Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 108 checked references that resolve
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resolves10.1016/j.lfs.2011.05.018Identification of cytochrome P450 enzymes responsible for metabolism of cannabidiol by human liver microsomes
resolves10.1124/dmd.109.026898Characterization of Human Hepatic and Extrahepatic UDP-Glucuronosyltransferase Enzymes Involved in the Metabolism of Classic Cannabinoids
resolves10.1089/can.2015.0012Human Metabolites of Cannabidiol: A Review on Their Formation, Biological Activity, and Relevance in Therapy
resolves10.1016/j.lfs.2006.12.032Cytochrome P450 enzymes involved in the metabolism of tetrahydrocannabinols and cannabinol by human hepatic microsomes
resolves10.3109/03602532.2013.849268Exogenous cannabinoids as substrates, inhibitors, and inducers of human drug metabolizing enzymes: a systematic review
resolves10.1016/j.lfs.2011.02.017Potent inhibition of human cytochrome P450 3A isoforms by cannabidiol: Role of phenolic hydroxyl groups in the resorcinol moiety
resolves10.1124/dmd.111.041384Cannabidiol, a Major Phytocannabinoid, As a Potent Atypical Inhibitor for CYP2D6
resolves10.1177/0897190019828920The Potential Clinical Implications and Importance of Drug Interactions Between Anticancer Agents and Cannabidiol in Patients With Cancer
resolves10.3390/jcm8070989Potential Adverse Drug Events and Drug–Drug Interactions with Medical and Consumer Cannabidiol (CBD) Use
resolves10.1080/14740338.2017.1397128Drug-drug interactions as a result of co-administering Δ<sup>9</sup>-THC and CBD with other psychotropic agents
resolves10.1159/000507998Delta-9-Tetrahydrocannabinol and Cannabidiol Drug-Drug Interactions
resolves10.1016/j.ajog.2013.08.005Cannabidiol enhances xenobiotic permeability through the human placental barrier by direct inhibition of breast cancer resistance protein: an ex vivo study
resolves10.1038/sj.bjp.0707467The multidrug transporter ABCG2 (BCRP) is inhibited by plant‐derived cannabinoids
resolves10.1016/j.bcp.2005.12.033The effects of cannabinoids on P-glycoprotein transport and expression in multidrug resistant cells
resolves10.7717/peerj.2081ABC transporters P-gp and Bcrp do not limit the brain uptake of the novel antipsychotic and anticonvulsant drug cannabidiol in mice
resolves10.7717/peerj.153Cannabidiol changes P-gp and BCRP expression in trophoblast cell lines
resolves10.1111/epi.13852Interactions between cannabidiol and commonly used antiepileptic drugs
resolves10.1111/epi.13060Drug–drug interaction between clobazam and cannabidiol in children with refractory epilepsy
resolves10.1002/cpdd.665A Phase 1, Open‐Label, Pharmacokinetic Trial to Investigate Possible Drug‐Drug Interactions Between Clobazam, Stiripentol, or Valproate and Cannabidiol in Healthy Subjects
resolves10.1111/ajt.15398Evidence of a clinically significant drug-drug interaction between cannabidiol and tacrolimus
resolves10.1007/s00204-018-2244-6Opioid analgesic drugs and serotonin toxicity (syndrome): mechanisms, animal models, and links to clinical effects
resolves10.1038/clpt.1990.2Morphine and metabolite behavior after different routes of morphine administration: Demonstration of the importance of the active metabolite morphine-6-glucuronide
resolves10.1124/dmd.32.4.447QUANTITATIVE CONTRIBUTION OF CYP2D6 AND CYP3A TO OXYCODONE METABOLISM IN HUMAN LIVER AND INTESTINAL MICROSOMES
resolves10.1016/j.clpt.2006.01.009Pharmacokinetics and pharmacodynamics of oral oxycodone in healthy human subjects: Role of circulating active metabolites
resolves10.1016/j.drugalcdep.2014.11.031Experience of adjunctive cannabis use for chronic non-cancer pain: Findings from the Pain and Opioids IN Treatment (POINT) study
resolves10.1089/can.2017.0012Cannabis as a Substitute for Opioid-Based Pain Medication: Patient Self-Report
resolves10.1038/s41386-018-0011-2Impact of co-administration of oxycodone and smoked cannabis on analgesia and abuse liability
