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Dexamethasone interactions

Full monograph for DexamethasoneCheck it against another medicine

Medicines

824 documented

Medicines documented to interact with Dexamethasone, worst severity first.
MedicineSeverityMechanismEffectSources
AdalimumabMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
Amiodarone HydrochlorideMajorMetabolismCoadministration with inducers of CYP450 3A4, such as rifamycins and St. John's wort, may decrease the serum concentrations of amiodarone and its metabolite…7 sources — open the full entry
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
BaricitinibMajorOthersCoadministration of baricitinib or tofacitinib with other immuno- or myelosuppressive agents may potentiate the risk of infections as well as lymphoma and…6 sources — open the full entry
Bempedoic acidMajorSynergyConcomitant administration of bempedoic acid may potentiate the risk of tendon rupture or injury associated with fluoroquinolones and corticosteroids. The…2 sources — open the full entry
Bempedoic acid + EzetimibeMajorSynergy · UnknownConcomitant administration of bempedoic acid may potentiate the risk of tendon rupture or injury associated with fluoroquinolones and corticosteroids. The…2 documented mechanisms2 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
Bupropion HydrochlorideMajorSynergyThe use of bupropion is associated with a dose-related risk of seizures. The risk may be further increased when coadministered with selective serotonin…19 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
Caspofungin AcetateMajorMetabolismCoadministration with inducers or mixed inducer/inhibitors of certain metabolic pathways may produce clinically meaningful reductions in the plasma…1 sources — open the full entry
CiprofloxacinbaseOphthalmicMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Ciprofloxacin + DexamethasoneMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Ciprofloxacin + Hydrocortisone AcetateMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Clobetasol Propionate + Ofloxacin + Ornidazole + TerbinafineMajorSynergy · UnknownConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…3 documented mechanisms7 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
DarolutamideMajorMetabolismCoadministration with potent or moderate inducers of CYP450 3A4 that also induce P-glycoprotein (P-gp) may significantly decrease the plasma concentrations of…6 sources — open the full entry
DasatinibMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of dasatinib, which is primarily metabolized by the…11 sources — open the full entry
DeferasiroxMajorSynergyCoadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…3 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
DelafloxacinMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Desmopressin AcetateMajorSynergyCoadministration of desmopressin with loop diuretics or systemic or inhaled corticosteroids may increase the risk of severe hyponatremia. Loop diuretics and…9 sources — open the full entry
Dexamethasone + LevofloxacinMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Dextromethorphan + BupropionMajorSynergy · UnknownThe use of bupropion is associated with a dose-related risk of seizures. The risk may be further increased when coadministered with selective serotonin…2 documented mechanisms19 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
EtanerceptMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
EverolimusMajorMetabolismCoadministration with potent inducers of CYP450 3A4 and/or P-glycoprotein (P-gp) may significantly decrease the blood concentrations and pharmacologic effects…6 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
GatifloxacinMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Gatifloxacin + DexamethasoneMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
GemifloxacinMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
GolimumabMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
InfliximabMajorSynergyThe use of tumor necrosis factor (TNF) blockers with other immunosuppressive or myelosuppressive agents may increase the risk of infections. Serious infections…6 sources — open the full entry
IohexolMajorOthersCoadministration of corticosteroids with iodinated contrast media by the intrathecal route may be associated with a high incidence of radiographic…5 sources — open the full entry
IopamidolMajorOthersCoadministration of corticosteroids with iodinated contrast media by the intrathecal route may be associated with a high incidence of radiographic…5 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
LeflunomideMajorSynergyThe use of leflunomide with other immunosuppressive or myelosuppressive agents may increase the risk of infections. The risk is thought to extend to…2 sources — open the full entry
Levofloxacin (Eye/Ear)MajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Levofloxacin HemihydrateMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
LomefloxacinMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 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
Loteprednol Etabonate + GatifloxacinMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 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 inducers of CYP450 2C19 and/or CYP450 3A4 may significantly decrease the plasma concentrations and therapeutic…1 sources — open the full entry
MifepristoneMajorAntagonism · MetabolismMifepristone is a potent antiglucocorticoid and may antagonize the effects of corticosteroids. Pharmacokinetically, mifepristone may increase the plasma…4 sources — open the full entry
Mifepristone + MisoprostolMajorAntagonism · Metabolism · UnknownMifepristone is a potent antiglucocorticoid and may antagonize the effects of corticosteroids. Pharmacokinetically, mifepristone may increase the plasma…2 documented mechanisms4 sources — open the full entry
Moxifloxacin HydrochlorideInjectionOphthalmicTabletMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Moxifloxacin Hydrochloride + DexamethasoneMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry
Moxifloxacin Hydrochloride + Xanthan GumMajorSynergyConcomitant administration of corticosteroids may potentiate the risk of tendinitis and tendon rupture associated with fluoroquinolone treatment. The mechanism…7 sources — open the full entry

Conditions

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

Therapeutic duplication

Drug classes that overlap with Dexamethasone, so taking both doubles up the same effect. This source publishes no per-row citations for duplication.