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Albendazole interactions

Full monograph for AlbendazoleCheck it against another medicine

Medicines

68 documented

Medicines documented to interact with Albendazole, worst severity first.
MedicineSeverityMechanismEffectSources
ClozapineMajorSynergyCoadministration of clozapine with other agents that can cause neutropenia or agranulocytosis may increase the risk and/or severity of hematologic toxicity.9 sources — open the full entry
AbametapirModerateMetabolismBased on in vitro inhibition data, a single topical application of abametapir lotion may increase plasma concentrations of drugs that are substrates of CYP450…1 sources — open the full entry
ApalutamideModerateAbsorption · MetabolismCoadministration with apalutamide may decrease the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 3A4, 2C9, 2C19, breast…5 sources — open the full entry
AprepitantModerateMetabolismCoadministration with aprepitant or its prodrug, fosaprepitant, may increase the plasma concentrations of drugs that are primarily metabolized by CYP450 3A4…2 sources — open the full entry
AsciminibModerateMetabolismCoadministration with asciminib may increase the plasma concentrations of drugs that are primarily metabolized by the CYP450 3A4 isoenzyme. The mechanism is…1 sources — open the full entry
BendamustineModerateMetabolismCoadministration with inducers of CYP450 1A2 may decrease the plasma concentrations of bendamustine and increase the plasma concentrations of its…1 sources — open the full entry
Bosentan MonohydrateModerateMetabolismCoadministration with bosentan may decrease the plasma concentrations of drugs that are substrates of the CYP450 2C9 and/or 3A4 isoenzymes. The mechanism is…5 sources — open the full entry
BrigatinibModerateMetabolismCoadministration with brigatinib may decrease the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. Brigatinib has been shown in…6 sources — open the full entry
CarbamazepineModerateMetabolismCoadministration with anticonvulsant drugs such as carbamazepine, phenytoin, phenobarbital, and primidone may decrease the plasma concentrations and half-life…8 sources — open the full entry
CenobamateModerateMetabolismCoadministration with cenobamate may decrease the plasma concentrations and pharmacologic effects of CYP450 3A4 substrates. The proposed mechanism is…1 sources — open the full entry
DasatinibModerateMetabolismCoadministration with dasatinib may increase the plasma concentrations of drugs that are substrates of CYP450 3A4. The mechanism is decreased clearance due to…8 sources — open the full entry
DeferasiroxModerateMetabolismCoadministration with deferasirox may decrease the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism may involve…3 sources — open the full entry
Diltiazem HydrochlorideModerateMetabolismCoadministration with diltiazem may increase the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism is decreased…11 sources — open the full entry
EfavirenzModerateMetabolismCoadministration with efavirenz may decrease the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism is accelerated…2 sources — open the full entry
EnzalutamideModerateMetabolismCoadministration with enzalutamide may decrease the plasma concentrations of drugs that are substrates of CYP450 3A4, 2C9, 2C19, and/or P-glycoprotein (P-gp)…4 sources — open the full entry
Fluvoxamine MaleateModerateMetabolismCoadministration with fluvoxamine may increase the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism is decreased…6 sources — open the full entry
Fosphenytoin SodiumModerateMetabolismCoadministration with anticonvulsant drugs such as carbamazepine, phenytoin, phenobarbital, and primidone may decrease the plasma concentrations and half-life…8 sources — open the full entry
GanciclovirModerateSynergyThe use of ganciclovir with other potentially myelotoxic and/or nephrotoxic agents may increase the risk and severity of hematologic toxicity and/or…7 sources — open the full entry
ItraconazoleModerateMetabolismCoadministration with itraconazole may significantly increase the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism…19 sources — open the full entry
Lamivudine + Zidovudine + NevirapineModerateMetabolismCoadministration with nevirapine may decrease the plasma concentrations and therapeutic efficacy of drugs that are substrates of CYP450 3A4. The proposed…4 sources — open the full entry
LapatinibModerateMetabolismCoadministration with lapatinib may increase the plasma concentrations of drugs that are substrates of the CYP450 2C8 isoenzyme, CYP450 3A4 isoenzyme, and/or…6 sources — open the full entry
LarotrectinibModerateMetabolismCoadministration with larotrectinib may increase the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme.4 sources — open the full entry
Lefamulin AcetateModerateMetabolismWhen administered orally, lefamulin may increase the plasma concentrations of drugs that are primarily metabolized by CYP450 3A4. Based on interaction with…6 sources — open the full entry
Lopinavir + RitonavirModerateMetabolismCoadministration with ritonavir may decrease the plasma concentrations of the benzimidazoles, albendazole and mebendazole, as well as the active metabolite of…5 sources — open the full entry
LorlatinibModerateMetabolismCoadministration with lorlatinib may decrease the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The proposed mechanism is…3 sources — open the full entry