resolves10.2174/156802611795371288Opioid Analgesics and P-Glycoprotein Efflux Transporters: A Potential Systems-Level Contribution to Analgesic Tolerance
resolves10.3390/pharmaceutics10040192Modulation of Opioid Transport at the Blood-Brain Barrier by Altered ATP-Binding Cassette (ABC) Transporter Expression and Activity
resolves10.1002/jps.20893Oxycodone induces overexpression of P‐glycoprotein (ABCB1) and affects paclitaxel's tissue distribution in Sprague Dawley rats
resolves10.1211/0022357022782Effect of P-glycoprotein inhibition on methadone analgesia and brain distribution in the rat
resolves10.1007/s00213-003-1718-1Brain penetration of methadone (R)- and (S)-enantiomers is greatly increased by P-glycoprotein deficiency in the blood?brain barrier of Abcb1a gene knockout mice
resolves10.1097/ADM.0000000000000118Safety and Pharmacokinetics of Oral Cannabidiol When Administered Concomitantly With Intravenous Fentanyl in Humans
resolves10.1159/000374090Acetaminophen: Dose-Dependent Drug Hepatotoxicity and Acute Liver Failure in Patients
resolves10.1093/toxsci/kfi211Phenobarbital and Phenytoin Increased Acetaminophen Hepatotoxicity Due to Inhibition of UDP-Glucuronosyltransferases in Cultured Human Hepatocytes
resolves10.3390/molecules24122256Paradoxical Patterns of Sinusoidal Obstruction Syndrome-Like Liver Injury in Aged Female CD-1 Mice Triggered by Cannabidiol-Rich Cannabis Extract and Acetaminophen Co-Administration
resolves10.1258/acb.2009.009003Depressive effect of an antidepressant: therapeutic failure of venlafaxine in a case lacking CYP2D6 activity
resolves10.1016/j.forsciint.2012.12.020A poor metabolizer of both CYP2C19 and CYP2D6 identified by mechanistic pharmacokinetic simulation in a fatal drug poisoning case involving venlafaxine
resolves10.3109/15563650.2011.626421Severe acute cardiomyopathy associated with venlafaxine overdose and possible role of CYP2D6 and CYP2C19 polymorphisms
resolves10.1002/cpt.597Clinical pharmacogenetics implementation consortium guideline (CPIC) for <i>CYP2D6</i> and <i>CYP2C19</i> genotypes and dosing of tricyclic antidepressants: 2016 update
resolves10.1007/s40262-015-0310-2Reliability of In Vitro and In Vivo Methods for Predicting the Effect of P-Glycoprotein on the Delivery of Antidepressants to the Brain
resolves10.1016/j.cgh.2014.06.021Use of Selective Serotonin Reuptake Inhibitors and Risk of Upper Gastrointestinal Bleeding: A Systematic Review and Meta-analysis
resolves10.1016/j.jphs.2016.01.002P-glycoprotein inhibitors improve effective dose and time of pregabalin to inhibit intermittent cold stress-induced central pain
resolves10.1016/S1474-4422(03)00409-5Clinically important drug interactions in epilepsy: general features and interactions between antiepileptic drugs
resolves10.1016/S0006-2952(03)00076-5The effect of valproic acid on drug and steroid glucuronidation by expressed human UDP-glucuronosyltransferases
resolves10.1155/2016/2920108Carnitine and/or Acetylcarnitine Deficiency as a Cause of Higher Levels of Ammonia
resolves10.1016/S0140-6736(18)30136-3Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial
resolves10.1124/jpet.106.102491Valproic Acid Is Not a Substrate for P-glycoprotein or Multidrug Resistance Proteins 1 and 2 in a Number of in Vitro and in Vivo Transport Assays
resolves10.1111/head.13615Lamotrigine in the Prevention of Migraine With Aura: A Narrative Review
resolves10.1124/dmd.106.009340IN VITRO CHARACTERIZATION OF LAMOTRIGINE N2-GLUCURONIDATION AND THE LAMOTRIGINE-VALPROIC ACID INTERACTION
resolves10.1021/tx0000825Metabolism of Lamotrigine to a Reactive Arene Oxide Intermediate
resolves10.1016/j.tox.2003.09.004Drug hypersensitivity reactions in skin: understanding mechanisms and the development of diagnostic and predictive tests
resolves10.1007/BF03191157Lamotrigine and valproate pharmacokinetics interactions in epileptic patients
resolves10.1155/2018/5371854Lamotrigine-Valproic Acid Interaction Leading to Stevens–Johnson Syndrome
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