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Cenobamate interactions

Full monograph for CenobamateCheck it against another medicine

Medicines

385 documented

Medicines documented to interact with Cenobamate, worst severity first.
MedicineSeverityMechanismEffectSources
AxitinibMajorMetabolismCoadministration with potent and moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of axitinib, which is primarily…9 sources — open the full entry
BrigatinibMajorMetabolismCoadministration with moderate inducers of CYP450 3A4 may decrease the plasma concentrations of brigatinib, which is partially metabolized by the isoenzyme.5 sources — open the full entry
Capmatinib HydrochlorideMajorMetabolismCoadministration with strong or moderate CYP450 3A4 inducers may decrease the plasma concentrations and anti-tumor activity of capmatinib. The proposed…5 sources — open the full entry
Citalopram HydrobromideMajorMetabolismCoadministration with CYP450 2C19 inhibitors may increase the plasma concentrations of citalopram, which is partially metabolized by the isoenzyme. Cases of QT…9 sources — open the full entry
DaclatasvirMajorMetabolismCoadministration with moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of daclatasvir, which is primarily metabolized by…2 sources — open the full entry
Daclatasvir + SofosbuvirMajorMetabolismCoadministration with moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of daclatasvir, which is primarily metabolized by…2 sources — open the full entry
DeflazacortMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of 21-desdeflazacort, the active…6 sources — open the full entry
ElacestrantMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of elacestrant, which is primarily…1 sources — open the full entry
ErdafitinibMajorMetabolismCoadministration with moderate inducers of CYP450 2C9 or 3A4 may decrease the plasma concentrations and therapeutic effects of erdafitinib. The mechanism is…7 sources — open the full entry
Fentanyl CitrateMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of opioids that are primarily metabolized by the isoenzyme such as…12 sources — open the full entry
FinerenoneMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of finerenone, which is primarily…3 sources — open the full entry
Fosphenytoin SodiumMajorMetabolismCoadministration of cenobamate and phenytoin may lead to increased plasma concentrations of phenytoin and reduced plasma concentrations of cenobamate. The…17 sources — open the full entry
Lefamulin AcetateMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 and/or P-glycoprotein (P-gp) may significantly decrease the plasma concentrations of lefamulin…3 sources — open the full entry
LorlatinibMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of lorlatinib, which has been found to be metabolized primarily by CYP450…4 sources — open the full entry
LurbinectedinMajorMetabolismCoadministration with a strong or moderate CYP450 3A4 inducer is predicted to decrease lurbinectedin systemic exposure, which may reduce its efficacy.3 sources — open the full entry
MavacamtenMajorMetabolismCoadministration with moderate to potent inhibitors of CYP450 2C19 or potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of…1 sources — open the full entry
Neratinib MaleateMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of neratinib, which is primarily…6 sources — open the full entry
OlaparibMajorMetabolismCoadministration with potent and moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of olaparib, which is primarily…7 sources — open the full entry
Phenytoin SodiumMajorMetabolismCoadministration of cenobamate and phenytoin may lead to increased plasma concentrations of phenytoin and reduced plasma concentrations of cenobamate. The…17 sources — open the full entry
RanolazineMajorMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of ranolazine, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
RimegepantMajorMetabolismCoadministration with strong or moderate inducers of CYP450 3A4 may significantly reduce the plasma concentrations and therapeutic effects of rimegepant, which…3 sources — open the full entry
SelpercatinibMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of selpercatinib, which is primarily…3 sources — open the full entry
Sofosbuvir + VelpatasvirMajorMetabolismCoadministration with potent or moderate inducers of CYP450 isoenzymes may decrease the plasma concentrations of velpatasvir, which has been shown in vitro to…3 sources — open the full entry
Ulipristal Acetate [For emergency contraception]MajorMetabolismCoadministration with potent and moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of ulipristal acetate and its…6 sources — open the full entry
Ulipristal Acetate [For uterine fibroids]MajorMetabolismCoadministration with potent and moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of ulipristal acetate and its…6 sources — open the full entry
VenetoclaxMajorMetabolismCoadministration with potent and moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of venetoclax, which is primarily…8 sources — open the full entry
AbemaciclibModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of abemaciclib and its pharmacologically active metabolites, all of which…2 sources — open the full entry
Abiraterone AcetateModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
AcalabrutinibModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of acalabrutinib, which is primarily metabolized by the isoenzyme.2 sources — open the full entry
Acyclovir + HydrocortisoneModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
AlbendazoleModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
AlpelisibModerateMetabolismCoadministration of alpelisib with inducers of CYP450 3A4 may reduce the plasma concentrations of alpelisib. The proposed mechanism, based on in vitro data, is…2 sources — open the full entry
AlprazolamModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amiodarone HydrochlorideModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amitriptyline HydrochlorideModerateSynergyCentral nervous system- and/or respiratory-depressant effects may be additively or synergistically increased in patients taking multiple drugs that cause these…44 sources — open the full entry
Amitriptyline Hydrochloride + ChlordiazepoxideModerateSynergyCentral nervous system- and/or respiratory-depressant effects may be additively or synergistically increased in patients taking multiple drugs that cause these…2 documented mechanisms44 sources — open the full entry
Amlodipine BesilateModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amlodipine Besilate + AtenololModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amlodipine Besilate + AtorvastatinModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…2 documented mechanisms13 sources — open the full entry
Amlodipine Besilate + Benazepril HydrochlorideModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amlodipine Besilate + Olmesartan MedoxomilModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amlodipine Besilate + TelmisartanModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
Amlodipine Besilate + ValsartanModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
ApixabanModerateMetabolismCoadministration with inducers of CYP450 3A4 and/or P-glycoprotein (P-gp) may decrease the plasma concentrations of apixaban, which is a substrate of both the…11 sources — open the full entry
ApremilastModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of apremilast, which is primarily metabolized by the isoenzyme in vitro.1 sources — open the full entry
AprepitantModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of aprepitant, which is primarily metabolized by the isoenzyme.12 sources — open the full entry
AripiprazoleModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of aripiprazole, which is partially metabolized by the isoenzyme.10 sources — open the full entry
ArmodafinilModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of modafinil (the racemate) and armodafinil (the R-enantiomer), which are…14 sources — open the full entry
Artemether + LumefantrineModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of artemether and lumefantrine, both of which are primarily metabolized by…2 documented mechanisms19 sources — open the full entry
Asenapine MaleateModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry

Food & lifestyle

Conditions

Conditions in which Cenobamate needs care, as documented in this source.