0220.000730%Not Available
Clear cell renal cell carcinoma20.01.04.008; 16.08.02.0040.000571%Not Available
Oedematous kidney20.01.02.0170.000730%Not Available
Abdominal lymphadenopathy07.11.01.018; 01.09.01.0200.000730%Not Available
Internal haemorrhage24.07.01.0720.001460%Not Available
Cholangitis infective11.01.18.006; 09.02.01.0070.000190%Not Available
Gastrointestinal wall thickening07.01.06.0320.001460%Not Available
Kidney angiomyolipoma20.01.04.009; 16.27.01.0040.001460%Not Available
Tongue discomfort07.14.02.0190.000381%Not Available
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