MavacamtenModerateMetabolismCoadministration with mavacamten may decrease the plasma concentrations of drugs that are primarily metabolized by CYP450 3A4, 2C9, and/or 2C19. The proposed…1 sources — open the full entry
MifepristoneModerateMetabolismBased on in vitro inhibition data, coadministration with mifepristone may increase the plasma concentrations of drugs that are substrates of the CYP450 3A4…10 sources — open the full entry
Mifepristone + MisoprostolModerateMetabolismBased on in vitro inhibition data, coadministration with mifepristone may increase the plasma concentrations of drugs that are substrates of the CYP450 3A4…10 sources — open the full entry
NelfinavirModerateMetabolismCoadministration with nelfinavir may increase the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism is decreased…1 sources — open the full entry
NilotinibModerateMetabolismBased on in vitro inhibition data, coadministration with nilotinib may increase the plasma concentrations of drugs that are substrates of the P-glycoprotein…6 sources — open the full entry
Nirmatrelvir + RitonavirModerateMetabolismCoadministration with ritonavir may decrease the plasma concentrations of the benzimidazoles, albendazole and mebendazole, as well as the active metabolite of…5 sources — open the full entry
OcrelizumabModerateSynergyThe use of the CD20-directed cytolytic antibody ocrelizumab with other immune-modulating or immunosuppressive therapy, including immunosuppressant doses of…1 sources — open the full entry
OxcarbazepineModerateMetabolismCoadministration with oxcarbazepine may decrease the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism is…9 sources — open the full entry
PhenobarbitalModerateMetabolismCoadministration with anticonvulsant drugs such as carbamazepine, phenytoin, phenobarbital, and primidone may decrease the plasma concentrations and half-life…8 sources — open the full entry
Phenytoin SodiumModerateMetabolismCoadministration with anticonvulsant drugs such as carbamazepine, phenytoin, phenobarbital, and primidone may decrease the plasma concentrations and half-life…8 sources — open the full entry
PosaconazoleModerateMetabolismCoadministration with posaconazole may significantly increase the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The mechanism…6 sources — open the full entry
PrimidoneModerateMetabolismCoadministration with anticonvulsant drugs such as carbamazepine, phenytoin, phenobarbital, and primidone may decrease the plasma concentrations and half-life…8 sources — open the full entry
RibociclibModerateMetabolismCoadministration with ribociclib may increase the plasma concentrations and pharmacologic effects of drugs that are substrates of CYP450 3A4. The proposed…10 sources — open the full entry
SelpercatinibModerateMetabolismCoadministration with selpercatinib may increase the plasma concentrations of drugs that are primarily metabolized by the CYP450 3A4 isoenzyme. The mechanism…6 sources — open the full entry
SomatropinModerateMetabolismCoadministration with human growth hormone may decrease the plasma concentrations of drugs that are metabolized by CYP450 3A4.4 sources — open the full entry
SotorasibModerateMetabolismCoadministration with sotorasib may decrease the plasma concentrations of drugs that are substrates of the CYP450 3A4 isoenzyme. The proposed mechanism is…2 sources — open the full entry
Tacrolimus MonohydrateOralTopicalModerateMetabolismCoadministration of sirolimus or tacrolimus with other drugs that are also metabolized by CYP450 3A4 may result in elevated plasma concentrations of the…7 sources — open the full entry
Tea tree oil + Echinacea + Geothermal waterModerateMetabolismCoadministration with echinacea may alter the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 3A4. Echinacea appears to…2 sources — open the full entry
TucatinibModerateMetabolismCoadministration with tucatinib may increase the plasma concentrations of CYP450 3A4 substrates. The mechanism involves tucatinib-mediated inhibition of CYP450…1 sources — open the full entry
VoriconazoleModerateMetabolismCoadministration with voriconazole may increase the plasma concentrations of drugs that are substrates of CYP450 2C19, 2C9, and/or 3A4. The mechanism is…9 sources — open the full entry
ArmodafinilMinorMetabolismCoadministration with modafinil (the racemate) or armodafinil (the R-enantiomer) may decrease the plasma concentrations of drugs that are substrates of the…11 sources — open the full entry
Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + LidocaineMinorMetabolismCoadministration with inducers of CYP450 1A2 and/or 3A4 may decrease the plasma concentrations of lidocaine, which is primarily metabolized by these isoenzymes.4 sources — open the full entry
Betamethasone + Phenylephrine + LignocaineMinorMetabolismCoadministration with inducers of CYP450 1A2 and/or 3A4 may decrease the plasma concentrations of lidocaine, which is primarily metabolized by these isoenzymes.4 sources — open the full entry
Calcium Dobesilate + Lidocaine + DexamethasoneMinorMetabolism · OthersCoadministration with inducers of CYP450 1A2 and/or 3A4 may decrease the plasma concentrations of lidocaine, which is primarily metabolized by these isoenzymes.2 documented mechanisms11 sources — open the full entry
Chloramphenicol + Lidocaine HydrochlorideMinorMetabolismCoadministration with inducers of CYP450 1A2 and/or 3A4 may decrease the plasma concentrations of lidocaine, which is primarily metabolized by these isoenzymes.4 sources — open the full entry

Food & lifestyle

Conditions

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