scholarly journals Evidence of a clinically significant drug‐drug interaction between cannabidiol and tacrolimus

2019 ◽  
Vol 19 (10) ◽  
pp. 2944-2948 ◽  
Author(s):  
Abbie D. Leino ◽  
Chie Emoto ◽  
Tsuyoshi Fukuda ◽  
Michael Privitera ◽  
Alexander A. Vinks ◽  
...  
2013 ◽  
Vol 68 (6) ◽  
pp. 1415-1422 ◽  
Author(s):  
C. T. M. M. de Kanter ◽  
A. P. H. Colbers ◽  
M. I. Blonk ◽  
C. P. W. G. M. Verweij-van Wissen ◽  
B. J. J. W. Schouwenberg ◽  
...  

PEDIATRICS ◽  
2020 ◽  
Vol 145 (6) ◽  
pp. e20193256 ◽  
Author(s):  
Kevin Madden ◽  
Kimberson Tanco ◽  
Eduardo Bruera

2017 ◽  
Vol 32 (1) ◽  
pp. 106-108 ◽  
Author(s):  
Janna C. Beavers

Purpose: Ticagrelor and atorvastatin are commonly used medications in the management of acute coronary syndrome and percutaneous intervention. This is a report of a patient case of a potential drug interaction leading to the use of alternative therapy. Case Report: A 58-year-old male presented for cardiac catheterization following an abnormal stress test. He underwent placement of a drug-eluting stent and was started on ticagrelor. Three months later, he was noted to have elevated creatine kinase (CK), thought to be related to a potential drug–drug interaction between ticagrelor and atorvastatin. Ticagrelor was discontinued and he was successfully transitioned to clopidogrel. CK returned to normal within weeks of this change. Discussion: Pharmacokinetic studies have demonstrated a potential interaction between ticagrelor and atorvastatin but have not been deemed clinically significant. To date, only one other case report has been published discussing this interaction and consideration of alternative therapy. This case report is unique, with ticagrelor being the only new medication added prior to the abnormal CK finding. Conclusions: A probable drug–drug interaction occurred with concomitant ticagrelor and atorvastatin. While this interaction may not always be clinically significant, it is reasonable to consider in patients who present with signs and symptoms of adverse effects.


2019 ◽  
Vol 85 (3) ◽  
pp. 540-550 ◽  
Author(s):  
Sa'ad T. Abdullahi ◽  
Adeniyi Olagunju ◽  
Julius O. Soyinka ◽  
Rahman A. Bolarinwa ◽  
Olusola J. Olarewaju ◽  
...  

2019 ◽  
Vol 26 (10) ◽  
pp. 934-942 ◽  
Author(s):  
Adam Wright ◽  
Dustin S McEvoy ◽  
Skye Aaron ◽  
Allison B McCoy ◽  
Mary G Amato ◽  
...  

Abstract Objective The study sought to determine availability and use of structured override reasons for drug-drug interaction (DDI) alerts in electronic health records. Materials and Methods We collected data on DDI alerts and override reasons from 10 clinical sites across the United States using a variety of electronic health records. We used a multistage iterative card sort method to categorize the override reasons from all sites and identified best practices. Results Our methodology established 177 unique override reasons across the 10 sites. The number of coded override reasons at each site ranged from 3 to 100. Many sites offered override reasons not relevant to DDIs. Twelve categories of override reasons were identified. Three categories accounted for 78% of all overrides: “will monitor or take precautions,” “not clinically significant,” and “benefit outweighs risk.” Discussion We found wide variability in override reasons between sites and many opportunities to improve alerts. Some override reasons were irrelevant to DDIs. Many override reasons attested to a future action (eg, decreasing a dose or ordering monitoring tests), which requires an additional step after the alert is overridden, unless the alert is made actionable. Some override reasons deferred to another party, although override reasons often are not visible to other users. Many override reasons stated that the alert was inaccurate, suggesting that specificity of alerts could be improved. Conclusions Organizations should improve the options available to providers who choose to override DDI alerts. DDI alerting systems should be actionable and alerts should be tailored to the patient and drug pairs.


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