Skip to content
Med Rx.

Caffeine Citrate interactions

Checked as Caffeine in this data source.

Full monograph for Caffeine CitrateCheck it against another medicine

Medicines

79 documented

Medicines documented to interact with Caffeine Citrate, worst severity first.
MedicineSeverityMechanismEffectSources
Tizanidine HydrochlorideMajorMetabolismCoadministration with inhibitors of CYP450 1A2 may significantly increase the plasma concentrations and pharmacologic effects of tizanidine, which is a…8 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
AdenosineModerateAntagonismINTERVAL: Methylxanthines (e.g., caffeine, theophylline) are nonspecific, competitive antagonists of adenosine receptors. As such, they may interfere with the…10 sources — open the full entry
Adenosine + Cytochrome-C + Sodium Succinate + NicotinamideModerateAntagonismINTERVAL: Methylxanthines (e.g., caffeine, theophylline) are nonspecific, competitive antagonists of adenosine receptors. As such, they may interfere with the…10 sources — open the full entry
Aspirin + DipyridamoleModerateAntagonism · OthersINTERVAL: Methylxanthines (e.g., caffeine, theophylline) are nonspecific, competitive antagonists of adenosine receptors. As such, they may interfere with the…2 documented mechanisms13 sources — open the full entry
BendamustineModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of bendamustine, which has been shown in vitro to be metabolized by the…1 sources — open the full entry
Bupropion HydrochlorideModerateSynergyTranslated with DeepL4 sources — open the full entry
Capmatinib HydrochlorideModerateMetabolismCoadministration with capmatinib may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 1A2. The proposed…1 sources — open the full entry
CiprofloxacinbaseOphthalmicModerateMetabolismCoadministration with certain quinolones may increase the plasma concentrations and pharmacologic effects of caffeine due to inhibition of the CYP450 1A2…26 sources — open the full entry
Ciprofloxacin + DexamethasoneModerateMetabolismCoadministration with certain quinolones may increase the plasma concentrations and pharmacologic effects of caffeine due to inhibition of the CYP450 1A2…26 sources — open the full entry
Ciprofloxacin + Hydrocortisone AcetateModerateMetabolismCoadministration with certain quinolones may increase the plasma concentrations and pharmacologic effects of caffeine due to inhibition of the CYP450 1A2…26 sources — open the full entry
DeferasiroxModerateMetabolismCoadministration with deferasirox may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is decreased…2 sources — open the full entry
Dextromethorphan + BupropionModerateSynergyTranslated with DeepL4 sources — open the full entry
DipyridamoleModerateAntagonismINTERVAL: Methylxanthines (e.g., caffeine, theophylline) are nonspecific, competitive antagonists of adenosine receptors. As such, they may interfere with the…10 sources — open the full entry
Duloxetine HydrochlorideModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of duloxetine, which is a substrate of the isoenzyme. Theoretically, high…5 sources — open the full entry
Fluvoxamine MaleateModerateMetabolismCoadministration with fluvoxamine may increase the plasma concentrations of caffeine in a dose-dependent manner. The proposed mechanism is fluvoxamine…49 sources — open the full entry
Hydroxyprogesterone CaproateModerateMetabolismCoadministration with hydroxyprogesterone may decrease the plasma concentrations of drugs that are metabolized by CYP450 1A2, 2A6, and/or 2B6.1 sources — open the full entry
Lithium CarbonateModerateExcretionOne study has suggested that caffeine withdrawal may significantly increase blood lithium levels. The mechanism may be involve reversal of a caffeine-induced…47 sources — open the full entry
MethotrexateModerateAntagonismLimited data suggest that consumption of greater than 180 mg/day of caffeine may interfere with the efficacy of methotrexate (MTX) in patients with rheumatoid…4 sources — open the full entry
Nalidixic AcidModerateMetabolismCoadministration with certain quinolones may increase the plasma concentrations and pharmacologic effects of caffeine due to inhibition of the CYP450 1A2…26 sources — open the full entry
Obeticholic AcidModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
OlaparibModerateMetabolismCoadministration with olaparib may decrease the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 1A2 and/or 2B6. The…10 sources — open the full entry
OsimertinibModerateMetabolismCoadministration with osimertinib may decrease the plasma concentrations of drugs that are primarily metabolized by CYP450 1A2. In vitro, osimertinib has been…1 sources — open the full entry
RamelteonModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations and pharmacologic effects of ramelteon, which is primarily metabolized by…2 sources — open the full entry
RasagilineModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of rasagiline, which is primarily metabolized by the isoenzyme.14 sources — open the full entry
RopiniroleModerateMetabolismCoadministration with drugs that are inhibitors of CYP450 1A2 may increase the plasma concentrations of ropinirole, which is metabolized by the isoenzyme.7 sources — open the full entry
Tea tree oil + Echinacea + Geothermal waterModerateMetabolismCoadministration with echinacea may increase the plasma concentrations and the risk of adverse effects of drugs that are substrates of CYP450 1A2. The proposed…1 sources — open the full entry
TheophyllineModerateMetabolismCoadministration with caffeine may increase the serum concentrations of theophylline. The proposed mechanism involves competitive inhibition of theophylline…7 sources — open the full entry
AspirinMinorOthersOne study has reported that coadministration of caffeine and aspirin lead to a 25% increase in the rate of appearance and 17% increase in maximum concentration…3 sources — open the full entry
Clobetasol Propionate + Ofloxacin + Ornidazole + TerbinafineMinorOthersTerbinafine may decrease the clearance of intravenously administered caffeine by 19% to 21%. The mechanism of the interaction has not been delineated. Although…6 sources — open the full entry
Clopidogrel + AspirinMinorOthersOne study has reported that coadministration of caffeine and aspirin lead to a 25% increase in the rate of appearance and 17% increase in maximum concentration…3 sources — open the full entry
ClozapineMinorOthersCaffeine may increase clozapine serum concentrations and exacerbate psychotic symptoms. The mechanism is unknown but may be related to competition for the same…10 sources — open the full entry
DiazepamMinorOthersOne study has reported a 22% reduction in diazepam plasma levels when coadministered with caffeine. The exact mechanism of this interaction has not been…37 sources — open the full entry
MelatoninMinorMetabolismOral caffeine may significantly increase the bioavailability of melatonin. The proposed mechanism is inhibition of CYP450 1A2 first-pass metabolism.4 sources — open the full entry
RiluzoleMinorMetabolismCaffeine may increase the serum concentration of riluzole. Riluzole is metabolized by the CYP450 1A2 isoenzyme. Caffeine inhibits this particular isoenzyme…3 sources — open the full entry
Ropivacaine HydrochlorideMinorMetabolismRopivacaine serum concentrations may increase when given with drugs metabolized by the CYP450 isoenzyme 1A2. The theorized mechanism is via competitive…1 sources — open the full entry
Terbinafine HydrochlorideMinorOthersTerbinafine may decrease the clearance of intravenously administered caffeine by 19% to 21%. The mechanism of the interaction has not been delineated. Although…6 sources — open the full entry
TopotecanMinorOthersThe cytotoxic and cytostatic activity of topotecan may be diminished in the presence of caffeine. The mechanism is probably formation of complexes between…3 sources — open the full entry

Food & lifestyle

Conditions

Conditions in which Caffeine Citrate needs care, as documented in this source.