Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Binimetinib
Drug ID BADD_D02535
Description Binimetinib, also known as _Mektovi_, is a potent and selective oral mitogen-activated protein kinase 1/2 (MEK 1/2) inhibitor which is combined with [Encorafenib] [A34275,L3335]. On June 27, 2018, the Food and Drug Administration approved the combination of [Encorafenib] and binimetinib (BRAFTOVI and MEKTOVI, from Array BioPharma Inc.) in combination for patients with unresectable or metastatic melanoma with the BRAF V600E or V600K mutations, as detected by an FDA-approved test.[L3335]
Indications and Usage On June 27, 2018, the Food and Drug Administration approved encorafenib and binimetinib in combination patients with unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test [L3335].
Marketing Status approved; investigational
ATC Code L01EE03
DrugBank ID DB11967
KEGG ID D10604
MeSH ID C581313
PubChem ID 10288191
TTD Drug ID D0C4LF
NDC Product Code 70255-010; 54893-0119
UNII 181R97MR71
Synonyms binimetinib | Mektovi | MEK162
Chemical Information
Molecular Formula C17H15BrF2N4O3
CAS Registry Number 606143-89-9
SMILES CN1C=NC2=C1C=C(C(=C2F)NC3=C(C=C(C=C3)Br)F)C(=O)NOCCO
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)
Asthenia08.01.01.0010.000224%Not Available
Chills15.05.03.016; 08.01.09.0010.000246%
Death08.04.01.0010.000839%
Diarrhoea07.02.01.0010.000112%
Dyspnoea02.11.05.003; 22.02.01.0040.000112%
Fatigue08.01.01.0020.000851%
Malaise08.01.01.0030.000112%
Memory impairment17.03.02.003; 19.20.01.0030.000381%
Muscular weakness17.05.03.005; 15.05.06.0010.000112%
Nausea07.01.07.0010.000302%
Pyrexia08.05.02.0030.000168%
Rash23.03.13.0010.001444%Not Available
Visual impairment06.02.10.0130.000246%Not Available
Vomiting07.01.07.0030.000302%
Peripheral swelling08.01.03.053; 02.05.04.0150.000168%Not Available
Neoplasm progression16.16.02.0050.000437%Not Available
Decreased appetite14.03.01.005; 08.01.09.0280.000302%
Serous retinal detachment06.09.03.0370.000168%Not Available
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